Aculife Healthcare Pvt. Ltd., a growing pharmaceutical company committed to quality healthcare solutions, is hiring for the role of RA Support at its facility near Sachana, Ahmedabad.
Established to serve domestic and international markets, Aculife focuses on manufacturing a wide range of pharmaceutical products with cGMP compliance, employing over 150 professionals across its operations.
About Aculife Healthcare
Located at Near Railway Crossing (Sanand-Viramgam Highway), Village: Sachana, Taluka: Viramgam, District: Ahmedabad – 382150, Gujarat, Aculife Healthcare is dedicated to producing high-quality pharmaceuticals.
The company adheres to Good Manufacturing Practices (GMP) and aims to expand its footprint in the industry, offering a supportive work environment for career growth.
Job Opportunity: RA Support
We’re seeking a skilled professional to join our Regulatory Affairs team in Sachana.
| Job Details | Information |
|---|---|
| Designation | RA Support |
| Qualification | M.Pharm / M.Sc. / B.Pharm |
| Experience | 1–5 years in RA/QA Documentation in Pharmaceutical Industries |
| Location | Aculife Healthcare Pvt. Ltd., Near Railway Crossing (Sanand-Viramgam Highway), Village: Sachana, Taluka: Viramgam, District: Ahmedabad – 382150, Gujarat |
| Vacancies | Not specified (apply based on eligibility) |
| Note | Male and female candidates can apply |
Key Responsibilities
- Collect required documents as per Regulatory Affairs (RA) requests from cross-functional teams, verify, and provide them for filing or product registration.
- Review analysis of API, finished products, and stability samples.
- Assess method development and method validation, including PDR (Pharmaceutical Development Report) reviews.
- Evaluate specifications and methods of analysis for raw materials and finished products.
- Review process validation, cleaning validation protocols, and reports.
- Ensure compliance with GMP/GDP and Standard Test Procedures (STP).
Qualifications & Skills
- Education: M.Pharm, M.Sc., or B.Pharm with a focus on pharmaceutical sciences.
- Experience: 1–5 years in RA or QA documentation within the pharmaceutical industry.
- Technical Expertise:
- Knowledge of regulatory documentation and filing processes.
- Experience with API, stability, and method validation reviews.
- Familiarity with GMP, GDP, and validation protocols.
- Skills:
- Strong attention to detail and analytical skills.
- Effective communication and coordination with cross-functional teams.
- Proficiency in documentation and regulatory compliance.
Why Join Aculife Healthcare?
Aculife offers a rewarding career in a growing pharmaceutical company. Benefits include:
- Competitive Salary: RA Support roles earn ₹3–6 LPA in Sachana, with potential for growth.
- Career Growth: Training in regulatory documentation, GMP compliance, and validation processes.
- Supportive Environment: A collaborative culture with opportunities for skill enhancement.
- Challenges: Employees may face high-pressure timelines and evolving regulatory demands.
Why This Role Matters
As an RA Support professional, you’ll play a critical role in ensuring regulatory compliance and product registration, supporting Aculife’s expansion into global markets. Your work will contribute to Ahmedabad’s thriving pharma ecosystem with over 1,800 jobs.
Growth Opportunities
Training includes regulatory guidelines, documentation skills, and process validation, with potential for advancement into RA leadership roles.
Work Environment
The Sachana facility features modern production and documentation units, fostering a quality-driven culture. Expect a desk-based role with possible field coordination.
How to Apply
Interested candidates should send their updated CV to recruitment@aculife.co.in or rajeshthakor@aculife.co.in by June 21, 2025, 12:30 PM IST. Include:
- Updated CV highlighting 1–5 years of RA/QA documentation experience.
- Educational certificates (M.Pharm/M.Sc./B.Pharm).
- Experience letters or relevant project details.
Shortlisted candidates will be contacted for interviews, which may include technical assessments (e.g., documentation review, regulatory knowledge).
Application Tips
- Highlight experience in RA documentation, method validation, or GMP compliance.
- Specify familiarity with API or stability analysis.
- Prepare for questions like “How do you ensure regulatory compliance?” or “What steps do you take for document verification?”
Important Disclaimer
Aculife Healthcare maintains a transparent recruitment process. We do not charge fees or use free email services (e.g., Gmail, Yahoo) for job offers. Verify opportunities through recruitment@aculife.co.in or rajeshthakor@aculife.co.in. Report suspicious activities to HR.
Stay Safe from Fraud
- Confirm offers through official Aculife channels.
- Avoid sharing personal or financial information with unverified sources.
- Contact HR for clarifications.
Why Sachana, Ahmedabad?
Sachana, near Ahmedabad, is part of Gujarat’s pharma hub with over 1,800 jobs, hosting Aculife’s growing facility. Its proximity to Ahmedabad (50 km) and industrial growth make it ideal for pharma careers.
Join Aculife’s Mission
Aculife Healthcare is dedicated to delivering quality pharmaceutical solutions. Join our Sachana team to support regulatory excellence. Apply now to be part of our 150+ strong workforce!
Next Steps
Submit your CV to recruitment@aculife.co.in or rajeshthakor@aculife.co.in by June 21, 2025, 12:30 PM IST. The selection process may include interviews and document verification. Successful candidates will receive further communication.
Contact Us
For queries, email recruitment@aculife.co.in or rajeshthakor@aculife.co.in. Visit Aculife Careers for updates (if available).
Innovate with Aculife
Join Aculife Healthcare to advance regulatory support in Sachana. Apply today and drive innovation in healthcare!
