Job Opportunity: Shape the Future of Pharmaceuticals at Safetab Life Science
Summary:
Safetab Life Science, a rapidly expanding pharmaceutical company located in Puducherry, is seeking talented and motivated individuals to join our Analytical Research & Development (AR&D), Formulation Research & Development (FR&D), and Quality Assurance (QA) teams. We offer a dynamic and supportive work environment where you can contribute to cutting-edge pharmaceutical development and manufacturing. If you have a strong foundation in pharmaceutical sciences and a passion for quality, we encourage you to apply.
About Safetab Life Science:
At Safetab Life Science, we are committed to developing and manufacturing high-quality pharmaceutical products that improve patient lives. Our state-of-the-art facility in Puducherry is equipped with the latest technology and staffed by a team of experienced professionals. We are dedicated to fostering a culture of innovation, collaboration, and continuous improvement.
We are currently hiring for the following positions:
1. Junior Scientist – AR&D (Analytical R&D)
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Responsibilities:
- Perform analytical method development, validation, and routine analysis using Shimadzu HPLC.
- Review raw data and Certificates of Analysis (COA).
- Maintain accurate documentation according to regulatory standards.
- Collaborate with other team members to ensure project success.
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Qualifications:
- B.Pharm / M.Pharm / M.Sc Chemistry
- 3–5 years of hands-on experience in analytical method development and validation within a regulated pharmaceutical environment.
- Proficiency in operating and troubleshooting Shimadzu HPLC systems.
- Strong understanding of cGMP and regulatory guidelines.
- Excellent documentation skills and attention to detail.
2. Document Reviewer – AR&D
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Responsibilities:
- Review analytical method validation (AMV) protocols and reports to ensure accuracy and compliance with regulatory requirements.
- Maintain awareness of current regulatory guidelines and industry best practices.
- Ensure GMP documentation practices are followed.
- Collaborate with AR&D team members to address any documentation-related issues.
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Qualifications:
- B.Pharm / M.Pharm / M.Sc Chemistry
- Minimum 5 years of experience in reviewing analytical documentation within a regulated pharmaceutical environment.
- In-depth knowledge of AMV protocols, regulatory compliance, and GMP documentation.
- Excellent attention to detail and ability to identify discrepancies in documentation.
3. Junior Scientist – FR&D (Formulation R&D)
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Responsibilities:
- Conduct pre-formulation studies and compatibility studies to support formulation development.
- Develop solid oral and topical formulations.
- Prepare trial batches for evaluation.
- Participate in stability studies and scale-up activities.
- Maintain accurate records of experiments and results.
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Qualifications:
- B.Pharm / M.Pharm (Pharmaceutics)
- 3–5 years of experience in solid oral/topical formulation development within a regulated pharmaceutical environment.
- Experience with pre-formulation studies, stability testing, and scale-up processes.
- Strong understanding of pharmaceutical manufacturing processes.
4. QA Executive – Quality Assurance
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Responsibilities:
- Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) to ensure compliance with procedures and regulations.
- Perform In-Process Quality Assurance (IPQA) checks on the manufacturing floor.
- Handle Quality Management System (QMS) elements such as deviations, Out-of-Trend (OOT) investigations, change control, and Corrective and Preventive Actions (CAPA).
- Ensure shop-floor compliance with cGMP guidelines.
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Qualifications:
- B.Pharm / M.Pharm / M.Sc
- 2–4 years of experience in Quality Assurance within a regulated pharmaceutical environment.
- Familiarity with BMR/BPR review, IPQA, change control, deviation management, CAPA, QMS, and cGMP principles.
General Requirements:
- Strong knowledge of cGMP, GDP, ICH, and other relevant regulatory guidelines.
- Excellent documentation and communication skills.
- Ability to work both independently and collaboratively within a fast-paced environment.
- Strong problem-solving and analytical skills.
Benefits:
- Competitive salary package (best in industry for the Puducherry location).
- Comprehensive health insurance plan.
- Opportunities for professional development and career advancement within a rapidly expanding organization.
- Exposure to cutting-edge pharmaceutical technology and regulatory submissions.
- A supportive and collaborative work environment.
How to Apply:
Interested candidates are encouraged to submit their updated resume to [email protected]. Please include the specific position you are applying for in the subject line of your email (e.g., “Application for Junior Scientist AR&D”).
Contact Information:
- Email: [email protected]
- Phone: +91-9092625656
- Location: Puducherry
Application Deadline:
While we will accept applications until all positions are filled, we encourage you to apply as soon as possible. Early applications are preferred and will be reviewed promptly.
Additional Information:
- All positions are full-time and onsite at our manufacturing facility in Puducherry.
We look forward to receiving your application and exploring how you can contribute to the success of Safetab Life Science!