Aculife Hiring Regulatory Affairs

Aculife Hiring Regulatory Affairs
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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:

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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