Process Validation Jobs

Post: Supplier Quality Engineer / Senior EngineerJob Location: FaridabadCompany: Aktive Technologies Pvt. Ltd.Support regulatory compliance related to ISO 13485, MDR, and customer-specific requirements.Required Candidate profileEnsuring all supplied materials, components, and services meet Aktiv Technologies quality, compliance, and regulatory standards.Experience with medical devices, automotive, aerospace industry.

Job Opening: Quality Assurance (QA) Officer with IPQA ResponsibilitiesLocation: On-site Nalagarh, Himachal PradeshExperience: 3+ years mandatory experienceQualification: B. Pharm / M. PharmLanguage & Software Skills: Proficiency in English and Microsoft Office (Word, Excel, PowerPoint) MandatoryAbout the Role:We are hiring a knowledgeable and proactive Quality Assurance (QA) Officer to join our pharmaceutical manufacturing unit in Nalagarh. This role combines core QA responsibilities with In-Process Quality Assurance (IPQA) oversight on the production floor. The ideal candidate will ensure regulatory compliance, documentation accuracy, and continuous quality improvement throughout the production lifecycle.Key Responsibilities: Core QA Functions:Review and approve Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).Manage deviations, validations (mandatory), change controls, CAPAs, and maintain documentation as per regulatory norms.Conduct internal quality audits and assist in external audits by clients or regulatory agencies.Maintain and update SOPs, manuals, and master documents in accordance with current regulations.Oversee document control systems and archival processes.Train employees on cGMP practices and quality systems.In-Process QA (IPQA) Responsibilities:Monitor critical stages of manufacturing and packing operations to ensure GMP compliance.Line clearance before batch start-up and between changeovers.Sampling of in-process materials and verification of critical process parameters.Real-time review and recording of BMR/BPR entries during production.Ensure proper gowning, hygiene, and sanitation compliance on the shop floor.Immediate reporting and documentation of any deviation or non-conformance observed.Desired Profile:B. Pharm / M. Pharm with a strong academic and technical background.Minimum 3 years of QA experience in a regulated pharmaceutical manufacturing unit.Hands-on experience with IPQA activities and on-floor quality monitoring.Excellent written and spoken English communication skills MandatoryProficiency in Microsoft Office (Word, Excel, PowerPoint) MandatoryGood understanding of WHO-GMP, Schedule M, and other applicable quality regulations.Strong coordination skills, attention to detail, and documentation accuracy.Join a team committed to delivering excellence through quality-first manufacturing.If you're passionate about compliance, process integrity, and hands-on QA work we invite you to apply!#QualityAssurance #IPQA #PharmaJobs #QAOfficer #BPharmJobs #MPharmJobs #PharmaCareers #GMPCompliance #NalagarhJobs #QualityFirst #IndianPharma #HimachalPharmaJobs #AuditReady

Senior Quality Assurance OfficerExecutive: (Vapi) Job Location: VapiQualification: M.Sc. (Chemistry) or B.Pharm or M.Pharm. Experience: 5 to 7 years experience in a Cosmetic/API/Pharmaceutical Product manufacturing company. He has to review and prepare SOPs.He is responsible for deviation management.He is also responsible for change control management.He is responsible for CAP management.He has to prepare and review BPR & BMR.He is responsible for in process quality assurance.He has to prepare market complaint investigation report/He has to prepare annual quality product review.He has to prepare protocol and report for process validation.He is also responsible for qualification of equipments and manufacturing process.He has to conduct internal audits.Salary: Best in Industry.Share me resume on career.talenthunt.th@gmail.com / cv.talenthunt1@gmail.com Whatsapp me on 7016504771 / 9998137070.

QA validation qms microbiology chemist HPLC all b pharma m pharma b tech biotech candidate call us . Fresher and experienced both can apply for this job .

Thermal/ Equipment Validation Steam Quality Testing Compressed Air/ Nitrogen Gas Testing Plc Validation Hvac/ Clean Room/ Laf/ Rlaf Validation Calibration

Delhi, Delhi: Reliably commute or planning to relocate before starting work (Required)Candidates Having The Central Drugs Standard Control Organization(CDSCO) experience and similar with these organizations can apply .Informing strategic regulatory controls and providing the worldwide regulatory policy for product development, manufacturing, and registration: It aids the applicant in advancing a universally accepted product.Development of proper leaflets like a summary of product characteristics, patient information, etc.To complete record data of the companys products and maintain the records of therapeutic products in agreement with current regulations and guidelines.To prepare data about a new product for doctors and other healthcare professionals for harmless and effective practice of medicine and maintain records, and reports of post-marketing surveillance of the new product. It also helps to prepare the leaflets and advertising material for existing as well as new drugs.IMMEDIATE JOINERS CAN APPLY.