Are you a skilled pharmaceutical professional looking for a rewarding career in API manufacturing? Centaur Pharmaceuticals Pvt. Ltd., a leading name in the pharmaceutical industry, is hiring for multiple roles at its state-of-the-art API manufacturing facility in Ambernath, Thane, Maharashtra. With a focus on quality and innovation, Centaur offers exciting opportunities in Quality Assurance (QA), Quality Control (QC), and Analytical R&D for candidates with API experience in USFDA, EDQM, and MHRA-regulated facilities. Explore these pharma jobs and take your career to the next level!
Job Responsibilities
Quality Assurance (QA)
- Analytical QA Lead (Dy. Manager): Oversee analytical quality processes, ensure compliance with regulatory standards, and lead investigations for deviations.
- Analytical QA (Sr. Officer/Executive): Review analytical data and ensure adherence to Good Manufacturing Practices (GMP).
- Microbiology QA Reviewer (Sr. Officer/Executive): Validate microbiological testing procedures and ensure compliance with regulatory guidelines.
- Engineering QA & ITQA (Executive/Sr. Executive): Monitor engineering and IT quality systems for compliance.
- Customers/Marketing Support (Executive/Sr. Executive): Provide technical support to customers and marketing teams.
- Control & Stability Sample Management (Sr. Officer/Executive): Manage control and stability samples per regulatory requirements.
- Investigation Lead (Dy. Manager): Conduct root cause analysis and draft detailed investigation reports.
Quality Control (QC)
- Chromatography & Non-Chromatography Analyst (Officer/Sr. Officer): Perform analytical testing using HPLC, GC, and titration techniques.
- QMS & Investigation (Sr. Executive/Asst. Manager): Implement Quality Management Systems and lead investigations for non-conformances.
- Section Incharge (Asst./Dy. Manager): Oversee stability, raw material, finished product, and intermediate testing sections.
- Documentation (Sr. Officer/Executive): Prepare and review LIMS, SOPs, specifications, and test procedures.
- Training Coordinator (Executive): Develop and deliver training programs for QC staff.
- Investigation Lead (Asst./Dy. Manager): Lead investigations and draft technical reports for QC processes.
Analytical Method Validation & R&D
- Analytical Validation (Executive/Officer): Validate analytical methods using HPLC, GC, titration, and PSD techniques.
- Analytical Method Development (Executive/Officer): Develop and optimize methods for HPLC, GC, titration, and LCMS.
Qualifications
- Education: B.Sc. or M.Sc. in Chemistry (mandatory for all positions).
- Experience: 3-15 years of API pharmaceutical experience in USFDA, EDQM, or MHRA-regulated facilities.
- Skills: Excellent communication and drafting skills for technical and investigation reports.
- Availability: Willingness to work in all shifts.
Benefits
- Competitive salary ranging from INR 4,00,000 to INR 12,00,000 per annum, based on position and experience.
- Opportunities for career growth in a leading API manufacturing company.
- Work in a USFDA, EDQM, and MHRA-regulated facility, ensuring global standards.
- Supportive work environment with a focus on innovation and quality.
How to Apply
Interested candidates should send their updated CV to apihrd@centaurlab.com or contact 0251 6611900 for further details. Ensure your CV highlights your API experience and regulatory exposure. Shortlisted candidates will be contacted for interviews at our Ambernath facility.
FAQs
1. What qualifications are required for these pharma jobs at Centaur Pharmaceuticals?
Candidates must hold a B.Sc. or M.Sc. in Chemistry and have 3-15 years of API pharmaceutical experience in USFDA, EDQM, or MHRA-regulated facilities.
2. How can I apply for these positions?
Send your updated CV to apihrd@centaurlab.com or call 0251 6611900 to express interest. Ensure your CV includes relevant API experience.
