Quality Manager Job Vacancies in Baddi

Location: On-site Nalagarh, Himachal PradeshExperience: 12 years (Mandatory)Qualification: B.Sc. in Chemistry / Microbiology / Biotechnology / Life SciencesAbout the Role:We are looking for a dedicated Quality Control (QC) Officer to join our pharmaceutical manufacturing team at our Nalagarh facility. The ideal candidate will have hands-on experience with laboratory testing and strong documentation practices in a GMP-regulated environment.Key Responsibilities:Conduct testing of raw materials, in-process samples, and finished products.Operate and maintain analytical instruments like HPLC, UV, IR, pH meter, etc.Ensure accurate and timely documentation as per cGMP and GLP guidelines.Perform stability studies and environmental monitoring (if required).Participate in lab audits, calibration, and equipment qualification.Maintain safety and hygiene in the lab environment.Desired Profile:B.Sc. in Chemistry / Microbiology / Biotechnology or relevant field12 years of QC experience in a pharmaceutical formulation unit (mandatory)Sound knowledge of GMP practices and analytical techniquesAttention to detail, good documentation habits, and strong analytical skillsMandatory Proficiency in written and verbal EnglishJoin a team committed to delivering high-quality, affordable medicines.Apply now to become part of our quality-driven organization!#QualityControl #PharmaJobs #ChemistryJobs #QCOfficer #PharmaceuticalIndustry #HimachalJobs #BScJobs #NalagarhJobs #PharmaCareers #GMPCompliance

QA manager ,QA validation, Qms , Injection and osd both

IVPEX PARENTERAL PVT. LTD. Urgent requirements for QC departments.Job Posted date- 17/02/2023Last Date- 25/02/2023.Quality Control Job Opening For Tr. Officer / Officer With 0 Years to 1.5 YEARS OF EXPERIENCE. JOB LOCATION BADDI.IVPEX PARENTERAL PVT. LTD.71/1 ,Vill.- Dhela , Near Super Hoze , Teh. - Baddi, Distt. Solan(H.P.) 173205

Responsibilities and DutiesAssist in QC stability testing, prepare and maintain stability records and summaries.Involve in training and transfer of methods to and from QC and contract manufacturers as assigned.Modify and validate analytical procedures to meet QCs needs.Support design and development of experimental protocols, SOPs, etc., consistent with cGMP/GLP.Participate in special projects and department meetings via input, feedback and execution of assigned tasks.Execute special projects on analytical and instrument problem solving.Conduct all quality QC chemical tests.Perform non radioactive and biological QC on time and record quality of product.Adapt, maintain and operate analytical instrumentation.Involve in procedure review and propose modifications and updates.Ensure work environment is clean and safe complying with safety and pharmaceutical regulation.Conduct radiation safety duties conforming to regulations.Report monthly on supplies for QC orders involving devices and reagents.Contribute to industrial, R&D qualification and validation activities and support routine maintenance.Conduct various analytical testing procedures as per manufacturing/QC SOPs.

We have vacant of 2 QC Officer Jobs in Baddi Experience Required : 1 Year Educational Qualification : B.Pharma, B.Sc, M.Pharma, M.Sc Skill QA-Quality Assurance,QC - Quality Control,HPLC etc.

We have vacant of 3 MANAGER QUALITY ASSURANCE PHARMA Jobs in Baddi Experience Required : 10 Years Educational Qualification : M.Pharma, M.Sc Skill QMS , VALIDATION,IPQA AND OTHER ACTIVITIES OF QA etc.

Hi,we have an urgent vacancy for QC Manager for pharmaceuticals industryLocation:- BaddiDesignation:- Managerinterested candidate, please share your resume on

We are looking for 3 QC Officer Posts in Baddi,Baddi Chandigarh with deep knowledge in QTP-Quick Test Professional,QA-Quality Assurance,QC - Quality Control,Biotechnology,Quality Control,HPLC and Required Educational Qualification is : B.Pharma, B.Sc, M.Pharma, M.Sc

Production Chemists are requiredMinimum Qualification B- PharmaShould have minimum one years experience in Production

We are looking for 2 IPQA Officer Posts in Baddi with deep knowledge in QA-Quality Assurance,QC - Quality Control,Market Complaints,Bpr Review,IPQC,Apr and Required Educational Qualification is : B.Pharma, B.Sc, M.Pharma

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