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32,000+ live jobsQuality Data Associate Specialist
On-site in Haarlem·Full-time·Added 5 days ago (last checked 31 Oct)
Our summary
- Work mode
- On-site, Haarlem
- Contract
- Full-time
- Languages
- Dutch
Skills
Nice to have
This job advert was originally written in Dutch.
Requirements
What we're looking for
- A Bachelor's or Master's degree in pharmacy, life sciences, process technology, or chemistry
- At least 1 year of relevant work experience within a quality role in a GMP environment
Nice to have
- Experience with SAP, LIMS, and Veeva is a plus
- Affinity with packaging technology and/or registration of medicines is a plus
- You are accurate, result-oriented, flexible, and work independently
Current Employees apply HERE
Current Contingent Workers apply HERE
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.
Languages
- You possess strong communication skills in both Dutch and English
Pay & benefits
What you'll get
- A competitive salary
- 35.5 vacation days
- 8% holiday allowance and a 3% year-end bonus
- Incentive Plan
- An excellent pension
- In-house sports facilities
- Various training modules
The role
Job Description
Do you want to contribute to the quality of medicines that reach patients worldwide? Are you analytically strong and do you get energy from ensuring and improving quality processes? Then this might be the perfect role for you!
For our location in Haarlem, we are looking for a:
Quality Data Associate Specialist (QAL2) - Blister
What you'll do
You will have a lot of contact with various departments and systems and ensure that quality guidelines are correctly applied and implemented. In doing so, you will have a direct impact on compliance, product quality, and patient safety.
Tasks and responsibilities
- You support departments in implementing changes to guidelines via, among others, Veeva, Veeva Registrations, and Change Control processes
- You actively contribute to increasing quality awareness within the organization and act as a representative of Quality within various systems
- You participate in the introduction of new products, where you are responsible for the quality aspects
- You are Quality Assurance responsible for a number of products
- You check and approve master data (ZERT, ZERP, and ZDSB)
- You assess and set up Quality Standards within systems such as GLIMS and SAP
- You perform material control reviews and approvals in SAP
- You review Certificates of Analysis (CoAs), both manually and in SAP
- You lead, if necessary, investigations within deviation management
- You write and maintain QMS procedures
Your profile
We offer
Working at our organization means working together for health in an international working environment with dedicated colleagues. You will get all the space to develop yourself and show who you are. Furthermore, you can count on attractive employment conditions:
Do you have questions about this vacancy?
Send your question together with the vacancy number and the title of the vacancy to: RecruitmentNL@MSD.com.
Applications can only be submitted via the website.
Required Skills
Analytical Problem Solving, Analytical Problem Solving, Aseptic Filling, cGMP Compliance, Complaint Management, Data Quality Assurance, Decision Making, Deviation Investigations, Deviation Management, Good Manufacturing Practices (GMP), New Product Introduction (NPI), Pharmaceutical Packaging, Product Quality Assurance, Quality Assurance (QA), Quality Assurance (QA) Standards, Quality Assurance Engineering, Quality Assurance Systems, Quality Auditing, Quality Compliance, Quality Management, Quality Management Standards, Quality Management Systems (QMS), Quality Policy, Quality Reporting, Quality Standards {+ 5 more}
Employee Status
Project Temps (Fixed Term)
Flexible Work Arrangements
Not Applicable
Job Posting End Date
11/11/2026
About MSD
- Industry
- Pharma
- Founded
- 1891
- Employees
- 50,000–100,000
- Headquarters
- Rahway, USA
In their own words
About the company & team
Welcome to our team
Within our Quality Release department, we ensure that all our products are produced, processed, tested, packaged, stored, and distributed according to the highest quality standards and applicable laws and regulations.
Within this department, the Quality Release Blister team is part of a close-knit group of 11 colleagues. Together, you will support the entire Haarlem site in the areas of quality assurance, product release, and the introduction of new products. In this role, you will work closely with various disciplines and contribute directly to a reliable supply of medicines worldwide.
About the position
Our Quality Release team in Haarlem is looking for a Quality Data Associate Specialist, who plays a key role in managing and ensuring quality data and processes. In this role, you will work on-site in a committed team where quality and collaboration are central.
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