Aculife Hiring Regulatory Affairs
- Company Overview
- Job Role & Responsibilities
- Regulatory Affairs – Trainee Officer
- Eligibility / Qualifications
- Required Education
- Relevant Courses
- Experience
- Skills Required
- Location & Salary
- Job Location:
- Salary:
- Application Process
- Why You Should Apply
- FAQs
- Who can apply for this role?
- Is this role suitable for freshers?
- What markets will I work on?
- What is the job location?
- How can I apply?
- Summary Table
Aculife Healthcare Regulatory Affairs Fresher Jobs 2026 – Trainee Officer Hiring in Ahmedabad
Aculife Healthcare Pvt. Ltd. (a part of the Nirma Group) is hiring for the Regulatory Affairs department, offering an excellent opportunity for freshers and early-career professionals. The company is recruiting for the Trainee Officer role at its Ahmedabad head office, targeting candidates with 6 months to 1 year of experience, including internships or apprenticeships in regulatory affairs.
This is a strong entry-level opportunity for M.Pharm graduates who want to build a career in global regulatory submissions, dossier preparation, and pharmaceutical compliance across international markets such as LATAM and Europe.
Company Overview
Aculife Healthcare Pvt. Ltd., a flagship pharmaceutical company under the Nirma Group, is known for its leadership in sterile formulations and parenteral manufacturing. The company has a strong presence in global markets and is recognized for its commitment to quality, innovation, and regulatory excellence.
With advanced manufacturing facilities and a focus on injectable products, Aculife serves regulated and semi-regulated markets worldwide. Its emphasis on regulatory compliance, documentation accuracy, and global standards makes it a preferred employer for professionals aiming to grow in regulatory affairs.
Working at Aculife Healthcare offers:
- Exposure to international regulatory markets including LATAM and EU
- Hands-on experience in dossier preparation and submission management
- Opportunity to work with global regulatory teams and documentation systems
- Career growth in pharmaceutical regulatory affairs and compliance
Job Role & Responsibilities
Regulatory Affairs – Trainee Officer
- Compile and review registration dossiers as per country-specific regulatory guidelines
- Support regulatory submissions for LATAM markets including Brazil and Mexico
- Assist in EU market submissions and submission management systems
- Review technical documents such as DMF, Product Development Reports, BMR, BPR, AMV reports, STP, stability data, and BE study reports
- Prepare responses for regulatory deficiencies and backlog dossiers
- Assist in post-approval changes, variations, and lifecycle management activities
- Coordinate with overseas regulatory teams, agents, and distributors for timely submissions
- Review packaging artworks and regulatory comments for product launches
- Maintain regulatory databases and update central depository records
These responsibilities are critical in ensuring regulatory compliance, timely approvals, and successful product launches in international pharmaceutical markets.
Eligibility / Qualifications
Required Education
M.Pharm
Relevant Courses
Regulatory Affairs, Pharmaceutics, Pharmaceutical Analysis, Industrial Pharmacy
Experience
- 6 months to 1 year (including internship or apprenticeship in regulatory affairs)
Skills Required
- Basic understanding of global regulatory guidelines (LATAM, EU)
- Knowledge of dossier preparation and submission processes
- Strong documentation and communication skills
- Attention to detail and willingness to learn in a regulated environment
Location & Salary
Job Location:
- Ahmedabad (Head Office)
Salary:
- Best in the industry for entry-level regulatory roles
Application Process
Interested candidates can apply by sending their updated resume to:
- Email: satabdeerath@aculife.co.in
Ensure your resume highlights any internship or hands-on experience in regulatory affairs, documentation, or pharmaceutical compliance.
Why You Should Apply
- Excellent entry point into global regulatory affairs
- Exposure to LATAM and EU regulatory markets
- Work with a reputed pharmaceutical company under the Nirma Group
- Strong career growth in regulatory submissions and compliance
FAQs
Who can apply for this role?
M.Pharm graduates with 6 months to 1 year of experience or relevant internships.
Is this role suitable for freshers?
Yes, candidates with internship or apprenticeship experience are encouraged to apply.
What markets will I work on?
LATAM (Brazil, Mexico) and European markets.
What is the job location?
Ahmedabad head office.
How can I apply?
Send your updated resume to the provided email ID.
Summary Table
| Company | Aculife Healthcare Pvt. Ltd. |
|---|---|
| Vacancies | Trainee Officer – Regulatory Affairs |
| Required Education | M.Pharm |
| Experience | 6 months – 1 year |
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