Consultant QC Analytical Method Validation

☞ Trevalco BV

View: 125

Update day: 11-11-2025

Location: Willebroek Antwerp

Category: Quality Assurance / Quality Control

Industry:

Position: Associate

Job type: Full-time

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Job content

Job position: consultant QC analytical method validation

Location: Belgium

You are a hands-on expert familiar with a broad range of analytical methodologies? You have great attention to detail? Then a job as consultant specialized in analytical method validation is something for you.

As consultant you support and execute routine and project related analytical method validation activities with clients in the pharmaceutical industry. You support the development, improvement and/or transfer of analytical methods and assist in the writting of reports. You support the organization during internal and external audits.

For this position we are looking at all levels of experience, although experience with analytical method development such as HPLC is required.

Your Responsibilities As Analytical Method Validation Consultant Include
  • write analytical method validation protocols and reports
  • review and approve lab results
  • coördinate activities of lab technicians, and supervise lab experiments
  • implement new and change existing lab methods in a controlled and documented manner
  • lab methods transfer to new equipment, new laboratories, new sites in a controlled and documented manner
  • manage quality records such as deviations, CAPA’s and change controls
HPLC is an analytical method often used in pharmaceutical QC laboratories. Experience with HPLC method development from a previous job, master thesis or internship is required for this position.

Qualifications

Must have
  • fluent in English, at least intermediate in Dutch
  • good knowledge of and experience with analytical method development, especially HPLC
  • strong analytical skills, well organized, studious and precise
  • you enjoy managing documentation: creating documents, reviewing and updating, getting approval on documents
  • master degree in science, or equivalent through experience
Nice to have
  • experience working in a GMP or GLP environment
  • experience with validation in a regulated environment (e.g. on lab equipment)
  • knowledge of pharmaceutical regulations
Our offer

Attractive salary package

including CAO90 bonus, hospitalization and dental care insurance, meal vouchers and much more

Company car or mobility budget

you choose what works best for you: company car, (e)bike, public transportation or a cash bonus

Training and development

coaching, classroom and digital online training, professional memberships, or whatever way is working best for you

Interesting projects

we don’t decide this for you, we decide with you what your next project or assignment will be

A fair, respectful employer

the right company culture is important to us: fair, respectful, transparent, being there for our employees

Work / life balance

because we have a family to take care of or non-professional commitments after working hours
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Deadline: 26-12-2025

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