Centaur Pharmaceuticals is inviting applications from experienced B.Sc and M.Sc Analytical Chemistry professionals for multiple Quality Control (QC) positions at its API manufacturing facility in Ambernath, Maharashtra.
This is an excellent opportunity for candidates with API pharmaceutical experience seeking career growth in chromatography, analytical method validation, QMS investigations, documentation, and stability management. Interested professionals can share their updated resumes directly with the company.
About Centaur Pharmaceuticals
Centaur Pharmaceuticals is a reputed pharmaceutical organization known for its commitment to quality, innovation, and healthcare excellence. The company is currently expanding its Quality Control team and looking for experienced professionals across multiple QC functions.
Job Details
| Position | Experience Required |
|---|---|
| Chromatography Analyst – Officer/Sr. Officer | 5–7 Years |
| Non-Chromatography Analyst | 3–5 Years |
| Reviewer | 8–10 Years |
| QMS & Investigation – Sr. Executive | 10 Years |
| Section Incharge (Stability/Raw Material/Finished Goods/Intermediate) – Asst./Dy. Manager | 10–15 Years |
| Documentation (LIMS, Specifications, Test Procedures, SOP Preparation) – Sr. Officer/Executive | 5–8 Years |
| Analyst – Analytical Method Validation | 2–6 Years |
Key Responsibilities
Chromatography Analysts
- Perform HPLC, GC, and related chromatographic analysis.
- Execute testing of raw materials, intermediates, and finished products.
- Maintain analytical records as per GMP requirements.
Analytical Method Validation Analysts
- Conduct method validation and method transfer activities.
- Prepare validation protocols and reports.
- Ensure compliance with regulatory guidelines.
QMS & Investigation Professionals
- Handle OOS, OOT, deviations, and CAPA investigations.
- Maintain quality systems documentation.
- Support audit and compliance activities.
Documentation Executives
- Prepare and review SOPs, specifications, and test procedures.
- Manage LIMS documentation and data integrity requirements.
- Ensure compliance with GMP documentation standards.
Section Incharge Roles
- Supervise stability, raw material, finished product, and intermediate testing activities.
- Lead teams and ensure timely completion of QC operations.
- Drive quality compliance and laboratory efficiency.
Eligibility Criteria
Educational Qualification
- B.Sc (Analytical Chemistry)
- M.Sc (Analytical Chemistry)
Experience
- 2 to 15 years depending on the position applied for.
Mandatory Requirement
- Candidates must have API Pharmaceutical Industry Experience.
Job Location
Ambernath, Maharashtra, India
Benefits of Joining Centaur Pharma
- Opportunity to work in a reputed API pharmaceutical organization.
- Exposure to advanced analytical instruments and quality systems.
- Career growth opportunities in Quality Control and Quality Assurance functions.
- Competitive salary package based on experience and role.
- Professional work environment focused on quality and compliance.
How to Apply
Interested and eligible candidates can send their updated resume to:
