Are you an experienced pharma professional seeking pharma jobs in Analytical Development and QC jobs? Accuprec Research Labs Pvt. Ltd. is hiring a Sr. Research Associate (5-7 years experience) in Ahmedabad, Gujarat. This is a great opportunity for pharmaceutical careers in India with a leading CRO focused on regulatory compliance and innovation.
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About the Company
Accuprec Research Labs Pvt. Ltd. is a NABL-accredited Contract Research Organisation (CRO) established in 2012, headquartered in Ahmedabad, Gujarat. The company offers comprehensive testing and research solutions for pharmaceuticals, bio-products, food, nutraceuticals, cosmetics, agrochemicals, and medical devices under one roof.
With a strong emphasis on accuracy, precision, and regulatory compliance, Accuprec supports global clients for NDA, ANDA, USFDA QC release, and DMF filings. It maintains a global footprint, including a branch in Hamilton, Canada, and serves over 650 pharmaceutical clients worldwide through cutting-edge analytical services and innovation-driven processes.
Job Details
- Company Name: ACCUPREC RESEARCH LABS PVT. LTD.
- Experience: 5-7 Years
- Qualification: B.Pharm, M.Pharm
- Location: Ahmedabad, Gujarat (Head Office: Opp. Pharmez, Changodar – Bavla Highway, Nr. Matoda Patia, Post: Matoda, Ahmedabad – 382213)
Job Description
Accuprec Research Labs Pvt. Ltd. is expanding its team in the Analytical Development & Quality Control Department. We are looking for a talented Sr. Research Associate to contribute to stability studies, analytical method development, and regulatory-compliant quality control activities in a fast-paced CRO environment.
Sr. Research Associate
- Department: Analytical Development & Quality Control
- Experience: 5-7 Years
- Education/Qualification: B.Pharm, M.Pharm
Skills/Qualifications
- In-depth knowledge of ICH Q1A/Q1B guidelines
- Experience in stability study design, protocols, and execution
- Hands-on expertise with HPLC, GC, UV, and Dissolution apparatus
- Proficiency in handling stability chambers (Temperature/RH control)
- Strong understanding of GDP, GLP, and ALCOA+ principles
- Expertise in data trending, OOT/OOS evaluation, and investigation
- Ability to prepare stability reports and estimate shelf-life
- Familiarity with USFDA and EMA regulatory guidelines
- Proficient in LIMS, Empower software, and MS Excel
- Excellent communication and teamwork skills
Key Responsibilities
- Design and execute stability study protocols as per ICH guidelines
- Perform analytical testing using HPLC, GC, UV, and Dissolution
- Monitor and maintain stability chambers for Temp/RH conditions
- Ensure compliance with GDP, GLP, and ALCOA+ documentation standards
- Conduct data trending and evaluate OOT/OOS results
- Prepare stability reports and support shelf-life estimation
- Review data in LIMS and Empower for regulatory submissions
- Collaborate with team members for timely project delivery
Benefits/Perks
- Professional growth and career advancement opportunities
- Collaborative and supportive work environment
- Comprehensive benefits package
- Exposure to global regulatory standards and international projects
- Learning opportunities in advanced analytical techniques and compliance
How to Apply
Interested candidates can send their updated resume to career@accuprec.in or contact the HR team at 7600138060 / 9099932105. Mention the reference 2026-27/04-01 in the subject line. For more pharma jobs and opportunities in the industry, explore listings on PharmaRecruiter.in.
We encourage quick applications as this is a time-sensitive hiring for the Analytical Development & Quality Control team. Join a dynamic CRO and advance your pharmaceutical careers in India.
Why You Should Join
Accuprec Research Labs fosters a culture of excellence, innovation, and regulatory integrity. Employees benefit from long-term career stability in a growing CRO with global clientele. You will gain hands-on experience with advanced analytical tools while working in a compliant, collaborative environment that values continuous learning and professional development.
This role offers the perfect platform to build expertise in stability studies and quality control for international regulatory submissions.
FAQs
1. What is the experience required for the Sr. Research Associate position?
Candidates need 5-7 years of relevant experience in analytical development or quality control, preferably in a pharma or CRO setup.
2. What qualifications are needed for this pharma job?
B.Pharm or M.Pharm graduates with strong knowledge of ICH guidelines and analytical instruments are eligible.
3. Is this a walk-in interview or application-based role?
Applications are accepted via email. Shortlisted candidates will be contacted for further process. No specific walk-in date is mentioned.
4. What growth opportunities does Accuprec offer?
The company provides professional growth, exposure to global projects, and skill enhancement in regulatory-compliant analytical work, supporting long-term career progression in the pharmaceutical industry.
