Eurofins: Associate - Formulation Analytical — Bengaluru, KA, India

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 Associate - Formulation Analytical in Bengaluru, KA, India, under reference REF81282K. The details below separate the work described by the employer from essential conditions, preferred experience and practical preparation advice.

• Department: R&D
• Employment type: Full-time
• Employer listing date: 15 September 2026
• Legal Entity: CIN014 - Eurofins Advinus BioPharma Services India Private Limited
• Sub-Business Line: BioPharma Development and Manufacturing
• Contract Type: Permanent
• Business Lines: Biopharma Services

Responsibilities and work described

• Analytical Method Development & Validation
• Develop, optimize, and validate analytical methods for New Chemical Entities (NCEs) and generic compounds using advanced instrumentation including HPLC-UV, GC, LC-MS/MS, and ICP-MS
• Quality / delivery: all methods meet regulatory requirements and are suitable for intended applications
• **Preclinical Analysis & Quality Assurance**
• Execution: dose verification analysis on preclinical dose formulation samples utilizing HPLC-UV, GC, and LC-MS/MS techniques
• Generate Certificates of Analysis (CoA) for Investigational New Drug (IND) submissions with accuracy and attention to regulatory compliance
• **Equipment Calibration & Maintenance**
• Research / execution: routine calibration and maintenance of laboratory equipment including HPLC systems, pH meters, analytical balances, and pipettes in accordance with established protocols
• Maintenance: detailed calibration records and ensure all instruments remain within acceptable operating parameters
• **Regulatory Compliance & Documentation**
• Maintenance: comprehensive and secure raw data management practices in compliance with GLP/GMP standards
• Preparation: and develop study protocols and Standard Operating Procedures (SOPs) to ensure consistency and regulatory adherence
• Maintenance: laboratory facilities and operations in full compliance with Good Laboratory Practice (GLP) guidelines
• **Laboratory Operations**
• Support: day-to-day laboratory operations while adhering to all quality and safety standards
• Collaboration: with cross-functional teams to ensure timely completion of analytical projects

Essential requirements and candidate background

• Master's degree (M.Sc. or M
• Pharm.) in Chemistry, Pharmaceutical Sciences, or related discipline
• Minimum 3-4 years of professional experience in analytical chemistry, pharmaceutical formulation analysis, or related laboratory environment
• Demonstrated expertise in analytical instrumentation, including HPLC-UV, GC, LC-MS/MS, and ICP-MS
• Comprehensive knowledge of regulatory compliance standards, including GLP and GMP guidelines
• Proficiency: analytical method development, validation, and documentation in accordance with regulatory requirements
• Technical competency in data management and regulatory documentation practices
• Experience: IND submissions and preclinical analytical support
• Familiarity: pharmaceutical quality assurance protocols and Certificate of Analysis (CoA) preparation
• Track record of maintaining compliance with regulatory standards in a pharmaceutical or contract research organization (CRO) setting

Preferred experience and additional strengths

• Preferred:

Location, schedule and contract conditions

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

Employer details to confirm

• The employer’s seniority category and its stated experience requirements do not agree. Follow the role-specific requirements above rather than assuming this is a fresher opening.

Pay and application dates

A verified salary figure is not established in this article. An online estimate for another Associate - Formulation Analytical vacancy is not an offer for reference REF81282K; 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 REF81282K.

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: GMP

GMP references concern work performed within a controlled manufacturing or quality environment. In an application, explain your actual involvement with procedures, records, deviations or other controls relevant to the post.

Relevant skills

• GMP
• quality assurance
• maintenance
• GLP
• laboratory testing
• HPLC
• compliance
• chemistry