Are you a skilled Analytical Method Development professional with 1-2 years of hands-on experience in Analytical Method Validation (AMV) for solid oral dosage forms? Acme Group, one of India’s fastest-growing pharmaceutical organizations, is actively hiring a Senior Officer – Analytical Method Development at its state-of-the-art facility in Ahmedabad, Gujarat.
This is a golden opportunity for M.Sc / B.Pharm / M.Pharm graduates who want to grow their career in analytical R&D with a reputed formulation company.
Key Responsibilities
- Develop and validate analytical methods for solid oral dosage forms (tablets, capsules)
- Perform forced degradation studies and establish impurity profiles
- Handle instruments like HPLC, UV, Dissolution, GC, and IR
- Prepare method development reports, validation protocols, and technology transfer documents
- Ensure compliance with ICH guidelines, USP, and current regulatory requirements
- Troubleshoot analytical issues during routine and stability analysis
- Coordinate with formulation development and QA/QC teams
Qualifications & Experience Required
- M.Sc Chemistry / M.Pharm / B.Pharm
- 1 to 2 years of hands-on experience in Analytical Method Validation (AMV) specifically in solid orals
- Strong knowledge of HPLC method development and validation
- Familiarity with 21 CFR compliance and data integrity practices
- Good documentation skills (SOPs, protocols, reports)
Salary & Benefits
- Competitive salary range: ₹4.2 – 6.8 LPA (based on experience & interview performance)
- Provident Fund, gratuity, health insurance, and performance bonus
- Cab facility, subsidized canteen, and modern work environment
- Excellent career growth in analytical R&D
How to Apply
Interested candidates should send their updated resume to career@acmegrp.in Mention “Senior Officer – Analytical Method Development” in the subject line. Contact: +91 72270 26128 Location: Ahmedabad, Gujarat (work from office only)
Apply within 10 days for priority processing!
Frequently Asked Questions (FAQ)
1. Is this job open for freshers? No, the position requires minimum 1–2 years of relevant experience in analytical method validation for solid oral dosage forms.
2. What is the interview process? It typically includes a technical written test followed by HR and technical panel interviews.
