Qualification and Validation Specialist for NIRAS Life Science

2 days ago

Allerød, Allerød Kommune, Denmark PARETO SECURITIES AS Full time

Qualification and Validation Specialist for NIRAS Life Science

Are you an experienced qualification and validation specialist looking for a dynamic role within the pharmaceutical and life science industry? We're seeking a highly skilled individual to join our team

About Us

NIRAS is a leading consulting engineering firm in Northern Europe, specializing in providing expert support to global pharmaceutical and life science companies. Our team of professionals delivers high-quality solutions across a broad spectrum of projects.

Your Role

As a Qualification and Validation Specialist, you'll play a critical role in ensuring the successful execution of qualification and validation activities across various projects. Your expertise will be instrumental in advising both clients and colleagues, driving quality-related activities, and facilitating effective communication between stakeholders.

Key Responsibilities

  1. Establishing and delivering all qualification and validation activities within projects.
  2. Acting as an expert and supervisor, providing guidance to colleagues and clients.
  3. Directly engaging with clients and their Quality Assurance teams, addressing GMP-related queries.
  4. Facilitating and planning quality-related activities such as User Requirement Specifications (URS), Risk Workshops, Commissioning and Qualification activities (DQ, IQ, OQ, PQ).
  5. Collaborating with other NIRAS departments to integrate client requirements into project deliverables.
  6. Engaging in knowledge sharing, sales, and networking activities.

Qualifications

As a team player, you thrive in collaborative environments and contribute to fostering a positive project atmosphere. Your ability to work autonomously and appreciate autonomy with accountability is essential for success in this role.

  1. Solid technical background in engineering, chemical engineering, pharmacy or similar fields.
  2. Minimum of 5-10 years of operational experience in qualification and validation of equipment, facilities, or processes within the pharmaceutical and life science industries.
  3. Proven track record of independently delivering qualification documentation according to V/SRV models.
  4. Ability to work both independently and collaboratively with NIRAS and clients.
  5. Excellent communication skills, with the ability to translate and present client needs effectively within the project.
  6. Analytical mindset and adept at navigating dynamic project environments.
  7. Fluency in spoken and written English.
  8. A European working permit is required.

Join Us

If you're experienced within qualification and validation and looking for a new challenging role where you can make a significant impact, we encourage you to apply.

Let's talk about the possibilities...

Are you interested in hearing more about this position and your possibilities with NIRAS? Then give Head of Department, Marina Blanco Leon a call on +4531447516 to learn more about your potential future

or apply directly from this page.

We are looking forward to hearing from you

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