Biodeal Pharmaceuticals Limited, a fast-growing USFDA-approved manufacturing facility located in Baddi, Himachal Pradesh, has announced urgent hiring for 5 positions in the Quality Control department. If you have hands-on expertise in HPLC operations and Analytical Method Validation (AMV) in the pharmaceutical industry, this is your chance to join a reputed organization known for quality and compliance.
Key Responsibilities – Sr. Officer / Executive Quality Control
- Perform routine and stability testing using HPLC, GC, UV, and other advanced instruments
- Execute Analytical Method Validation (AMV), method transfer, and verification protocols as per ICH/USP guidelines
- Prepare and review QC documentation: COA, SOPs, protocols, reports, and deviations
- Handle calibration and maintenance of QC instruments
- Ensure compliance with cGMP, GLP, and regulatory requirements (USFDA, MHRA, etc.)
- Participate in internal audits and regulatory inspections
- Investigate OOS/OOT and implement CAPA
Required Qualifications & Experience
- B.Pharma / M.Pharma / M.Sc (Chemistry)
- 3–8 years of relevant experience in pharmaceutical Quality Control
- Mandatory hands-on experience in HPLC operations and Analytical Method Validation (AMV)
- Sound knowledge of current regulatory guidelines (ICH, USP, EP)
- Excellent documentation and computer skills
- Ability to work in shift duties at Baddi plant
Benefits Offered by Biodeal Pharmaceuticals
- Competitive salary package with performance incentives
- Subsidized food and transport facility
- Group medical & accidental insurance
- Provident Fund and gratuity benefits
- Career growth opportunities in a USFDA-approved unit
How to Apply
Interested candidates should send their updated resume with the subject line “Application for Sr. Officer / Executive – QC (HPLC & AMV)” to: 📧 hr4@biodealpharma.com
Last date to apply: January 03, 2026 (or till positions are filled)
Frequently Asked Questions (FAQs)
1. What is the exact experience required for Sr. Executive QC role at Biodeal Baddi? Candidates must have 3–8 years of hands-on experience specifically in HPLC and Analytical Method Validation (AMV) in a pharmaceutical QC lab.
2. Is this QC job in Baddi open for female candidates? Yes, Biodeal Pharmaceuticals encourages applications from both male and female candidates. Transport and accommodation support is provided.
