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Eurofins

Global lab testing and analytics network

Associate Formulation Analytical

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeBengaluru, Karnataka, IndiaNo salary listedIn-person

About the Job

Requirements

  • A Master's degree (M.Sc. or M. Pharm.) in Chemistry, Pharmaceutical Sciences, or a related discipline is required.
  • A minimum of 3–4 years of professional experience in analytical chemistry, pharmaceutical formulation analysis, or a related laboratory environment is required.
  • Demonstrated expertise in analytical instrumentation, including HPLC-UV, GC, LC-MS/MS, and ICP-MS, is required.
  • Comprehensive knowledge of regulatory compliance standards, including GLP and GMP guidelines, is required.
  • Proficiency in analytical method development, validation, and documentation in accordance with regulatory requirements is required.
  • Technical competency in data management and regulatory documentation practices is required.

Responsibilities

  • Develop, optimize, and validate analytical methods for New Chemical Entities (NCEs) and generic compounds using HPLC-UV, GC, LC-MS/MS, and ICP-MS.
  • Ensure analytical methods meet regulatory requirements and are suitable for their intended applications.
  • Perform dose verification analysis on preclinical dose formulation samples using HPLC-UV, GC, and LC-MS/MS.
  • Generate Certificates of Analysis (CoA) for Investigational New Drug (IND) submissions in compliance with regulatory requirements.
  • Conduct routine calibration and maintenance of laboratory equipment, including HPLC systems, pH meters, analytical balances, and pipettes, in accordance with established protocols.
  • Maintain detailed calibration records and ensure instruments remain within acceptable operating parameters.
  • Maintain comprehensive and secure raw data management practices in compliance with GLP/GMP standards.
  • Prepare and develop study protocols and Standard Operating Procedures (SOPs) to ensure consistency and regulatory adherence.
  • Maintain laboratory facilities and operations in compliance with Good Laboratory Practice (GLP) guidelines.
  • Support day-to-day laboratory operations while adhering to quality and safety standards.
  • Collaborate with cross-functional teams to ensure timely completion of analytical projects.

Desired Qualifications

  • Experience with IND submissions and preclinical analytical support is preferred.
  • Familiarity with pharmaceutical quality assurance protocols and Certificate of Analysis (CoA) preparation is preferred.
  • A proven track record of maintaining regulatory compliance in a pharmaceutical or contract research organization (CRO) setting is preferred.

About the Company

Eurofins

Global lab testing and analytics network

Eurofins provides global laboratory testing and analytical services to verify the safety, authenticity, and quality of products across food, water, medicine, and the environment. It operates a network of more than 900 laboratories in over 60 countries, offering access to more than 200,000 analytical methods. Its product work involves running specialized tests—using chemistry, biology, and other scientific techniques—to confirm origin, composition, and compliance of samples, such as detecting wine fraud or contaminant presence. The company differentiates itself through its massive, distributed lab network and broad portfolio, enabling standardized testing at scale and fast turnaround across many industries, rather than relying on a single specialty or location. Its goal is to protect public health and safety by delivering accurate, comprehensive testing data and helping clients meet regulatory and quality requirements.

Company size
10,001+
Company stage
IPO
Headquarters
Luxembourg
Founded
1987

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