Job Title: Sr. Officer / Executive – Quality Control (HPLC & AMV)
Summary:
Biodeal Pharmaceuticals Limited, a USFDA-approved pharmaceutical manufacturing facility located in Baddi, Himachal Pradesh, is seeking highly motivated and experienced Quality Control professionals to join our growing team. We have multiple immediate openings for Sr. Officer/Executive positions, focused on HPLC operations and Analytical Method Validation (AMV). If you possess a strong understanding of pharmaceutical quality control principles, hands-on experience with analytical instrumentation, and a commitment to quality and compliance, we encourage you to apply. This is an excellent opportunity to contribute to a dynamic organization committed to excellence and offering a competitive compensation and benefits package.
About Biodeal Pharmaceuticals Limited:
Biodeal Pharmaceuticals Limited is a leading pharmaceutical manufacturer committed to producing high-quality medications that improve patient lives. Our state-of-the-art manufacturing facility in Baddi, Himachal Pradesh, adheres to the highest standards of quality and compliance, including USFDA regulations. We foster a culture of innovation, collaboration, and continuous improvement, providing our employees with opportunities for professional growth and development.
Responsibilities:
As a Sr. Officer / Executive in our Quality Control department, you will be responsible for the following:
- Performing routine and stability testing of pharmaceutical products using HPLC, GC, UV spectrophotometers, and other advanced analytical instruments.
- Executing Analytical Method Validation (AMV), method transfer, and method verification protocols in accordance with ICH/USP guidelines.
- Preparing and reviewing comprehensive QC documentation, including Certificates of Analysis (COAs), Standard Operating Procedures (SOPs), analytical protocols, reports, and deviation investigations.
- Handling the calibration, qualification, and maintenance of all QC instruments and equipment.
- Ensuring strict compliance with current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and all relevant regulatory requirements (USFDA, MHRA, etc.).
- Actively participating in internal audits and regulatory inspections.
- Thoroughly investigating Out-of-Specification (OOS) and Out-of-Trend (OOT) results, and implementing Corrective and Preventive Actions (CAPA) to prevent recurrence.
- Contributing to a continuous improvement environment within the QC department.
- Assisting in the training and mentoring of junior QC staff members.
Qualifications:
To be considered for this role, you must meet the following requirements:
- Education: Bachelor of Pharmacy (B.Pharma), Master of Pharmacy (M.Pharma), or Master of Science (M.Sc) in Chemistry.
- Experience: 3 to 8 years of relevant experience in a pharmaceutical Quality Control laboratory.
- Technical Skills: Mandatory hands-on expertise in High-Performance Liquid Chromatography (HPLC) operations and Analytical Method Validation (AMV).
- Regulatory Knowledge: Sound understanding of current regulatory guidelines, including ICH, USP, and EP.
- Documentation Skills: Excellent documentation practices and proficient computer skills.
- Flexibility: Ability to work in rotational shift duties at our Baddi plant.
Benefits:
Biodeal Pharmaceuticals offers a competitive compensation and benefits package to attract and retain top talent:
- Competitive salary commensurate with experience and qualifications.
- Performance-based incentives.
- Subsidized food and transportation facilities.
- Comprehensive Group Medical and Accidental Insurance coverage.
- Provident Fund and Gratuity benefits.
- Significant opportunities for career growth and advancement within a USFDA-approved manufacturing unit.
How to Apply:
If you are a qualified and motivated individual seeking a challenging and rewarding career opportunity, we encourage you to apply. Please send your updated resume to [email protected]. In the subject line of your email, please clearly indicate “Application for Sr. Officer / Executive – QC (HPLC & AMV)”.
Application Deadline: January 03, 2026 (or until positions are filled).
Biodeal Pharmaceuticals Limited is an equal-opportunity employer and values diversity at all levels. We encourage applications from all qualified individuals.
Frequently Asked Questions (FAQs):
1. What is the exact experience required for the Sr. Officer / Executive QC role at Biodeal Baddi?
Candidates must have 3–8 years of hands-on experience specifically in HPLC operations 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.