3773 Pharma Jobs - Page 50

About the role QSC- Quality Supply Chain is a core function of Haleon manufacturing and supply chain. Under QSC there are 24 manufacturing sites integrated within BUs and regions which allows far more flexibility and faster response to local needs. QSC HQ team supports the Global Quality, Category & Technical, EHS & Engineering, Strategy Leadership Teams and have global P&L ownership for entire QSC central functions. Role of QSC HQ Team is critically important in supporting large-scale global innovation, technical and digital activities, and other opportunities to leverage scale where cross BU decision making is required. It will also set the standards and build capability in quality, health, safety and wellbeing, engineering, and manufacturing excellence, and drive longer term strategy. MUST HAVES Cost Accounting/ Chartered Accountant or similar Analyse the Data and create reports and Dashboard, Check/analyse Data. Reconcile and Validate the Data The QSC Senior Finance Manager Role is to provide Financial & System support to the QSC HQ team and ensure the Data quality & system compliance. This role provides key financials, analytical support and reporting responsibilities to ensure smooth closing of the financial books. Scope includes accounting, analysis and reporting as well as finance governance of ad-hoc projects (Business cases, Capital project, etc.) Global QSC HQ team is composed of team members spread across the globe, it is therefore spread between many different legal entities and cost centres resulting in crucial alignment with finance & non-finance stakeholders across the globe. This role has key elements to empower senior finance team and business leaders for decision making on P&L, Cashflow and BS by creating reporting dashboards and ensuring quality analytics and insights into the financial numbers. Reporting and updates of non-Core cost (OE & NCI) link to synergies & Network Key responsibilities Create enhanced QSC Reports & Dashboards to support CSO & CFO QSC Reporting requirements P/L & B/S consolidation monthly for the QSC HQ Team Provide support to aid the review of actuals vs. budget and investigated major variances. COGS & Supply Chain reporting / Main Power-Bi support for the QSC team Provide system support to analysis & review Actuals, CMF, Plan (LRP & ABP) in ONEPLAN, SIERA & Bison and provide monthly, QTD & YTD variances and support commentary, investigate, and fix the reconciling items. Monthly reconciliation of EGOLS from finance reporting system (Bison) and ensure corrections done wherever needed. Follow up with QSC Site Siera & ONEPLAN submission and ensure Siera/ONEPLAN ties to Bison. Support Journal postings in Bison & Data loads from Siera & ONEPLAN. CAPEX reporting and follow ups to ensure timely capitalisation and review of the CAPEX spend. Other Responsibilities for ad hoc requests Qualifications and skills Essential Degree and/or internally recognized accounting or professional finance qualification University degree in business/finance. Working knowledge of multiple systems apps e.g. SAP, Bison, ONEPLAN, SIERA and strong understanding of reporting tools: SAC, Lumira, AO, Power-BI, Qlik Good working knowledge of Power-Bi, and good communication skills to drive the Power-Bi reporting suite. Prior supply chain experience required while Pharma, FMCG, industry experience is preferable. Able to effectively manage time against agreed deadlines for activities for both self & matrix team Advanced financial analysis skills Curious, self-starter, proactive, pragmatic, and dynamic .

MAIN PURPOSE OF 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) Experience/Background Experience Experience Details No Experience #LI-DNI LOCATION: India > Chennai : Padmini Building t

Asst. Business Manager OR Business Manager for Bangalore Post: Asst. Business Manager OR Business Manager Qualification: Biotechnology/Microbiology or equivalent in any bioscience stream. Masters with MBA will be preferred. Nature of experience : Must be having experience in Research institutes and Biotechnology sectors. Job Description: Complete coverage of the assigned territory Candidate has to cover Research Institutes, industries, pharma, diagnostic centers, hospitals etc. To promote product ranges of high technology such as PCR, Gel Electrophoresis units, Gel Doc Systems, Centrifuges and knowledge about Laboratory Chemicals and Plasticwares. day to day field visit - meeting customers and distributors to fulfill the assigned target. To keep an eye on business potential - thru personal visit, tender bulletins, GEM enquiries. To extend distributor network and customer segment. To make sure Product wise target achievement Experience: 2-5 years SKILLS: Individual must be having good marketing and technical knowledge. To manage distributor networks, existing customers and finding new avenues Good communication, verbal and written. Well versed with Product technicalities in the segments of Plasticwares, chemicals and instruments, excellent command on online tools - excel, word, power point.

Manage Sales & Business Dev of Pharma Excipients/API business in assigned territory. Identify new customers & businesses opportunities. Make product presentations to customers. Resolve customer complaints & queries, follow up for timely payments Required Candidate profile Looking for Candidate with excellent communication skill along with pleasant personality. Min 7 years experience in sales of Pharma Excipients. Should have good contacts in pharma industry/companies.

Responsible for driving exponential growth in food ingredients in large enterprise accounts and PAN India Identify market trends & developing strategies Data analysis Manage and drive applications for products. Required Candidate profile Min 8 years of exp in Sales and Marketing role of Specialty Chemicals , food Ingredients segment Good Communication skills

Manage Key accounts for Pharma Excipients in Maharashtra/Nepal/Sri Lanka/Bangladesh. Identify new customers & businesses opportunities. Make product presentations to customers. Resolve customer complaints & queries, follow up for timely payments Required Candidate profile Looking for B.Pharma/M.Pharma Candidates with good technical knowledge and excellent communication skills. Minimum 5 years experience in techno commercial role in Pharma Excipients.

Overseeing production planning ensuring optimal capacity utilization, HSE compliance, coordinating with various departments , adhering to SOP made by QA /QC dept.Manpower, Capacity & Plant Occupancy Calculation. Monitor SAP WIP & HAZOP study. Required Candidate profile 15+yrs of exp in this role with major in operations Must be a B.Tech (Chemical only) Hands on exp on ESH ,Audits overseeing large teams of more than 500 employees Specialty Chemical Exp No job changes

ROLE SUMMARY In Pfizer Digital Research & Development, we work with our R&D partners to accelerate drug development and clinical trials through digital products and solutions. Within Digital R&D, the Veeva Platform & Services function is responsible for defining the strategy and leading the delivery of the Veeva product suite to end users of Veeva products within Digital R&D. This includes the operation, implementation, and integration of Veeva platform solutions that address R&D business processes effectively. Veeva solutions include Regulatory - RIM (Registrations, Submissions, and Publishing), Clinical (CTMS, eTMF, Study Start Up, and Site Connect), and Quality (QMS and Quality Docs). Your role as a Veeva Run Operations Associate involves contributing to the delivery of seamless operational support, system implementation, and system maintenance activities to support the ongoing operations of implementing the Veeva Platform across Pfizer s global business units. The Veeva Run Operations team is expected to develop, implement, and manage the technical support framework to provide timely, high-quality, value-added services to enhance user productivity. ROLE RESPONSIBILITIES Apply fundamental knowledge of technology principles, concepts, and theories to drive improvements in the implementation and operation of the Veeva platform. Manage day-to-day system activities, including business support & incident management by using knowledge of internal/external business challenges and established guidance. Resolve system development and/or maintenance activity issues and risks, escalating them as needed. Develop, test, and implement Veeva system enhancements Partner closely with business teams to implement changes, manage project plans, and drive operational improvements in our production systems. Learn and apply industry knowledge and build understanding of business processes to deliver robust technology support for Veeva systems. Leverage existing information and contribute to stakeholder engagement and communication. Participate in knowledge-sharing activities with others within team through existing knowledge sharing processes/systems. BASIC QUALIFICATIONS HS Diploma (or Equivalent) and 6 years of relevant experience OR an associates degree with 4 years of experience OR a bachelors degree with 0+ years of experience in Computer Science, Software Engineering, or a related technical field. Service delivery experience, preferably in pharmaceutical industry Technical support and operations management experience participating in robust, cost-effective, high-quality services for external and internal customers. Participating in cross-functionals teams including business subject matter experts, technical experts and compliance teams for project execution. Good knowledge of analytics, quantitative and problem-solving skills to drive decisions for optimized solutioning. Knowledge of stakeholder management, facilitation, influencing and negotiation skills. Strong working knowledge on MS Tools - Project, Word, PowerPoint, Excel. Information & Business Tech #LI-PFE

ROLE SUMMARY In Pfizer Digital Research & Development, we work with our R&D partners to accelerate drug development and clinical trials through digital products and solutions. Within Digital R&D, the Veeva Platform & Services function is responsible for defining the strategy and leading the delivery of the Veeva product suite to end users of Veeva products within Digital R&D. This includes the operation, implementation, and integration of Veeva platform solutions that address R&D business processes effectively. Veeva solutions include Regulatory - RIM (Registrations, Submissions, and Publishing), Clinical (CTMS, eTMF, Study Start Up, and Site Connect), and Quality (QMS and Quality Docs). Your role as Veeva Release Analyst involves working with a team of release managers/operations associates to plan, schedule, and manage software releases for Veeva platform solutions. To excel in this role, you should have a combination of strong technical background, people management skills, exceptional organizational skills, and the ability to collaborate effectively with cross-functional teams. ROLE RESPONSIBILITIES Participate in the planning, execution, and delivery of software releases, ensuring the smooth deployment of products and services to R&D stakeholders. Support release activities, including version control, feature branching, code merges, and deployment Develop release plans, progress, and status updates to stakeholders Manage day-to-day system activities and mitigate risks mitigate risks related to the release process, including addressing potential bottlenecks Prepare necessary documentation, release notes, and communication materials for each release Participate in post-release activities, such as issue tracking, bug fixes, and customer support BASIC QUALIFICATIONS HS Diploma (or Equivalent) and 6 years of relevant experience OR an associates degree with 4 years of experience OR a bachelors degree with 0+ years of experience in Computer Science, Software Engineering, or a related technical field. Service delivery experience, preferably in pharmaceutical industry Technical support and operations management experience participating in robust, cost-effective, high-quality services for external and internal customers. Participating in cross-functionals teams including business subject matter experts, technical experts and compliance teams for project execution. Good knowledge of analytics, quantitative and problem-solving skills to drive decisions for optimized solutioning. Knowledge of stakeholder management, facilitation, influencing and negotiation skills. Strong working knowledge on MS Tools - Project, Word, PowerPoint, Excel. Information & Business Tech #LI-PFE

VSM Software (P) Ltd is an ISO certified company catering to the global needs of Pharma and Banking industries. In both these verticals, we offer solutions and services in specific areas. VSM has Strong founding team based in India and the US A great leadership team who come with high levels of educational qualifications and relevant industry experience Skilled and trained IT and Subject Matter professionals We have a local presence in 5 countries and are further expanding our delivery reach. About the team The team is responsible for managing servers, networks, system backups, endpoint security, user support, and more. We support both in-house and remote operations, troubleshoot technical issues, ensure data integrity, and maintain business continuity. Responsibilities: Manage and monitor all installed systems and infrastructure. Install, configure, test, and maintain operating systems, application software, and system management tools. Ensure the highest levels of systems and infrastructure availability. Periodic preventive maintenance to be carried out. Troubleshoot hardware and software issues across desktop, server, and network environments. Administer user accounts, permissions, and access rights in Active Directory and related systems. Maintain backup, disaster recovery, and cybersecurity strategies. Monitor and test application performance for potential bottlenecks, identify possible solutions, and work with developers to implement fixes. Provide Level 1 and Level 2 support to internal users and escalate issues when needed. Maintain inventory of all hardware and software resources. Vendor Management with proper evaluation of the quality of the services being provided Cost Management. Stay current with the latest IT trends, technologies, and best practices. Document internal procedures and support manuals.

Regulatory Affairs Specialist II Job Details | Teva Pharmaceuticals Find a Career With Purpose at Teva Search by Postal Code Area of Interest Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: Regulatory Affairs Specialist II Jul 4, 2025 Navi Mumbai, India, 400706 Who we are The opportunity The Regulatory Affairs Specialist is a project manager, (PM) responsible for the RA lifecycle management on Medis dossiers for Teva s 3rd party client business (Medis), ensuring information flow and provision of supportive documents reaches the clients The PM is responsible for liaison with Teva s 3rd party client business (Medis) supply chain, Teva site RA and other relevant functions How you ll spend your day Lifecycle management on specific products for Europe and international market Responsible at all times that regulatory modules under Product Manager responsibility are up to date, in accordance with agreed procedure as applicable Inform, prepare and submit variations either directly to authorities or to Teva s 3rd party client business (Medis) Follow up on variation submissions, timelines and approvals, in accordance with agreed procedure as applicable Compile answers to any deficiency questions from authorities or clients Ensure outcomes of variations are communicated in timely manner and databases/lists are up to date at all times, in accordance with agreed procedure as applicable Regular status updates to management Goal setting and follow up together with his/her supervisor Professional communications with both internal and external stakeholders Work on other specialised projects as defined by managers of RA Your experience and qualifications M Pharm/ MSc: 0-1 years of experience in RA Good organisation skills Good communication and presentation skills Good written and verbal knowledge in English Strategic thinking and flexibility to adapt to changes Good team player Good computer skills Proactive way of working and able to work independently Reports To Group leader regulatory affairs Teva s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Tevas global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Finance Operation Admin I Job Details | Teva Pharmaceuticals Find a Career With Purpose at Teva Search by Postal Code Area of Interest Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: Finance Operation Admin I Jul 3, 2025 Bangalore, India, 560064 Who we are Finance Operation Admin I This section is where we attract the attention of potential candidates and sell the role. How has the role come aboutWhat makes it appealingWhat are the key responsibilitiesHow is the role better with Teva than with another companyWherever possible, we should bring through the essence of our EVP pillars, i. e. , we care, we re in it together, and we make work fulfilling. How you ll spend your day Manage and process Accounts payable transactions. Invoices processed in timely manner Manage the payment proposal creation and payment disbursement of scheduled payments timely Manage urgent payment requests on a timely basis Adhere to Internal controls prerequisite and ensure all approvals/ supporting are suitably documented Ensure compliance with company policies and procedures Create Payment batch for H2H payments processing. Collaborate with Treasury on payment cash flow forecasts required and to resolve payment issues Contribute to process improvements to improve process efficiency and drive automation Manage failed payments/ rejections Respond to Generic mailbox inquiries within the agreed Turnaround Time Positively and creatively influence change and champion mission critical change initiatives Participating in internal control testing and prepares documentation Prepare ad-hoc & operational reports, manage analytics & management reporting Support Accounts payable and periodic book close activities on time as per the close calendar Prepare an effective SOP to outline the procedure & scope in the prescribed template. Perform periodically review and sign off Your experience and qualifications Bachelor s/ Master s degree in Accounting 0-1 years of working experience in Accounts payable Invoice processing and payment disbursements Excellent written and verbal communication SAP Enterprise knowledge with FICO and MM modules High level of attention to detail Good working experience in SAP workflow, Readsoft and Vendor portal Advanced Microsoft Excel skills, proficiency in MS office (PPT, VBA preferred) Good interpersonal skills to establish and maintain effective working relationships with a diverse population; ability to interact professional and courteously. Detail-oriented with the ability to manage multiple tasks simultaneously Flexible and adaptable to change, with the ability to work under pressure to meet deadlines in a fast-paced office environment . Enjoy a more rewarding choice Make a difference with Teva Pharmaceuticals Already Working @TEVA The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Tevas global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Role: Lead Maintenance Engineer Job Location: Bangalore Department: Engineering & Maintenance About Syngene: Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation. Job Purpose: Leading EAM team & activities at SU3. Execute maintenance and Upgradation projects. Ensures Safety & GMP compliance at SU3. Common Responsibilities: Responsible for EAM activities in the Biologics Operations Unit Ensuring all assigned mandatory trainings related to data integrity, health and safety measures are completed on time. Develop and contribute to development of procedures, practices and setup that ensures safety operations compliant to company and regulatory norms. Specific Responsibilities: Leading engineering and maintenance team for GMP areas at Biologics Manufacturing and Biologics Process Development. Able to handle minor project, design review and execute and Facility modification in a GMP facility. Exposure in handling Process, Electrical, HVAC, Utilities and instrumentation teams. Ensuring the related facility, equipment and maintenance systems are in GMP compliance state. Adherence to established procedures and policies of the company on Quality and Safety, ensuring the team adheres the same. Responsible for managing maintenance activities within framework of Quality management systems. Ensuring work management through defined SOP s, Change control, deviations and CAPA, review and approval through Trackwise and EDMS. Represent the function during audits and ensuring agreed actions are acted upon timely. Ensure followings are complying: o Equipment master list, Preventive Maintenance and calibration planners are prepared timely. o Preventive maintenance and Calibration of equipment and facility are executed as per the planner. o Qualification of equipment and facility and area validation for GMP blocks as per schedule. o Operations and maintenance of Utilities to enable operations o Service contracts for equipment and Instruments are planned and executed. Ensure that team comprising of on-roll engineers and contract manpower are trained on GMP requirements. Evaluation, assessment and selection of vendors for providing services for maintenance, calibration and validation Overall maintenance management that includes handling unscheduled breakdowns and other general upkeep activities are as per requirement to enable operations. Identifying and maintaining Inventory of equipment spares required for maintaining continuous operations. Reviewing and analysing the energy and utility consumption like electricity units, water etc. and take measures for control. Implementing the energy saving initiatives. Facility design, detail engineering and execution of any new requirements for business growth. Preparing and presenting the MIS reports Maintaining and improving departmental operational performance, to meet the requirements of regulatory authorities, company procedures, internal and external customers with respect to quality, service, lead time and cost. Good exposure in Regulatory audit handling. Educational Qualification: BE/BTech in Mechanical or Electirical or Instrumentation. Technical/functional Skills: Responsible for EAM activities in the Biologics Operations Unit Ensuring all assigned mandatory trainings related to data integrity, health and safety measures are completed on time. Develop and contribute to development of procedures, practices and setup that ensures safety operations compliant to company and regulatory norms. Leading engineering and maintenance team for GMP areas at Biologics Manufacturing and Biologics Process Development. Able to handle minor project, design review and execute and Facility modification in a GMP facility. Ensuring the related facility, equipment and maintenance systems are in GMP compliance state. Experience: 15 years or above within Biologics manufacturing plant, with at-least 6-7 years of experience in Leading Engineering team, Projects & Maintenance. Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, colour, 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.

JOB DESCRIPTION Designation: Associate Scientist Job Location: Bangalore Department: DDS About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation. Key Responsibilities: Perform synthetic chemistry reactions, reaction workups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab equipmentEnsure 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 shipmentRecord 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. Ensure that the instrument / equipment s are calibrated, undergone preventive maintenance, and are kept clean before use and in case of any breakdown, report to maintenance immediatelyEnsure that they know the MSDS 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 normsAttend all mandatory trainings and update training records as and when trainings are completedAlways ensure confidentialityPrepare SOPs/IOPs/EOPs/OCPs when any new lab activity is identified or existing one requires updatingAny other lab responsibilities as indicated by the EHSQ team member/ supervisor / group leader. Understanding and demonstrating responsibility for safety of self & colleagues by following all safety protocols provided by SyngeneAdherence to all environment, health, and safety (EHS) policies & standards always in the workplaceWearing all PPE as required. Adherence to all procedures related to Syngene s data integrity policiesCompliance to Syngene s quality standards at all times. For running independent project(s) in the areas of immuno-oncologyFor driving the assigned project with full commitment, To champion the biology of project, establish all assays, models required to drive the project and work in collaboration with team members within the domain, across different domains and across departmentTo take active participation in running experiments, compiling the data in required format and prepare study reportsTo train and mentor other scientists in a timely mannerTo work in a collaborative fashion with research scientists from various disciplines Educational Qualification: MSc (Chemical Sciences). Experience: 5 - 8 Years Required Skills: Should be familiar with concepts of chemical synthesisFamiliar with operations of relevant apparatus - instrument / equipment. Good Knowledge of analytical techniques and analytical data interpretation. Good communication skills Behavioral Skills: Good communication skills, good presentation skills, hardworking, sincere and a team player. Must demonstrate integrity and take accountability of their work 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 about 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.

Job Role: Discovery Chemistry Scientist Job location: Bangalore Job grade: 7-II/6-I 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 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 Key Responsibilities: Supervise the subordinates for timely completion of assigned projects. Responsible for periodic reports updating to both internal and external clients Ensure the optimum resource utilization and cost efficiency Responsible for project planning and execution Ensure the implementation of regulatory compliances Troubleshoot the problem areas of project(s) Responsible for clear individual derivable Possess the knowledge and exposure to environment, health, and safety (EHS) practices Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety Attend training on environment, health, and safety (EHS) measures imparted company Behavioral Skills: Strong commitment to exceptional customer experience, and a high level of dedication Excellent speaking-listening-writing skills, attention to details, proactive self-starter Ability to work successfully in a dynamic, ambiguous environment. Ability to meet tight deadlines and prioritize workloads. Ability to develop new ideas and creative solutions. Exceptional influencing and leadership skills. Enthusiasm, motivation, and persuasive ability in a team and cross-functional environment. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience: 2-8 years Education: Ph. D in organic chemistry / Medicinal chemistry from reputed universities in India / abroad. Skills and Capabilities: Candidate should have a experience in drug discovery from pharmaceutical or biotech industry. Excellent understanding of the concepts of drug discovery, preferably having prior experience of progressing a project from hit identification to lead optimization. Has prior experience working with a cross-functional team, comprising assay biologists, Structural biologists, DMPK scientists, computational chemists, and safety pharmacologists. Familiarity with molecular modelling concepts and tools is desirable. Strong knowledge of data analysis (SAR/SPR) and informatics tools. Familiarity with cGMP and regulatory knowledge. Strong Client communication and presentation skills. Extensive knowledge and experience in synthesis planning, synthetic methods and use of modern chromatographic and analytical tools. Behavioral / Managerial skills: Proven ability to lead and motivate the teams. Excellent written and verbal communication skills. A team player / works well in multi-discipline teams Builds strong plans to provide clarity for others, and utilizes time management tools and capabilities. Equal Opportunity Employer: It s 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.

JOB DESCRIPTION Designation: Executive Job Location: Bangalore Department: EAM About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation . Job Purpose This role focuses on the engineering and maintenance of formulation injectable and OSD facility systems, supporting the engineering team in optimizing performance and enhancing organizational competency while adhering to delivery, quality, and safety standards. Responsibilities include ensuring the timely resolution of equipment breakdowns, analyzing instrument failures, and reviewing PLC and SCADA systems to ensure the seamless operation of manufacturing equipment and systems. Key Responsibilities: Ensure functionality of automation related to process and equipment s, which are installed in Formulation units (OSD tablet and Capsule facility). Preventive and Breakdown maintenance of Compression machine, FBE, Auto coater, Blenders, Shifter, RMG. Preventive maintenance and Breakdown of HMI and PLS systems Adherence to Standard Operating procedures, Safety, cGMP, QMS & EHS Requirements. Co-ordination with OEM for required automation and instrument issues. Educational Qualification: BE in Electronics and instrumentation engineering (EIE) Technical/functional Skills: Proficiency in programming languages PLC programming & HMI Programming. Hands-on experience with SCADA, DCS, and other industrial control systems. Knowledge of sensors, actuators, signal processing, and control theory. Familiarity with relevant standards like IEC, ISA, or ISO. Experience: 4-6 years in Formulation or Injectable Facility. Behavioral Skills: Strong problem-solving and analytical abilities. Excellent communication and teamwork skills. Ability to manage multiple projects and meet deadlines. Equal Opportunity Employer: .

JOB DESCRIPTION Designation: AQA Reviewer Job Location: Bangalore Department: Analytical Quality Assurance About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation . 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 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 Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Job Purpose: To review the data & reports generated from GMP Laboratory (Stability) and to monitor the GMP Lab compliance. Key responsibilities: 1) Online Sequence & Document review in HPLC, GC, KF, PXRD, ICPMS, LCMS & other all analytical instruments. (CD & FC - Intermediate, FP & Stability) 2) Offline Raw Data review in ELN (CD & FC - IPQC, Intermediate, FP & Stability) and release of IPQC TI sheets in 24/7 3) Daily verification data review, PM reports and Lamp intensity report review in ELN. 4) Compiled Report review (CD & FC - IPQC, Intermediate, FP & Stability). 5) Calibration sequence, data review of HPLC (S17) and release of instrument. Raw material data review and release in LIMS & SAP. 6) Reconciliation of EDMS issued prints (formats). 7) Audit trial review of Standalone systems and chromeleon application. 8) Monthly Date & Time verification of approximately 20 standalone instruments. 9) Review of analytical raw data generated by analyst, protocols/ reports pertaining to the section as per the standard operating procedure and specification. 10) Ensuring, verifying and reviewing the instrument usage log periodically and accordingly checking the labels as per SOP. 11) Review of Outsourced analytical report. 12) Review of logbooks with respect to all activity performed in the lab. 13) Responsible for taking any other job allocated by Department Head / Department In charge. 14) Review of technical data in analytical document viz. Calculations, Chromatograms, method parameters, integration, logbook entries, WS/RS and Column usage records, method parameters, reconciliation, vendor COA and other technical data in analytical document. 15) Reviewer shall ensure the documents physically for availability of all the pages of ODS and supporting documents. 16) Review the documents for completeness, compliance to Good documentation practices, test results against specification limits or acceptance criteria as mentioned in protocol and reconciliation of forms issued as applicable 17) In case of any discrepancy, immediately notify to the reporting manager or his designee or Head or designee GMP Analytical Laboratory. 18) Ensuring of conducting regular GMP rounds at Quality Control Laboratory. Educational Qualification: M. Sc. Chemistry or Analytical or equivalent Technical/functional Skills: The candidate should possess good communication, leadership and technical skills in Laboratory instruments like HPLC, GC, GCMS, LCMS, PXRD, KF etc. , . He / she should have working knowledge in quality, conducting investigations and quality management systems. He / she should have experience in review of data generated from QC team of QA professional. Experience: 4 to 8 years Equal Opportunity Employer: .

JOB DESCRIPTION Designation: AQA Reviewer Job Location: Bangalore Department: Quality Assurance About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation . 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 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 Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Job Purpose: To review the data & reports generated from GMP Laboratory (Stability) and to monitor the GMP Lab compliance. Key responsibilities: Review of analytical raw data generated by analyst, protocols/ reports pertaining to the section as per the standard operating procedure and specification. Ensuring, verifying and reviewing the instrument usage log periodically and accordingly checking the labels as per SOP. Review of Outsourced analytical report Review of logbooks with respect to all activity performed in the lab. Responsible for taking any other job allocated by Department Head / Department In charge. Review of technical data in analytical document viz. Calculations, Chromatograms, method parameters, integration, logbook entries, WS/RS and Column usage records, method parameters, reconciliation, vendor COA and other technical data in analytical document Reviewer shall ensure the documents physically for availability of all the pages of ODS and supporting documents. Review the documents for completeness, compliance to Good documentation practices, test results against specification limits or acceptance criteria as mentioned in protocol and reconciliation of forms issued as applicable Review of all the tests as specified in the specification/Request for analysis /validation protocol/sampling protocol have been carried out Review of all supporting documents like chromatograms, balance print outs, Instrument printouts are enclosed in sequential manner to the parent report with signature as applicable Responsible to ensure review and approval of analytical calibration reports and Review of method validation protocol and method transfer protocols. Review of the test results in COA against specification along with other relevant sample information before approval. In case of any discrepancy, immediately notify to the reporting manager or his designee or Head or designee GMP Analytical Laboratory. Ensuring of conducting regular GMP rounds at Quality Control Laboratory. Educational Qualification: M. Sc. Technical/functional Skills: The candidate should possess good communication, leadership and technical skills. He / she should have working knowledge in quality, conducting investigations and quality management systems. He / she should have experience in review of data generated from QC team of QA professional. Experience: 9 to 12 years Equal Opportunity Employer: .

Hire, train, and manage Financial advisors to generate business Guide advisors in achieving sales goals Monitor and report advisor performance Builds long-term client relationships and ensures satisfaction Required Candidate profile 2+ years of experience in field sales Bachelor’s degree in any stream Having Good Local network and Own vehicle Good Communication and presentation skill Call : 78620 87265 | Rupa Perks and benefits Speedy Growth Attractive incentive structure

Requirement for B.sc/Msc Chemistry, BioChem, Microbilogy, Dip/BE/Btech Chem/Petro/Biotechnology / Bpharm / Mpharm Location - Chennai/Kovai/Cuddalore/Pondy Field - Pharma/Water Treatment/Paint/Chemical Industry Designation - QC / P Chemist /Lab Asst

Exciting Opportunity at India's Fastest-Growing Medical Devices Company Meril at Telangana. Meril is a global leader with 14,000+ employees and a presence in 150+ countries. We are hiring District Managers in Telangana to represent all Meril businesses in their district. If you are willing to commit for long term and are from Asifabad, Bhadradri Kothagudem, Jagtial, Jangaon, Jayashankar Bhupalapally, Jogulamba Gadwal, Kamareddy, Karimnagar, Khammam, Mahabubabad, Mahabubnagar, Mancherial, Medak, Medchal-Malkajgiri, Mulugu, Nagarkurnool, Nalgonda, Narayanpet, Nirmal, Nizamabad, Peddapalli, Rajanna Sircilla, Ranga Reddy, Sangareddy, Siddipet, Suryapet, Vikarabad, Wanaparthy, Warangal, and Yadadri Bhuvanagiri. If you have a long term vision and want to make a career within your own district, this is your chance to get in medical devices industry Who can apply? 3-7 years of Pharma/Surgical experience Local candidate with a stable career history (minimal job hops) Strong sales & relationship-building skills CTC: 4 to 6 LPA, Based on experience & performance in the interview. Interested? Send your CV to akshay.revankar@merillife.com Be a part of Indias revolutionary healthcare journey with Meril!

Recruit a team of advisors Generate business through the team Lead the team of advisors Motivate them to achieve targets Provide training and guidance to them Directly Company payroll Required Candidate profile Experience: 2+ years in Any Field Sales Graduation Complete Local candidate Product Knowledge

India's Leading Company is looking for a Sales Executive Develop a sales strategy to achieve organizational sales goals and revenues. Built Potential Sales Team & Train Them. Set individual sales targets with the sales team. Required Candidate profile Graduation is required Must have 1+ years of experience in any Sales, Banking, finance/insurance sector. Good Communication skills Location : All Imp City of West Bengal

Talk to customers, explain products, and solve doubts. Use company leads and get more through referrals. Follow up with leads and close sales on time. Keep records of calls, leads, and sales. Meet targets and support your team if needed. Required Candidate profile Graduate in any field. 2+ years of sales experience (BFSI exp is a plus) Good communication &convincing skills Local candidates preferred. Goal-oriented & self-motivated Kevisha Lathiya | 88490 20556

Education : Any Degree in safety Location:- Umargam Male candidates consider. Note:- Candidate must have experience in Safety department with manufacturing Industry. Call on +91 9033020100 Required Candidate profile Thanks Ms. Bharti +91 9033020100 (Call & Whatsapp) hr.mgr@creativehr.in Creative HR Services Visit Us on: SA-05, Solitaire Business Centre, GIDC Char Rasta, Vapi.