- Regulatory Documentation
- Dossier Preparation
- Strong knowledge of various International Regulatory Guidelines
- Excellent attention to detail
- Ability to work independently and as part of a team
- Strong organizational and time management skills
- At least a Bachelor's degree in Pharmacy, M.Sc., Life Sciences, or a related field
- Prior experience in the pharmaceutical industry is a plus
- People from QA, QC or Manufacturing departments are welcome to apply.
- Freshers are more than welcome to join us if they show willingness to learn, work and show stability.
Regulatory Affairs Executive - Ahmedabad, India - Swiss Pharma Pvt. Ltd.
Description
Company Description
Swiss Pharma Pvt. Ltd. is one of India's leading pharmaceutical companies based in Ahmedabad. With a focus on exports to regulated and semi regulated markets, Institution & Tender Business and Contract Development and Manufacturing Organizations (CDMO), Swiss Pharma is known for manufacturing various dosage forms, including injections, tablets, capsules, suspensions, and dry powder. The company has 3 manufacturing units and offers products in general, cephalosporin, and carbapenem categories. Swiss Pharma exports its products to more than 16 countries across Asia, Africa, Middle East, and Latin & Central America. The company values quality, integrity, and invests heavily in its facilities, processes, people and their training.
Role Description
This is a full-time on-site role for a Regulatory Affairs Executive at Swiss Pharma Pvt. Ltd. located in Ahmedabad. The Regulatory Affairs Executive will be responsible for preparing dossiers, regulatory documentation, ensuring compliance with regulatory requirements, and managing overall regulatory affairs for the company within the timeframe and along with the team.
We expect the following skills from the candidate