Flamingo Pharmaceuticals Ltd., founded in 1985 by Mr. Ashwin Thacker, is a trusted global leader in affordable, high-quality therapeutics. With a presence in 50 countries across five continents, our products meet rigorous standards like WHO-GMP, UK-MHRA, USFDA, and EU-GMP. Our state-of-the-art facilities in Taloja and Nanded drive innovation in oral solid dosage (OSD) forms and analytical development. We’re excited to announce a Walk-In Interview Drive on April 13, 2025, for dynamic professionals to join our team.
Why Work with Flamingo Pharmaceuticals?
At Flamingo, we believe healthy living is a right, not a privilege. Joining us means:
- Contributing to therapeutics trusted worldwide.
- Growing in a supportive, quality-driven environment.
- Working in facilities compliant with global regulatory standards.
- Being part of a legacy serving millions across continents.
Open Positions
We’re hiring for roles in Formulation Research & Development (FRD), Analytical Research & Development (ARD), Packaging Development, Quality Control (QC), Quality Assurance (QA), and Production at our Taloja and Nanded facilities. Here’s a snapshot:
Formulation Research & Development (FRD) – Taloja
- FRD: M.Pharm/B.Pharm, 2-7 years in FRD/technology transfer for OSD.
- FRD Group Leader: M.Pharm/B.Pharm, 12-17 years leading OSD FRD teams.
Packaging Development – Taloja
- Packaging Development: PGPPST/BE (Packaging), 2-7 years in packaging R&D.
Analytical Research & Development (ARD) – Taloja/Nanded
- ARD: M.Sc/B.Pharm, 1-10 years in method development/validation.
- ARD Documentation: M.Sc/B.Pharm, 3-7 years in validation protocols/ARD review.
- ARD Group Leader: M.Sc/M.Pharm, 15-20 years in method development/validation.
Quality Control (QC) – OSD Plant
- QC: M.Sc/B.Pharm/B.Sc, 2-10 years in HPLC, GC, IR, LIMS, microbiology, stability, and method validation.
Quality Assurance (QA) – OSD Plant
- QA: M.Pharm/B.Pharm, 2-10 years in QMS, audit compliance, validation, IPQA, documentation.
- QA Head – IPQA (Taloja): M.Pharm/B.Pharm, 10-15 years in IPQA leadership.
- CQA – Analytical Experts: M.Pharm/B.Pharm, 10-15 years in analytical compliance.
- CQA – Training & QMS: M.Pharm/B.Pharm, 10 years in training/QMS.
Production – OSD Plant
- Officer/Shift In-Charge: M.Pharm/B.Pharm, 2-10 years in manufacturing/packing.
- Operators: ITI/Diploma, 1-3 years in granulation, compression, packing (BQS).
Walk-In Interview Details
Mark your calendar for our Walk-In Interview Drive and take the next step in your career!
- Date: Sunday, April 13, 2025
- Time: 10:00 AM to 5:00 PM
- Venue: Hotel Woodlands, National Highway No. 8, Near Tejpal Motors, Balitha, Vapi, Gujarat – 396191
- What to Bring: Updated resume, passport-size photo, educational certificates, experience letters, last 3 months’ payslips
How to Apply
- Walk-In: Join us at Hotel Woodlands, Vapi, with your documents.
- Email: Can’t attend? Send your resume to hr@flamingopharma.com.
- Contact: Reach out via hr@flamingopharma.com or visit www.flamingopharma.com for more info.
Tips for Success
- Showcase Your Skills: Highlight experience in OSD, method validation, or QMS, depending on the role.
- Know Our Standards: Be familiar with USFDA, EU-GMP, or WHO-GMP requirements.
- Be Professional: Dress formally and arrive by 9:45 AM to register.
- Prepare to Discuss: Expect questions on HPLC, technology transfer, or audit compliance.
About Flamingo Pharmaceuticals
Since 1985, Flamingo has grown from a small enterprise to a global pharmaceutical leader. Our focus on quality therapeutics and affordability has earned us a loyal customer base and approvals from top regulatory bodies. With advanced manufacturing units, we’re dedicated to making healthcare accessible to all.
Take Your Career to New Heights
Flamingo Pharmaceuticals offers a platform to thrive, whether you’re innovating in FRD, ensuring quality in QA/QC, or driving production. Join us on April 13, 2025, in Vapi, or email hr@flamingopharma.com to apply.
We can’t wait to meet you and build a healthier future together!