Looking for pharma jobs in India with global exposure? Explore this exciting opportunity in regulatory affairs for injectable products with a leading pharmaceutical company.
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About the Company
Swiss Parenterals Ltd. is a well-established pharmaceutical organization known for its excellence in sterile manufacturing and injectable formulations.
The company emphasizes innovation, regulatory compliance, and global market expansion.
With a strong presence across international markets, Swiss Parenterals continues to build credibility through quality-driven operations and a commitment to growth.
Their focus on regulatory excellence makes them a preferred employer in pharmaceutical careers in India.
Job Details
- Company Name: Swiss Parenterals Ltd.
- Experience: 7 to 10 years
- Qualification: B.Pharm / M.Pharm
- Location: Ahmedabad, Gujarat, India
- Work Type: On-site
Job Description
Swiss Parenterals Ltd. is hiring an experienced Regulatory Affairs professional to manage injectable product registrations across the LATAM region.
The role focuses on regulatory lifecycle management, submissions, and compliance.
Regulatory Affairs Manager / Senior Manager
- Department: Regulatory Affairs
- Market: LATAM (Latin America)
- Role: End-to-end regulatory lifecycle management for injectable products
- Experience: 7–10 years
- Education/Qualification: B.Pharm / M.Pharm
Skills/Qualifications
- Strong expertise in CTD/eCTD dossier preparation
- Experience with injectable (parenteral) product registrations
- Knowledge of LATAM regulatory guidelines
- Familiarity with countries like Chile, Peru, Colombia, Panama
- Excellent communication and coordination skills
- Ability to manage regulatory queries and deficiencies
- Proficiency in English (Spanish/Portuguese preferred)
- Cross-functional collaboration skills
Key Responsibilities
- Develop regulatory strategies for LATAM product registrations
- Prepare and submit CTD/eCTD dossiers
- Handle regulatory submissions and approvals
- Liaise with LATAM health authorities
- Monitor regulatory changes and ensure compliance
- Coordinate with R&D, QA, and Manufacturing teams
- Manage deficiency responses and agency queries
- Maintain regulatory documentation systems
- Support audits and inspections
- Mentor junior regulatory professionals
Benefits/Perks
- Opportunity to work in global pharmaceutical markets
- Strong career growth in regulatory affairs
- Exposure to international compliance standards
- Competitive salary package
- Collaborative and innovation-driven work culture
- Continuous learning and development opportunities
How to Apply
Interested candidates can apply by sending their updated resume to:
- Email: hroffice1@swiss.in
- Alternate Email: hroffice@swiss.in
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Apply now and take the next step in your regulatory affairs career with a globally recognized pharmaceutical company.
Why You Should Join
Swiss Parenterals Ltd. offers a strong platform for professionals seeking international exposure in regulatory affairs.
The company promotes a culture of compliance, innovation, and continuous improvement.
Working here ensures long-term career stability, global learning opportunities, and involvement in high-impact pharmaceutical projects across LATAM markets.
FAQs
What is the eligibility for this role?
Candidates must have B.Pharm or M.Pharm with 7–10 years of regulatory affairs experience.
Is LATAM experience mandatory?
Experience with LATAM regulatory markets is highly preferred but not always mandatory.
How can I apply for this job?
You can send your resume to the official HR email IDs mentioned above.
What are the growth opportunities?
This role offers global exposure, leadership opportunities, and career advancement in regulatory affairs.
