Are you a skilled professional in pharmaceutical quality control looking to advance your career? Flamingo Pharmaceuticals Ltd, a leading name in the pharmaceutical industry, is hiring for Senior Officer, Officer, Executive, and Analyst roles in its Quality Control (QC) Department at Taloja MIDC, Panvel. This is your chance to join a dynamic team committed to excellence in a regulatory-compliant environment. Walk-in interviews are scheduled for 21-22 September 2025. Don’t miss this opportunity to grow with a trusted pharmaceutical company!
Job Responsibilities
As a Quality Control professional at Flamingo Pharmaceuticals Ltd, you will play a critical role in ensuring product quality and compliance. Key responsibilities include:
- Conducting Analysis and Testing: Perform testing of Raw Materials, Packing Materials, In-process, Finished Products, and Stability Samples per GLP, GMP, and SOP guidelines.
- Method Validation and Transfer: Execute method validation and method transfer activities to ensure accuracy and reliability.
- Regulatory Compliance: Adhere to MHRA, WHO, and other regulatory standards, ensuring compliance with cGMP, GLP, and GDP requirements.
- Documentation: Maintain accurate records and documentation in line with Good Documentation Practices (GDP).
- Instrument Operation: Utilize analytical instruments such as HPLC, GC, UV-Vis Spectrophotometer, IR, KF, Potentiometer, pH Meter, and AAS for testing.
Qualifications and Skills
To excel in these Quality Control roles, candidates must meet the following criteria:
- Education: M.Sc, B.Pharm, or equivalent in a relevant field.
- Experience: Proven experience in a pharmaceutical QC laboratory compliant with MHRA, WHO, or other regulatory bodies.
- Technical Skills: Hands-on expertise with analytical instruments (HPLC, GC, UV-Vis, IR, KF, Potentiometer, pH Meter, AAS).
- Documentation Skills: Strong understanding of quality systems and GDP standards.
- Availability: Preference for immediate joiners.
Benefits of Joining Flamingo Pharmaceuticals Ltd
- Career Growth: Work in a dynamic, growth-oriented environment with opportunities for professional development.
- Regulatory Exposure: Gain experience in a regulatory-compliant setting, enhancing your expertise in cGMP, GLP, and GDP.
- Competitive Salary: Earn a competitive salary ranging from INR 3,00,000 to INR 6,00,000 per annum, based on experience and role.
- Team Collaboration: Join a supportive team dedicated to maintaining high-quality standards in pharmaceuticals.
How to Apply
Interested candidates can attend the walk-in interviews on:
- Date: 21 & 22 September 2025
- Time: 10:00 AM to 5:00 PM
- Venue: Flamingo Pharmaceuticals Ltd, E28, Opp. Firebrigade, Near Water Tank, Tondara Village, Taloja MIDC, Panvel-410208
Alternatively, email your resume to talojahr@flamingopharma.com. For more details, visit Flamingo Pharmaceuticals Ltd.
FAQs
Q: What documents should I bring to the walk-in interview?
A: Bring your updated resume, educational certificates, experience letters, and a valid ID proof.
Q: Is prior registration required for the walk-in interview?
A: No registration is required. Simply attend the interview at the specified venue and time with your documents.
