Accuprec Research Hiring QA, R&D, AD, IT & Mechanical

Accuprec Senior Roles – QA, R&D, AD – Ahmedabad

Accuprec Research Labs hiring senior professionals for QA, R&D, AD, IT & Mechanical roles in Ahmedabad. 8–20 years experience.

Accuprec Research Labs Pvt. Ltd. has announced senior-level job openings at its Ahmedabad facility for highly experienced professionals across Quality Assurance, Analytical Development, R&D, Pharmacology & Toxicology, Mechanical Engineering, IT, and GLP Quality Assurance functions. These opportunities are intended for professionals who have built strong technical careers and are now ready to lead, mentor teams, and drive regulated scientific operations.

This hiring initiative is well suited for candidates with extensive exposure to pharmaceutical research, testing laboratories, regulatory compliance, and advanced instrumentation. Accuprec offers a mature, compliance-driven environment where senior professionals can directly influence quality systems, innovation pipelines, and commercialization strategies.

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Company Overview

Accuprec Research Labs Pvt. Ltd. is a recognized research, testing, and analytical services organization supporting pharmaceuticals, medical devices, and healthcare products. The company operates under stringent regulatory frameworks including NABL ISO 17025 and GLP, delivering high-precision analytical, validation, and research solutions.

With advanced laboratories, multidisciplinary scientific expertise, and a strong compliance culture, Accuprec serves global clients across API research, formulation development, toxicology, pharmacology, nanotechnology, and medical device testing. The organization is known for its technical depth, documentation discipline, and regulatory alignment.

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Job Role & Responsibilities

Accuprec is hiring for multiple senior and leadership positions. Responsibilities vary by department but require a strong balance of technical expertise, regulatory understanding, and people management.

AGM / DGM – Quality Assurance

• Lead the Quality Assurance department and oversee QA systems
• Ensure compliance with GLP, GMP, and applicable regulatory standards
• Review and approve SOPs, protocols, validation documents, and reports
• Manage internal and external audits and continuous improvement initiatives
• Drive quality culture and risk-based compliance strategies

Manager – Analytical Development (LC / LC–MS)

• Lead analytical method development using LC and LC–MS platforms
• Review method validation protocols, analytical reports, and data packages
• Ensure data integrity, ALCOA+ compliance, and regulatory readiness
• Guide analytical teams and support client-facing technical discussions

Manager – Pharmacology & Toxicology

• Oversee pharmacology and toxicology study execution
• Review study protocols, reports, and scientific interpretations
• Ensure GLP compliance and data integrity throughout study lifecycle
• Coordinate with clients and regulatory stakeholders as required

Manager – Mechanical Department

• Manage design and development of machinery and instruments for medical device testing
• Maintain NABL ISO 17025 documentation and compliance for the Mechanical Department
• Review protocols, reports, and compiled data for assigned projects
• Approve SOPs, STPs, and departmental documentation
• Lead mechanical testing activities and technical teams

Manager – R&D Department

• Lead R&D projects involving synthesis, formulation, and material analysis
• Characterize nanomaterials using advanced techniques such as NMR, EPR, XRD, AFM, CRYO-TEM, and SEM
• Identify niche APIs and KSMs through market research, patent analysis, and technology landscape studies
• Establish lab-scale and pilot-scale processes for selected APIs and KSMs
• Support commercialization, scale-up, and technology transfer activities

Manager – IT Department (Pharma Experience)

• Manage IT infrastructure supporting laboratory and pharma operations
• Ensure system validation, data security, and regulatory compliance
• Support laboratory informatics, digitalization, and system integration initiatives

Assistant Manager – QAU / GLP

• Support GLP Quality Assurance Unit activities
• Review study documentation, SOPs, and compliance records
• Assist in audits, inspections, deviations, and CAPA management

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Eligibility / Qualifications

Required Education

M.Sc, M.Pharm, Ph.D (Nanotechnology), M.Tech, B.Tech, Diploma (Mechanical/Biomedical), M.Sc Physics, BE (IT/CS/EC/IC)

Experience Requirements

• AGM / DGM – QA: 15–20 years
• Manager – AD (LC / LC–MS): 10–15 years
• Manager – Pharmacology & Toxicology: 10–15 years
• Manager – Mechanical: 10–15 years
• Manager – R&D: 10–15 years
• Manager – IT: 10–15 years (Pharma experience mandatory)
• Assistant Manager – QAU / GLP: 8–10 years

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Location & Salary

• Job Location: Ahmedabad, Gujarat
• Employment Type: Full-time
• Salary: No bar for the right candidate. Compensation will be commensurate with experience, expertise, and leadership scope.

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Application Process

Interested candidates should send their updated resumes via email, clearly mentioning the position applied for.

• Email: career@accuprec.in

Candidates should include the following details:

• Current CTC
• In-hand salary
• Expected CTC
• Notice period

For inquiries:

• Contact: 7600138060 / 9099932105

Company website:

• Website: www.accuprec.com

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Frequently Asked Questions (FAQs)

Who should apply for these roles?

Senior professionals with extensive pharma, CRO, laboratory, or research experience should apply.

Are these purely managerial roles?

These are senior technical leadership roles with both hands-on and managerial responsibilities.

Is salary negotiable?

Yes. Salary is not a limiting factor for suitable candidates.

Where are these roles based?

All positions are based in Ahmedabad, Gujarat.

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Summary Table

Company	Accuprec Research Labs Pvt. Ltd.
Vacancies	Multiple Senior Positions
Required Education	M.Sc, M.Pharm, Ph.D, M.Tech, B.Tech, Diploma, BE
Experience	8–20 years (Role-dependent)