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Project Manager Qualification & Validation

Job in 1000, Amsterdam, North Holland, Netherlands
Listing for: QbD Group
Full Time position
Listed on 2026-08-28
Job specializations:
  • Pharmaceutical
    Quality Engineering, Regulatory Compliance Specialist, Validation Engineer
Salary/Wage Range or Industry Benchmark: 70000 - 110000 EUR Yearly EUR 70000.00 110000.00 YEAR
Job Description & How to Apply Below
QbD Group offers knowledge & tailored solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD.

Currently we are looking for Project Managers (PM) in Qualification & Validation to make sure we can keep track of all ongoing and upcoming high-level projects. We offer training and internal support to make sure our experts can grow in their roles and evolve as a professional PM in life sciences.

What you’ll be doing as a Project Manager?
As a  Project Manager Qualification & Validatio n, you will be responsible for the planning, execution, and delivery of qualification and validation projects within life sciences

Depending on your industry expertise you will l ead qualification & validation projects  within pharmaceutical, ATMP or medical device industries.

Develop and manage  project plans , including scope, timeline, resources, and budget.

Act as the  primary point of contact  for clients, ensuring alignment on project goals and expectations.

Collaborate with internal departments (Sales, HR, Division Head) to support  business development and resource planning.

Organize and lead  Steering Committees  (Steer Co) to report on project progress, risks, and mitigation strategies.

Ensure compliance with GMP, FDA, EMA, and other relevant regulatory requirements.

Oversee validation activities  including IQ/OQ/PQ for equipment, clean rooms, utilities, HVAC systems, and processes.

Support and guide validation specialists, providing  coaching and training  when necessary.

Represent QbD Group during internal and external audits.

What you bring

BSc/MSc degree  in Life Science & Technology, Exact Science, Engineering, or a related field

At leas t 5 years of experien ce i n Commissioning & Qualification  (C&Q) within life sciences

Fluent  in Dutch and English

Strong  project management  skills, with experience managing multiple stakeholders

Excellent  communication and leadership skills , capable of managing client relationships

Problem-solving mindset  with a proactive and detail-oriented approach

Ability to work independently and as part of a team

A true QbD’er  can be recognized by the following qualities

Resilient :
Your strong and positive attitude helps you overcome any challenge

Hungry for knowledge :
You are always open to learn ing

No non-sense mentality : you can be straightforward in a respectful way

Innovative :
You are constantly looking for new and better soluti ons

(Not too) serious : your job is serious, but you don’t take yourself too serio us.

Who you are
Our culture is driven by values If this sounds like you, you’ll fit right in:

You’re  resilient  and tackle challenges with a positive mindset

You’re  curious  and always up for learning something new

You have a  no non-sense approach  honest, clear, respectful

You’re  innovative  and bring ideas, not just opinions

And above all, you’re  serious about your work, but not too serious about yourself

We support life sciences companies from idea to patient, offering tailored solutions in development, clinical, regulatory, compliance, production, and distribution. With 500+ experts across 8 countries, we help drive innovation in ATMP, biotech, medical devices, diagnostics, digital health, and pharma.

We believe in  JPEG :

Joy. Partnership. Going the Extra Mile. Getting Things Done.

You won’t just be taking a job, you’ll be joining a community where people grow, laugh, build, and contribute to something bigger.

#J-18808-Ljbffr
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