About us At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you re our kind of person. In assigned therapeutic area and geographical territory, engages in clinical and scientific exchange with medical and scientific experts, including Healthcare Professionals, and where appropriate non-traditional stakeholders (e.g. policy and decision makers, PAGs, government, innovative solution providers) consistent with medical objectives. Scientific Expertise: Maintain clinical/scientific expertise in disease state management, AstraZeneca products, emerging therapies, and the competitive landscape. Contribute to the development and provide project leadership/ management of the therapeutic area Field MedicalStrategic Plan (FMSP). Act as a subject matter expert/resource for internal and external stakeholders. Work with internal stakeholders in the development and delivery of appropriate training and mentoring needs within therapeutic area. Scientific Exchange: Engage in peer-to-peer level dialogue with key customers and deliver appropriate clinical/scientific content through utilizing the correct channel mix, which will differentiate AstraZeneca products from those of other companies. Respond to unsolicited customer inquiries and provide focused and balanced clinical / scientific information that supports the safe and appropriate use of AstraZeneca s products and services. Provide scientific/clinical support and deliver presentations to internal and external stakeholders. Identify and establish relationships with key customers and other scientific thought leaders for engaging them in ongoing scientific dialogue on AstraZeneca products and unsolicited discussions about compounds in development. Organize and facilitate scientific events such as MSL events, Symposiums, Scientific Exchanges, Advisory Boards/Expert Panels, non-promotional standalone events, Meet the Professor sessions, etc., with KEEs and HCPs. Prioritize these events based on their relevance in the patient journey for the related disease. Deliver informative lectures at scientific events tailored to healthcare professionals, aligning with the field medical Communication strategy. Collaborate with KEEs on study proposals (ESR or Local Study) and/or publications of interest to AstraZeneca. Customer Insight: Effectively identify, gather, analyze, synthesize, report and forward relevant new knowledge about the external scientific/medical environments to internal stakeholders Provide internal stakeholders with actionable items related to medical / product strategy or clinical development based on customer perspectives. Partner with traditional and non-traditional stakeholders to identify gaps in the patient experience journey as insights to be included in the medical / product strategies. Strategic Relationship: Develop peer-level relationships with medical and scientific experts, including Healthcare Professionals and collaborate with other internal teams for other key external stakeholders (e.g. policy and decision makers, PAGs, government, innovative solution providers) consistent with Medical objectives. Identify pre-clinical, clinical, and post-marketing study investigators in alignment with Medical Plans. Support data generation activities including participating in reviews of Investigator sponsored studies. Looks to broaden the My MA contact list where appropriate to include non-traditional KEEs from government, payer groups, researchers and clinical advisors who may support practice change initiatives. Establish win-win partnerships with traditional and non-traditional stakeholders to deliver on strategic, scalable and sustainable solutions addressing patient healthcare access gaps within the ecosystem. Other: Responsible for leveraging digital and innovation / technology as enablers for scientific exchange and creating patient centric solutions. Possesses a solid grasp of pharmacovigilance and GxP principles, showcasing a clear understanding of their significance. This includes practical knowledge of Good Clinical Practice (GCP), various types of clinical studies, and requirements for reporting adverse events (AEs). Possesses a solid grasp of pharmacovigilance and GxP principles, showcasing a clear understanding of their significance. This includes practical knowledge of Good Clinical Practice (GCP), various types of clinical studies, and requirements for reporting adverse events (AEs). Exhibits a robust understanding of the Ethical Interactions Policy, along with relevant standards, local laws, and regulations. Moreover, possesses the ability to provide training to others in this domain. Adherence to internal processes and AstraZeneca Global Field Medical Standards and the external regulations including but not limited to clinical trials, promotional activity (e.g. Local Code of Conduct) and pharmacovigilance activities to meet internal SOP and local regulations. Education, Qualifications, Skills and Experience Doctoral degree in a scientific discipline (e.g. M.D., Ph.D., Pharm.D.) Experience in pharmaceutical industry, regulatory environment, clinical or preclinical research, and knowledge of a therapeutic area disease state and treatment. Experience with basic research, drug discovery, drug development and KEE interactions. Why AstraZeneca? At AstraZeneca we re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We re on an exciting journey to pioneer the future of healthcare. Date Posted 28-Feb-2025 Closing Date 27-Mar-2025

Achieving assigned territory/ geography wise sales target Carrying out effective field work without direct day-to-day supervision Report field work in daily basis on assigned online system Meeting Call Average, Coverage, Frequency coverage Norms of assigned division Core Job Responsibilities Generate maximum prescriptions & increase market share Promote the Division s products as per strategy Relationship Building with the Stake holders (Doctors, Chemists, Stockiest etc) Facilitating Strategy building A good Brand Ambassador Minimum Education BSc/B. Pharma. Experience/Training Required 2+ Yrs of experience Fresher with good communication and analytical skill may also consider Candidate with prior/current experience in same therapy. Candidate from MNC and top Indian Pharma companies will have added advantage. Fluent and confident in communication

MAIN PURPOSE OF ROLE Summarize the main purpose of the role. Conduct market research and feasibility studies to analyze the viability of alternative business development opportunities. MAIN RESPONSIBILITIES Collect, compile, verify, and analyze financial, competitive, sales, marketing, and other information about potential business partners, new markets, products and services, or other business opportunities so that senior management has accurate and timely information for making strategic and operational decisions. Prepare documents and materials (for example, reports, presentations, information packages) for meetings and negotiations with potential clients and business partners so that the information provided is accurate and appropriate for external distribution. QUALIFICATIONS Education Education Level Major/Field of Study Or Education Level Associates Degree ( 13 years)

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines. Our 109,000 colleagues serve people in more than 160 countries. CORE JOB RESPONSIBILITIES 1. To analyse and prepare working plan for the territory basis the data provides/ market research 2. To be able to follow up, monitor and achieve targets of the territory 3. Implementation execution of all strategies 4. Stakeholder engagement- doctors, stockist, retailers, chemists and institutions pharmacy 5. Discipline and punctual with set timelines for multiple internal processes 7. Basic computer skills- excel working, word email exchanges 6. Fast learner and adaptable to change in market 7. Strong communication skills (verbal)- English and local language 8. Effective in-clinic performance 9. Basic understanding and ability to explain anatomy physiology and product portfoli0 10. Organizing Camps (CME) as per the division strategy and customer needs 11. Prescription audit for Abbott brands and other competitors brands 12. Generate POBs for Abbott brands as per the business plan REQUIRED EXPERIENCE Experience 2+ years of experience Fresher with good communication skills and analytical skills may also consider Required Qualification B.Sc. / B.Pharma.

1. Product registrations /Submissions -Leads and coordinates project registrations for complex filings, including new product introductions -Identifies and collects data needed, or delegates where appropriate -Seeks and evaluates expert advice and technical support where necessary -Prepares responses to deficiency letters 2. Relationships Cross Functional team work -Represents Regulatory Affairs at relevant meetings and presents agreed RA position -Provides expert advice and technical support to cross-functional colleagues -Monitors actual versus planned activities and timelines. -Proactively identifies, communicates and mitigates risks and issues impacting project progression. 3. Affiliate Coordination -Maintains strong working relationships with Regional Product leads and Affiliate colleagues -Finds ways to improve ways of working and knowledge sharing 4. Compliance across Life-Cycle -Assesses and approves change requests and ensures files are updated accordingly -Has expert knowledge of legislation and current developments across different areas of business -Acts as a subject matter expert -Manages corrective action plans and drives to completion within agreed timelines 5. Strategy -Leads and coordinates the development of regulatory product strategies for assigned products and projects -Identifies, communicates and mitigates regulatory risks 6. Process Improvement -Identifies opportunities and proactively takes steps to implement improvements -Leads the development of position papers work aids etc 7. Health Agency Interaction -Takes a leading role in preparing for and attending Health Agency meetings as appropriate -Liaises (including acting as the single point of contact if necessary) with Notified Bodies and other medical device organisations (may not be applicable to all staff) 8. Licensing Reviews -Leads and coordinates regulatory due diligence activities for assigned projects 9. Technical competency -Has expert knowledge of global regulatory requirements -Has specialist regulatory knowledge across multiple countries, region, product class requirements -Has expert knowledge across product protfolios -Ensures knowledge remains current CORE COMPETENCIES Anticipation -Develops scenario and contingency plans that ensure achievement for results under changing conditions and situations -Proactively implements change to mitigate risks, solve issues or improve processes and ways of working. -Actively gathers customer inputs in order to anticipate and fulfill their needs and requirements -Manages internal/external stakeholders to identify and address issues -Understands the situation or audience and adjusts approach to achieve desired outcomes Adaptability -Effectively prioritizes and plans long-term (months/years) work tasks and projects, including the work of others -Has big picture thinking to Identify synergies and opportunities across the organisation -Regularly reviews commitments and re-prioritises activities or negotiates timelines as necessary -Reacts quickly to solve problems and issues as they arise -Provides guidance, advice and mentoring to colleagues Initiative -Understands the organisation and the roles of other functions -Proactively anticipates, mitigates and avoids problems and issues -Proactively seeks feedback from manager and team members and adapts behaviour to improve performance -Maintains strong customer focus. Innovation -Uses intrapreneurial skills to identify and execute new or unique ways to address work problems and opportunities -Creates an environment of experimentation and uses failure as an opportunity to learn and take alternate action -Challenges current thinking and generates new ideas. Encourages others to do the same -Integrates information from multiple sources to generate unique insights or new solutions that increase competitiveness -Leverages diversity of people and thinking to create a competitive advantage -Collaborates across boundaries to create cross-business opportunities Integrity -Delivers high quality results -Meets agreed deadlines -Exhibits honesty and presents complete impartial information -Displays consistency between words and actions -Acknowledges and responds constructively to failures and mistakes -Expresses dissatisfaction constructively, without over-reacting Teamwork -Uses leadership skills drives completion of individual and shared goals and to develop the skills of others LEADERSHIP COMPETENCIES Set Vision and Strategy -Uses influencing and negotiation skills to drive strategic alignment of key cross-functional stakeholders -Drives the generation of robust regulatory strategies for complex global projects Build Organization and Inspire People -Mentors junior team members -Provides training and support on areas of subject matter expertise -Demonstrates strong leadership skills every day and encourages the same others to do the same -Provides insight, knowledge and leadership to improve functional area and build the business Drive Results -Displays energy and persistence to drive the organization forward -Delivers what is promised; holds self and others accountable for results, commitments and behaviors -Takes appropriate accountability for failure; does not blame others -Takes action in a timely manner, with urgency or caution as appropriate, but always in a planful way -Balances short-term and long-term priorities and maximizes the opportunities for both -Addresses organizational or cultural barriers that could prevent success Make Difficult Decisions -Identifies crisis situations and elevates appropriately Encourage an Open Environment and Knowledge Sharing -Provides accurate, frequent and constructive feedback to subordinates, peers and leaders -Openly shares information with peers and managers -Challenges and expects to be challenged Supervisory/Management Responsibilities: Direct Reports : None (individual contributor) Indirect Reports: None (individual contributor) Minimum Education: Bachelors Degree in pharmacy, biology, chemistry, pharmacology, or related subject Minimum Experience/Training Required: 10+ years experience in Regulatory Affairs, RD, Manufacturing or related area. By exception, less experience is acceptable, e.g. if supplemented by other relevant knowledge such as a higher degree in a related discipline. JOB FAMILY: Regulatory Operations LOCATION: India > Mumbai : BKC Building t SIGNIFICANT WORK ACTIVITIES: Keyboard use (greater or equal to 50% of the workday)

Primary Job Function Achieving assigned territory/ geography wise sales target Carrying out effective field work without direct day-to-day supervision Report field work in daily basis on assigned online system Meeting Call Average, Coverage, Frequency coverage Norms of assigned division Core Job Responsibilities Generate maximum prescriptions increase market share Promote the Division s products as per strategy Relationship Building with the Stake holders (Doctors, Chemists, Stockiest etc) Facilitating Strategy building A good Brand Ambassador Minimum Education BSc/B. Pharma. Experience/Training Required 2+ Yrs of experience Fresher with good communication and analytical skill may also consider Candidate with prior/current experience in same therapy. Candidate from MNC and top Indian Pharma companies will have added advantage. Fluent and confident in communication

Roles & Responsibilities: This role will be responsible for technical Solutioning for clients across the Life-Sciences domain and help build their Business Transformation Road Map. Focus is mainly on pharmaceutical industry w. r. to enterprise solutions e. g. : SAP. Expected to have technical knowledge on Emerging technologies associates with Healthcare, Biotechnology, Pharmaceutical, AI for Life Sciences, Digital and I4. 0 solutions for Life Sciences Present overall technical capabilities in life science portfolio (Pharma+ Biotech+ MedTech+ Healthcare) to clients during initial connects, post which involve SME to get into technical depth & build RFP/RFI/RFQs Create and stich a winning business transformation solution. Build and nurture positive working relationships with clients with the intention of win more for Bosch . Partner with senior leadership to define and implement overall target future state and capabilities for the clients life sciences programs/projects. Design and develop life sciences strategic solution responses for the complex RFP/ requirements. Develop and tailor solution approaches, methods, and 3rd party tools/software to support client s life sciences programs and initiatives. Collaborate with cross-functional teams to define architecture for client environment in aligned to its Industry and local compliance related to healthcare/pharma domain. Should be open to engage in multiple Presales opportunities across Geo and work internally towards its solution building with support of SME. Collaborate with industry and latest market trends to understand and leverage latest life sciences offerings, capabilities to clients! Strong in presentation, creating artifacts, reusable contents, used cases, conduct demos, technical workshop. Open for short travels domestic/international. Flexible to support global opportunities.

Regional Medical Advisor THE OPPORTUNITY The RMA (Regional Medical advisor) will be a valued representative at our company working in the field to interact and engage key stakeholders. Our medical affairs team objective is to provide scientific expertise across their identified regions/products/therapy areas to these valued customers. WHAT YOU WILL DO: The RMA will have the following key responsibilities: Developing and implementing medical strategies: Scientific leader identification development and engagement to build regional, national or international relationships to contribute to understanding of diseases, scientific trends, practice guidelines, and treatment patterns in areas relevant to our business Support to the health care providers by providing accurate and up-to-date medical information Education, training and periodic medical updates to the commercial team as demanded Ensuring compliance with local regulations and industry standards in all medical activities Responsibilities and Primary Activities: Scientific Expertise: Developing and maintaining an in-depth understanding of the companys products, therapeutic areas, and relevant scientific research. Staying updated on the latest medical and scientific advancements, clinical guidelines, and treatment protocols. SL KDM Engagement: Building and maintaining relationships with Scientific Leaders (SLs), Key decision makers (KDMs) healthcare professionals, and academic institutions. Engaging in scientific discussions, presenting clinical data, and providing educational support to KOLs regarding the companys products and therapeutic areas. Support to medical strategy: In alignment with the line manager, provide strategic inputs, and expertise, to product management towards ethical promotion of assigned products Medical Education: Providing scientific and medical education to internal stakeholders, including sales teams, marketing teams, and other cross-functional colleagues. Collaborating with the Medical Affairs team to develop and deliver training materials, presentations, and scientific symposia. Scientific Exchange: Facilitating scientific exchange and knowledge transfer between the company and external stakeholders. Participating in medical conferences, advisory boards, and scientific meetings to gather insights, share data, and contribute to the scientific community. Clinical Data Communication: Interpreting and communicating clinical trial data, real-world evidence, and other scientific information to healthcare professionals, regulators, and other relevant stakeholders. Ensuring accurate and compliant dissemination of scientific information in accordance with regulations and company policies. Clinical Research: Provide medical support for local studies, including need-based visits to identify study sites Lead Investigator Initiated Trials Cross-functional Collaboration: Collaborating closely with cross-functional teams, including Clinical Development, Regulatory Affairs, Marketing, and Market Access, to provide scientific input, support clinical trial design, contribute to regulatory strategies, and align on medical communication plans. Facilitate access to scientific leaders as appropriate. Support as well as own medical initiated projects in line with therapy area that would involve a strong stakeholder interface Provide scientific support to sales team Medical Information: Addressing medical inquiries and providing timely and accurate responses to healthcare professionals, patients, and other stakeholders. Ensuring that medical information materials, such as medical letters and FAQs, are up to date and compliant. Sales Force Training: Provide medical training to sales colleagues on the therapy areas assigned Assist in pre-launch and launch training to sales staff for new products. Compliance: Adhering to relevant legal, regulatory, and compliance guidelines, including the organizations code of conduct and industry-specific regulations. Ensuring all activities and interactions are conducted ethically and in compliance with applicable laws and regulations. Overall, RMA in Medical Affairs acts as a scientific expert and liaison between the company and external stakeholders, playing a crucial role in building scientific credibility, fostering relationships, and supporting the companys strategic objectives in the healthcare industry. Values and Behaviors: Consistently adhere to/demonstrate all company Values with focus on excellence Work in harmony with internal and external stakeholders WHAT YOU MUST HAVE To be successful in this role, you will have strong marketing skills as well as business capabilities Educational Background: A strong academic background in life sciences, such as a medical degree (MD), doctorate (Ph.D.). Other relevant degrees in biology, pharmacology, or related fields may also be considered. Industry Experience: 1 year experience in the pharmaceutical, biotechnology, or medical device industry is often preferred. This could include experience in clinical research, medical affairs, or related roles that have exposed the candidate to scientific and medical aspects of the industry. Therapeutic Area Expertise: Demonstrated knowledge and expertise in the specific therapeutic area relevant to the position. This may involve experience working on clinical trials, publications, or direct patient care in that therapeutic area. Scientific and Clinical Knowledge: A strong understanding of medical and scientific principles, including knowledge of clinical trial design, data analysis, and interpretation. Familiarity with relevant disease states, treatment guidelines, and emerging trends in the therapeutic area is also important. Communication and Relationship-Building Skills: Excellent interpersonal, communication, and presentation skills are crucial for a RMA role. The ability to effectively communicate scientific information to various stakeholders, including Key Opinion Leaders (KOLs), healthcare professionals, and internal teams, is essential. Analytical and Problem-Solving Skills: RMAs are often required to analyze complex scientific data, identify insights, and provide recommendations. Strong analytical and problem-solving skills are valuable for interpreting clinical trial results and addressing medical inquiries. Adaptability and Flexibility: RMAs often work in dynamic and fast-paced environments, requiring the ability to adapt to changing priorities and work independently. Flexibility to travel frequently to engage with external stakeholders is also often required. Regulatory and Compliance Knowledge: Familiarity with relevant legal, regulatory, and compliance guidelines, such as Good Clinical Practice (GCP), the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines, and local regulations governing medical communications. We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we follow the science that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe. Our Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry professionals ensuring the scientific value of our products is realized. We engage and train internal employees to ensure that they thoroughly comprehend the science behind the medicine and review further unmet medical needs to bolster collaboration and further differentiate our portfolio. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Employee Status: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Not Applicable Shift: Valid Driving License: Hazardous Material(s): Job Posting End Date: 04/20/2025 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

JOB TITLE: Assistant Research Scientist (Product Engineering) JOB FUNCTION: Research and Development WORK LOCATION: Unilever Bangalore With 3. 4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and improve the lives of our consumers and the communities around us. We are driven by our purpose: to make sustainable living commonplace, and it is our belief that doing business the right way drives superior performance. At the heart of what we do is our people - we believe that when our people work with purpose, we will create a better business and a better world. At Unilever, your career will be a unique journey, grounded in our inclusive, collaborative, and flexible working environment. We don t believe in the one size fits all approach and instead we will equip you with the tools you need to shape your own future. Unilever is reimagining the future of cleaning, and it starts with reinventing a century-old history of chemistry. Billions of people around the world are asking for products that are tough on germs and stains, and ever more convenient to use. But now, people also want these products to be kinder to the planet. CATEGORY OR FUNCTION INTRODUCTION The Purpose of the Science & Technology, Home care team is to provide Unilever with world class capability to develop next generation formats like powders, bars, liquids, capsule products with superior performance, great value, and sustainable technology. Within the S&T, team is responsible for exploring upstream/novel process and product technologies. This includes the development of new analytical methodologies to create data spaces and digital models of previously unknown interactions. These technology insights are used to develop deep domain expertise that ultimately supports the product design and delivers competitive advantage. JOB PURPOSE: The role requires individuals to develop a comprehensive understanding of product engineering principles, as well as in-depth knowledge of manufacturing technology and the interactions between materials, processes, and products in the home care sector. Areas of expertise should include product microstructure, rheology, and structure-property relationships. This knowledge must then be translated into decisions, actions, and initiatives that align with and support the divisional strategy, targets, and plans. Material Engineers are not merely technology specialists; they are integrators who combine consumer and business needs into effective technical solutions. JOB RESPONSIBILITIES: 10+ years experience in materials, polymers background either in FMCG or extended industries like Pharma Experience in basic unit operations, processing and product engineering is preferred Strong analytical including physio-chemical characterization is critical for this role. 10+ years experience in materials, polymers background Work with international and interdisciplinary teams (Unilever R&D, Academics, material and equipment suppliers) to develop next generation solid formats. Develop a deep understanding of how-to materials/process/structure products that deliver against consumer needs. Generate ideas for new products and for improvement of existing products. Must have a hands-on approach to pilot plant and laboratory scale-up activities. Need to be able to work in a safe, disciplined manner. Lead workstreams/projects WHAT YOU NEED TO SUCCEED: In depth knowledge of material science, thermodynamics, equipment principles and practices Computer literate and digital savvy (experience of DoE and statistical data analysis) Project management (communication and presentation) Experience in product/process development, and technology transfer desirable. EXPERIENCES AND QUALIFICATIONS Essential Experience: ME, MTech in Materials/Chemical Engineering with specialization in Polymer Science from reputed institutes Our commitment to Equality, Diversity & Inclusion Unilever embraces diversity and encourages applicants from all walks of life! This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity.

As a Senior Advanced Software Engineer here at Honeywell, you will play a critical role in developing and implementing advanced software solutions for our industry-leading products. You will be accountable for designing, coding, testing, and debugging complex software applications, as well as collaborating with cross-functional teams to ensure the successful delivery of high-quality software solutions. Your expertise and contributions will drive innovation and position Honeywell as a global technology leader in the industry. You will report directly to our Sr Engineering Manager and you'll work out of Bangalore location on a hybrid work schedule. In this role, you will have the opportunity to make a significant impact on the development of cutting-edge software solutions that will shape the future of our products and enhance the quality of life for people around the world. At Honeywell, our people play a critical role in developing and assisting our employees to help them perform at their best and drive change across the company. Help to build a strong, diverse team by recruiting talent, identifying and developing successors, driving retention and engagement, and fostering an inclusive culture. KEY RESPONSIBILITIES Design, develop, and implement advanced software solutions for our products Design, develop, and implement advanced software solutions for our products Work with cross-functional teams to gather requirements and define software specifications Write clean, efficient, and maintainable code Conduct thorough testing and debugging of software applications Participate in code reviews and provide feedback to team members Stay up to date with the latest industry trends and technologies Contribute to the continuous improvement of software development processes and best practices Manage/Lead the team as SW Lead, conducting daily standups, helping the team resolve program software issues, and delegating work effectively. YOU MUST HAVE Bachelor s degree from an accredited institution in Computer Science, Software Engineering, or a related field Minimum 8 years of experience in software development Strong proficiency in programming languages such as, C or C++, or Python with Java Experience with software development methodologies and best practices Strong problem-solving and thoughtful skills WE VALUE Masters degree in Computer Science or a related field Experience with cloud technologies and distributed systems Knowledge of software security ethics and best practices Experience with Agile development methodologies Strong communication and collaboration skills

Job Location: Bangalore Job Title: Project Manager Reporting to: Program Lead, Operating Unit Job Grade: 7 Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022) is the leading integrated research, development and manufacturing services company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. Syngenes more than 5200 scientists offer both skills and the capacity to deliver great science, robust data management and IP security and quality manufacturing at speed to improve time to market and lower the cost of innovation. With a combination of dedicated research facilities for Amgen, Baxter and Bristol Myers Squibb as well as 2 Mn sq. ft of specialist discovery, development and manufacturing facilities, Syngene works with biotech companies pursuing leading edge science as well as multinationals, including GSK, Zoetis and Merck KGaA. For more details, visit www.syngeneintl.com Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time The Role: To manage the allotted projects through the Syngene way of execution to achieve the desired level of project performance, revenue, profitability, and customer satisfaction in collaboration with the cross functional project teams, grounded in the Syngene values of Integrity, Excellence and Professionalism. Key Responsibilities: Adhere to safe practices and procedures for self and the team members; contribute to the development of procedures, practices, and systems that ensure safe operations and compliance with the company s integrity and quality standards and hold self and the project team members accountable for the achievement of safety goals Ensure all mandatory assigned training related to data integrity, health, and safety measures are completed on time; and promptly report incidents and near misses Understand and engage with customers to not only deliver the expected project performance (quality on time in full within budget) but to delight them Develop a complete understanding of the contract and ensure fulfillment of contract obligations; provide effective initiation by creating a charter, bringing an appropriate set of stakeholders together, and by completing system requirements for initiation Prepare planning documents, including schedule, and secure requisite approvals; proactively identify risks and manage them; enable resolution of issues in a timely manner Identify the key stakeholders, build and maintain a strong relationship with them and ensure alignment to project objectives; communicate effectively Ensure effective execution by running review meetings at desired frequency through adequate agenda setting, capturing decisions and action items, and actively following up on action items to completion Ensure the right level of control through effective use of governance frameworks and established escalation mechanisms; ensure timely and transparent sharing of information, including appropriate dashboards and status updates Ensure systematic closure of project tasks as needed Analyze data to pick patterns toward enabling continuous improvement and organizational learning Foster a culture of cross functional collaboration across the project team by promoting we before I, shared vision, and common metrics Build a strong relationship with allotted customers, ensure periodic formal and informal communication/feedback and manage escalations by facilitating required actions; accurately assess, track and report customer sentiment Specific requirements for this role: Education and Experience Degree in disciplines relevant to the life sciences industry; preferably with qualifications in management A globally recognized project management certification is highly desirable Overall 12 15 years of experience, Five years of relevant experience from reputed CRO / CDMO / Product / Services / Consulting with at least three years as a project manager and a current portfolio of over USD 1 million in a multi cultural setting Masters in life sciences, with a background in large molecules (Biological) process development and manufacturing like Biosimilars, antibodies, Biotherapeutics, Vaccines, etc., or Masters in Business administration with Program/Project management experience in the Biopharma industry. PMP certification or six sigma/Prince 2/ Agile certifications. Technical/ Functional Skills : Must possess full fluency in MS Office (Word, Outlook, PowerPoint) with knowledge of using Microsoft Project (MS Project, Primavera) to monitor, control, and provide overall visibility to the organization. Knowledge of manufacturing (process, equipment, facility, automation) quality (GLP, cGMP, 21 CFR Part 11 validation, etc.). Good understanding of product development lifecycle. Knowledge of Quality Assurance, CAPA, Change Control, Document Control, Training Systems The operational excellence attitude is critical as projects and processes in the Biologics operating unit need PM to coordinate cross functional resources in Operations, Quality, and other supporting functions. Exceptions can be made for candidates with extraordinary credentials with commensurate adjustments in job grade. Leadership Competencies (for leading self, leading with others, and leading a team as required) Partners with customer Provides clarity and focus Drives performance against outcomes Drives accountability Works collaboratively Develops self and others Professional Skills and Capabilities Comprehensive knowledge of project management disciplines Thorough knowledge of project management software (preferably Microsoft Project and Project Online) and analytics using Microsoft Excel (preferably with exposure to AI/ML) Fair knowledge of the business landscape, the scientific landscape, and the compliance frameworks Fair understanding of finance, modeling, and simulation Demonstrated experience managing cross functional projects with empathy in a fast paced, innovative, dynamic environment while remaining flexible, proactive, resourceful, and efficient; ability to resolve conflicts in a win win manner Fluent in English, with excellent verbal and written communication; proficient in Microsoft PowerPoint Collaborative team player with the ability to influence irrespective of hierarchies Problem solver; anticipates and develops solutions relevant to customers Specialization and scientific knowledge relevant to operating unit Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodation for qualified individuals with disabilities. Pls visit us at https://syngeneintl.com/ to know more about us and what we do.

Job Location: Bangalore Reporting to: Program Lead, Global Program Office About Syngene Syngene is an integrated research, development, and manufacturing organization providing scientific services from early discovery to commercial supply. We offer services in a wide range of industrial sectors, including pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical companies. Our culture of scientific innovation is driven by the expertise of our highly qualified team of 5,000 employees and is supported by state of the art infrastructure and market leading technology. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and SOPs, in letter and spirit. Core Purpose of the Role: To manage the allotted projects through the Syngene way of execution to achieve the desired level of project performance, revenue, profitability, and customer satisfaction in collaboration with the cross functional project teams, grounded in the Syngene values of Integrity, Excellence and Professionalism. Role Accountabilities: Adhere to safe practices and procedures for self and the team members; contribute to the development of procedures, practices, and systems that ensure safe operations and compliance with the company s integrity and quality standards and hold self and the project team members accountable for the achievement of safety goals Ensure all mandatory assigned training related to data integrity, health, and safety measures are completed on time; and promptly report incidents and near misses Understand and engage with customers to not only deliver the expected project performance (quality on time in full within budget) but to delight them Develop a complete understanding of the contract and ensure fulfillment of contract obligations; provide effective initiation by creating a charter, bringing an appropriate set of stakeholders together, and by completing system requirements for initiation Prepare planning documents, including schedule, and secure requisite approvals; proactively identify risks and manage them; enable resolution of issues in a timely manner Identify the key stakeholders, build and maintain a strong relationship with them and ensure alignment to project objectives; communicate effectively Ensure effective execution by running review meetings at desired frequency through adequate agenda setting, capturing decisions and action items, and actively following up on action items to completion Ensure the right level of control through effective use of governance frameworks and established escalation mechanisms; ensure timely and transparent sharing of information, including appropriate dashboards and status updates Ensure systematic closure of project tasks as needed Analyze data to pick patterns toward enabling continuous improvement and organizational learning Foster a culture of cross functional collaboration across the project team by promoting we before I, shared vision, and common metrics Build a strong relationship with allotted customers, ensure periodic formal and informal communication/feedback and manage escalations by facilitating required actions; accurately assess, track and report customer sentiment Specific requirements for this role: Education and Experience Degree in disciplines relevant to the life sciences industry; preferably with qualifications in management A globally recognized project management certification is highly desirable For job grade 6: Ten years of relevant experience from reputed CRO / CDMO / Product / Services / Consulting , with at least five years as a project manager and a current portfolio of over USD 5 million in a multi cultural setting Exceptions can be made for candidates with extraordinary credentials with commensurate adjustments in job grade Leadership Competencies (for leading self, leading with others, and leading a team as required) Partners with customer Provides clarity and focus Drives performance against outcomes Drives accountability Works collaboratively Develops self and others Professional Skills and Capabilities Comprehensive knowledge of project management disciplines Thorough knowledge of project management software (preferably Microsoft Project and Project Online) and analytics using Microsoft Excel (preferably with exposure to AI/ML) Fair knowledge of the business landscape, the scientific landscape, and the compliance frameworks Fair understanding of finance, modeling, and simulation Demonstrated experience managing cross functional projects with empathy in a fast paced, innovative, dynamic environment while remaining flexible, proactive, resourceful, and efficient; ability to resolve conflicts in a win win manner Fluent in English, with excellent verbal and written communication; proficient in Microsoft PowerPoint Collaborative team player with the ability to influence irrespective of hierarchies Problem solver; anticipates and develops solutions relevant to customers Specialization and scientific knowledge relevant to operating unit Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

: In this position you will be dealing with requests regarding our Pharma Chemicals and Process Solution Products.You are the entry point for the first level commercial and regulatory questions from our internal and external clients received by mail, phone or fax.In your dedicated area of responsibility, you act as an interface between the sales organization in the field, supply chain, regulatory affairs, marketing and all other interfering interfaces.Also you continuously support the sales representatives in their daily activities in order to meet the sales objectives.You will be responsible for dealing with all quotations in close collaboration with the sales representative, you will enforce our price policy and develop special prices for a specific category of clients.You ll be in charge of handling requests for all types of commercial documents intended for our customers, such as brochures, sample requests, literature, product datasheets etc.You handle product orders, check inventory availability or status of shipment, verify customer pricing, prepare and process customer return goods for credit and/or replacement, handle and resolve customer complaints, escalate requests and unresolved issues to the designated resource and file records of customer interactions and transactions. Who you areMinimum 4-6 years professional experience in a customer facing environment, a first experience in chemicals, pharmacy or biochemical is an assetFluent English conversational and written.Organized, multitasking, open-minded, flexible in a changing environment and able to adjust accordinglyStrong verbal and written communication skills, promotes good relationship in the team, ensures 2-ways communication and teamworkEnjoy working in an international teamA positive outlook on dealing with our important customers and driven by great sensibility for customer satisfactionExcellent computer skills with experience on Microsoft Office, SFDC, SAP is a plus Basic/ Minimum Qualifications Any graduation - Science preferred Preferred Qualifications: Commerce and science background

Summary of Position: Alcon is looking to hire a Territory Sales Executive -DEOH (Dry Eye and Ocular Health) at Bangalore is the head quarter with major coverage in Mangalore Udupi as well . To achieve target sales of in-line products within budgets for the designated territory. Key Responsibilities: To deliver individual performance plan by meeting or exceeding the assigned target. To gain increased usage for promoted products in all relevant accounts. To prepare implement account development territory business plans. To attain minimum benchmark in terms of product knowledge, selling skill, marketing knowledge and knowledge on competitor products and promotion. To apply science behind the molecule and concept behind managing the Therapeutic Area for effective customer influencing. To identify facilitate/collaborate to develop key opinion leaders for advocacy and increased product usage. Timely completion of all online training. Timely submission of sales reports, tour plan, secondary sales data to reporting manager and/or any automated system deployed by the organization. Daily reporting of field work activities and complying with all sales force effectiveness (SFE) KPI s. Adherence and complying with executional KPI s as guided by the Marketing team. To operate within the relevant codes of practice. Responsible for adverse event and product complaint handling related activities at a local level including the collection, intake and forwarding the information to the Local Vigilance Representative). Adherence to all corporate compliance guidelines corporate programs by self . Key Requirements/Minimum Qualifications: Bachelor s degree in Pharma/ Science 2 years of handling Pharma Product, Managed Science based selling with a proven record of sales performance. Knowledge of the health care system and its changing environment. Selling skills in an account development role. Proficient in English - both written and spoken ATTENTION: Current Alcon Employee/Contingent Worker If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site. Find Jobs for Employees Find Jobs for Contingent Worker Alcon is an Equal Opportunity Employer and takes pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital status, disability, or any other reason.

Job description Job title: Synthetic Chemistry Scientist Job location: Bangalore Hyderabad About Syngene: Syngene ( www.syngeneintl.com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned. Contributing to development of procedures, practices and systems that ensure safe operations and compliance to company s integrity quality standards. Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals. Govern and Review safety metrics from time to time. Core Purpose of the Role: Personnel handling this profile will be responsible for conducting reactions and delivering final compounds within a fast turnaround time, meeting the specific requirements of both the project and Syngene. The candidate should be capable of independently designing the synthetic scheme for any target and solve chemistry problems. He or she should ensure that the experimental observations are recorded contemporaneously and in compliance with the Electronic Laboratory Notebook (ELN) policies of the project and Syngene. Role Accountabilities: Expected to design a synthetic scheme for any given target and to be proactive in identifying rate limiting steps along with the mitigation strategy. The candidate should be well versed in using literature search engines and predictive synthesis tools Perform synthetic chemistry reactions, reaction workups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab equipment s Ensure that the samples generated during synthesis are given for analysis and record subsequent results obtained and update the supervisor / group leader on the progress of synthesis and ensure samples are packed appropriately for shipment Record the observations of experiment/reaction, results, utilization of resources and other activities related to the reaction in the laboratory or e-notebook following guidelines and in timely manner and ensure that the same is handled safely and confidentially. The candidate should be capable of meeting Syngene s productivity expectations (# of compounds/month, # of steps/month and productivity index of around 1.5) without compromising on safety and quality. The candidate should be capable of synthesizing the final compounds at a faster turnaround time. The candidate should have excellent analytical interpretation and purification skills. Ensure that they know the SDS of the chemicals they are handling and aware of emergency response procedures in case of accidental spillage, leakage or fire and ensure proper waste segregation as per EHS norms. Always follow EHS and quality system requirements in the workplace ensuring individual safety and lab safety. Attend all mandatory trainings and update training records as and when trainings are completed. Always ensure confidentiality. Syngene Values All employees will consistently demonstrate alignment with our core values. Excellence Integrity Professionalism Specific requirements for this role Experience 3-12 years. Skills and Capabilities: Should have deeper knowledge with concepts of organic synthesis and reaction mechanisms. Should be capable of designing synthetic schemes and troubleshooting synthesis problems independently. Should be excellent in purification and analytical interpretation skills. Familiar with operations of relevant apparatus - instrument / equipment. Education M.Sc in general or organic chemistry / M.Pharma

At PwC, our people in data and analytics focus on leveraging data to drive insights and make informed business decisions. They utilise advanced analytics techniques to help clients optimise their operations and achieve their strategic goals. In business intelligence at PwC, you will focus on leveraging data and analytics to provide strategic insights and drive informed decisionmaking for clients. You will develop and implement innovative solutions to optimise business performance and enhance competitive advantage. Why PWC At PwC, you will be part of a vibrant community of solvers that leads with trust and creates distinctive outcomes for our clients and communities. This purposeled and valuesdriven work, powered by technology in an environment that drives innovation, will enable you to make a tangible impact in the real world. We reward your contributions, support your wellbeing, and offer inclusive benefits, flexibility programmes and mentorship that will help you thrive in work and life. Together, we grow, learn, care, collaborate, and create a future of infinite experiences for each other. Learn more about us . s Design, develop, and maintain scalable data pipelines using Azure data services such as Azure Data Factory, Azure Databricks, and Apache Spark. Implement efficient Extract, Transform, Load (ETL) processes to move and transform data across various sources. Knowledge about data warehousing concepts Extensive working experience in Azure Databricks Utilize Azure SQL Database, Azure Blob Storage, Azure Data Lake Storage, and other Azure data services to store and retrieve data. Performance optimization and troubleshooting capabilities Experience in working in pharma and/or healthcare clients will be a plus Technology SQL, ADF, Azure Databricks, ADLS, Synapse, PySpark Desired Candidate Profile B.E./B.Tech. (preferably in Computer Science) or MCA or Statistics/Applied Mathematics Experience in designing solutions with IaaS, PaaS, and SaaS. Proficient in data modeling and ETL pipeline implementation. Strong knowledge of Azure services. Proven track record in business development and client relationship management. Excellent communication and interpersonal skills. Mandatory skill sets Azure DE Preferred skill sets Azure DE

About us At AstraZeneca we are guided in our work by a strong set of values, and we re resetting expectations of what a biopharmaceutical company can be. By truly following the science, we pioneer new methods, new thinking and bring unexpected teams together. From scientists to sales, lab techs to legal, we re on a mission to turn ideas into life changing medicines that transform lives. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world. If you re swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you re our kind of person. At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you re our kind of person. Roles & Responsibilities: Ensure Zero breach in the SOTC Process Agility in purchase order execution with mitigation of Risks Detailed reading of Tender, Rate Contract and Purchase Orders terms and conditions and mitigate the risks with right external & internal consents. Validate the Purchase Orders with internal references and Regularization of the Purchase Orders Coordinate with CFTs (Tender / Sales / Finance / Distribution / and Quality) for the execution of Purchase Orders Timely communications to the internal and external stakeholders on the purchase order related issues/Status Ensuring to keep sufficient stock inventories at the sales depots by coordinating with the Sales Team. Prepare and submit the documents as per terms of tender, rate contract and purchase orders with all the supplies for the payment realization against the purchase order. Preparation of m onthly dashboards on the purchase order executions and pending order details with the internal stakeholders. Coordinate with Tender Support for the Security Deposits for the Rate Contract finalization and Purchase Order Execution. Filing all the purchase order related documents and support the internal and external audit process. Skills Required: Assertive ness : follow the process and execute the job within the SOP Attention to details & Problem Solving : should be able to understand the challenge in hand and support with the solutions as an option to the CFT. Communication : effective in verbal and written communication. Collaboration : Person should have the good collaboration mindset and a great team payer. Proactiveness & Time Management : Should be able to pre-empt the next bottle necks and work proactively to resolve the issue in timely manner with race against the time mindset. Essential Education al Qualification: B Pharmacy/ bachelor s degree with relevant experience in the SOTC Advance d Microsoft O ffice Desirable : Experience in Pharma SOTC process will be an advantage. Experience in tender operations/Pharma Operations (Supply chain/procurement) will be an advantage. Why AstraZeneca? At AstraZeneca we re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We re on an exciting journey to pioneer the future of healthcare. Date Posted 18-Mar-2025 Closing Date 17-Apr-2025

- Drive business development thru collaboration withexternal businesses, partners, distributors (noncompeting) to drive the bottom line - Develop exportmarket for ITCs beverage brands Responsibilities Building customer base for External Business and Exports - In-line withbusiness plan and technical capability, scouting for external businessopportunities for capacity utilization of PET production line - Develop exportbusiness thru collaboration with partners (in Carton and PET portfolio) todrive bottom line Requirements - Preferably from Pharma, Foods or FMCG background - Know-how of export value chain - B.Sc or B Tech or equivalent technical background withexposure in Techno-Commercial role, exposure in business development would beadded benefit (PG in foreign trade/Management)

About us At AstraZeneca we are guided in our work by a strong set of values, and we re resetting expectations of what a biopharmaceutical company can be. By truly following the science, we pioneer new methods, new thinking and bring unexpected teams together. From scientists to sales, lab techs to legal, we re on a mission to turn ideas into life changing medicines that transform lives. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world. If you re swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you re our kind of person. At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you re our kind of person. Typical Accountabilities : Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality. Leads Local Study Team consisting of Study Start-up Manager(s), Contract Manager(s), CRA(s), CSA(s), for assigned study/studies. Leads and optimizes the performance of the Local Study Team(s) at country level ensuring compliance with AZ Procedural Documents, ICH-GCP and local regulations. Ensures, as required, that clinical and operational feasibility assessment of potential studies is performed to the highest quality. Leads the site selection process by identifying potential sites/investigators with Feasibility Lead (and (acting) Site Engagement Lead- where applicable) , performing initial Site Quality Risk Assessment in collaboration with CRA, and conducting or overseeing Site Qualification Visits to evaluate suitability and quality risks. Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study. Works together with Regulatory Affairs to ensure timely delivery of application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations. Ensures timely preparation of country financial Study Management Agreement (fSMA) and maintains accurate study budget in AZ clinical studies financial system by regular checks of the system and financial reports (as agreed with Director, SMM/ Director, Country Head). Ensures timely preparation of local Master CSA (including site budget) and amendments as needed. Ensures timely preparation of country level Master Informed Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant AZ SOPs and local regulations. Ensures all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with AZ SOPs. Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction). Sets up and maintains the study in CTMS at study country level as well as local websites as required by local laws and regulations. Oversees, manages and coordinates monitoring activities from site activation through to study closure at country and site level in accordance with the Monitoring Plans in collaboration with Clinical Research Associate Director as appropriate. Reviews or oversees the review of monitoring visit reports (as required and following AZ SOPs) and pro-actively advices the monitor(s) on study related matters. Performs any required co-monitoring, Accompanied Site Visits/training visits with study CRAs. Proactively identifies risks and facilitates resolution of complex study problems and issues. Organizes regular Local Study Team meetings on an agenda driven basis. - Is responsible to coordinate LST and specific meetings with the local medical affairs team through ECPLIPSE2.0 Actively works towards achieving good personal relationships with all Local Study Team members, sites staff, local (eg medical affairs) and global stakeholders. AstraZeneca Job Profile. Is responsible to pro-actively share Reports study progress/update, risks and mitigation plan to the Global Study Associate Director/ Global Study Team, including SMM Lead. Contributes to patient recruitment strategy including regular communication with participating Investigators as necessary and set-up of recruitment vendor solutions. Develops, maintains and reviews risk management plan on country study level: proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed. Communicates and co-ordinates regularly with National Co-ordinating Investigator / National Lead Investigator on recruitment and other study matters, if applicable. Plans and leads National Investigator meetings, in line with local codes, as required. Assists in forecasting study timelines, resources, recruitment, budget, study materials and drug supplies. Ensures relevant systems required to facilitate business critical, license to operate activities (for example, Safety Reporting, Regulatory submissions, Clinical Trial Transparency) are set-up, updated and access is organized at country level. Ensures accurate payments related to the study are performed according to local regulations and agreements. Participates in training and coaching new members of the Local Study Team ensuring compliance with ICH-GCP and AZ Procedural Documents. Ensures completeness of the eTMF and ensures essential documents are uploaded in a timeline manner to maintain the eTMF Inspection Ready . Ensures that all study documents are ready for final archiving and completion of local part of the eTMF. Plans and leads activities associated with audits and regulatory inspections in liaison with CQAD and QA. Provides input to process development and improvement. Provides regular information to Line Managers at country level on studies and planned study milestones/key issues. Updates Line Managers about the performance of the CRAs/CSAs. Ensures that study activities at country level comply with local policies and code of ethics. Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market. Ensures compliance with AstraZeneca s Code of Ethics, company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment). Collaborates with local Medical Affairs team on the study execution and delivery. Supports SMM in different initiatives (local, regional or global) as agreed with the SMM Line Management. May act as Site Management & Monitoring Lead for the study Education, Qualifications, Skills and Experience Bachelor s degree in relevant discipline. Significant experience in Study Management within a pharmaceutical or clinical background. Thorough knowledge of Patient Safety processes and local regulations Advanced degree within field Professional certification Clinical study delivery operational experience Project management experience Why AstraZeneca? At AstraZeneca we re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We re on an exciting journey to pioneer the future of healthcare. Date Posted 18-Mar-2025 Closing Date 30-Mar-2025

Job Title: Manager, Global Clinical Solutions Introduction to role Global Clinical Solutions (GCS) drives the delivery of services and technology for AstraZeneca for its internal and external partners. The Manager, GCS supports teams to improve process effectiveness and performance in operational processes/procedures within the department, as well as providing support and guidance in the development of processes owned by Global Clinical Solutions. Individuals with this job will coordinate/lead and deliver GCS services across projects and/or other activities that enable delivery of Clinical Development programs to time, cost, and quality across all delivery models. They may be assigned one or more roles relating to the development and maintenance of processes, systems, and services. All Managers, GCS will lead and project run improvement projects as needed. Accountabilities As a member of a specific activity team, the Manager, GCS: Coordinates and delivers GCS services and coordinates life cycle management and business continuity for projects, services, and technology. Provides authority support to user communities including: I. Conducting relevant process/system/tool trainings II. Facilitating knowledge sharing III. Establishing standard methodologies IV. Ensuring communication with relevant partners across GCS and AZ Conducts critical analyses of processes and tools to define business usage and finds opportunities to improve efficiency/effectiveness of systems/services/processes whilst reducing business continuity risks. Chips in to and/or develops cases for continuous improvement projects. Leads or handles business improvement projects according to lean principles, including planning, prioritizing, implementing, and tracking delivery. Acts as a source of knowledge in one or more areas of GCS. Supports the implementation of changes to improve the way various functions and teams perform. Evaluates and monitors the performance and efficiency of programs to ensure that program implementation is on target. Responsible for training colleagues to use continuous improvement in the new ways of working and embed change culture. Grows capabilities, applies new approaches to improve work; and has a positive impact on team performance creating learning opportunities for others. Responsible for knowledge management of continuous improvement activities and ensuring that the knowledge is used in the selection and execution of future activities. Essential Skills/Experience University degree in related subject area, preferably in biological science or healthcare-related fields, such as medicine, nursing, or equivalent experience Ability to work collaboratively; shown organizational and analytical skills, and shown skills to deliver to time, cost, and quality Good project management skills Excellent knowledge of spoken and written English Strong business communication, partner management, and presentation skills Well-developed organizational and social skills Ensures risks and issues management to ensure effective delivery. Authoritatively applies issue routes and governance to gain traction and deliver rapid solutions Shares lessons learned and standard methodology recommendations with relevant partners to drive continuous improvement Builds relationships and achieves results without line management input Curious and self-motivated Desirable Skills/Experience Expert in their relevant service Experience of utilizing standard process improvement methodologies (e.g., Lean Six Sigma) to identify root causes of process issues and identify areas of process improvement Some experience of Quality Systems and Quality Management, including process definition and process improvement, ideally within an Information Systems environment Experience in multiple fields of clinical development At least 2 years experience in Drug Development within a pharmaceutical or clinical background Understanding ICH GCP guidelines in relation to study delivery Experience of working in a global organization with complex/geographical context When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace, and challenge perceptions. Thats why we work, on average, a minimum of three days per week from the office. But that doesnt mean were not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. Date Posted 12-Mar-2025 Closing Date 29-Apr-2025

Introduction to role Join our dynamic team as an Associate Director, Pharmacovigilance Processes, where you will work closely with the PV Processes Manager, Associate Director, and Director. You will be responsible for handling assigned AstraZeneca projects and processes, including implementation, communication, compliance, performance, and inspection readiness. You will develop relationships across Patient Safety and other relevant areas of AstraZeneca to complete the delivery of the processes strategy and priorities, alongside governance and management of current procedural documents. Accountabilities Find opportunities for and drive the enhancement of existing processes through knowledge of internal and external environments. Work with Process Managers, Associate Directors, Patient Safety, and Regulatory authorities to develop, establish, monitor, report, and assess global KPIs related to safety and regulatory data reporting. Lead the management of process updates in Patient Safety; initiate updates, project manage the delivery of new documents, work with the BPO for content updates, address comments, and release the document. Be an expert in the ECMS tool and associated processes. Support PS Process owners with guidance, advice, and support on PD processes. Use safety and regulatory knowledge to maintain and support the global inspection readiness strategy. Provide process or compliance support to regulatory teams and submissions using a deep understanding of pharmacovigilance processes and regulations. Establish a culture of continuous improvement, high performance, flexibility, and quality emphasizing a can do attitude and innovative approaches. Contribute to the overall management and oversight of the Pharmacovigilance Quality System. Develop and maintain a vision and strategy for nominated pharmacovigilance or regulatory processes. Coordinate and own the lifecycle management of nominated processes, enabling business continuity and compliance. Find opportunities to improve and simplify methodologies in processes and guidance, provide practical solutions, and drive implementation. Promote innovation and new ways of working to drive efficiency and improved deliverables in all processes and partnerships. Lead the development or enhancement of standards or techniques to improve the quality, compliance, and efficiency of deliverables for the overall group. Develop and improve reporting tools and analysis processes and technology. Perform monitoring, analysis, and trending of data. Identify issues and risks and propose options to mitigate them. Monitor, interpret, and validate current, new, and changing legislation, handling the impact of changes. Ensure appropriate, up-to-date records are maintained for compliance. Participate in or support activities for GVP, GCP, GRP, and GMP audits/inspections. Deliver on project assignments supporting the business, e.g., representation or leadership on global cross-functional task forces. Provide process training to relevant functional groups. Seek personal and professional development opportunities and share knowledge gained in open forums. Represent AstraZeneca on industry bodies when appropriate. Serve as the delegate for Process Directors where appropriate. Contribute to communication and change management activities associated with process initiatives. Build relationships with stakeholders and customers to support pharmacovigilance and regulatory activities and responsibilities including successful partnerships. Work collaboratively to provide expertise and share best practices across all regions and partnerships. Essential Skills/Experience A science/pharmacy/nursing degree with at least 5 years relevant experience (pharmaceutical, regulatory, safety, and partnership) Experience in working cross-functionally Leadership skills, including proven leadership of project teams experience Thorough scientific knowledge sufficient to understand all aspects of regulatory/pharmacovigilance and partnership issues Thorough knowledge of the drug development process Good attention to detail Excellent written and verbal communication skills Proven track record to work across cultures Knowledge of AZ Business and processes Able to influence whilst maintaining an independent and objective view Strong collaboration skills Strong negotiation, conflict management, and interpersonal skills Relationship builder Able to work effectively as a member of a cross-functional or global team Understanding of change management process Desirable Skills/Experience MSC/PhD in scientific field Knowledge of new and developing regulatory and pharmacovigilance expectations Knowledge of existing AstraZeneca external alliances and collaborative projects Knowledge of CoE and CMO operating model Experience working with third-party suppliers Experience working in a global organization, preferably within the pharmaceuticals industry, with knowledge of the drug development life cycle and commercial aspects of the industry

NNE is looking for a people with a curious consulting mindset and solid knowledge and skills within Utility & solvents Generation & Distribution design. Join us in delivering the largest and most advanced pharmaceutical projects, while learning from some of the smartest people within process utilities. In the Process Systems Intelligence department, we are 20+ dedicated members working with Clean Utility, Black Utility, Process Waste, and CIP within the pharma & biopharma industry. We aim to inspire our customers with new technologies and help them find the optimal solutions when building new facilities, expanding, or renovating existing facilities. You will have the opportunity to explore new, smarter, and more sustainable technologies. As a specific initiative in our area, we have biweekly knowledge sharing activities where you learn from colleagues - examples hereof are: Digital twin, sustainability initiatives in a specific project, new technology within department connected to regulatory requirements, discussion with technology suppliers, and how to execute projects smarter. You will also get the opportunity to further grow your competencies through internal/external courses and conferences. Our office is in Bangalore, India and in Virum, Denmark where we have an open and flexible office environment, which provides space and opportunities for knowledge sharing, dialogue, and of course - to have fun. We also work from NNE s office in Kalundborg site and depending on current projects the workplace will be there or at customer site. Required Skill Set Excellent verbal and written communication skills with success in building trustful relationships and influencing others in cross-functional areas including customer management Experience in Pharma, Biotech industry is a must. Coordination with other disciplines & conducting design review for engineering activities. Have experience in the perform the Gemba / quality checks for the required discipline. Estimation of Generation Capacities for Utility (Clean, Black, CIP, Waste & Exhaust), Gases and solvents Prepare URS for Utility (Clean, Black, CIP, Waste & Exhaust), Gases and solvents generation skids/equipment & Distribution package Knowledge in Defining concept, designing, sizing and testing of clean & black utility systems and process gases & Solvents and distributions systems on both existing and new facilities. Experience with regulatory requirements, authority applications, GMP impact and calculation of energy consumption. optimization of design solutions to meet specific project technical & commercial requirements. Prepare, Evaluate & Finalize the tender for the utility & Solvents packages. Have experience in qualification of the vendor and equipment (validation life cycle) Have experience in Planning & Estimation of the project deliverables in the different phase of project. Preferred Competencies We care about who you are as a person. In the end, how you work, and your energy is what impacts the effort we do as a team. As a person, you: Are determined and have a solid customer understanding and a consultative mindset Have an interest in technological developments and trends in the field. Are an eager project member and are excited for solving complex tasks Able to collaborate and work with cross disciplinary. Understanding of your colleagues personal and cultural differences Fluent in English, spoken and written. Education and Work Experience In all positions there are some things that are needed, and others a bonus. We believe these qualifications are needed for you to do we'll in this role: BE / B. Tech or M.Sc. / ME / M. Tech in Mechanical, Chemical or equivalent, with relevant experience Must have experience in CD, BD, DD & Construction phases of project execution. Must have good knowledge of the current relevant Engineering & Pharma legislation / regulations / guidelines / standards. Knowledge/ work experience in MS VISIO, AUTO CAD, NAVISWORK are preferred.

Provides input for Budget Planning Likely to oversee contingent workers and/or vendors; Likely to provide training to others Primarily works at the project level Delivers assignments with quality and within timelines Contributes strategy under moderate supervision Provides strong programming support to CDISC based e-submission. Develop, review, and/or perform validation of generic macros. Develop, debug, and enhance SAS programs to support quality control of safety or efficacy derived datasets Has good knowledge and understanding of the statistical models in efficacy data analysis Responsible for the standardization of Clinical Programming deliverables within a project Extends existing or develops new clinical programming methods to solve complex problems Your experience and qualifications Bachelor s Degree/ Master s Degree/ PhD in Science, Statistics, Information Technology or equivalent combination of education and related work experience. Bachelor s + 5 years or Master s + 4 years of professional experience in a pharmaceutical or clinical research setting as a programmer Experience in SDTM and ADaM acquainted with CDISC Guidelines and requirements.

Primarily works at project level May oversee contingent workers and/ or vendors; may provide training to others as needed Offers leadership and basic accountability, provides strategic assistance, and planning support for clinical regulatory documents Writers and edits clinical regulatory documents, including submission summaries and other complex documents Ensures that these documents include the proper content and context (from a regulatory medical writing perspective) and clear and consistent medical/scientific messaging, are accurate and complete, and adhere to applicable regulatory guidelines and departmental and editorial standards May participate in the preparation/revision of document templates Your experience and qualifications Phd or PharmD in life sciences (or other related field), or Master s degree in life sciences (or other related field) PhD or PharmD with a minimum of 2 years of experience OR Master s degree with a minimum of 4 years of experience

Technical/functional knowledge in Intercompany Accounting, Closing and reporting process area Handle various types of intercompany transactions such as sales of products, Transfer pricing agreement (TPA) transactions, services, inventory sales/purchases, cost allocations, royalties, Inhouse banking transactions. Ensure that accruals are properly recorded and analyzed Preparation of Journal Entries Supporting schedule Perform Support monthly and quarterly close activities of multiple entities Analysis of the various accounts and variances per legal entities, obtain explanation on deviations and prepare a summarized reporting on a monthly basis within scheduled time Preparation monthly Intercompany reconciliations clearance of reconciling/aged/disputed items. Hands on experience in submission of trial balance in HFM. Identify drive process improvement, standardization opportunities in of processes and tasks across the team. Acting as a key contact for local teams for record-to-report related questions Ensuring that accounting books and records comply with accounting policies and regulations Provide supporting documents and explanations for all internal and external audit as and when required Knowledge on Accounts payable (AP) and Accounts receivable (AR) books. Your experience and qualifications University education in Accounting or Finance required Masters degree is preferred Minimum experience of 3+ years of closing reporting, Intercompany experience Preferably familiar with USGAAP Working knowledge of internal controls Good working knowledge of SAP Good understanding of accounting processes and can follow accounting policies Good analytical skills and have hands on experience on working clearance of reconciling items Fluent verbal and written communication in English Experience in a multinational firm or within a GBS (Global Business Service) is preferred Hands-on and proactive; strong organizational skills Accustomed to working with deadlines, in a dynamic environment Results driven and service oriented to internal and external customers Excellent collaboration with colleagues within the local organization and with the colleagues of the global business service to support the overall Finance department s goals and objectives Flexible and able to work in a changing environment Strong focus on improvement opportunities Want to work in a new (to be) established team Process documentations and certifications will have to ensure that all process are appropriately documented and periodically certified by team members on regular basis The individuals must have hands on experience in preparing process flows