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Lab support Technician Quality Control – Microbiological

On-site in Boxmeer·Full-time·Added yesterday (last checked 12 Nov)

MSD

57 open roles

Our summary

Work mode
On-site, Boxmeer
Contract
Full-time
Languages
Dutch
Experience
2+ years

Skills

Nice to have

This job advert was originally written in Dutch.

Requirements

What we're looking for

  • You have a completed MBO education, preferably in the field of microbiology, laboratory technology, or a similar field of study.
  • You have several years of relevant work experience, preferably within a microbiological QC laboratory, including experience with sterility testing and environmental monitoring.
  • You have experience with deviation and/or non-conformance management.
  • You have knowledge of GMP (Good Manufacturing Practice) and other quality systems within a regulated environment.

Nice to have

  • Preferably, you have experience with SAP, LIMS, and electronic data processing within QC testing systems.
  • You are quality-oriented, have strong communication skills, and possess a proactive and solution-oriented attitude. Additionally, you enjoy collaborating and taking initiative.
  • You are able to maintain an overview within a complex environment, set priorities, identify risks in a timely manner, and escalate where necessary.
  • You possess good oral and written skills in both Dutch and English, including the drafting of technical documentation (technical writing).

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Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status: Regular

Pay & benefits

What you'll get

Working at our organization means working together for health in an international work environment with dedicated colleagues. You will be given all the space to develop yourself and show who you are. Furthermore, you can count on attractive employment conditions:

  • Competitive salary depending on your knowledge and experience.
  • 3% year-end bonus and an annual bonus based on individual and company results.
  • At least 35.5 vacation days.
  • Travel allowance and a solid pension scheme.
  • A high-quality company restaurant with fresh and healthy daily options.
  • Excellent accessibility: the train station is located directly at our main entrance and there is ample parking availability.
  • A contribution to your personal gym membership to support your vitality.
  • A beautiful private park on the premises, ideal for a walk, a break, or a moment of relaxation.
  • Mental wellbeing support via Lyra Health for you and your family members.
  • Access to a separate prayer/meditation room.
  • Extensive growth opportunities thanks to the size of the site and the presence of many disciplines and global departments represented in Boxmeer.
  • A workplace within an organization that is continuously growing and evolving.

The role

Job Description

Are you accurate and quality-oriented and do you find problem-solving an interesting challenge? Are you a team player who likes to take initiative and thereby serves as an example to others? Are you able to maintain an overview in a complex environment? Do you want to work in a professional organization where there is plenty of room for your own development?

What you'll do

  • Identifying, registering, investigating, and following up on deviations, including coordinating necessary actions in accordance with GMP procedures.
  • Supporting the execution of root cause analyses and the implementation of corrective and preventive actions (CAPAs).
  • Drafting, monitoring, and optimizing the laboratory schedule to ensure timely execution of microbiological analyses.
  • Managing laboratory supplies and handling orders for reagents, consumables, and other laboratory necessities.
  • Coordinating and supporting daily operational activities within the microbiological laboratory.
  • Initiating, guiding, and implementing improvement projects aimed at efficiency, quality, and compliance.
  • Supporting audits, inspections, changes, training, and documentation management.
  • Drafting, reviewing, and maintaining laboratory documentation, including SOPs, work instructions, and forms.
  • Acting as a point of contact for operational issues and collaborating with internal stakeholders to further optimize laboratory processes.
  • Monitoring KPIs, trends, and process performance and identifying opportunities for improvement.

Lab support Technician Quality Control - Microbiological

Welcome to our team
Quality Control Operations (QCO) is a dynamic team that supports all Integrated Process Teams (IPTs) in the timely execution of quality control testing. QCO is responsible for all physical, chemical, biological, and microbiological analyses of vaccines and pharmaceutical finished products, antigens, raw materials, APIs, and primary packaging materials within the Boxmeer location.

About the position
The Lab Support Specialist Microbiology QC fulfills an important role within the microbiological laboratory and ensures that daily activities are carried out efficiently, safely, and in accordance with GMP guidelines. In this supporting and coordinating role, you contribute to optimal planning, the availability of materials, and an effective handling of deviations and opportunities for improvement. You are an important link within the team and support microbiological analysts so that analyses can be carried out on time and according to schedule. Additionally, you work actively on improving processes, systems, and working methods within the laboratory. We continuously strive for further optimization of our processes and actively employ Lean/Six Sigma methodologies, such as Tier Meetings, Kaizens, and Root Cause Analyses. Therefore, we are looking for a proactive and structured professional who shows ownership, is open to change, and thinks in solutions.

Do you have questions about this vacancy?

Please send your inquiry, including the vacancy number and the vacancy title, to the following email address: RecruitmentNL@MSD.com Applications can only be submitted via our careersite.

Required Skills

Deviation Management, GMP Compliance, Good Laboratory Practices (GLPs), Good Manufacturing Practices (GMP), Laboratory Management, Laboratory Operations, Laboratory Quality Control, Microbiological Analysis, Microbiological Test, Microbiology

Travel Requirements

Flexible Work Arrangements: Not Applicable

Hazardous Material(s)

Job Posting End Date: 12/3/2026

About MSD

Industry
Pharma
Founded
1891
Employees
50,000–100,000
Headquarters
Rahway, USA

In their own words

About the company & team

Our Animal Health division is a trusted world leader in veterinary medicine, dedicated to preserving and improving the health, welfare, and performance of animals and the people who care for them. We are a global team of professionals working together to make a positive impact on animal care and the world's food supply, and we have a deep sense of responsibility to our customers, consumers, animals, society, and our planet. Through our commitment to The Science of Healthier Animals®, we offer veterinarians, farmers, pet owners, and governments one of the broadest ranges of veterinary medicines, vaccines, and health management solutions and services, as well as an extensive offering of digitally connected identification, traceability, and monitoring products. We invest in dynamic and extensive R&D resources and a modern, global supply chain. We are active in more than 50 countries, while our products are available in approximately 150 markets.

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