Looking for an exciting Regulatory Affairs career in the pharmaceutical industry? Bharat Parenterals Limited has announced a new recruitment drive for experienced Regulatory Affairs professionals. The company is inviting applications for the position of Executive to Assistant Manager – Regulatory Affairs. Candidates with relevant experience in international regulatory documentation, product registration, and dossier preparation can apply through email.

This is an excellent opportunity for professionals seeking long-term career growth in a reputed Indian pharmaceutical company engaged in manufacturing and global regulatory operations.

Job Highlights

• Company Name: Bharat Parenterals Limited
• Position: Executive to Assistant Manager – Regulatory Affairs
• Department: Regulatory Affairs
• Job Type: Full-Time
• Vacancies: 03
• Experience Required: 4–8 Years
• Job Location: Vadodara, Gujarat, India
• Application Mode: Email
• Selection Process: Shortlisting followed by Interview

About Bharat Parenterals Limited

Bharat Parenterals Limited is a well-established Indian pharmaceutical company engaged in the manufacturing and marketing of high-quality pharmaceutical formulations. The company serves domestic and international markets while maintaining strong regulatory compliance and quality standards. It offers excellent career opportunities for professionals who wish to contribute to global pharmaceutical operations.

Roles & Responsibilities

The selected candidates will be responsible for various Regulatory Affairs activities, including:

• Prepare and compile regulatory dossiers for submission to Asian, African, LATAM, and CIS markets.
• Maintain regulatory documentation in accordance with international guidelines.
• Respond to regulatory authority queries and coordinate with business partners.
• Review and approve packaging artworks, labels, and packaging materials for regulatory compliance.
• Verify product samples and supporting documentation before submission.
• Support new product registrations and regulatory strategy development.
• Prepare package inserts and coordinate artwork development for new products.
• Maintain regulatory databases and monitor submission status for different markets.
• Ensure compliance with applicable international regulatory requirements.

Required Qualifications

Candidates should possess any of the following qualifications:

• B.Pharm
• M.Pharm
• M.Sc. (Relevant Life Sciences)

Applicants should have 4 to 8 years of relevant Regulatory Affairs experience in the pharmaceutical industry.

Required Skills

The ideal candidate should have:

• Strong understanding of international regulatory guidelines
• Experience in dossier preparation and regulatory submissions
• Excellent documentation and communication skills
• Knowledge of product registration processes
• Ability to coordinate with regulatory authorities and business partners
• Good analytical and organizational skills

Salary

Based on industry standards and experience, the expected salary may range between:

₹6.5 LPA – ₹11 LPA

Actual salary will depend on the candidate’s qualifications, experience, and company policies.

Employee Benefits

Selected candidates may receive benefits such as:

• Competitive salary package
• Career growth opportunities
• Professional learning environment
• Exposure to international regulatory markets
• Employee welfare benefits as per company policy
• Long-term career development opportunities

Selection Process

The recruitment process may include:

• Resume Screening
• Technical Evaluation
• Personal Interview
• HR Discussion
• Final Selection

Important Note

The company has mentioned that the selected candidate should be willing to sign a 3-year long-term association agreement.

How to Apply

Interested and eligible candidates can send their updated resume to the official recruitment email mentioned below.

Email: recruitment@bplindia.in

Candidates are advised to mention the “Regulatory Affairs – Executive/Assistant Manager” position in the email subject line for easy identification.