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LabCorp

Global life sciences R&D services

Experienced QC Analyst - Bioanalysis

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

About the Job

Requirements

  • A bachelor's degree in science.
  • At least 5 years of analysis experience in the pharmaceutical industry or a regulated laboratory.
  • At least 4 years of experience with PCR, bioassay, and chemical testing, including compendial testing, capillary electrophoresis, and high-performance liquid chromatography.
  • Proficiency in English; Dutch is an added value.
  • Computing skills, including word processing and spreadsheet use such as Microsoft Office.
  • Ability to independently perform a wide variety of analytical techniques.
  • Understanding of health and safety policies, company policies, and procedures.
  • Strong written and spoken communication skills.
  • Flexibility to perform other laboratory-related tasks when needed.

Responsibilities

  • Perform and oversee analytical testing in accordance with Good Manufacturing Practice requirements, study protocols, and laboratory procedures.
  • Review and evaluate test results, investigate trends or deviations, and support problem-resolution activities.
  • Collaborate with QC Scientists and cross-functional teams to deliver studies on time and to quality standards.
  • Receive and register samples and keep the laboratory clean.
  • Support method troubleshooting, transfer, validation, and continuous improvement initiatives.
  • Maintain laboratory equipment, documentation, and quality records in line with regulatory requirements.
  • Ensure compliance with data-integrity standards and Good Manufacturing Practice regulations.
  • Contribute to audits, inspections, investigations, and quality-improvement activities.
  • Serve as a subject matter expert for analytical techniques and support execution of complex projects.
  • Complete analyses efficiently and effectively, maintaining study documentation and laboratory records.
  • Complete work according to the laboratory schedule, relevant standard operating procedures and policies, and scientific and technical standards, including Good Manufacturing Practice.
  • Carry out operational activities required for a wide variety of departmental studies and maintain a clean and safe laboratory work environment.

Desired Qualifications

  • At least 2 years of experience with Good Manufacturing Practice in a quality-control environment.
  • Dutch language skills.

About the Company

LabCorp

Global life sciences R&D services

Labcorp provides global life sciences and healthcare R&D services, supporting pharma, biotech, and crop protection clients with testing, safety assessments, and regulatory submissions. It conducts studies ranging from basic physicochemical tests to complex inhalation toxicology and uses specialized facilities to evaluate inhaled substances and ensure regulatory compliance. Its global presence and integrated suite of services enable clients to move projects from early development to product approval within one organization. Labcorp aims to help clients bring safe, effective products to market efficiently, advancing human health and scientific research.

Company size
10,001+
Company stage
IPO
Headquarters
Burlington, VT
Founded
1976

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