Swiss Parenteral Recruitment for Regulatory Affairs Executive to DGM
Swiss Parenteral Limited is a leading pharmaceutical company specializing in the development and manufacturing of high-quality injectable drugs. We are committed to providing affordable and innovative healthcare solutions to improve the quality of life for patients worldwide.
Job Overview
Swiss Parenteral Limited is seeking highly skilled professionals for our Regulatory Affairs team. We have openings ranging from Executive to Deputy General Manager (DGM) levels. This is a fantastic opportunity for individuals with a background in regulatory affairs to join a dynamic and growing company.
Key Responsibilities
- Regulatory Submissions: Prepare and submit regulatory documents for EU and emerging markets, including ASEAN, AFRICA, MENA, LATAM, and CIS regions.
- Compliance: Ensure all regulatory activities comply with relevant guidelines and standards.
- Documentation: Maintain and update regulatory files and documentation.
- Communication: Liaise with regulatory authorities and internal stakeholders to ensure smooth regulatory processes.
- Strategy Development: Develop and implement regulatory strategies to support product registrations and approvals.
Required Qualifications
- Education: B.Pharm or M.Pharm.
- Experience: 2 to 15 years in core regulatory affairs.
- Skills: Strong knowledge of regulatory requirements and guidelines for the specified regions.
How to Apply
Interested candidates can share their updated resumes with us via email at hroffice@swiss.in
