India Toxicologist Jobs – 6 Open Jobs Today

Sr. Executive / Assistant Manager, Toxicology | NCE
Amneal Pharmaceuticals —Ahmedabad, Gujarat
- Full-time
- Doctoral degree
- Master's degree
- EMR systems
Cosmetic toxicologist
Euverify —Calicut, Kerala
- From ₹20,000 a month
- Full-time
- Customer service
- English
- Master's degree
Quick apply
13d
Associate Scientist, Toxicology (174186)
Colgate-Palmolive —Mumbai, Maharashtra
- English
- Master's degree
- Travel
Eco Toxicologist
Global Product Compliance —Nagpur, Maharashtra
- Doctoral degree
- Master's degree
1700_Extracables & Leachables
Recruise —Bengaluru, Karnataka
- Full-time
- B.Sc
- Microsoft Office
- Master's degree
Quick apply
Head Animal Pharmacology Toxicology
Venus Remedies —Baddi, Himachal Pradesh
- Full-time

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Cosmetic toxicologist
Euverify —Calicut, Kerala
Work across the EU and UK cosmetic regulatory compliance lifecycle for international cosmetic brands. The role offers hands-on exposure across the full spectrum…
From ₹20,000 a month
Quick apply
13d

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Sr. Executive / Assistant Manager, Toxicology | NCE

Amneal Pharmaceuticals -
Ahmedabad, Gujarat

Apply Now

Job details

Full-time

Qualifications

Doctoral degree
Master's degree
EMR systems
Communication skills

Full job description

Key Responsibilities

Nonclinical safety and toxicology study design & execution -

1. Design, plan, and conduct in vivo and/or in vitro safety pharmacology and toxicology
studies in alignment with GLP principles.
2. Select appropriate species, study duration, and endpoints based on pharmacology,
pharmacokinetics and regulatory requirements.
3. Review study raw data, protocols, results and reports.
4. Oversee study execution, ensure data accuracy, and coordinate with CROs or internal cross
functional teams.
• Risk Assessment & Safety Evaluation -
1. Analyse and interpret the safety and toxicology data and integrate findings with pharmacokinetics and pharmacodynamics to assess potential safety risks.
2. Perform toxicological risk assessments including PDE/OEL/ADI derivations, impurity/excipient qualification assessments, extractables & leachables evaluations, and safety margin calculations.
3. Conduct exposure assessments for process materials, impurities, metabolites, degradation products and excipients.
• Regulatory & Documentation -
1. Prepare and review high-quality safety and toxicology study reports, technical summaries, and nonclinical sections of regulatory submission documents (IND, NDA/MAA, ANDA, eCTD Modules 2.4/2.6 & 4, briefing books and IB, etc.).
2. Support regulatory filings to USFDA, EMA, DCGI, and other global agencies.
3. Draft and review regulatory query responses, briefing documents, and expert justifications.
• Toxicology Informatics & Literature Research -
1. Perform comprehensive literature searches using toxicity databases (e.g., PubMed, TOXNET, ECHA, HSDB, etc.,).
2. Utilize modern toxicity prediction & risk assessment software/tools (e.g., DEREK Nexus, CASE Ultra, OECD QSAR Toolbox, etc.).
3. Interpret computational toxicology outputs and integrate them into safety evaluations.
• Compliance & Quality -
1. Ensure full adherence to global regulatory guidelines (ICH, OECD, EMA, and USFDA).
2. Support internal audits, regulatory inspections, and quality compliance activities related to toxicology studies.
• Cross-Functional Collaboration
1. Work closely with Pharmacology, ADME, DMPK, CMC, Clinical and Regulatory Affairs teams.
2. Represent toxicology in project meetings and contribute to risk/benefit evaluations.

Required Qualifications & Skills

Master’s or PhD in Toxicology, Pharmacology, Veterinary Sciences, or related biomedical science discipline.

8-10 years’ experience in preclinical toxicology with at least 5 years as a Study Director in a GLP-certified facility.

Strong understanding of regulatory toxicology for USFDA, EMA, and DCGI submissions.

Proven experience in designing, monitoring, and interpreting in vivo and/or in vitro safety pharmacology and toxicology studies.

Hands-on experience preparing toxicology study reports and regulatory documents.

Expertise in risk assessments, exposure limits, and safety justification documents.

Experience in handling regulatory queries or participating in agency interactions.

Familiarity with modern in silico computational toxicology and predictive safety tools will be a plus.

Strong scientific writing, analytical, problem-solving, and communication skills.

Board certification as toxicologist (DABT, ERT, or equivalent) is advantage, but not mandatory

Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion.

Apply Now

Refine Your Search

toxicologist jobs in india

Sr. Executive / Assistant Manager, Toxicology | NCE

Cosmetic toxicologist

Associate Scientist, Toxicology (174186)

Eco Toxicologist

1700_Extracables & Leachables

Head Animal Pharmacology Toxicology

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