22 job opportunities for cleaning validation in India updated today
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Sun PharmaRole & responsibilities Analytical Method Development & Validation. Assay, Related Substances, Dissolution cleaning validation analytical method transfer Preferred candidate profile B.Pharma / M.Sc with minimum 3 to 6 years experience in AMV, AMT, CV
USVRole & responsibilities Protocol & Reporting: Prepare, review, and execute Cleaning Validation Master Plans (CVMP), protocols, and summary reports. risk Assessment: Conduct Quality Risk Assessments (QRA) to identify hard-to-clean areas and determine re-validation frequencies. ross-functional
Apotex ResearchJob Description About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer heal
Job Description Description JOB DESCRIPTION The role is responsible for ensuring day-to-day compliance with global GMP (Good Manufacturing Practices) during manufacturing, packing, and dispensing activities at the site. The role provides on-floor quality assurance support, ensuring operations are pe
Job Description Job Description Process Validation Plan, execute, and document Process Validation (PV), Cleaning Validation (CV), and Re-validation for injectable products. Prepare and review validation protocols and reports (IQ, OQ, PQ). Equipment & Utility Validation Perform validation of: Aut
keybiz dashboards pvt ltdJob Description Hyderabad Save this job Upload File Key Responsibilities Execute and monitor validation activities for sterile injectable manufacturing processes. Prepare, review, and maintain validation protocols and reports. Perform qualification activities including: DQ, IQ, OQ, and PQ for equipm
Apotex ResearchJob Description About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer heal
Job Description Key Responsibilities Responsible for implementation of cGMP in the plant Responsible for following and ensuring GLP practices in the laboratories Responsible for preparation of STP, SOP & Specifications Responsible for handling of operations and calibrations of Instruments Respon
KeyBiz Dashboards Pvt LtdHyderabad Save this job Upload File Key Responsibilities Execute and monitor validation activities for sterile injectable manufacturing processes. Prepare, review, and maintain validation protocols and reports. Perform qualification activities including: DQ, IQ, OQ, and PQ for equipment and utilitie
Job Description Strategic and planning Support in compliance through various digitalization platform Functional Core Ensure good documentation practice Validation & Qualification of Machine and Equipment's Requalification of machine and equipment as per frequency Preparation and updating of site
Baxter Medical DevicesJob Description This is where your work makes a difference. At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delive
Job Description Job Title: Executive / Senior Executive – QA (DSQA) Department: Quality Assurance Experience: 2–9 Years Qualification: M.Sc / M.Pharm Location: Pune Job Purpose To ensure cGMP compliance at the shop floor for Drug Substance (DS) manufacturing through effective line clearance, documen
Job Description Be the First to Apply Job Description Manager - Quality AssuranceJob Description Candidate should have good communication skill Must have Regulatory Knowledge and audit handling exposure Must have working exposure of Cleaning Validation and respective work area's Must have sound know
JOB TITLE Assistant Manager- Quality Control, Chemistry REQUIREMENTS Education / Experience Post Graduate in Science (Organic or Analytical Chemistry ) 5 to 8 years in chemical & instrumental testing laboratory with exposure to GMP, GLP. Technical skills & Competencies / Language · Technical compete
Job Description Job Title : Senior Executive QA (DSQA) Department: Quality Assurance Experience: 6 to 9 Years Qualification: M.Sc / M.Pharm Job Purpose - To ensure cGMP compliance at the shop floor for Drug Substance (DS) manufacturing through effective line clearance, documentation review, in-proce
India, Hyderabad QA Qualification Specialist Location: Hyderabad, India Job Description Summary: As a QA Qualification Specialist, you will be responsible for supporting, reviewing, and approving qualification documentation for facilities, utilities, computerized systems, and equipment in accordance
the whole truth foodsJob Description Job Description: Process QA Lead Department: Quality Assurance Location: Andheri (Mumbai) | 6 Days Working Employment Type: Full-Time Reports To: Head of Quality Assurance Experience: 8–12 Years (Pharmaceutical / FMCG / Food & Beverage Manufacturing) Education: B.Sc / B.Tech / M.
Alkem LaboratoriesJob Description QUALITY COMPLIANCE AND SYSTEM: 1.1 Documentation 1.1.1 To ensure online documentation related to current good manufacturing practices (cGMP). 1.1.2 Continuous improvement and review for upgrading existing SOP's with respect to compliance to global standards. 1.2 Quality Management Sy
Start-To-Finish Solutions For Air Solutions For Water Solutions For Process Case Studies Projects Blog Function: Quality Assurance & Documentation Reports to: Assistant General Manager Location: Andheri (HO) Responsibilities FACILITIES, UTILITIES, PROCESSES, CLEANING AND EQUIPMENTS, DOCUMENTATION AN
Responsible for line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labelling, and packing. Responsible for Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per p
₹3,00,000 – ₹4,75,000per year
Estimation confidence: High
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