Executive Job at Amneal | Pharmacy Graduates Apply Now
Amneal Pharmaceuticals is hiring an Executive / Senior Executive – Formulation Development (Injectable) for its R&D hub in Ahmedabad City, Gujarat. This Executive Job is designed for M.Pharm (Pharmaceutics) professionals with at least 2 years of experience in parenteral product development. The successful candidate in this Amneal Job will manage the entire lifecycle of injectable formulations, from raw material indenting and study protocol preparation to supporting ANDA submissions and responding to CMC queries.
- Job Title: Executive / Senior Executive
- Location: Ahmedabad City, Gujarat, India
About the Company
Amneal Pharmaceuticals is a high-growth pharmaceutical company specializing in the development, manufacturing, and marketing of complex generic and specialty drug products. With a strong presence in Ahmedabad, Amneal is recognized for its robust R&D pipeline and its commitment to quality and innovation. The company fosters a workplace that values diversity and inclusion, ensuring equal opportunity for all employees.
Key roles
- Executive Role: Specialists in all aspects of people management. High-level input at the strategic level into all key business decisions.
- Audit Role: Ensures all areas of the organization are compliant with legal requirements AND best practice employment policies and procedures.
- Facilitator Role: Close partnership to support, advise, and extend the ability of all areas of the organization to meet their objectives through implementation of highly effective employment practices in areas such as Talent Acquisition, Learning and Development, Reward systems, Performance Management, Health and Wellbeing.
- Consultancy Role: Provide expert advice to the organization and its managers on any aspect of workforce management, employee relations, and performance.
- Service Role: Ensure the organization is fully aware of and is equipped to deal with developments impacting employment matters, such as changes in legislation and changes in the characteristics of the labor market.
Responsibilities
- Responsible for development related activities of all Parenteral Products.
- Responsible for the preparation and review of MFR for the exhibit batch of Parenteral products.
- Responsible for indenting the raw materials, RLD, Packaging Material, and other items required for product development as well as exhibit batches.
- Responsible for the preparation and review of the study protocol required for the exhibit batch of parenteral products.
- Responsible for review of specifications like API, Excipients, In-process, finished product, Shelf life, etc. of Parenteral products.
- Responsible for the review of the specification of primary packaging material.
- Responsible for the review of the BMR and BPR of the Exhibit batch.
- Responsible for supporting the Regulatory Affairs department for ANDA submission and responding to CMC queries.
- Responsible for the preparation and review of PDR and other necessary documents of parenteral products required for ANDA submission.
- Responsible for the preparation of SOP and different study protocols for product development.
- Responsible for reviewing GMP-related documents as applicable.
Qualifications
Master’s in pharmacy in Pharmaceutics with a minimum of 2 years of experience
