Looking for pharma jobs in India with global exposure? Swiss Parenterals Ltd is hiring experienced Regulatory Affairs professionals for LATAM markets. Explore this exciting pharmaceutical career opportunity and apply today.
Contents
About the Company
Swiss Parenterals Ltd is a well-established pharmaceutical company known for its expertise in manufacturing high-quality parenteral (injectable) formulations. The company operates with a strong commitment to regulatory compliance, innovation, quality assurance, and patient safety.
With a growing international presence, Swiss Parenterals serves multiple global markets and maintains high manufacturing standards aligned with international regulatory requirements.
The organization focuses on continuous improvement, operational excellence, and delivering reliable healthcare solutions worldwide.
Professionals seeking long-term pharmaceutical careers in India can benefit from the company’s dynamic work environment, global exposure, and growth-oriented culture.
Job Details
- Company Name: Swiss Parenterals Ltd
- Position: Manager / Senior Manager – Regulatory Affairs
- Experience: 7–10 Years
- Qualification: B.Pharm / M.Pharm
- Location: Ahmedabad, Gujarat, India
- Work Type: On-site
- Market Focus: LATAM (Latin America)
Job Description
Swiss Parenterals Ltd is seeking an experienced Regulatory Affairs professional to manage regulatory activities for injectable pharmaceutical products across Latin American markets.
The selected candidate will handle the complete regulatory lifecycle, ensuring timely approvals and compliance with regional regulations.
Manager / Senior Manager – Regulatory Affairs
- Department: Regulatory Affairs
- Market: LATAM (Latin America)
- Role: Regulatory Lifecycle Management for Parenteral Products
- Experience: 7–10 Years
- Education/Qualification: B.Pharm / M.Pharm
Skills/Qualifications
- Strong experience in parenteral (injectable) product registrations
- Expertise in CTD and eCTD dossier preparation
- Knowledge of LATAM regulatory requirements
- Experience with product registrations, renewals, and variations
- Familiarity with regulatory lifecycle management
- Ability to handle agency queries and deficiency responses
- Strong communication and stakeholder management skills
- Cross-functional coordination experience
- Documentation and regulatory database management
- Proficiency in English
- Spanish or Portuguese language knowledge preferred
- Understanding of international pharmaceutical regulations
Key Responsibilities
- Develop regulatory strategies for LATAM markets
- Prepare and submit CTD/eCTD dossiers
- Manage product registrations and renewals
- Coordinate regulatory submissions and approvals
- Liaise with LATAM health authorities
- Monitor regulatory guideline updates
- Ensure ongoing regulatory compliance
- Handle authority queries and responses
- Maintain regulatory documentation
- Support audits and inspections
- Collaborate with QA, R&D, Manufacturing teams
- Mentor junior regulatory professionals
Benefits/Perks
- Opportunity to work with a reputed pharmaceutical company
- Exposure to international LATAM markets
- Strong career growth opportunities
- Collaborative work culture
- Learning and professional development
- Competitive compensation package
- Regulatory leadership experience
- Cross-functional project exposure
- Long-term career stability
- Global pharmaceutical compliance experience
How to Apply
Interested candidates can submit their updated resume directly to the official recruitment email addresses:
- Email: hroffice1@swiss.in
- Email: hroffice@swiss.in
Candidates should mention the position title “Regulatory Affairs Manager / Senior Manager – LATAM” in the email subject line for faster processing.
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Apply now and advance your career with a leading global pharmaceutical organization.
Why You Should Join Swiss Parenterals Ltd
Swiss Parenterals offers professionals an opportunity to work in a highly regulated and globally recognized pharmaceutical environment. The company values innovation, compliance, quality, and continuous learning.
Employees gain exposure to international regulatory markets while working alongside experienced professionals.
The organization’s growth-focused culture, commitment to quality, and expanding global footprint make it an excellent destination for ambitious Regulatory Affairs professionals.
Working with Swiss Parenterals allows candidates to build specialized expertise in injectable product registrations while contributing to global healthcare solutions.
FAQs
Who can apply for this Regulatory Affairs position?
Candidates with B.Pharm or M.Pharm qualifications and 7–10 years of relevant Regulatory Affairs experience can apply.
Is experience in injectable products mandatory?
Yes. Hands-on experience with parenteral (injectable) product registrations is a key requirement for this role.
Which LATAM countries will the candidate handle?
The role involves regulatory activities for markets including Venezuela, Uruguay, Paraguay, Guatemala, Panama, Chile, Colombia, and Peru.
How can I submit my application?
Interested candidates can send their updated resume to hroffice1@swiss.in or hroffice@swiss.in.
