Acme Generics Pvt. Ltd., a leading pharmaceutical company with a 17-year legacy, is hosting a hiring drive for multiple roles in Production, Quality Assurance (QA), and Quality Control (QC) at our state-of-the-art facility in Baddi, Himachal Pradesh.
As one of the largest Oral Solid Dosage (OSD) manufacturers in Baddi, we are proud to hold certifications from USFDA, MHRA, EU-GMP, ANVISA Brazil, Health Canada, PICS Ukraine, and WHO Geneva.
Join our team of over 2,000 skilled professionals to contribute to high-quality pharmaceutical manufacturing in a regulatory-compliant environment. Apply now to advance your career in the pharmaceutical industry!
Job Openings Overview for Production, QA, and QC Roles
We are hiring for the following positions at our Baddi facility:
Officer/Executive – Quality Assurance (QMS/IPQA)
- Qualification: B.Pharm, M.Pharm
- Experience: 3–6 years
- Key Skills: QMS, IPQA, GMP compliance, regulatory audits
Operator/Officer – Production (Compression)
- Qualification: ITI, Diploma, B.Pharm
- Experience: 3–5 years
- Key Skills: Compression machines (Parle Hatta, Sejong, Fette), GMP
Officer – Quality Control (Microbiology/HPLC Analysis)
- Qualification: B.Sc, M.Sc, B.Pharm
- Experience: 2–5 years
- Key Skills: Microbiology, HPLC analysis, stability testing
- Job Location: Acme Generics Pvt. Ltd., Plot No. 115, HPSIDC Industrial Area, Davni, Baddi, Himachal Pradesh – 174101
- Note: Prior experience in USFDA, MHRA, or EU-GMP-approved plants is mandatory.
Job Description for QA, Production, and QC Roles
Qualifications
- QA (QMS/IPQA): B.Pharm or M.Pharm from a recognized institution.
- Production (Compression): ITI (Fitter, Mechanical), Diploma (Mechanical, Pharmacy), or B.Pharm.
- QC (Microbiology/HPLC): B.Sc (Microbiology, Chemistry), M.Sc (Microbiology, Analytical Chemistry), or B.Pharm.
- Strong academic background in pharmaceutical sciences or related fields.
Experience
- QA: 3–6 years in Quality Management Systems (QMS) or In-Process Quality Assurance (IPQA) in a pharmaceutical formulation plant.
- Production: 3–5 years operating compression machines (Parle Hatta, Sejong, Fette) in OSD manufacturing.
- QC: 2–5 years in microbiological analysis or HPLC analysis for pharmaceutical products.
- Mandatory experience in USFDA, MHRA, or EU-GMP-regulated facilities.
Skills
Officer/Executive – Quality Assurance (QMS/IPQA):
- Expertise in QMS (e.g., CAPA, Change Control, Deviations, APQR).
- Proficiency in IPQA activities, including line clearance, in-process checks, and batch record review.
- Strong knowledge of GMP, ICH guidelines, and regulatory audit compliance (USFDA, MHRA, EU-GMP).
- Skills in documentation, internal audits, and vendor qualification.
- Familiarity with SAP or ERP systems for QA processes.
Operator/Officer – Production (Compression):
- Hands-on experience with compression machines (Parle Hatta, Sejong, Fette) for tablet manufacturing.
- Knowledge of GMP and SOP compliance in OSD production.
- Ability to perform equipment setup, tooling, and troubleshooting during compression.
- Skills in preparing batch manufacturing records (BMR) and batch production records (BPR).
- Understanding of line clearance and cleaning validation procedures.
Officer – Quality Control (Microbiology/HPLC Analysis):
- Proficiency in HPLC (High-Performance Liquid Chromatography) for analytical testing of raw materials, finished products, and stability samples.
- Expertise in microbiological testing (e.g., microbial limit tests, environmental monitoring, sterility testing).
- Knowledge of GLP, GMP, and ICH guidelines for analytical and microbial analysis.
- Experience with method validation, stability studies, and OOS investigations.
- Familiarity with software like Empower or Chromeleon for HPLC data management.
Responsibilities
Officer/Executive – Quality Assurance (QMS/IPQA):
- Manage QMS activities, including CAPA, Change Control, Deviations, and APQR.
- Conduct in-process checks, line clearance, and batch record reviews during manufacturing.
- Ensure compliance with USFDA, MHRA, and EU-GMP standards during regulatory audits.
- Prepare and review SOPs, validation protocols, and audit reports.
- Train staff on GMP practices and support vendor qualification.
Operator/Officer – Production (Compression):
- Operate and maintain compression machines (Parle Hatta, Sejong, Fette) for tablet production.
- Perform tooling setup, machine cleaning, and line clearance per SOPs.
- Monitor critical process parameters to ensure product quality and yield.
- Document activities in BMR/BPR and ensure GMP compliance.
- Troubleshoot equipment issues and coordinate with Engineering for maintenance.
Officer – Quality Control (Microbiology/HPLC Analysis):
- Conduct HPLC analysis for raw materials, finished products, and stability samples.
- Perform microbiological tests (e.g., microbial limit, sterility, environmental monitoring).
- Validate analytical methods and support stability studies per regulatory guidelines.
- Investigate OOS, OOT, and laboratory incidents, preparing CAPA reports.
- Maintain GLP-compliant documentation and ensure readiness for regulatory audits.
How to Apply for Production, QA, and QC Jobs
Interested candidates can apply by submitting their resumes to the designated contact:
Email: deepak.sharma@acmegenerics.in
- Subject Line: “Application for [Position Name] – Baddi”
WhatsApp: 7018194189
- Include current CTC, expected CTC, and notice period in your message.
Documents to Submit:
- Updated resume
- Educational certificates (B.Pharm, M.Pharm, B.Sc, M.Sc, ITI, Diploma)
- Experience certificates
- Last 3 months’ salary slips
- Aadhar and PAN card copies
- One recent passport-size photograph
Website: Visit www.acmegenerics.in for more details about Acme Generics Pvt. Ltd. and career opportunities.
Note: Acme Generics Pvt. Ltd. does not charge any fees for recruitment. Beware of fraudulent offers requesting payments and report suspicious activities to hr@acmegenerics.in. Candidates must have prior experience in USFDA, MHRA, or EU-GMP-approved plants.
Why Join Acme Generics for Your Pharmaceutical Career
Acme Generics Pvt. Ltd., part of the Acme Group, is a global leader in OSD and injectable manufacturing, operating from USFDA-approved facilities in Baddi and Nalagarh, Himachal Pradesh. With a workforce of 1,001–5,000 and a production capacity of 15 billion tablets, 3 billion capsules, and 30 million ampoules annually, we serve top Indian and global pharmaceutical companies, including 5 MNCs. By joining our Baddi team, you will:
- Work in a USFDA, MHRA, and EU-GMP-certified facility with exposure to international regulatory standards.
- Contribute to a company rated 4.3/5 overall, with skill development rated at 4.4/5 and a strong focus on innovation.
- Gain hands-on experience with advanced equipment like HPLC, compression machines (Parle Hatta, Sejong, Fette), and microbiological testing systems.
- Benefit from a collaborative culture and opportunities for career growth in QA, QC, and Production.
- Be part of a legacy of excellence, supplying high-quality medicines to over 70 countries.
Don’t miss this opportunity to advance your career in quality assurance jobs, production jobs, or quality control jobs with Acme Generics Pvt. Ltd. Apply by sending your resume to deepak.sharma@acmegenerics.in or WhatsApp at 7018194189. Let’s build the future of pharma together in Baddi, Himachal Pradesh!