Accuprec Hiring Pharmacology, Toxicology & QAU

MPharm/MSc GLP Vacancies at Accuprec Ahmedabad

M.Pharm, M.Sc, B.Pharm GLP vacancies at Accuprec Ahmedabad. Multiple openings in Pharmacology, Toxicology & QAU.

Accuprec Research Labs Pvt. Ltd. is hiring experienced and entry-level professionals for its GLP-compliant research facility in Ahmedabad. If you are from Pharmacology, Toxicology, QA, Biotechnology, Chemistry, or Life Sciences background and looking for regulated GLP laboratory careers, this walk-in opportunity opens doors to high-growth research roles.

These openings are ideal for candidates searching for GLP pharmacology jobs, toxicology research vacancies, QA QAU executive roles, in-vivo research associate positions, genotoxicity biotechnology jobs, and agrochemical analytical research careers in Gujarat.

Company Overview

Accuprec Research Labs Pvt. Ltd. is a GLP-certified contract research organization (CRO) offering toxicology, pharmacology, genotoxicity, and agrochemical research services. The organization supports pharmaceutical, biotech, and agrochemical companies in generating regulatory-compliant preclinical data for global submissions.

Operating under Good Laboratory Practice (GLP) guidelines, Accuprec maintains strict documentation control, data integrity systems, validated protocols, and regulatory inspection readiness. The laboratory supports in-vivo and in-vitro studies, toxicology evaluation, pharmacokinetics research, and QAU oversight aligned with international regulatory expectations.

Working at Accuprec means contributing to preclinical research that directly supports drug development, agrochemical safety assessment, and global regulatory submissions.

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Job Role & Responsibilities

1. Manager – Pharmacology & Toxicology

Qualification: M.Pharm (Pharmacology & Toxicology)
Experience: 13–18 Years

Key Responsibilities:

• Lead GLP-compliant pharmacology and toxicology studies.
• Oversee in-vivo research protocols and study design.
• Ensure regulatory documentation and data integrity compliance.
• Guide scientific teams and manage project timelines.
• Support client audits and regulatory inspections.

This leadership role requires deep expertise in preclinical research, toxicology study management, and regulatory GLP compliance.

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2. Assistant Manager – QAU (GLP Department)

Qualification: M.Sc / M.Pharm (Quality Assurance)
Experience: 7–11 Years

Key Responsibilities:

• Conduct GLP audits and internal quality inspections.
• Review study protocols, raw data, and final reports.
• Ensure adherence to GLP documentation standards.
• Handle deviation reporting and corrective action tracking.
• Support regulatory inspection preparedness.

Strong experience in QAU documentation and GLP compliance systems is essential.

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3. Sr. Research Associate – AD Department (Agrochemical)

Qualification: M.Sc (Chemistry) or Equivalent
Experience: 5–8 Years

Key Responsibilities:

• Conduct analytical development studies for agrochemical research.
• Perform method validation and sample analysis.
• Maintain GLP-compliant documentation and instrument logs.
• Support regulatory submission data preparation.

Experience in analytical chemistry and regulatory laboratory environments is preferred.

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4. Research Assistant / Research Associate / Sr. Research Associate – Pharmacology & Toxicology (In-Vivo Department)

Qualification: M.Sc / M.Pharm (Pharmacology & Toxicology)
Experience: 0–8 Years

Key Responsibilities:

• Assist in in-vivo study execution and animal handling.
• Perform dosing, sample collection, and data recording.
• Maintain GLP documentation and study records.
• Support report compilation and scientific data analysis.

This role provides strong exposure to regulated preclinical pharmacology and toxicology research.

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5. Sr. Research Associate – Genotoxicity (In-Vitro Department)

Qualification: M.Sc (Biotechnology)
Experience: 5–8 Years

Key Responsibilities:

• Conduct in-vitro genotoxicity assays.
• Perform cell culture-based safety evaluation studies.
• Maintain laboratory compliance under GLP.
• Generate validated study reports for regulatory use.

Exposure to cytogenetic assays and molecular biology techniques is preferred.

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6. Data Entry Operator – QAU Department

Qualification: Any Graduation
Experience: 1–3 Years

Key Responsibilities:

• Maintain electronic documentation records.
• Support audit data compilation.
• Ensure accurate entry of regulatory study data.
• Maintain confidentiality and data integrity.

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7. Project Management – Pharmacology & Toxicology

Qualification: B.Sc, B.Pharm, M.Sc, M.Pharm
Experience: 0–2 Years

Key Responsibilities:

• Coordinate study timelines and documentation flow.
• Track project milestones.
• Support client communication and reporting.
• Assist senior scientists in documentation management.

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Eligibility / Qualifications

Eligible educational backgrounds include:
M.Pharm (Pharmacology & Toxicology), M.Sc (Chemistry), M.Sc (Biotechnology), M.Sc (QA), B.Pharm, B.Sc, Any Graduation (for data entry).

Candidates must have relevant GLP laboratory exposure for mid to senior roles.

Freshers may apply for entry-level research and project coordination positions.

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Location & Salary

Location: Ahmedabad, Gujarat
Salary: No bar for the right candidate (based on experience and expertise).

Compensation is aligned with GLP research industry standards in pharmacology, toxicology, and preclinical CRO environments.

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Application Process

Interested candidates must email their resumes to:
career@accuprec.in

Mention clearly:

• Position applied for
• Current CTC
• In-hand salary
• Expected CTC
• Notice period

For inquiries: 7600138060 / 9099932105

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Why Consider a GLP Career at Accuprec?

Working in a GLP-certified CRO strengthens your profile in:

• Preclinical toxicology studies
• Regulatory documentation for global submissions
• In-vivo and in-vitro research compliance
• Genotoxicity and safety pharmacology
• Quality assurance auditing under GLP

Experience in GLP environments significantly enhances long-term career growth in pharmaceutical research, regulatory toxicology, and global drug development programs.

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Frequently Asked Questions (FAQs)

1. Are freshers eligible?
Yes, for Research Assistant and Project Management roles.

2. Is GLP experience mandatory?
For senior roles, yes. Entry-level roles may consider freshers.

3. What location are the openings for?
Ahmedabad, Gujarat.

4. Are salaries negotiable?
Yes, salary is no bar for the right candidate.

5. How to apply?
Send your CV to career@accuprec.in mentioning the position applied.

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Summary

Company	Accuprec Research Labs Pvt. Ltd.
Vacancies	Manager (Pharmacology & Toxicology), Asst. Manager (QAU), Sr. Research Associate (AD Agrochemical), Research Assistant/Associate (In-Vivo), Sr. Research Associate (Genotox), Data Entry Operator (QAU), Project Management
Required Education	M.Pharm (Pharmacology & Toxicology), M.Sc (Chemistry/Biotechnology/QA), B.Pharm, B.Sc, Any Graduation
Experience	0–18 Years depending on role

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