Senior QA Professional

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Are you passionate about driving quality assurance in a dynamic environment? Do you aspire to be deeply involved in daily operations and act as Subject Matter Expert (SME) both in minor and major projects to ensure that we adhere to internal standards and regulatory requirements?If you are also eager to have an impact on the entire value chain, we look forward to welcoming you in the QA/Regulatory Affairs (RA) department at [xxxxx] Pharmatech. Submit your application today!The positionAs Senior QA Professional, you will play an important role in guaranteeing the effectiveness and compliance of our current processes but also throughout projects, which are essential for our growth strategy.Additionally, you will foster a culture of quality across the organization by ensuring that daily operations and project activities align with best practices and regulatory standards.Your primary responsibilities will include:
  • Managing approval of instructions, deviations, change requests, qualification, and validation documents, as well as release of products
  • Acting as a SME in projects, using your production and domain knowledge to ensure project compliance with both internal and external requirements
  • Collaborating with the project team and stakeholders, serving as a vital link between the project, the QA Project Coordinator (for larger projects), and the QA/RA department
  • Handling customer complaints, conducting both internal and external audits, and collaborating with the Sales and Marketing department on customer inquiries
    • We offer an exciting and challenging position in an amazing department where focus on collaboration and team spirit is key. As a new member of the team, we will prioritize your training and support you in gaining the competencies needed.
    QualificationsTo be successful in this role, we imagine you to:
  • Hold a master’s degree in Science, Pharmacy, Chemistry, Biotechnology, or a similar filed
  • Bring 3 to 5 years of experience in the pharmaceutical industry, preferably within QA
  • Demonstrate solid experience with deviations, change requests, and validation
  • Have experience in working with projects on new and existing products
  • Showcase the ability to build strong relationships with stakeholders across the organization,
  • Possess professional fluency in both spoken and written English
    • Experience with customer inquiries and customer complaint handling is an advantage, as is knowledge of Danish.On a personal level, you are a self-driven and strong team player with excellent problem-solving and communication skills; you are proactive and solution-oriented with a can-do attitude and strategic focus. Openness, honesty and focus on continuous improvements and quality mindset are natural parts of your personality and the way you work. Finally, you demonstrate a real interest in others' perspectives and engage actively in discussions as they arise.About the departmentThe team is a part of the QA/RA department at [xxxxx] Pharmatech A/S. The QA/RA department currently consists of 36 employees working diligently to support the entire value chain, from Research & Development to Production and finally Sales & Marketing. We also cover quality and regulatory affairs related communication with the authorities, our B2B customers, our distributors, and our suppliers.
    Working at [xxxxx] Pharmatech [xxxxx] Pharmatech A/S has approximately 540 employees and is 100% owned by [xxxxx] A/S. [xxxxx] Pharmatech A/S is a leading global supplier of high-quality ingredients for the biopharmaceutical and pharmaceutical industries, supplying products such as recombinant insulin for cell growth media and pharmaceutical grade quaternary ammonium compounds as well as raw materials for [xxxxx] A/S. [xxxxx] Pharmatech A/S is a growing company, which will provide many exciting projects in the future and good development opportunities in the job.ContactFor further information, you can contact the Director for Quality Assurance, Lene Berg Jørgensen (week 28 and 29) on +[xxxxx], QA Manager, Sara Melissa Plov Hoff (week 30) on +[xxxxx], or Hiring Manager Daniel Grundahl (week 31) on +[xxxxx].
    Deadline
    3 August 2025.You do not need to attach a cover letter to your application, but please include a few sentences about your motivation in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

    At [xxxxx] we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.


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    Jobbet er oprettet på vores service den 6.7.2025, men kan have været deaktiveret og genaktiveret igen.

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