Job Title: Formulation & Development Specialist – Injectables
Company: Eris Therapeutics Ltd.
Location: Bavla, Ahmedabad, Gujarat
About the Opportunity:
Eris Therapeutics Ltd. is actively seeking an experienced Formulation & Development Specialist to strengthen our Injectable function at our cutting-edge facility in Bavla, Ahmedabad, Gujarat. This pivotal role is designed for professionals with 3-5 years of dedicated, hands-on experience in developing sterile injectable products for diverse markets, including EU, ROW, and domestic. If you are passionate about driving pharmaceutical innovation and possess a robust background in injectable formulation, we encourage you to apply and contribute to our mission.
Key Responsibilities:
- Lead and execute comprehensive formulation development activities for various sterile injectable products, encompassing solutions, lyophilized products, and suspensions.
- Conduct thorough pre-formulation studies, optimize existing formulations, and manage the entire process development lifecycle.
- Oversee and facilitate efficient technology transfer activities for new and existing products.
- Prepare, review, and maintain critical development documentation, including Development Reports, Batch Manufacturing Records (BMR), Protocols, and regulatory submissions.
- Ensure strict compliance with cGMP, GLP, and aseptic manufacturing practices throughout all stages of product development.
- Collaborate effectively with cross-functional teams such as Analytical, Production, Quality Assurance (QA), and Regulatory Affairs to ensure successful product development and timely project execution.
- Exposure to analytical coordination, stability studies, and scale-up activities will be considered a significant advantage.
Required Qualifications & Experience:
- A Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, or a closely related scientific discipline.
- 3 to 5 years of practical, hands-on experience in Injectable Formulation and Development within the pharmaceutical industry.
- Proven experience in developing sterile injectable dosage forms, specifically solutions, lyophilized products, and suspensions, for global market requirements (EU, ROW, Domestic).
- Solid theoretical and practical knowledge of pre-formulation studies, formulation optimization, process development, and technology transfer principles.
- In-depth understanding and familiarity with cGMP, GLP, and aseptic manufacturing guidelines.
- Exceptional problem-solving capabilities, strong organizational and documentation skills, and excellent cross-functional communication abilities.
How to Apply:
If you meet these qualifications and are ready to take on a challenging and rewarding role within a leading pharmaceutical company, please submit your updated Curriculum Vitae (CV) to our Human Resources team.
Please note: This is an application opportunity. There are no walk-in interviews scheduled for this position.
