Explore high-paying pharmaceutical jobs at Aculife Healthcare in Ahmedabad. Apply now for Formulation & Development roles with salaries up to ₹8 LPA. Global exposure, USFDA-compliant sterile manufacturing, and career growth in parenterals.
🚀 Aculife Healthcare Hiring: Formulation & Development (F&D) Jobs in Ahmedabad 2025 – Apply Now!
If you are an experienced M.Pharm professional seeking high-paying pharmaceutical jobs in India 2025, your opportunity has arrived. Aculife Healthcare Pvt. Ltd., a global leader in sterile injectables and parenterals manufacturing, is conducting recruitment for Formulation & Development (F&D) Officer, Sr. Officer, and Executive positions in Ahmedabad, Gujarat.
With over 100+ country operations, Aculife Healthcare — a key subsidiary of the $5 billion Nirma Group — offers world-class manufacturing facilities with compliance across USFDA, EMA, ANVISA, Health Canada, WHO-GMP, ISO 13485, and more. This is your chance to join one of India’s largest injectable manufacturers with cutting-edge infrastructure, regulatory exposure, and international career growth opportunities.
🔎 About Aculife Healthcare Pvt. Ltd.
Aculife Healthcare, located in Ahmedabad’s Sanand-Viramgam Pharma Hub, is one of the world’s largest producers of parenterals. Spread over a 550-acre campus, it houses:
✅ BFS (Blow-Fill-Seal) & Glass Injectable Plants
✅ WHO-GMP Certified Sterile Manufacturing Units
✅ Advanced R&D Facilities with HPLC, UPLC, GCMS, LCMS
✅ Regulatory Compliance with USFDA, EMA, TGA, Health Canada, ANVISA
✅ Export to 100+ global markets with 1000+ product registrations
🏢 Current Openings: Formulation & Development (F&D) Roles
| Designation | Department | Qualification | Experience | Location |
|---|---|---|---|---|
| Officer / Sr. Officer / Executive | Formulation & Development (F&D) | M.Pharm (Pharmaceutics) | 1–7 Years | Ahmedabad, Gujarat |
👉 Application Emails:
📩 recruitment@aculife.co.in
📩 rajeshthakor@aculife.co.in
🔬 Key Job Responsibilities
- Develop sterile injectables (vials, ampoules, BFS) and non-sterile dosage forms (tablets, capsules).
- Conduct pre-formulation studies: solubility, stability, pKa, DSC, FTIR analysis.
- Perform compatibility studies with excipients and packaging components.
- Execute scale-up, process optimization, and technology transfer to commercial plants.
- Prepare documentation for regulatory submissions (PDR, protocols, validation reports).
- Collaborate with cross-functional teams (QA, QC, RA) for CGMP compliance.
- Support development for USFDA, EMA, ANVISA, Canada, and ROW markets.
✅ Eligibility Criteria
- Educational Qualification: M.Pharm (Pharmaceutics or equivalent)
- Experience: 1–7 Years in injectables/parenterals/OSD formulation development
- Technical Skills Required:
- USFDA, EMA, ANVISA, Health Canada compliance knowledge
- Literature search: PubMed, SciFinder
- Hands-on QbD, DOE, HPLC, UV, LCMS, GCMS
- Pre-formulation and compatibility studies expertise
- Strong documentation for regulatory filings
💸 Salary Package & Growth Opportunities
Average Salary Range (Ahmedabad, Gujarat): ₹4 LPA – ₹8 LPA
Benefits of Working at Aculife:
- Global exposure to regulated markets.
- Training in QbD, Regulatory Affairs, and Tech Transfer.
- Access to high-end analytical instrumentation.
- International product portfolio across critical care, parenteral nutrition, and large-volume infusions.
- Opportunity to collaborate on contract manufacturing for global pharma leaders.
⚠ Challenges to Consider
Some employee reviews highlight:
- Fast-paced work environment.
- Limited internal promotions and salary increments (2.7/5 rating on growth).
- Heavy compliance workload due to regulated markets focus.
🌍 Why Ahmedabad for Pharma Jobs?
Ahmedabad is India’s emerging pharmaceutical manufacturing hub. With over 2,500+ pharma jobs, NIPER proximity, excellent infrastructure, and multiple multinational companies (MNCs), Ahmedabad is ideal for pharma professionals seeking long-term career growth in sterile injectable formulation development.
📝 Application Process
Send your updated resume to:
Subject Line Format:F&D – [Designation] (e.g., F&D – Sr. Officer)
Documents to Attach:
- Updated CV detailing F&D experience
- Sterile/Non-sterile projects handled
- Regulated market (USFDA/EMA/ANVISA) exposure
- Educational qualification documents
Interview Process:
- Technical assessment in pre-formulation, scale-up, QbD.
- HPLC, analytical instrumentation, and regulatory process questions.
🔐 Stay Safe from Recruitment Frauds
Aculife maintains a transparent recruitment process. Do not engage with any recruiter requesting payments or offering unofficial employment letters. Verify job offers only through:
- recruitment@aculife.co.in
- official HR department contact
🚀 Why This Opportunity Matters
Joining Aculife Healthcare’s Formulation & Development team offers you:
- Hands-on regulatory experience with regulated market filings.
- Exposure to sterile injectable innovations.
- Direct involvement in global drug development programs.
- Stable career growth with a global pharmaceutical leader.
👉 Apply Now and Shape the Future of Global Healthcare with Aculife Healthcare Pvt. Ltd.
