Accuprec Walk-In Study Personnel, Study Director, Research Associate, Sr. Research Associate, Assistant Manager

Accuprec Research Labs Walk-In Drive 2026 Hyderabad – GLP Jobs for M.Pharm, MSc, PhD Candidates

Accuprec Research Labs Pvt. Ltd. is conducting a walk-in interview in Hyderabad for multiple GLP (Good Laboratory Practice) roles across departments such as Pharmacology & Toxicology, Pathology, Analytical Development (AD), Bioanalytical, QAU, and Biotechnology. The company is offering multiple vacancies for designations including Study Personnel, Study Director, Research Associate, Sr. Research Associate, and Assistant Manager.

This hiring drive is ideal for both freshers and experienced professionals, with opportunities ranging from 0 to 15 years of experience. The job location is Ahmedabad, Gujarat, while the walk-in interview will be held in Hyderabad.

Candidates with M.Pharm, M.Sc, PhD, B.Sc, DMLT, and MLT qualifications are eligible depending on the role. This is a strong opportunity for professionals aiming to build careers in clinical research, GLP toxicology studies, regulatory science, and pharmaceutical R&D.

Company Overview

Accuprec Research Labs Pvt. Ltd. is a reputed contract research organization (CRO) specializing in preclinical research, toxicology studies, and GLP-compliant analytical services. The company supports pharmaceutical, biotechnology, and agrochemical industries by delivering high-quality research solutions aligned with global regulatory standards.

With expertise in areas such as bioanalytical method validation, extractables and leachables, and chemical characterization, Accuprec plays a critical role in drug development and regulatory submissions.

Working at Accuprec offers:

• Exposure to GLP-certified laboratory environments
• Hands-on experience in toxicology and analytical research
• Opportunities in regulatory-driven pharmaceutical development
• Career growth in CRO and life sciences sectors

Job Role & Responsibilities

Pharmacology & Toxicology (Study Personnel / Study Director / Manager)

• Conduct and manage preclinical toxicology studies as per GLP guidelines
• Prepare study protocols, reports, and regulatory documentation
• Ensure compliance with ICH, OECD, and regulatory standards
• Supervise study execution and data integrity

Pathology (Research Associate)

• Perform histopathology and tissue analysis
• Maintain laboratory records and documentation
• Support toxicological evaluations and reporting

Analytical Development (AD-Agro / AD)

• Conduct physico-chemical studies and batch analysis
• Perform method validation as per ICH Q2 and ICH M10 guidelines
• Work on extractables & leachables and chemical characterization studies

QAU (Quality Assurance Unit)

• Monitor GLP compliance and audit study processes
• Handle QMS activities including deviation, CAPA, and documentation
• Support regulatory inspections and internal audits

Biotechnology (Genotox)

• Perform genotoxicity studies and bioanalytical assessments
• Maintain compliance with regulatory and GLP requirements

These roles are crucial in ensuring regulatory compliance, data integrity, and safety evaluation in drug development processes.

Eligibility / Qualifications

Required Education

M.Pharm (Pharmacology, Toxicology, QA), M.Sc (Chemistry, Microbiology, Biotechnology), PhD (Biotechnology), B.Sc, DMLT, MLT

Experience

• Freshers to 15 years depending on role

Skills Required

• Knowledge of GLP, ICH, OECD guidelines
• Experience in toxicology, analytical research, or QMS
• Strong documentation and regulatory compliance skills
• Attention to detail and scientific reporting ability

Location & Salary

Job Location:

• Ahmedabad, Gujarat

Interview Location:

• Hyderabad, Telangana

Salary:

• Competitive salary based on experience and role

Application Process

Walk-In Interview Details:

• Date: 5th April 2026 (Sunday)
• Time: 09:00 AM to 05:00 PM
• Venue: Hotel RCC Prime, Opp Andhra Bank, Moosapet X Road, Kukatpally, Hyderabad

Contact Details:

• Phone: +91 76001 38060, +91 90999 32105
• Email: career@accuprec.in

Candidates are advised to carry updated resumes, educational documents, and experience certificates.

Why You Should Apply

• Multiple vacancies across GLP and CRO domains
• Opportunity to work in regulatory-focused research environment
• Exposure to global pharmaceutical development standards
• Strong career growth in toxicology, bioanalytical, and regulatory research

FAQs

Who can apply for these roles?

Candidates with M.Pharm, M.Sc, PhD, B.Sc, DMLT, or MLT qualifications.

Is this suitable for freshers?

Yes, select roles are open for freshers with 0–2 years of experience.

What is the job location?

Ahmedabad, Gujarat.

Where is the interview conducted?

Hyderabad.

What domains are available?

GLP Toxicology, Analytical Development, QAU, Pathology, and Biotechnology.

Summary Table

Company	Accuprec Research Labs Pvt. Ltd.
Vacancies	Study Personnel, Study Director, Research Associate, Sr. Research Associate, Assistant Manager
Required Education	M.Pharm, M.Sc, PhD, B.Sc, DMLT, MLT
Experience	0–15 years