Eurofins: Study Director – Toxicology — Bengaluru, KA, India

Eurofins lists a Study Director – Toxicology opening in Bengaluru, KA, India. The position is listed as full-time. The job description covers data analysis, GLP, pharmacy, compliance, project management, communication.

Recruitment overview

OrganisationEurofins
Post / roleStudy Director – Toxicology
DepartmentTesting & Laboratory
Employment typeFull-time
Notification / job IDREF81328M
Job locationBengaluru, KA, India
Work arrangementOn-site
Educational qualificationDegree / qualification: Qualification: Ph.D./Master's in Veterinary Sciences, Biosciences, or related disciplines
Experience requiredExperience as a Study Director or in an equivalent role within a CRO or pharmaceutical organization
Salary / stipendSee employer notice for pay details
Last date to applySee official notice

About Eurofins

Eurofins provides analytical testing and laboratory services across life sciences and other industries. Its work includes assessing food, water, pharmaceutical and cosmetic products for qualities such as safety, authenticity, composition and accurate labelling. The employer also describes activities in genomics, clinical-study support, biopharmaceutical development and manufacturing, and diagnostic testing. Scientific methods and dependable information are central to this business, supported by the technology and operational functions used to deliver laboratory services.

The position and its setting

Eurofins lists Study Director – Toxicology in Bengaluru, KA, India, under reference REF81328M. The details below separate the work described by the employer from essential conditions, preferred experience and practical preparation advice.

  • Department: Testing & Laboratory
  • Employment type: Full-time
  • Employer listing date: 16 September 2026
  • Legal Entity: CIN014 - Eurofins Advinus BioPharma Services India Private Limited
  • Brands: Eurofins India Advinus

Responsibilities and work described

  • Position: Study Director – Toxicology
  • The Study Director – Toxicology will be responsible for designing, conducting, overseeing, and reporting non-clinical safety studies (GLP and non-GLP) to support drug development and regulatory submissions
  • The role involves scientific leadership, regulatory compliance, study management, and cross-functional collaboration to ensure the quality and integrity of toxicology studies

Essential requirements and candidate background

  • Experience: repeat-dose toxicity, teratology, and reproductive toxicity studies/processes
  • Understanding: pharmaceutical R&D and agrochemical testing processes
  • Knowledge: GLP and relevant regulatory guidelines
  • Experience as a Study Director or in an equivalent role within a CRO or pharmaceutical organization
  • Scientific writing and communication skills
  • Lead teams and manage multiple projects simultaneously
  • Proficiency: data analysis and scientific interpretation
  • Team-working and cross-functional collaboration skills
  • Behavioral Competencies
  • Oral and written communication skills
  • Flexibility to work effectively in a environment
  • Effective time and project management skills
  • Takes ownership of responsibilities and demonstrates a commitment to continuous learning and improvement
  • Well-organized, structured, and efficient approach to work
  • Qualification: Ph.D./Master's in Veterinary Sciences, Biosciences, or related disciplines

Location, schedule and contract conditions

  • Work arrangement: On-site
  • Advertised location: Bengaluru, KA, India

Pay and application dates

A verified salary figure is not established in this article. An online estimate for another Study Director – Toxicology vacancy is not an offer for reference REF81328M; use the employer’s own pay disclosure and recruitment communication.

A closing date is not confirmed in this article. Check the current employer page before submitting: an undated posting can change or be withdrawn.

How to apply to Eurofins

Applications follow the official employer page linked below.

Open the official Eurofins posting below and match the title and reference REF81328M.

Compare your qualifications and experience with the essential conditions for the Bengaluru, KA, India position, then read the preferred criteria separately.

Prepare an accurate CV and the supporting items requested in that employer’s application. Provide only information and documents you are authorised to share.

Use the employer’s application option, complete the required fields and review the submission. Retain the acknowledgement when one is provided. Job Alerts World does not receive the application.

Practical preparation: data analysis

An analysis example should start with the question and the available data. Explain cleaning, assumptions, checks and the conclusion, including any limits that affected what could reasonably be inferred.

Relevant skills

  • data analysis
  • GLP
  • pharmacy
  • compliance
  • project management
  • communication

Important links

Official notification / job descriptionOpen official page
Online application portalOpen official page

Read the complete official notice before applying. Availability and requirements can change.

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