Quality Control Manager Job Vacancies in Himachal Pradesh

Seeking a Senior Site Incharge with 5-10 years of experience in Shimla, India. Responsible for overseeing all on-site activities, managing construction projects, ensuring safety protocols are followed, and liaising with contractors and stakeholders. The ideal candidate should have a Post Graduate degree, strong leadership skills, excellent communication abilities, and a proven track record of successfully managing site operations. The role requires a male candidate who is able to work from the office location.

Quality Manager 17025 for NABL Lab in IMT Manesar Gurgaon MCPSKey Responsibilities:Maintain and update the laboratorys quality system in line with ISO/IEC 17025 and NABL requirements.Perform analytical tests in the laboratory and ensure accuracy, reliability, and validity of results.Assist in administrative duties to maintain smooth laboratory workflow.Obtain and renew laboratory certifications, handle audits, and maintain compliance documentation.Implement and monitor QA/QC programs and assignments.Ensure adherence to standard operating procedures (SOPs).Train, guide, and support laboratory staff in quality practices and compliance.Promote good customer service practices by ensuring timely and reliable delivery of results.Required Skills & Knowledge:Strong knowledge of ISO systems with proven track record of implementation in laboratories.Familiarity with NABL accreditation processes.Hands-on experience with GC (Gas Chromatography) and HPLC (High-Performance Liquid Chromatography) will be an added advantage.Excellent problem-solving, analytical, and organizational skills.Ability to manage audits, documentation, and continuous quality improvement.

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

Educate the operator about Kaizen, Shop Floor Losses, and Poke Yoke etc. Production planning, manpower planning, scheduling To ensure that all necessary aids to the production are available for smooth functioning of the Weld shop (Man, Machine, Method &Material) Ensuring safety measures in day to day working in the department. To initiate Kaizen activities in the department. Maintaining 5-S and to Train, Guide and Motivate personnel along with maintaining discipline on shop floor.

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 .

Job Openings for 5 Qc Officer/ Executive Jobs for Freshers in Kala Amb, having Educational qualification of : B.Pharma,B.Sc with Good knowledge in fresher or experience both are required etc.

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

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.

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

Walkin Interview Going On Baddi Pharmaceuticals Company..required Qa ( Ipqa ,Document Ion )production Executive /production Chemistqc Executive /microbiology qualification- Msc Chemistry ,Microbiologybsc,M Pharma/ B Pharmahr -luxmi

Hiring for 2 Manager QC Jobs in Baddi,Zirakpur with minimum 10 Years Experience,Required Educational Qualification is : B.Pharma, B.Sc, M.Pharma, M.Sc with Good knowledge in Approved in Micro instrument and chemical etc.

Candidate should have basic Software background and knowledge in one of the programming languages(C/C++/VB/Java/ .Net)Freshers with good communication and computer skills can applyExperience in Software Testing field is a plus

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

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

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