Looking for pharma jobs in Gujarat? Brooks Steriscience Limited is hiring experienced Regulatory Affairs professionals for its Vadodara facility.
This is an excellent opportunity for candidates seeking pharmaceutical careers in India with global regulatory exposure and long-term growth potential.
Contents
About the Company
Brooks Steriscience Limited is a leading pharmaceutical company known for its commitment to quality, innovation, and regulatory excellence.
The company specializes in manufacturing high-quality pharmaceutical products while maintaining strict compliance with international regulatory standards.
With a strong presence in global markets, Brooks Steriscience continues to expand its operations through advanced technologies, robust quality systems, and a highly skilled workforce.
The organization provides a dynamic environment for professionals looking to build successful careers in the pharmaceutical industry.
Job Details
- Company Name: Brooks Steriscience Limited
- Department: Regulatory Affairs
- Experience: 2–5 years or 7–10 years
- Qualification: B.Pharm / M.Pharm
- Location: Village Manglej, Nareshwar Road, Taluka Karjan, Vadodara, Gujarat – 391243
- Work Type: On-site
Job Description
Brooks Steriscience Limited is seeking skilled Regulatory Affairs professionals with strong experience in Rest of World (ROW) markets.
The selected candidates will be responsible for regulatory submissions, lifecycle management, deficiency responses, and maintaining compliance with global regulatory requirements.
Regulatory Affairs Officer / Senior Officer / Team Leader
- Department: Regulatory Affairs
- Market: ROW (Rest of World) Markets
- Role: Regulatory Affairs Professional
- Experience: 2–5 years or 7–10 years
- Education/Qualification: B.Pharm / M.Pharm
Skills/Qualifications
- Bachelor’s or Master’s degree in Pharmacy
- Strong experience in ROW regulatory markets
- Knowledge of CTD, eCTD, and ACTD submissions
- Understanding of global regulatory requirements
- Experience in dossier preparation and submission
- Expertise in lifecycle management activities
- Regulatory documentation and compliance knowledge
- Strong communication and coordination skills
- Analytical and problem-solving abilities
- Ability to work with cross-functional teams
- Excellent organizational and documentation skills
- Proficiency in regulatory tracking systems
Key Responsibilities
- Prepare regulatory dossiers for ROW markets
- Compile CTD, eCTD, and ACTD submissions
- Manage initial product submissions
- Handle deficiency responses effectively
- Coordinate with R&D, QA, and QC teams
- Support regulatory query resolution
- Maintain regulatory databases and trackers
- Process post-approval variations
- Manage product renewals and annual reports
- Track submission timelines and approvals
- Review regional labeling requirements
- Ensure regulatory compliance standards
Benefits/Perks
- Competitive compensation package
- Long-term career growth opportunities
- Exposure to international regulatory markets
- Professional learning and development
- Collaborative work environment
- Opportunity to work with industry experts
- Stable pharmaceutical career path
- Experience with global compliance standards
- Cross-functional learning opportunities
- Recognition-based performance culture
How to Apply
Interested candidates who meet the eligibility criteria can share their updated CV directly with the recruitment team.
Email: preeti.yadav@brookssteriscience.com
Candidates are encouraged to apply as early as possible to maximize their chances of consideration.
For more pharmaceutical job opportunities, career updates, and industry hiring news, visit Pharma Recruiter: https://pharmarecruiter.in
Apply today and take the next step in your pharmaceutical career with Brooks Steriscience Limited.
Why You Should Join
Brooks Steriscience offers a professional environment focused on innovation, quality, and continuous improvement. Employees gain valuable exposure to global regulatory practices while working alongside experienced industry professionals.
The company promotes career development through challenging projects, compliance-driven operations, and opportunities to contribute to international pharmaceutical markets.
Professionals seeking stability, learning, and growth will find excellent prospects within the organization.
FAQs
Who can apply for this Regulatory Affairs position?
Candidates with B.Pharm or M.Pharm qualifications and relevant Regulatory Affairs experience in ROW markets can apply.
How can I apply for the job?
You can send your updated resume directly to preeti.yadav@brookssteriscience.com.
Is this a walk-in interview opportunity?
No walk-in interview details have been announced. Interested candidates should apply via email.
What career growth opportunities are available?
Selected candidates can gain international regulatory exposure, leadership opportunities, and long-term growth within the organization.
