Caplin Point Laboratories Hiring for Regulatory Affairs Department

Caplin Point Laboratories, a prominent name in the pharmaceutical industry, is actively seeking talented professionals to join its Regulatory Affairs Department. With a commitment to excellence and innovation, Caplin Point Laboratories offers an exciting career opportunity for individuals passionate about regulatory affairs and compliance.

Company Overview: Caplin Point Laboratories is renowned for its high-quality pharmaceutical products and services. The company focuses on providing affordable healthcare solutions while adhering to the highest standards of quality and compliance.

Open Positions: Caplin Point Laboratories is looking to fill 6 positions in the Regulatory Affairs Department. This is a great opportunity for candidates with experience in regulatory affairs to join a dynamic and growing team.

Job Location: Hyderabad and Chennai

Key Responsibilities:

1. Responsible for Authoring and review of dossiers for submission to US, Canada, Europe, Australia, South Africa and other regulated markets
2. Review of DMF’s, technical documents and coordinate with CFT’s to ensure the submission requirements
3. Responsible for Change assessments and provide regulatory filling strategy for Post approval submissions
4. Responsible for authoring and review of PLCM submission to maintain compliance to approved MA’s

Qualifications and Experience:

• Experience: 2 to 6 years in Regulatory Affairs
• Educational Qualification: Relevant degree in pharmaceutical sciences or related field
• Market Exposure: Experience with US, Canada, and Europe markets is preferred

Skills Required:

• Strong knowledge of regulatory guidelines and requirements for various markets.
• Excellent written and verbal communication skills.
• Ability to work collaboratively with cross-functional teams.
• Detail-oriented with strong organizational skills.

Application Process:

Interested candidates are encouraged to send their CVs to careers@caplinpoint.net. Make sure to highlight your experience and qualifications relevant to the Regulatory Affairs Department.