Acme Generics Pvt. Ltd., a leading pharmaceutical CDMO (Contract Development and Manufacturing Organization), is seeking experienced Quality Assurance (IPQA) professionals for its Oral Solid Dosage (OSD) facility in Baddi, Himachal Pradesh.
Key Responsibilities:
- Conduct In-Process Quality Assurance (IPQA) checks to ensure compliance with USFDA, MHRA, and EUGMP standards.
- Monitor manufacturing processes, documentation, and SOP adherence.
- Support regulatory audits and implement corrective actions.
- Maintain quality systems in alignment with cGMP guidelines.
This role is ideal for candidates with 3–6 years of experience in pharmaceutical quality assurance, offering growth in a dynamic regulatory environment.
About Acme Generics Pvt. Ltd.
Established in 2005, Acme Generics is a trusted CDMO partner for Indian and global pharmaceutical companies. Headquartered in Baddi, the company specializes in high-quality, compliant manufacturing services. With a focus on innovation and regulatory excellence, Acme Generics has built a reputation for reliability in the pharma and healthcare industry.
Eligibility Criteria
Education & Experience:
- Qualification: B.Pharm / M.Pharm (Mandatory).
- Experience: 3–6 years in IPQA (Quality Assurance) within a pharmaceutical manufacturing unit.
- Regulatory Exposure: Hands-on experience with USFDA, MHRA, or EUGMP audits is required.
Preferred Candidates:
- Immediate joiners will be prioritized.
- Strong analytical and documentation skills.
How to Apply
Interested and eligible candidates can apply via:
- Email: Send your updated resume to deepak.sharma@acmegenerics.in.
- WhatsApp: Share your CV at 7018194189.
Ensure the subject line reads: “Application for QA (IPQA) Role – [Your Name]”.
Why Join Acme Generics?
- Work with a reputed pharmaceutical CDMO.
- Exposure to global regulatory standards.
- Career growth in quality assurance and compliance.
Explore this pharma job opportunity today!