Join exciting pharma jobs at Accuprec Research Labs Pvt. Ltd. in Ahmedabad! Multiple openings in Regulatory Affairs, Analytical Development, and QC for experienced professionals. Ideal for pharmaceutical careers in India with growth in a leading CRO. Apply now for these regulatory and analytical roles.
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About the Company
Accuprec Research Labs Pvt. Ltd. is a premier NABL-accredited, GLP-certified, and USFDA-recognized Contract Research Organization (CRO) based in Ahmedabad, Gujarat, India. Founded in 2012, Accuprec delivers comprehensive testing and research services for pharmaceuticals, medical devices, herbal products, food, nutraceuticals, and agrochemicals.
With global offices in the USA and Canada, the company supports over 650 clients worldwide in NDA, ANDA, DMF filings, and compliance with ICH, ISO, USP, and other international standards. Accuprec emphasizes innovation, accuracy, precision, and strict regulatory adherence, creating an ideal environment for professional excellence and career advancement in the pharma sector.
Job Details
- Company Name: Accuprec Research Labs Pvt. Ltd.
- Experience: 3–7 years (varies by role)
- Qualification: M. Pharm / M. Sc (in Regulatory Affairs, Analytical Chemistry, or related fields)
- Location: Ahmedabad, Gujarat (Head Office: Opp. Pharmez / Zydus Pharmez, Changodar – Bavla Highway, Nr. Matoda Patia, Post: Matoda, Ahmedabad – 382213)
- Work Type: On-site
Job Description
Accuprec Research Labs Pvt. Ltd. is actively expanding its team for new ventures and high-impact projects. The company is hiring talented professionals across Regulatory Affairs, Analytical Development (AD), and Analytical Development & Quality Control (AD&QC) departments.
These roles involve critical work in global dossier submissions, advanced analytical techniques, impurity profiling, and ensuring compliance with international regulatory guidelines.
Regulatory Affairs
- Department: Regulatory Affairs
- Role: Regulatory Affairs professional
- Experience: 3–5 years
- Education/Qualification: M. Pharm (Regulatory Affairs)
Study Director – Analytical Development
- Department: Analytical Development
- Role: Study Director
- Experience: 4–6 years
- Education/Qualification: M. Pharm, M. Sc
Sr. Research Associate – LCMS (AD&QC)
- Department: AD&QC (Analytical Development & Quality Control)
- Role: Sr. Research Associate – LCMS
- Experience: 4–6 years
- Education/Qualification: M. Sc, M. Pharm (Analytical Chemistry)
Research Associate / Sr. Research Associate – HPLC AMV (AD)
- Department: Analytical Development (AD)
- Role: Research Associate / Sr. Research Associate – HPLC (Analytical Method Validation)
- Experience: 3–7 years
- Education/Qualification: M. Sc, M. Pharm
Skills/Qualifications
- Strong expertise in CTD/eCTD dossier compilation and submission per country-specific and EAEU requirements
- Hands-on experience with LC-MS/MS for trace-level impurity detection, especially nitrosamines
- Proficiency in HPLC, UV, Dissolution, IC, and instrument calibration
- Knowledge of ICH guidelines (Q2, M10), ISO, USP for method validation, forced degradation, extractables & leachables
- Experience in nitrosamine risk assessment, NDSRI evaluation, and control strategy development
- Ability to perform gap analysis, monitor regulatory/pharmacopoeial updates (CIS/EAEU focus)
- Skills in bioequivalence study planning, raw data review, and compliance with ICH-GCP
- Excellent documentation, coordination, and problem-solving abilities
Key Responsibilities
- Compile, review, and submit product registration dossiers in CTD/eCTD format
- Prepare Site Master File (SMF) and support GMP inspection documentation for CIS/EAEU approvals
- Conduct gap analysis of existing CTD dossiers against EAEU unified standards
- Track CIS/EAEU pharmaceutical regulations, pharmacopoeial changes, and submission guidelines
- Lead nitrosamine impurity assessments and LC-MS/MS method development/validation
- Perform analytical method development, verification, validation, and forced degradation studies
- Ensure studies comply with approved protocols, ICH guidelines, and regulatory standards
- Verify raw data, review reports, and coordinate bioanalytical/PK and BE studies
- Oversee chemical characterization, extractables/leachables, and dose formulation analysis
Benefits/Perks
- Strong focus on professional growth and career progression
- Collaborative and innovative work environment
- Comprehensive benefits package
- Exposure to cutting-edge global regulatory and analytical projects
- Opportunity to work with advanced instruments and international compliance standards
How to Apply
Send your updated resume to career@accuprec.in or contact via phone/WhatsApp at 7600138060 / 9099932105. Include the relevant job reference code (e.g., Ref: 2025-26/02-06 for Regulatory Affairs) in the subject line or message.
Verified Post
Verification: Directly Shared by HR.
Shortlisted candidates will be invited for interviews. Seize these pharma jobs in a dynamic CRO—apply today!
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Why You Should Join
Accuprec Research Labs provides a supportive culture rooted in accuracy, precision, and regulatory excellence within a GLP and NABL-accredited facility. Enjoy long-term career stability, continuous learning through diverse global projects, and the satisfaction of contributing to high-quality, compliant pharmaceutical solutions.
This is the perfect platform for professionals eager to advance in pharmaceutical careers in India while working in an innovative and growth-oriented setting.
FAQs
What qualifications do these pharma jobs at Accuprec require?
Roles typically need M. Pharm or M. Sc in relevant specializations (e.g., Regulatory Affairs, Analytical Chemistry) with 3–7 years of experience.
How do I apply for these positions in Ahmedabad?
Email your CV to career@accuprec.in or call/WhatsApp 7600138060 / 9099932105, mentioning the job reference.
Are these on-site roles only?
Yes, all positions are full-time on-site at the Ahmedabad head office in Matoda.
What career growth can I expect at Accuprec?
The company prioritizes professional development, collaborative culture, and exposure to international projects for sustained career advancement.
