Accuprec Research Labs Pvt. Ltd., a leading Contract Research Organization (CRO) based in Ahmedabad, Gujarat, is hiring for multiple roles with immediate joining. Established in 2012, Accuprec is FDCA, OECD-GLP, NABL, ISO 9001:2015, and USFDA-accredited, offering comprehensive testing and research solutions for pharmaceuticals, chemicals, phytochemicals, and medical devices.
With a state-of-the-art 85,000+ sq. ft. facility and a team of 150+ skilled professionals, we are committed to accuracy, precision, and innovation. Join us to advance your career in the pharmaceutical industry at our Ahmedabad location.
Job Openings Overview for Pharmaceutical Roles
We are hiring for the following positions with immediate joining at our Ahmedabad facility:
Research Associate (CQA – Corporate Quality Assurance)
- Qualification: M.Pharm (Quality Assurance)
- Experience: 2–4 years
Executive (CSV – IT Department)
- Qualification: M.Sc/B.E (Instrumentation & Control/Electronics & Communication)
- Experience: 3–5 years
Research Associate (Formulation & Development Department)
- Qualification: M.Pharm (Pharmaceutics)
- Experience: 3–5 years
Executive/Jr. Executive (Store – Engineering Department)
- Qualification: ITI/Diploma in Mechanical or Electrical
- Experience: 2–4 years
Research Assistant (QA Department)
- Qualification: B.Pharm/B.Sc
- Experience: Fresher (2023–2025 pass-outs)
- Job Location: Ahmedabad, Gujarat
- Salary: No bar for the right candidate
Job Description for CQA, CSV, Formulation & Development, Store, and QA Roles
Qualifications
- Research Associate (CQA): M.Pharm in Quality Assurance from a recognized institution.
- Executive (CSV): M.Sc or B.E in Instrumentation & Control or Electronics & Communication.
- Research Associate (F&D): M.Pharm in Pharmaceutics.
- Executive/Jr. Executive (Store): ITI or Diploma in Mechanical or Electrical engineering.
- Research Assistant (QA): B.Pharm or B.Sc in Chemistry, Biotechnology, or related sciences.
- Strong academic records are required for all roles.
Experience
- CQA: 2–4 years in Corporate Quality Assurance, preferably in a CRO or pharmaceutical setting.
- CSV: 3–5 years in Computer System Validation within the pharmaceutical or IT domain.
- F&D: 3–5 years in Formulation & Development of pharmaceutical dosage forms.
- Store: 2–4 years in store management or inventory control in an engineering or pharmaceutical context.
- QA: No experience required (freshers welcome).
Skills
- Research Associate (CQA):
- Expertise in reviewing Change Control, Deviations, OOS, CAPA, and investigation reports.
- Knowledge of GLP, GMP, and QMS for establishing quality systems.
- Proficiency in preparing and reviewing QA SOPs and coordinating with cross-functional teams.
- Executive (CSV):
- Proficiency in Computer System Validation (CSV) for pharmaceutical IT systems (e.g., LIMS, ERP).
- Knowledge of GAMP 5, 21 CFR Part 11, and EU Annex 11 guidelines.
- Experience in validation protocols, risk assessments, and IQ/OQ/PQ documentation.
- Research Associate (F&D):
- Expertise in developing oral solid dosage (OSD), liquid, or semi-solid formulations.
- Familiarity with pre-formulation studies, process optimization, and scale-up.
- Knowledge of GMP and regulatory requirements for formulation development.
- Executive/Jr. Executive (Store):
- Skills in inventory management, material handling, and store documentation.
- Familiarity with SAP or ERP systems for store operations.
- Basic understanding of mechanical/electrical components in a pharmaceutical setting.
- Research Assistant (QA):
- Basic knowledge of GMP, GLP, and quality assurance processes.
- Strong documentation skills and attention to detail for SOP preparation and audit support.
- Willingness to learn QA compliance and regulatory standards.
Responsibilities
- Research Associate (CQA):
- Review and close Change Control, Deviations, OOS, and CAPA reports.
- Participate in internal audits and ensure compliance with GLP/GMP standards.
- Prepare and review QA SOPs and coordinate with cross-functional teams.
- Executive (CSV):
- Develop and execute CSV protocols for IT systems in compliance with 21 CFR Part 11.
- Conduct risk assessments and prepare IQ/OQ/PQ documentation.
- Support system validation and maintain audit-ready documentation.
- Research Associate (F&D):
- Design and develop pharmaceutical formulations (e.g., tablets, capsules, liquids).
- Conduct pre-formulation studies, process optimization, and stability testing.
- Prepare technical documents for regulatory submissions and GMP compliance.
- Executive/Jr. Executive (Store):
- Manage inventory of engineering materials, tools, and spares in the store.
- Maintain accurate stock records using SAP/ERP and ensure timely material availability.
- Support procurement and vendor coordination for engineering supplies.
- Research Assistant (QA):
- Assist in QA documentation, including SOPs, batch records, and audit reports.
- Support internal audits and compliance activities under senior guidance.
- Learn and apply GMP/GLP standards in daily operations.
How to Apply for Pharmaceutical Jobs
Interested candidates can apply by sending their resumes to the designated email address:
Email: career@accuprec.in
- Subject Line: “Application for [Position Name] – Ahmedabad”
- Details to Include:
- In-Hand Salary
- Current CTC
- Expected CTC
- Notice Period
Documents to Submit:
- Updated resume
- Educational certificates (M.Pharm, M.Sc, B.E, B.Pharm, B.Sc, ITI, Diploma)
- Experience certificates (for non-freshers)
- Last 3 months’ salary slips (if applicable)
- Aadhar and PAN card copies
Contact for Inquiries:
- Phone: 90999 32105 / 90999 37398
- Email: career@accuprec.in
- Website: Visit www.accuprec.com for more details about Accuprec Research Labs and career opportunities.
Note: Accuprec Research Labs Pvt. Ltd. does not charge any fees for recruitment. Beware of fraudulent offers requesting payments and report suspicious activities to career@accuprec.in. Salary is no bar for the right candidate.
Why Join Accuprec Research Labs for Your Pharmaceutical Career
Accuprec Research Labs Pvt. Ltd. is a globally recognized CRO with accreditations from USFDA, NABL, OECD-GLP, and ISO 9001:2015, serving clients in pharmaceuticals, medical devices, and phytochemicals. With a 3.3/5 employee rating on AmbitionBox and a workforce of 150+, we offer a dynamic and innovative workplace. By joining our Ahmedabad team, you will:
- Work in a USFDA-approved facility with cutting-edge instrumentation and exposure to global standards.
- Contribute to 11 patented polyherbal formulations for chronic diseases like diabetes and arthritis.
- Benefit from a general shift schedule, free food, staff bus, mediclaim, and cooperative HR (rated 3.4/5 for work-life balance).
- Gain hands-on experience in CQA, CSV, F&D, store management, or QA with opportunities for skill development.
- Be part of a team driving innovation in 14 verticals, including analytical testing, preclinical studies, and formulation development.
Don’t miss this opportunity to advance your career in pharmaceutical jobs with Accuprec Research Labs Pvt. Ltd. Apply by sending your resume to career@accuprec.in and join our team in Ahmedabad for immediate openings