Quality Manager for Pharma IT and Automation Engineering Projects

Job-Link A/S
Quality Manager for Pharma IT and Automation Engineering Projects

Quality Manager for Pharma Engineering Projects (PQM's)

Job-Link is looking for a highly skilled Project Quality Manager to join our client's engineering team in IT and Automation.
Your role will be pivotal in securing the highest quality in all aspects of the word, relating to engineering projects under IT and Automation.This interesting project is based in in the Zealand area of Denmark, less than one hour from Copenhagen, offering you this unique opportunity to work on-site -and be part of groundbreaking advancements in the pharmaceutical industry.
About the job:
Key Tasks and Responsibilities

• Quality Management in Pharma Engineering Projects:
  • Lead and coordinate quality activities for cross-disciplinary pharma engineering projects.
  • Develop and implement verification strategies, for aligning with customer QMS and validation concepts, relating to Automation and IT Projects.
• Manage Suppliers:
  • Facilitate and coordinate supplier management activities.
  • Guide, review, and ensure compliance with suppliers' quality deliverables.
• Team and Process Coordination:
  • Actively contribute to the department's project management team.
  • Collaborate with other disciplines to ensure compliance with relevant codes, regulations, and project procedures.
• Project Oversight:
  • Review team deliverables to ensure quality standards are met.
  • Take financial responsibility for the quality related deliverables within the project.

Qualifications, Skills and Personal Qualities:(If you have other related skills, to the same effect and feel confident that you would be a close match, then please go ahead and send us your CV, in many cases a position can be tailored to your unique combination of skill-set, if relevant to the overall department needs)

• Qualifications and experience
  • Degree in engineering (e.g. automation, process, chemistry, biotechnology, pharmaceutical production, or a relevant field).
  • GMP knowledge and experience
  • Minimum of 3 years of experience with quality management and project execution from the life sciences or biotech industry.
• Professional Skills:
  • In-depth knowledge of quality planning, verification, and validation.
  • Strong experience with project execution in engineering environments.
  • Fluent in spoken and written English.
• Personal Attributes:
  • Strong at problem-solving and collaboration.
  • Results-oriented and enthusiastic approach to work.
  • Thrives in a fast-paced environment with multiple project interfaces.
  • Builds strong, trusting relationships with all stakeholders.
  • Good at open communication.

• Not needed but nice to have knowledge about:
  • S-88
  • 21 CFR Part
  • Batch production and related requirements in the pharmaceutical industry

The job is a contract of 1-3 years, with possibilities of renewal and steppingstone for further oportunities.
We invite you to apply and join our client’s highly professional team.
We can also accept consultants through their own company.

Please add your CV by clicking below.
References, although not mandatory at this stage, are always welcomed in a separate file during upload.

For further information about the vacancy please contact,

Ønsker du at høre mere om stillingen, er du velkommen til at kontakte Donny Mistarz
Donny@job-link.dk
Tlf.: 40602022
Ansøgningsfrist:
Snarest muligt