3748 Pharma Jobs - Page 6

Hiring for Sales Development Manager Identify potential customers through field visits Pitch products and services effectively Convert leads into successful sales Build and maintain strong client relationships Meet monthly sales targets Required Candidate profile Min. 1 year of experience in field sales Graduation Mandatory Excellent communication & interpersonal skills Strong negotiation & closing abilities Contact For more Info: +91 95379 91823 | Nikita

Associate Director - Disaster Recovery Officer Job Details | Teva Pharmaceuticals Find a Career With Purpose at Teva Search by Postal Code Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: Associate Director - Disaster Recovery Officer Date: Jul 25, 2025 Location: Bangalore, India, 560064 Company: Teva Pharmaceuticals Job Id: 62885 Who we are The opportunity The Disaster Recovery Officer is responsible for developing, implementing, and managing the organizations disaster recovery plans and procedures. This role ensures the organization can effectively respond to and recover from disruptive events, minimizing downtime and data loss. Key responsibilities include overseeing data recovery management for all virtual, physical, cloud, and on-premises environments, conducting risk assessments and mitigation procedures, and raising awareness and training employees on disaster recovery protocols. The DR Officer ensures that the disaster recovery plan is aligned with the business strategy and closely connected with the corporate risk plans. Additional duties include conducting DR drills according to the planned calendar, creating dashboards to monitor overall risk posture, and generating reports to communicate with stakeholders. The DR Officer will also be responsible for directing disaster response or crisis management activities, creating a risk register, providing disaster preparedness training, and preparing emergency plans for various scenarios, including natural disasters (e.g., hurricanes, floods, earthquakes), wartime situations, and technological emergencies. Responsible to develop incident management plans and implement procedures for disaster situations and security breaches, ensuring the integrity of data, assets, databases, information systems, and technology. How you ll spend your day Develop and Maintain DR Plans: Create, update, and test disaster recovery plans to ensure they are effective and align with business continuity strategies. Define BIA, Recovery Time Objective (RTO) and Recovery Point Objective (RPO). Ensure that the RTO & RPO for critical assets is aligned with business requirements. Risk Assessment: Conduct risk assessments to identify potential threats and vulnerabilities that could impact the organizations operations. Coordination and Communication: Coordinate with various departments to ensure all critical functions are covered in the DR plans. Communicate DR strategies and procedures to all stakeholders. Conduct DR drills and tabletop Exercise: Conducting regular DR drills according to the planned calendar to ensure the effectiveness of the DR solution Training and Awareness: Conduct regular training sessions and drills to ensure staff are aware of their roles and responsibilities during a disaster. Compliance: Ensure that DR plans comply with relevant regulations and industry standards. Incident Response: Lead the response to actual disaster events, coordinating recovery efforts and communicating with senior management. Documentation: Maintain detailed documentation of all DR plans, polices procedures, and recovery activities. Maintain industry standard and best Practices Ensure the team follows best practices and maintains service level agreements. Ensure compliance with relevant regulations and standards. Understand Business Processes Analyse data trends and share recommendations with stakeholders. Continuous Improvement: Regularly review and improve DR plans based on lessons learned from drills and actual incidents. Your experience and qualifications MSc/B.Tech. /B.E. (Computer Science/IT). Total of 15-20 years of experience. Preferred to have Certified Business Continuity Professional (CBCP) or similar certifications Certifications like ITIL, PMP etc. would be an added advantage. Exposure to ISO standards, TQM and other Quality methodologies/systems. Familiarity with industry compliance standards and regulations. Teva s Equal Employment Opportunity Commitment

For over 30 years, Beghou Consulting has been a trusted adviser to life science firms. We combine our strategic consulting services with proprietary technology to develop custom, data-driven solutions that allow life sciences companies to take their commercial operations to new heights. We are dedicated to client service and offer a full suite of consulting and technology services, all rooted in advanced analytics, to enhance commercial operations and boost sales performance. As a Forecasting Manager, you will lead and manage forecasting engagements across a range of pharmaceutical and biotech clients. You will be responsible for building high-quality, therapy-specific forecasting models that support commercial decision-making across the product lifecycle from pipeline through post-launch. You will work closely with cross-functional client teams (insights, marketing, finance, market access) and internal stakeholders to drive strategic forecasts, scenario planning, and evidence-based recommendations. This role requires deep expertise in pharmaceutical forecasting, experience in claims and epidemiology data, and an understanding of therapeutic dynamics, patient journeys, and commercial analytics. Well trust you to: Lead therapy-area-specific forecasting engagements, ensuring delivery of high-quality, well-documented, and strategically relevant models Design and develop custom forecast models using patient-based, analog-based, and market-based approaches depending on product lifecycle stage Apply deep understanding of disease epidemiology, treatment flow, claims data, and analogs to support robust assumptions Manage structured forecast processes- including assumption alignment, validation with stakeholders, and scenario modeling Lead discussions with clients on forecast inputs, model drivers, and commercial implications Collaborate with internal stakeholders including patient analytics, market research, and advanced analytics teams to enrich forecasts Drive innovation and consistency in forecasting methodology, template standardization, and reusable frameworks Support forecasting input into strategic deliverables including brand planning, launch readiness, market access strategy, and business case development Supervise and mentor a team of consultants/analysts on forecast building, QA, documentation, and client communication Support business development efforts through proposal development and forecast solutioning You ll need to have: 9+ years of experience in commercial pharma analytics, with a proven track record of delivering impactful solutions in the pharmaceutical and life sciences industry (Hands-on experience is preferred). Atleast 5 years of direct experience in pharmaceutical forecasting, preferably in a consulting environment (ZS, Axtria, IQVIA, or similar) Bachelor s or Master s degree in Life Sciences, Pharmacy, Economics, Engineering, or a quantitative field; MBA or MPH preferred Strong familiarity with forecasting approaches across early, pre-launch, launch, and in-market assets. Experience working across multiple therapeutic areas including specialty care, rare diseases, or oncology Advanced proficiency in statistical forecasting methods (time series analysis, regression modeling, predictive analytics) is a must. Experience with forecasting software and tools (SAS, R, Python, SPSS, or specialized platforms like Anaplan, Oracle EPM, SAP IBP) is good to have Knowledge of demand planning, sales forecasting, and financial modeling techniques is required. Understanding of seasonality, trend analysis, and scenario planning methodologies is a must. Advanced Excel modeling skills; ability to build, audit, and refine structured forecast models. Understanding of core statistical and analytical techniques used in forecasting (sensitivity analysis, back-casting, calibration) Strong Excel skills including advanced functions, pivot tables, and VBA/macros is required Experience in dashboarding tools (Power BI, Tableau) and scripting tools (R, Python) is a plus Ability to communicate complex model assumptions clearly and persuasively to both technical and non-technical audiences. Strong storytelling and slide development skills to communicate forecast outputs and implications Demonstrated leadership skills, with experience in managing and mentoring a team of consultants and collaborating with other stakeholders Excellent communication and collaboration skills, with the ability to translate complex technical concepts into clear, actionable insights for diverse audiences. Client management experience is a plus Strong problem-solving and critical-thinking abilities, with a research-oriented mindset and passion for tackling challenging problems, driving innovation in healthcare using ever evolving AI techniques. What you should know: - We treat our employees with respect and appreciation for both their contributions and their individuality. - We value our employees diverse talents and abilities, fostering a supportive, collaborative, and dynamic work environment that encourages professional and personal growth. - You will have the opportunity to collaborate with and learn from colleagues at all levels of the organization, promoting teamwork and success in every project. - We have had steady growth throughout our history because the people we hire are committed not only to delivering quality results for our clients but also to becoming leaders in sales and marketing analytics.

Select with space bar to view the full contents of the job information. Senior Specialist - Quality Hypercare (Biosimilars QC) Job Details | AdvanzPharma We use cookies to offer you the best possible website experience. Your cookie preferences will be stored in your browser s local storage. This includes cookies necessary for the websites operation. Additionally, you can freely decide and change any time whether you accept cookies or choose to opt out of cookies to improve the websites performance, as well as cookies used to display content tailored to your interests. Your experience of the site and the services we are able to offer may be impacted if you do not accept all cookies. Modify Cookie Preferences Reject All Cookies Accept All Cookies Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: Senior Specialist - Quality Hypercare (Biosimilars QC) Andheri (East), IN, Mumbai 400 ADVANZ PHARMA is a global pharmaceutical company with the purpose to improve patients lives by providing and enhancing the specialty, hospital, and rare disease medicines they depend on. Our ambition is to be a partner of choice for the commercialisation of specialty, hospital, and rare disease medicines in Europe, Canada, and Australia. In line with our ambition, we are partnering with innovative biopharma and pharmaceutical development companies to bring medicines to patients. Headquartered in London, UK, we have c700 employees based across more than 20 countries, including key countries in Europe, the US, Canada, and Australia. Our Centre of Excellence in Mumbai, India, as well as an established global distribution and commercialisation partner network complement our global operations. ADVANZ PHARMA s product portfolio and pipeline comprises innovative medicines, specialty generics & biosimilars, and originator brands. Our products and pipeline cover a broad range of therapeutic areas, including hepatology, gastroenterology, anti-infectives, critical care, endocrinology, CNS, and, more broadly, rare diseases. We can only achieve our ambition with the passion of our dedicated and highly qualified people, acting in line with our company values of entrepreneurship, speed, and integrity. About the Role The Senior Specialist, Biosimilars will provide technical support to the Associate Director, Biosimilar Quality on all aspects of biological products and the development and enhancement of the Pharmaceutical Quality System to ensure it meets Health Authority expectations. The portfolio will consist of a range of products including in-licensed and development projects. This role will involve exposure to management across the business and requires an individual with a dynamic and collaborative approach. The maintenance of the Pharmaceutical Quality System to ensure it remains fit for purpose with respect to Biologics/Biosimilar products. To support the Associate Director, Biosimilars and the Strategic Quality team in the assessment of several new pipeline products in support of ADVANZ PHARMA s strategic initiatives and objectives. Support the necessary Quality activities to ensure on time delivery and launch of all pipeline projects. Proactively identify and highlight potential Quality risks, hurdles or issues which may impact project scope, and ensure practical resolution or escalation where necessary. Participate during the interactions with Competent Authorities (EMA, National EU Authorities, Health Canada, TGA and others). Address issues/requests by the Agency during MAA. Support in the preparation for Quality Review Meetings with our partners, escalating risks/issues appropriately to remove barriers to success or advise of delays and other changes which may impact Quality and or supply. Provide QA oversight of analytical method development, validation, qualification, and transfer activities for the biologic/biosimilar portfolio. Review protocols and reports for analytical method validation, comparability studies, and bioassays (e.g., potency, identity, purity, and stability). Evaluate and support resolution of laboratory investigations, OOS/OOT results, and method performance issues. Collaborate with external testing partners to ensure analytical approaches meet regulatory and scientific expectations for biologics/biosimilars. Act as subject matter expert in support of the Quality team in the review of Quality System records, incidents and changes. Review analytical methods, procedures, protocols Perform and oversee the lot disposition process Perform change control assessments including document management Review and approve/reject change controls Approve Deviations and CAPAs and ensure all they are appropriately documented and investigated to determine and address root cause Perform detailed risk assessments Thrive in an entrepreneurial environment and take accountability for results. Embrace challenge and change, applying a growth mindset approach. Have a bias for action and fast decision making. Consistent demonstration and embodiment of company core values: Entrepreneurship, Speed, and Integrity. Drive the spirit of One Team by working collaboratively across all business functions with an open, honest, and respectful cooperation. Contribute to making ADVANZ PHARMA a desired place to work. We are looking for highly motivated individuals who are passionate about making a meaningful difference to patients lives. For this role, you will also have the following: Qualifications: Tertiary qualification in any discipline within Life sciences or Pharmaceuticals Additionally professional qualifications. Knowledge, Skills & Experience: Must be a subject matter expert in quality assurance of Biosimilars, with significant relevant experience. Should possess strong experience in biopharmaceutical active substance production and analytics. Experience working with Biologic and Biosimilar applications Experience interacting with EU regulatory authorities Scientific advice meetings Broad knowledge and awareness of the European regulatory guidelines and legislation. Have a good understanding of early development and validation programs for Biosimilars. Excellent people management skills. Sense of urgency / willingness to operate within tight deadlines. Ability to work with colleagues across a broad range of disciplines and functions. Ability to communicate clearly and concisely and use strong writing and verbal skills to communicate facts, figures, and ideas to others. A positive and can-do approach, biased towards finding solutions and embracing change. Inspired by our values of entrepreneurship, speed and integrity. Learning agility and scalability , with a desire to continuously improve and develop as ADVANZ grows. Work collaboratively across all business functions with an open, honest, and respectful cooperation. Ability to have fun and thrive in a growing, unique, and inclusive work environment. The success of any company is driven by its people, and we are no different. At ADVANZ PHARMA, we believe in empowering our people to be entrepreneurs and embrace challenges to enable personal and company growth in an agile and fast-paced environment. We strive to do that inclusively and responsibly, treating all employees with integrity whilst rewarding outcomes and impact. Our teams are made up of people from all walks of life and backgrounds. We thrive in an environment where uniqueness is celebrated, but we are all united by the same passion to help improve patients lives by providing and enhancing the specialty and hospital medicines they depend on. But there s more to you and us than just work, which is why our culture, vision and values are so high on our agenda. We believe in gender equality and actively encourage women into senior roles we have an active ADVANZ PHARMA Women s Network; almost 40% of our managers are women. We work hard to recognise and reward talent, and we actively promote from within - last year, approximately 25% of our people across the company achieved promotions. In addition, we recognise talent with our annual Impact Awards, in which our top performers are rewarded for their hard work and dedication. 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Intellectual Property (IP) Paralegal Sartorius is a global leader in pharmaceutical and laboratory equipment, driving biopharmaceutical advancements with innovative solutions. It supports efficient vaccine and drug production, investing heavily in R&D to accelerate scientific progress. Committed to sustainability, Sartorius implements eco-friendly practices and products. With a presence in over 110 countries, it impacts various industries, including pharmaceuticals and biotechnology. Known for quality and compliance, Sartorius ensures safe and effective biopharmaceutical products. Overall, it plays a crucial role in advancing global healthcare and life sciences. Job Title: Intellectual Property (IP) Paralegal Department: Intellectual Property Management - Trade Mark & IP Services Employment Type: Full-time and On-site at the Bangalore Campus Overview: We are seeking a skilled and detail-oriented Intellectual Property (IP) Paralegal to support the entire lifecycle of IP rights for the Intellectual Property Management Group. This role is critical in ensuring compliance with legal frameworks, managing deadlines, and supporting both internal and external stakeholders on IP matters. You will collaborate with global teams and play a key role in the administrative handling of patent, trademark, and design portfolios. Main Responsibilities & Tasks: Administer and manage all formal IP procedures during the lifecycle of IP rights (patents, trademarks, designs). Implement Sartorius administrative IP workflow, ensuring alignment with internal and official deadlines. Coordinate and support application, registration, grant, opposition, and appeal proceedings in collaboration with internal IP managers and external patent law firms. Monitor and manage due dates and internal deadlines using PatOrg and other docketing systems. Administer and pay maintenance/renewal fees using tools such as PAVIS. Process invoices and manage cost-related documentation efficiently. Maintain and upgrade Sartorius internal electronic file management systems for IP (e.g., PatOrg). Support the integration of new IP portfolios during M&A activities. Ensure compliance with relevant jurisdictional legal frameworks (e.g., German Employee Invention Act). Liaise with global IP offices such as EPO, EUIPO, USPTO, and WIPO. Qualification & Skills: Formal training or qualification in IP/Patent Paralegal or a comparable certification/experience (Indian equivalents accepted in lieu of European standards). Minimum 3 years of professional experience in IP administration within a corporate IP department or law firm. Experience supporting legal proceedings before EPO, EUIPO, USPTO, WIPO is required. Proficient with IP management tools such as PatOrg, PAVIS, EPO Online Filing, ePCT, or other similar platforms. Excellent organizational and workflow optimization skills; a strong focus on accuracy, compliance, and customer service. Strong written and verbal English communication skills. High level of reliability, meticulous attention to detail, resilience, and team collaboration.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position Senior UX/UI Designer Roche India Roche Services & Solutions Hyderabad A healthier future. It s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That s what makes us Roche. We are seeking a highly experienced Senior UX/UI Designer to join our team, focusing on designing intuitive and visually compelling experiences for AI-driven tools and data visualization. Your work will transform complex datasets and AI-powered insights into clear, accessible, and engaging user experiences, empowering users to make data-driven decisions with confidence. As part of our team, you ll play a key role in shaping cutting-edge analytics tools and dashboards used globally across the pharmaceutical industry. You ll collaborate closely with cross-functional teams to ensure AI-driven solutions are both powerful and user-friendly. Your Opportunity Design and deliver user-friendly dashboards, AI-powered tools, and interfaces that simplify complex data and insights Work closely with product managers, data scientists, and developers to align designs with business and user needs Develop wireframes, prototypes, and high-fidelity mockups using Figma Transform AI-generated insights and large datasets into digestible visual narratives for non-technical users Collaborate with our in-house UX researcher to conduct usability testing and iterate designs based on user feedback Contribute to and evolve our design system, ensuring consistency across AI and data visualization tools Advocate for accessibility and inclusivity in AI-driven UI/UX design Work autonomously, taking ownership of projects while knowing when to raise questions if something is unclear Deliver efficient and high-quality work, ensuring that designs are both effective and scalable Who you are You have experience designing for AI-powered analytics platforms or machine learning applications with 7+ years of experience in UX/UI design with a strong portfolio showcasing data visualization and AI-driven applications Proficiency in Figma (required; other design tools not needed) Strong understanding of user-centered design principles and UX methodologies Excellent English communication skills ability to articulate design decisions, collaborate effectively, and present to stakeholders Experience translating complex AI insights and large datasets into intuitive charts, graphs, and dashboards Familiarity with accessibility standards and best practices in UI design A proactive, problem-solving mindset with the ability to balance user needs with business goals Ability to work independently and efficiently, while being proactive in asking for clarification when needed Must be able to work Central European hours Experience in the pharmaceutical or healthcare industries is a plus. Why Join Us Be part of a dynamic team driving innovation in AI-driven analytics and data visualization. Work on impactful projects used by global teams in over 80 countries Enjoy opportunities for growth, learning, and collaboration with talented colleagues Who we are A healthier future drives us to innovate. Together, more than 100 000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let s build a healthier future, together. Roche is an Equal Opportunity Employer. "

Requisition ID: 60126 Position Type: FT Permanent Workplace Arrangement: About Kerry Kerry is the worlds leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment. Key responsibilities Innovation - Lead projects in the bakery application to deliver topline innovation revenue Lead resource allocation for the End Use Market Lead understanding, approval, project management and stakeholder management Provide key technical inputs to team to ensure timely delivery of applications. Work with manager to manage costs for the function and ensure positive ROI. Work towards bringing in novel ideas to innovation funnel & New to Kerry ideas. Productivity - Lead the productivity agenda to deliver profitability improvement Existing Business support - Support existing business via high quality application support,training, and development of extended team. Actively work with Regulatory team to alwaysensure compliance for portfolio. Team development Understanding motivators, strengths and weakness of team members and work towards developing team. Use the objective setting process and review mechanismseffectively to develop the team Develop self Develop self to take up new challenges in the field of food science. Keep abreastwith latest trends and technologies, market dynamics, customer & stakeholder challenges andactively seek solutions from & beyond Kerry portfolio. Qualifications and skills Must have s Technical background with M. Tech/ M.Sc. in food science/ technology & relevant professional experience of minimum 12 years B. Tech food science/ technology with Minimum 15 years of experience. Ability to manage a team of minimum 5 team members towards project delivery. Knowledge of handling industrial manufacturing/processing especially for trials at customer place Expert level knowledge of Bakery products like hard bakes, soft bakes and wafers/ rolls Aware of business and commercial understanding and how RDA impacts the ROI. Experience in customer interaction and customer driven technical support. Ability to manage internal stakeholders like regulatory, marketing, sales, and project managers. Technical understanding of Good Lab Practices Good to have s Knowledge of plant processes, quality, supply chain, project management areas Front end innovation, Design to value and general management area. PMP certification/ other project management certifications Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a starter kit, investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name. Recruiter: #LI-AA1 Posting Type: LI

Career Category Quality Job Description ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world s toughest diseases, and make people s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what s known today. ABOUT THE ROLE Role Description: In this vital role, you will lead the Amgen India, Quality Control Technical Resources Team. This is a unique opportunity to support the global Quality Control network and to learn about the testing of Amgen products through various stages of the product lifecycle. In addition, as this is a newly formed team, the Senior Manager will have the opportunity to develop new business processes and to strategically develop the team structure. The QC Technical Resources team will primarily provide centralized document management support for the global QC Network. This will include the creation and/or revision of controlled documents within Amgen s enterprise document management system for a variety of QC processes. The Senior Manager Quality Control will provide management oversight of this team while fostering a culture of innovation, quality and collaboration. The Senior Manager will report directly to Amgen India Quality Leadership. This candidate will primarily work during regular working hours (9 AM 6 PM local time) to enable the business in delivering Amgen s mission to serve patients and may lead a shift-based team that provides coverage in support of the Amgen network across multiple time zones. The candidate may need to work outside of his/her routine workday to support business needs and will be responsible for determining the same for their staff. The individual will be required to work from our office located in Hyderabad India (Amgen India-AIN). The candidate will also lead the remote support from AIN to Amgen sites across multiple time zones globally. Roles & Responsibilities: The Senior Manager Quality Control will be accountable for the following activities: Daily management of the Quality Control Technical Resources team Responsible for organizing team resources to ensure that agreed upon due dates are met for QC Network requests Responsible for creating and maintaining business processes and tools that will facilitate the management and visibility of QC network requests Responsible for ensuring that the Technical Resources team has access to the required laboratory information management and enterprise systems needed to carry out document management tasks (for example, LIMS, electronic laboratory notebook). Responsible for leading issue resolution and problem-solving exercises within the team and cross-functionally, as needed Support staff training, career development and performance management Responsible for ensuring compliance with safety guidelines, cGMPs and other applicable regulatory requirements. Additional Responsibilities: Participate in Amgen global network teams Establish and enable LEAN principles across area of responsibility Establish and enable department goals, strategies and KPIs Champion site and QC global process improvements Interfaces with management on significant matters, often requiring the coordination of activity across organizational units Plans and organizes project assignments of substantial variety and complexity Translates complex data into actionable information and applies strong technical knowledge to meet business objectives Identifies process gaps, introduces innovative solutions, and leads operational excellence projects to improve efficiency and productivity, while decreasing expense/operating costs. Leads root cause analysis discussions for more complex problems to develop and efficiently implement effective permanent solutions. Basic Qualifications and Experience: Master s degree with 12-16 years of Pharma and Biotech commercial or clinical manufacturing Quality Control experience AND 5 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources Functional Skills: Must-Have Skills: Experience working and leading teams in a cGMP laboratory environment. Strong technical writing skills within a highly regulated environment. Working knowledge of cGMP regulations, practices, and trends pertaining to Quality Control. Experience managing staff and/or leading teams, projects, programs or directing the allocation of resources. Good-to-Have Skills: Track record of building or participating as a member of high performing team. Experience with various laboratory computer systems and applications. Strong leadership and negotiation skills with a demonstrated ability to influence different styles. Demonstrated innovative thinking and ability to transform work organizations. Exposure to Operational Excellence initiatives. Understanding of quality management systems and quality control processes related to drug substance and drug product for clinical and commercial operations. Demonstrated ability to navigate through ambiguity and provide structured problem solving. Demonstrated ability to coordinate multi-functional project teams and deliver on schedule. Demonstrated ability to coordinate and lead cross-functional teams. Demonstrated ability to find opportunities and implement new technologies and services to transform the business into a more agile, efficient and effective organization. Demonstrated skills in staff motivation, coaching/mentoring and professional development. Great teammate who can collaborate and provide leadership through influence to achieve the required results. EQUAL OPPORTUNITY STATEMENT .

Are you ready for a new beginning We need your talent, knowledge and dedication to better our world with biology. Our purpose points the way In Novonesis, we know that solutions rooted in biology can help solve humanity s biggest challenges. Since we began more than a century ago, this has been our guide. It s how weve gotten so far. And it s how well impact the future. Now, more than ever, the world needs change. And with biosolutions, the possibilities for transformation are endless. We re here to better our world with biology. GLOBAL JOB DESCRIPTION Job Title Process Engineer Job Description Responsible for, Responsible for User Management profile as active team member for team of Supply chain plant user management. This includes plant sizing, Equipment sizing, Plant Lay out studies, overall Engineering review of the green Field Project. Tasks and responsibilities Formulation/Standerdisation Process flow PFD preparation with desired battery limit (connection points to downstream process) support to engineering Company. Responsible for Co-ordination with all relevant stake holders from the project Team, Engineering/consultanting company and SCM Operation Teams for the project delivery. Best sutaible Plant Layout preparation support to Engineering company for Supply chain Operation Plant. Material and Man Movement plan preparation for new SCM plant in co-ordination with Project Engineering and Management Team. Sizing calculations for Liquid and Solid storage with internal plant vehicle Transport layout preparation. Plant Sizing-Formulation / Standerdisation capacity calculations with LTP/MTP plans with SCM Management team. Equipment sizing and design reviews of the detail Engineering drawings prepared by Engineering company. Compliance to all Food safety/Regulatory/EHS requirements during early design phase. Preparation/Review of PFD s (Process flow diagrams) for the SCM process with Engineering company. Support in preparation and reviewing deatil sizing of RM and PM storage with all the RM/PM material requirement and Movement plan. Review of DQ, IQ, HQ & OQ for new equipment s and delivery of the same for the process. Review of Mechanical & Piping P&ID Closely work with SCM- India Operations head on complex decisions considering Plant Scalability and Flexibility in Operation of the Plant prior to Design confirmation/Approvals. Basic Qualifications Bachelor of Engineering Chemical/Mechanical with 5-8 years of experience in process industry- Food/Pharma/biotech/Chemical Supervisor responsibilities All stake Holder Management. Reporting lines Supply Chain Operations Head Physical requirements ( For M umbai India positions Only) Novozymes Mumbai Inida, Input for job advertisement Candidate profile The Person should be having eexperience in big size standerdisation/Formulation plant (SCM) process Engineering with the green Field project. Challenges in position This position requires dedication and eye for detailing with effective stake holder management skills. Language of job advertisement (English default) English Could our purpose be yours Then apply today! At Novonesis we commit to an inclusive recruitment process and equality of opportunity for all our job applicants. We recommend you not to attach a cover letter to your application. Instead, please include a few sentences in your resume/CV about why you are applying. To ensure a fair recruitment process, please refrain from adding a photo in your resume/CV. Novonesis is dedicated to fostering a unique community by embracing and respecting differences. We make all employment decisions based on business needs, ensuring that every individual can thrive, regardless of identity or background such as ethnicity, religion, gender, sexual orientation, age, disability, or veteran status. Want to learn more Learn more about Novonesis, our purpose, and your career opportunities at novonesis.com Not the right fit for you Even if this job isnt the right fit for you, perhaps you know someone who might find it interesting. If so, please feel free to share the job link and encourage them to apply. Thank you for your referral! Please check out our other open positions. The right fit for you could just be a few clicks away. Stay alert: Avoid recruitment scams At Novonesis, we are committed to maintaining a safe and transparent recruitment process. Please be aware of potential scams targeting job seekers and take note of the following: Novonesis will never ask for sensitive personal information, such as bank account details, Social Security numbers, or passwords, at any stage of the hiring process. Novonesis does not make employment offers without conducting interviews with candidates. If you receive suspicious communication claiming to be from Novonesis, please do not share any personal or financial information. We encourage you to verify the legitimacy of the message by contacting us directly through our official channels.

Experience in Plant Scale up, Technology Transfer Strong understanding of key chemical engineering subjects (Heat transfer, mass transfer and Chemical reaction engineering) Exposure on process optimization, debottlenecking, process intensification, scaleup studies ","vacancyKeyroles":" Technology transfer of process for scaleup from Lab scale to commercial scale. Preparation of BFD, PFD, Mass balance , energy balance, MOC compatibility and design basis Involves Process optimization, scaleup and scale down of unit operations (reaction, filtration, drying, crystallization, distillation etc.) Process modification and improvement for optimized capex and opex (achieving target norms) Process Intensification using next generation techniques of flow chemistry and working on reaction kinetics Close collaboration with process safety team to study process for thermal safety (DSC, ARC, RC1E) etc. Close collaboration with R&D scientist for optimizing and conceptualizing process flow at plant scale. Anticipating problems of commercial scale and resolve during process development stage Close collaboration with Engg. Lab team for process scale-up, scale down and engineering optimization, engineering data generation (VLE data, crystallization PSD, filtration rate, drying curve, extraction studies etc.) Close collaboration with pilot team for piloting activities, BEP preparation, P&ID preparation, participating in hazop, and successful piloting activity. Close collaboration with MPP and Dedicated design team for transfer of finalized process (tech transfer package) Working on established plants and processes for troubleshooting and eliminating process challenges Optimizing process with minimum effluents and maximum productivity

":"B.Sc, M.Sc, Phd/ Doctorate. " , "process_Name":"R&D" , "vacancyKeyskills":" Ensure cost effective process development. Ensure that laboratory work is carried out in a safe manner. Ensure that the R&D unit complies with relevant statutes. Ensure that knowledge generated is captured in an easily retrievable form. Ensure that all data captured in the PLM system. ","vacancyKeyroles":" Execution of experimental work for the assigned project as per plan - Interpretation of experimental results and propose directions for further work Troubleshoot the problems in process development - Record the experimental observations - Interact with the analytical division for the analysis - Follow safety practices and procedures. - Follow the practices and procedures as laid down by statutes. - Follow systems for knowledge capture. - Follow PLM system and guideline ","vacancyBackground"

":"Phd/ Doctorate, M.Sc. " , "process_Name":"R&D" , "vacancyKeyskills":" Ensure accurate analysis of samples in time Ensure that laboratory work is carried out in a safe manner. Ensure that equipment are in working condition all the time. Ensure that analytical division complies with relevant statutes. Ensure that knowledge generated is captured in an easily retrievable form. Ensure compliance of systems implemented. Ensure timely completion of Projects. ","vacancyKeyroles":" Execution of analytical plan for the assigned projects. Interpretation of analytical results and prepare analytical reports. Record and report the observations during analysis. Documentation of analytical work. Interact with synthesis division for the analytical requirements. Follow safety practices and procedures. Prepare and implement maintenance schedule. Maintain required level of spares and consumables. Propose AMC/CMC contracts and implement AMC/CMC contracts. Follow the practices and procedures as laid down by statutes. Follow systems for knowledge capture. Follow the systems. Data and report sharing Customer discussion Analytical requirement Response to customer queries

Experience in R&D focusing on enzyme development and modification. Proficiency in molecular biology techniques such as PCR, gene cloning, and site-directed mutagenesis. Expertise in protein expression, purification, and characterization. Experience with enzyme kinetics and activity assays. Knowledge of biocatalysts and enzyme engineering principles. ","vacancyKeyroles":" Design and conduct experiments for enzyme discovery, modification, and functional optimization. Purify enzymes using advanced techniques and ensure high activity and purity. Study enzyme kinetics, substrate specificity, and stability under different conditions. Research and implement enzyme applications in industries such as pharmaceuticals, agriculture, bioenergy, and food processing. Collaborate with cross-functional teams, including engineers and scientists, to integrate biocatalysts into broader biochemical processes. Maintain laboratory equipment in good condition and ensure a safe working environment by adhering to safety protocols and procedures. Stay updated with advanced technologies in the field of enzyme and coenzyme development and provide innovative solutions. Assist in scaling up biocatalytic processes from laboratory to production scale, ensuring consistency and quality.

Ensure cost effective process development. Ensure that laboratory work is carried out in a safe manner Ensure that the R&D unit complies with relevant statutes. Ensure that knowledge generated is captured in an easily retrievable form Ensure that all data captured in the PLM system ","vacancyKeyroles":" Execution of experimental work for the assigned project as per plan. Interpretation of experimental results and propose directions for further work Troubleshoot the problems in process development. Interact with the analytical division for the analysis. Record the experimental observations. Follow safety practices and procedures. Follow the practices and procedures as laid down by statutes. Follow systems for knowledge capture. Follow PLM system and guideline

Proficiency in molecular biology techniques such as PCR, gene cloning, and site-directed mutagenesis. Expertise in protein expression, purification, and characterization. Experience with enzyme kinetics and activity assays. Knowledge of biocatalysis and enzyme engineering principles. Experience with techniques for enzyme immobilization and stabilization. Familiarity with computational tools for enzyme design and modeling. ","vacancyKeyroles":" Design and conduct experiments for enzyme discovery, modification, and functional optimization. Purify enzymes using advanced techniques and ensure high activity and purity. Study enzyme kinetics, substrate specificity, and stability under different conditions. Research and implement enzyme applications in industries such as pharmaceuticals, agriculture, bioenergy, and food processing. Collaborate with cross-functional teams, including engineers and scientists, to integrate biocatalysts into broader biochemical processes. Maintain laboratory equipment in good condition and ensure a safe working environment by adhering to safety protocols and procedures. Stay updated with advanced technologies in the field of enzyme and coenzyme development and provide innovative solutions.

Ensure cost effective process development. Ensure that laboratory work is carried out in a safe manner Ensure that the R&D unit complies with relevant statutes. Ensure that knowledge generated is captured in an easily retrievable form Ensure that all data captured in the PLM system ","vacancyKeyroles":" Execution of experimental work for the assigned project as per plan. Interpretation of experimental results and propose directions for further work Troubleshoot the problems in process development. Interact with the analytical division for the analysis. Record the experimental observations. Follow safety practices and procedures. Follow the practices and procedures as laid down by statutes. Follow systems for knowledge capture. Follow PLM system and guideline

Process Development for new products Preparation of Basic Engineering Package (BEP) Co-ordination during Detailed Engineering / Procurement Plant Erection and Commissioning Plant Start-up to attain rated capacity ","vacancyKeyroles":" Providing Engineering inputs to R&D groups/Pilot Plant. Compilation and preliminary analysis of data for scale-up studies Carrying out design calculations and preparation of engineering documents and drawings. Preparation of process engineering documents to make BEP. Preparation of documents for HAZOP study. Check Detailed Engineering documents from Engineering Contractor to ensure that BEP requirements are met. Provide clarifications to the consultant on process engineering related issues. Check vendor documents to ensure that BEP requirements are met. Carrying out checks in plant to ensure that the erection is done as per P&ID s and other guidelines set by BEP. Provide process engineering support to Production department for pre-commissioning and commissioning of the plant. Providing inputs for preparation of Plant Operating Manual. Identifying area for process improvements to attain or exceed the targeted capacity or Yield or Product Specifications. Identifying bottlenecks in achieving the targets and suggest the solution for the same. Complete the necessary formalities for carrying out changes during plant commissioning.

Refrigerants" , "vacancyKeyskills":" Development of processes in R&D Scale up of Process in Pilot Plant Capability development in Tech Transfer Team Statutory Compliance for Pilot Plant ","vacancyKeyroles":" Collaborating with the R&D team to understand the complexities of the proposed process and plan the scale-up accordingly. Carry out the changes as required for the set up with the help Mechanical / Electrical / Instrument engineers Train the manpower for different types of processes. Compile the experimental observations and results for Tech Transfer Report. Preparation of Pilot SOP and Batch Card as per PDS and data required for Process Scale up Tracking the Projects as per Time planning Conducting training for Pilot Operation team. Preparation of Umbrella System document for Pilot Plant System " , "vacancyBackground":"Candidate should be from Pharmaceutical/ Chemical Industry" , "vacancyRemarks":"Candidate should have scored 60% throughout (10th, 12th, B.Tech, M.Tech) He should be open to travel.He Should have done B.Tech or M.Tech with specialization in ChemistryHe should be willing to relocate.","disAllRemarks":"No.

Process Development for new products Preparation of Basic Engineering Package (BEP) Co-ordination during Detailed Engineering / Procurement Plant Erection and Commissioning Plant Start-up to attain rated capacity ","vacancyKeyroles":" Providing Engineering inputs to R&D groups/Pilot Plant. Compilation and preliminary analysis of data for scale-up studies Carrying out design calculations and preparation of engineering documents and drawings. Preparation of process engineering documents to make BEP. Preparation of documents for HAZOP study. Check Detailed Engineering documents from Engineering Contractor to ensure that BEP requirements are met. Provide clarifications to the consultant on process engineering related issues. Check vendor documents to ensure that BEP requirements are met. Carrying out checks in plant to ensure that the erection is done as per P&ID s and other guidelines set by BEP. Provide process engineering support to Production department for pre-commissioning and commissioning of the plant. Providing inputs for preparation of Plant Operating Manual. Identifying area for process improvements to attain or exceed the targeted capacity or Yield or Product Specifications. Identifying bottlenecks in achieving the targets and suggest the solution for the same. Complete the necessary formalities for carrying out changes during plant commissioning.

We are looking to hire Lead - RPO (Deployment at client location) for one of our Ahmedabad based client (Industry - Pharma) Preferred candidate profile Candidate should have experience in Pharma manufacturing hiring Must have catered Pharma clients and requirements from Mid - senior level of positions Good communication skills Client management skills should be very strong Immediate joiner or early joiners only If interested, share profiles at pallavi.chauhan@stmpl.co.in

As a Sales Executive , you will be responsible for generating prescriptions and increasing product sales by promoting pharmaceutical products to doctors, hospitals, pharmacies, and stockists. This role demands strong interpersonal skills, product knowledge, and the ability to build long-term professional relationships. Location: 1) Pune City 2) Shirur territory Experience: Science Background with minimum 6 months experience.

Job Description Your mission at IntegriChain: To help ensure success of high quality and on time delivery of rebate claims processing for IntegriChain s BPSaaS Customers. What this role entails: Processing of Managed Care and/or Medicaid Rebates Download, log and track data and contract submissions Run and create reports/analysis in Excel spreadsheets and other software packages to support payment reviews and approvals Ensure calculations are in compliance with contractual terms Reconcile and document any rebate variances Resolve errors and disputes within the rebate system based on defined set of rules and procedures Follow and ensure compliance with defined business processes and pre-established guidelines to perform the functions of the job Provide updates to management as required on delivery status of assigned work Ensure department SLA s are met for delivery Prepare and analyze ad hoc reporting Support ad hoc projects What success looks like in this role: Rebate claims are delivered on time and are of high quality Data and contracts are downloaded within required SLAs Compliance with department business processes Proactive and clear communication with Team Lead and other business partners Qualifications What you ll need to thrive in this role: Ability to prioritize and manage multiple tasks effectively and work in a fast paced environment Attention to detail, along wi

Career Category Operations Job Description Join Amgen s Mission of Serving Patients At Amgen, if you feel like you re part of something bigger, it s because you are. Our shared mission to serve patients living with serious illnesses drives all that we do. Since 1980, we ve helped pioneer the world of biotech in our fight against the world s toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. As a member of the Amgen team, you ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. What will you do Let s do this. Let s change the world. We are seeking an individual who thrives in ambiguity, capable of shaping the global R2O and Supplier Enablement strategy with speed and precision. This Global Product Owner role will lead and oversee key global processes and systems that drive our ability to engage with our supplier network though vendor onboarding, vendor enablement and the purchase order creation process. This global leader will be responsible for providing oversight and strategic direction to staff on the design, testing, deployment and maintenance of key global Amgen systems, including the Supplier On-boarding platform and our Requisition to Order platform. This role is part of the Global Procurement Center of Excellence (COE) and will be a key member of the Procure-to-Pay (P2P) Leadership team, responsible for helping meet the annual organizational goals as well as driving the multi-year transformational roadmap. Primary responsibilities will include: Develop and implement global standards related to Supplier On-boarding, Vendor Master Data, and Requisition to Order around which over 25K global staff will operate. Moreover, identify and recommend revisions to current procedures, programs and strategic initiatives, where necessary, consistent with best-in-practice procurement strategies Develop, champion, and ensure implementation of ideas that will focus on maximizing efficiency, improving customer service and user satisfaction, standardization / globalization, robust compliance, and compliance. Contribute to the design and development of global systems including the Supplier On-boarding platform and the R2O platform (Ariba) Align operational plans for processes and systems to align with corporate strategy (i.e. volume growth, geographical reach, technology enablement) Ownership of global Policies and Procedures specific to scope of role; ensure such policies and procedures are SOX compliant Serve as the Global Subject Matter Expert (SME) on all matters relating to the scope of Supplier On-boarding, Vendor Master Data, and the Requisition to Order process and their corresponding systems. Act as an advisor to management or senior professionals, as needed Independently determine the approach to project timelines and assignments and be accountable for alignment of results to objectives Work closely with global team peers (i.e. US, India, etc.) to complete global project activities; this includes functions outside of P2P including Technology, GSS, Compliance, etc. Accomplish results through the direct and indirect management of global teams Utilize judgement to resolve system or process issues when they arise in a timely and compliant manner Ensure compliance with all Amgen internal control and compliance policies. Define continuous reporting capabilities on compliance and performance across R2O process. Work closely with the Finance and Corporate Compliance functions to ensure compliance with controls is built into Supplier Onboarding and R2O processes and reports Identify user friendly / centric solutions to drive compliance by collaborating with Procurement Digital Lead and IT function Functional Skills: Must-Have Skills: Proficiency in defining and implementing best-in-class R2O & Supplier Enablement procurement processes. Experience in developing balanced scorecards to track procurement performance and key KPIs. Deep knowledge of the requisition-to-order (R2O) process, including requisition creation, supplier selection, and order placement. Strong analytical skills to analyze complex business systems and identify areas for improvement. Manage relationship with key stakeholders to enable development and execution of R2O processes that effectively address business needs. Good-to-Have Skills: Analytical mindset with a focus on continuous improvement and value delivery. Must have experience with analytical tools (Tableau, Power BI etc.) Experience with Global Procurement e-Sourcing (Ariba, Coupa, Jaggaer, iValua, etc.) and CLM Tools (e.g., Workday Strategic Sourcing, Sirion Labs), as well as Supplier Onboarding Platforms 12 + years of progressive finance / accounting / business process ownership experience 4+ years leadership experience directly managing and/or leading teams, projects, programs or directing the allocation of resources Pharmaceutical/Biotech experience Professional Certifications (please mention if the certification is preferred or mandatory for the role): CPA or MBA preferred, but not required Soft Skills: Strong written, verbal communication and presentation skills Strong interpersonal skills; ability to influence personnel across functions and levels Ability to thrive in ambiguous situations and help their team operate successfully a dynamic environment Ability to think strategically Ability to work effectively with global, virtual teams Ability to navigate ambiguity High degree of initiative and self-motivation Ability to manage multiple priorities successfully Team-oriented, with a focus on achieving team goals Influencing and Change Management skills Basic Qualifications: Doctorate degree and 3 years of procurement process management or related experience, OR Master s degree and 10 to 14 years of procurement process management or related experience, OR Bachelor s degree and 14 to 16 years of procurement process management or related experience, OR Diploma and 18 to 20 years of procurement process management or related experience What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. .

Job Title: Quantity Survey Engineer HVAC & MEP Projects Location: Bangalore Company: Envigaurd Engineering Pvt Ltd Experience Required: 6 to 8 years Employment Type: Full-Time About Envigaurd Envigaurd is a leading engineering solutions company specializing in HVAC, MEP, laboratory ventilation, and cleanroom systems . With a team of experienced professionals and a client-centric approach, we deliver turnkey solutions for pharmaceutical labs, R&D centers, hospitals, commercial complexes, industrial kitchens, IT parks, and more. We are committed to safety, innovation, and sustainable engineering practices. At Envigaurd, we value precision, accountability, and high-performance project delivery. Role Overview We are looking for a detail-oriented and experienced Quantity Survey Engineer with a strong background in HVAC and MEP projects . The ideal candidate will handle RA bill processing, subcontractor bill certification, quantity reconciliation, and internal/external reporting, ensuring timely and accurate documentation across all stages of project execution. Key Responsibilities RA Bill Preparation & Processing : Prepare and verify RA (Running Account) bills as per site progress and contract terms. Subcontractor Bill Certification : Evaluate and certify subcontractor bills based on executed work, BOQ, and terms of engagement. Client Quantity Approval : Coordinate with client representatives for quantity approvals and ensure measurement records are maintained. Documentation & Reconciliation : Maintain accurate records of site measurements, cost breakdowns, invoices, and project reconciliation reports. Reporting : Prepare cost and billing reports for internal teams and external clients, highlighting progress, variance, and reconciliation data. Coordination : Collaborate with the project team, site engineers, and procurement department for quantity inputs and validations. Variation & Change Order Management : Support cost assessments of variations and prepare necessary documentation for client submission. Skills & Qualifications B.E./MTech in Mechanical/Civil Engineering or related field. 6 8 years of experience in quantity surveying in HVAC and MEP environments. Strong understanding of BOQ, billing processes, HVAC and MEP systems. Experience with billing tools/software (MS Excel, AutoCAD, ERP, etc.). Excellent knowledge of cost control, material tracking, and subcontractor coordination. Strong documentation and communication skills. Why Join Envigaurd Work with a fast-growing company in specialized HVAC and MEP domains. Exposure to prestigious industrial and commercial infrastructure projects. A professional and collaborative team environment. Opportunities for career growth and skill enhancement. Reporting To: Project Manager / Commercial Head Job Category: Quantity Survey Site Operation Job Type: Full Time Job Location: Bangalore

Job Title: Costing & Estimation Engineer HVAC & MEP Projects Company: Envigaurd Location: Bangalore Experience: 6 8 Years (Mandatory in HVAC & MEP Projects) Industry: HVAC, MEP, Industrial Ventilation, Lab Infrastructure About Envigaurd Envigaurd is a leading solutions provider in laboratory infrastructure, HVAC systems, and industrial ventilation projects across India. Backed by ISO 9001:2015, EMS 14001, and OHSAS 45001 certifications, we cater to R&D labs, pharma, chemical, biotech, institutional, and industrial clients with precision and safety at the core. Job Summary We are seeking a Costing and Estimation Engineer with 4 5 years of hands-on experience in HVAC and MEP projects. The ideal candidate must be able to independently handle cost estimation, quantity take-offs, pricing, and tendering processes. If you do not have relevant HVAC/MEP experience, please do not apply. Key Responsibilities BOQ & Cost Estimation Prepare accurate cost estimates for HVAC, electrical, plumbing, and fire-fighting systems based on project drawings and technical specifications. Conduct quantity take-offs for all MEP components from GFC/IFC drawings. Tender Review & Analysis Analyze tender documents, scope of work, and technical requirements. Identify cost-impacting factors and prepare a strategic response. Vendor & Subcontractor Management Float enquiries, obtain competitive quotes, and prepare comparative statements. Negotiate with vendors for pricing and delivery to ensure budget compliance. Rate Analysis & Cost Benchmarks Develop and maintain internal pricing databases. Perform unit rate analysis for labor, materials, and equipment across HVAC & MEP systems. 5. Variation & Change Order Management Assess cost implications of design changes, site instructions, and client-initiated changes. Prepare change order documentation and submit for approval. 6. Pre-Bid Engineering & Value Engineering Coordinate with design and technical teams for optimal cost-effective design options. Offer value engineering suggestions without compromising technical integrity. 7. Post-Bid Support Handle technical and commercial clarifications raised by clients during evaluation. Revise proposals based on negotiated changes and conditions. 8. Project Cost Monitoring Assist the project team in tracking actuals vs. estimated costs. Raise alerts for budget overruns and recommend corrective actions. 9. Contract & Procurement Support Draft subcontractor scopes and commercial terms in alignment with project estimates. Participate in vendor finalization discussions and procurement processes. 10. Client & Consultant Coordination Attend review meetings for cost-related discussions and design clarifications. Ensure alignment with consultant specifications and compliance needs. 11. Technical Proposal Documentation Prepare technical-commercial proposals, bid compliance documentation, and presentations for internal and client reviews. 12. Market Intelligence & Cost Optimization Monitor industry pricing trends and material fluctuations. Recommend cost-saving alternatives and strategic sourcing methods. Essential Skills & Qualifications Education B.E./B.Tech/M.Tech in Mechanical, Electrical, or Civil Engineering. Experience 6 8 years specifically in HVAC & MEP quantity surveying, estimation, and cost control. Technical Knowledge In-depth understanding of HVAC, electrical, and plumbing systems including ductwork, piping, chillers, AHUs, FCUs, pumps, VRF systems, etc. Contract & Cost Management Experience in contract drafting, billing, and subcontractor management with strong command over cost estimation and budgeting. Analytical & Documentation Skills Strong analytical mindset to assess cost trends, prepare reports, and support decision-making. Software Proficiency Hands-on experience with MS Excel (advanced), AutoCAD, and quantity takeoff/costing tools. Communication & Team Collaboration Ability to interact with engineers, site teams, vendors, and clients with professionalism and clarity. Ability to read and interpret technical drawings and specifications. Preferred Candidate Profile Must have site-level and office-level experience in MEP cost estimation. Should have worked in sectors like labs, pharma, healthcare, commercial, tech parks, institutional or industrial projects. Self-starter, result-oriented, with a strong attention to detail. Should be based in Bangalore or willing to relocate. Note Applications without HVAC or MEP field experience will not be considered. Please apply only if you meet the criteria.