Average salary: Rs550,000 /yearly
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- ...About Sun Pharma: Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company... ...countries across the globe. Job Summary LIMS Testing & Documentation Specialist will be responsible for the thorough testing of LIMS...Suggested
- ...About Sun Pharma: Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the... ...Documentum D2 LSQM application, including custom workflows and document management solutions. • Collaborate with senior developers to...Suggested
- ...Title: Pharma / Scientific Recruiter Company: Rangam Consultants Inc. Location: Vadodara, Gujarat (100% On-Site) Shift: Night... ...high quality. Data Integrity: Maintain accurate documentation in our internal ATS/database. Required Skills & Qualifications...SuggestedPermanent employmentFull timeContract workWork at officeUS shiftShift workNight shift
- ...Description Pharma Product leader Requirements Position: Pharma Product Leader Must have domain: Pharma Business Analyst... ...Description Facilitate requirement-gathering sessions to document requirements in an Agile way Possess Good consulting and pre...SuggestedWork at office
- ...currently looking for an Engineering Project Manager, experienced in Pharma Sector ( freelancer ONLY ) to support our projects India.... ...to senior management and stakeholders. Overseeing project documentation, including protocols, reports, and regulatory submissions....SuggestedFull timeContract workFreelance
- ...setup time and changeover losses 3. Quality & Compliance (Pharma Focus) * Ensure compliance with GMP, GDP, ISO, and customer quality... ...* Control mix-ups, traceability, line clearance, and batch documentation * Coordinate with QA for in-process and final inspections *...SuggestedShift work
- Sun Pharma, we commit to helping you ' Create your own sunshine'— by fostering an environment where you grow at every step, take charge... .... Authorized to sign as a checker/verifier in following document, Finished product logbook etc. To prepare new BMR, revise...Suggested
- ...Job Description Manager - Production- Any work allocated by seniors. 1. To review Batch manufacturing record. 2. To prepare QMS documents and upload it in Track wise system. 3. To Handle Change control, SOP, incident, Deviation, and CAPA in Track wise. 4. To maintain the...Suggested
- ...Job Title: Assistant Manager – Production, Pharma Educational Qualification And Experience M. Pharm / B. Pharm from a reputed... ...compliance with GQS, HSE, and ISO guidelines/standards and maintaining documentation for the same, including process validation and qualification....SuggestedContract workFixed term contractShift work
- ...per the protocol. - Checks and cross-verify line clearance during Batch/Product changeover. - Maintains c-GMP practices along with documentation in various records. - To maintain good hygiene, safety practices and disciplines. - Fills in-process parameters/Reconciliation in...SuggestedFull timeImmediate startShift work
- ...Authoring/ reviewing of process/ QMS/ process part of regulatory filing documents. Participate and lead in cross-functional root cause analysis... ...M Tech in Biotech / Biochemical / Chemical or MSc Biotech / M Pharma A min of 8 years of relevant experience with Biopharma MSAT...Suggested
- ...department. Responsible for preparation & review of the master documents of production. Responsible for preparation and review of... ...& Team Leadership | Beginner Qualifications Education: B.Pharma, M.Pharma Total Experience - 15 - 18 Year in sterile manufacturing...Suggested
- ...quality standards. Coordinate with QA, QC, Engineering, and Warehouse departments for smooth production flow. Ensure proper documentation and compliance with USFDA, MHRA, and other regulatory guidelines. Train and guide operators and technicians on GMP practices and...Suggested
- Qualification: B.Pharma Experience: 5+ years Job Responsibilities Authorized to sign as a doer and verifier in: Batch Manufacturing... .... Authorized to sign as a checker/verifier in following document, Finished product logbook etc. To prepare new BMR, revise...Suggested
Rs 1 - 3 lakhs p.a.
...Job Title: Pharma Aid (Non-Pharmacist) Location: Kalyan Nagar, Bengaluru Experience: 0-5 years Qualification: Any qualification... ...ensure proper storage of medicines Handle billing and basic documentation Support in receiving and stocking new supplies Maintain...SuggestedShift work- ...Job Title: Apprentice Leader – Pharma Experience: 6–10 years Location: Bangalore (Onsite) Industry: Pharmaceutical / Biotechnology... ..., or PMDA. Experience in preparing and reviewing regulatory documentation, including CMC sections, clinical study reports, and safety...Long term contractFull time
- ...Job Description – Pharmacist / Pharma Aid Location: Stepcare Pharmacy, Whitefield, Bangalore Job Type: Full-time Experience... ..., dosage accuracy, and drug interactions. Maintain complete documentation and adherence to pharmacy laws and compliance standards....Full time
- ...planning while ensuring strong execution. SAP, Trackwise & Documentation Management Review and approve BMRs and BPRs in Trackwise.... ...coordination,crystallization,drying,api production,operations management,pharma,centrifuges,filtration,manufacturing,bprs,production targets,...Full timeShift work
- ...Regulatory Affairs Job Grade G12A Location Baroda At Sun Pharma, we commit to helping you 'Create your own sunshine'— by... ...maintain critical data records for regulatory audits. To prepare document for Technology Transfer like sheet II, Master Formula, Risk...
- At Sun Pharma, we commit to helping you ' Create your own sunshine'— by fostering an environment where you grow at every step, take charge... ...monitoring records, house keeping records and BPR and any GMP documents. Supervision and controlling of CPD First Floor (Block F)...Contract work
- ...Job Grade G12A / G12B Location : Vadodara At Sun Pharma, we commit to helping you 'Create your own sunshine'— by fostering... ...of Quality processes in application. To perform QMS & Documentation activities related to system/application (i.e. Change control,...
Rs 6 - 10 lakhs p.a.
...laboratory associates Write, review and/or approve analytical documentation in timely and high-quality manner, such as releases, analytical... ...chemistry or equivalent and a minimum 6 years experience or M. Pharma/M. Sc with a minimum of 12 years experience in the...Work at office- ...Supervises the line operations and participate in Validation activities as per the protocol. Maintains c-GMP practices along with documentations in various records. Fills and checks BMR / BPR before submission to the superiors. Handles minor parametric setting issues...Full timeImmediate startShift work
- ...Pharmaceutical Quality Assurance (QA) role ensures drug products meet safety, efficacy, and regulatory standards by overseeing documentation, processes, audits, and batch release, focusing on building quality into manufacturing (cGMP) through activities like SOP review,...
- ...Regulatory Affairs Job Grade G12A Location Baroda At Sun Pharma, we commit to helping you ' Create your own sunshine '— by... ...-up & Exhibit batches – Troubleshooting & Technology transfer Documentation i.e. Master Formula Record, Stability Protocol & Development P...
- ...Import & Export function especially in the field of medical device/Pharma industries. Manage import & export forwarding shipments from... ...Shipment, and Shipment clearance under Bond with 100% complied document management. Manage documentation recording for Exim return...
- ...and operators of the department. 10 To follow the cGMP, Good Document Practice and discipline in the department. 11 Responsible for... ...packing, and inspection. Qualifications Education: B.Sc., B.Pharma, M.Sc., M.Pharma Total Experience - 2 - 7 Year in sterile manufacturing...
- At Sun Pharma, we commit to helping you ' Create your own sunshine'— by fostering an environment where you grow at every step, take charge... ...She/he is authorize to sign (as a doer): Engineering GMP documents Break down/Preventive maintenance report. Incident and Investigation...
- ...Regulatory Affairs Job Grade G12A Location Baroda At Sun Pharma, we commit to helping you 'Create your own sunshine'— by... ...interpretation using MINITAB software. To prepare Technology Transfer documents like MF, Risk Assessment based upon CPP & CQA, To prepare...
- ...Title of Position ~ Executive – Warehouse, Pharma Basic & Minimum Qualification ~ Graduate in Science / Commerce... ...done on time to time. Carry out day-to-day maintenance of GMP documents/logbooks and formats as applicable. Statutory Compliances...
