swiss pharma job openings – Regulatory Affairs

We (Swiss Pharma Pvt. Ltd.) have urgent immediate openings for the following posts for the Vatva location, Ahmedabad.

International Regulatory Affairs job information;

An international regulatory affairs officer in the pharmaceutical industry is responsible for ensuring that a company’s products comply with all relevant laws and regulations in the countries where they are sold. This may involve coordinating with regulatory agencies in different countries, preparing and submitting regulatory documents, and conducting research to ensure compliance with local laws and regulations.

As an international regulatory affairs officer, you may be responsible for developing and implementing regulatory strategies to ensure that a company’s products can be successfully brought to market in different countries. This may involve working closely with other teams within the company, such as research and development, manufacturing, and quality control.

The specific tasks and responsibilities of an international regulatory affairs officer will depend on the size and structure of the company and the products being developed. It is typically a fast-paced and challenging role that requires strong attention to detail, excellent organizational skills, and the ability to work effectively in a team.

Positions: Officer to Sr. Executive
No of Vacancies: 5
Market: ROW
Qualification: B Pharm / M Pharm
Eligibility: Fresher – Candidate should be M Pharm /  M.Pharm in regulatory affairs would be an advantage.

Regulatory affairs is a field within the pharmaceutical industry that is responsible for ensuring that a company’s products comply with all relevant laws and regulations. A regulatory affairs specialist in a pharmaceutical company plays a key role in helping the company bring its products to market by coordinating with regulatory agencies and preparing the necessary documentation.

As a regulatory affairs fresher, you may be responsible for supporting more experienced regulatory affairs staff in preparing and submitting regulatory documents and conducting research to ensure compliance with relevant laws and regulations. You may also be responsible for maintaining regulatory databases and tracking the progress of regulatory submissions.

Candidates must have experience between 2 – 6 years in the ROW market in Tablet, Capsule, Dry Syrup and Parenteral dosage forms. Local candidates are preferred who can join on an immediate basis.

Graphic designer

No. of Vacancies: 1

Experience: Fresher to 1-year experience in the Pharma field is compulsory.
Eligibility: Any Graduate. A local candidate is preferred who
can join on an immediate basis.
Desired skills: Proficient in using Corel Draw, Photoshop & Illustrator. Good IT skills, especially with design and photo-editing software. Creativity and innovation. Local candidates are preferred who can join on an immediate basis.

APPLICATION PROCESS; Interested candidates having relevant experiences only can apply and send their updated CV to [email protected] or [email protected] along with their Current CTC, Expected CTC, and notice period.