Vice President API MSAT QC in CMC & Product Supply, Kalundborg (Denmark)

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Kalundborg

Vice President API MSAT Quality Control in CMC & Product Supply, Kalundborg (Denmark)Are you an experienced leader of large-scale quality control organisations in technically complex lab and analytical settings? Can you combine strategic vision with hands‑on execution to drive innovation, operational excellence, and uncompromising API quality control? If so, we invite you to join [xxxxx] as our new Vice President of Quality Control (QC) within Active Pharmaceutical Ingredient (API) Manufacturing Science & Technology (MSAT). Read on and apply today to make an indispensable difference in the consistent, high-quality production of our life-saving medicines.The position
As the Vice President of Quality Control, you will assume leadership over critical aspects of our Active Pharmaceutical Ingredient (API) manufacturing pipeline. This role demands a strong focus on compliance, process mastery, and future-proofing our operations through advanced technol-ogy adoption.Quality control (QC) within API MSAT is a newly created organisation consisting of four Director-led areas with 330 highly qualified lab technicians and professionals based in several facilitates in Kalundborg, Denmark. The task is to centralise the new organisation under the new leadership and ensure one smooth operation capable of handling the ever-increasing demands of a growing organisation and evolving pipeline.In this high-impact role, you will:
  • Oversee API Quality Control: Lead and manage API quality control operations, ensuring unwavering compliance with all internal standards, international cGMP, and regulatory requirements.
  • Drive Operational Excellence: Champion, innovate and implement process improvement initiatives to strategically optimize manufacturing efficiency, reduce costs, and enhance production scheduling across the API portfolio.
  • Strategic Leadership: Develop and implement critical strategic priorities that are tightly aligned with [xxxxx]’s overall global objectives and growth projections.
  • Champion Innovation: Drive sustainable and best-in-class manufacturing practices and accelerate the implementation of cutting-edge closed and continuous automation sys-tems.
  • Executive Representation: Represent the API quality control cluster in strategic decision-making forums, ensuring quality and compliance priorities are central to business strate-gy.
  • Develop Talent: Lead and mentor large, cross-functional teams, fostering robust collabo-ration, professional growth, and technical mastery.
    • The role is based in Kalundborg, Denmark.QualificationsWe are looking for an experienced and innovative leader with a proven track record of success in managing complex, compliant manufacturing environments.The successful candidate will possess:
  • Extensive Leadership Experience: Minimum of 10 years of leadership experience (includ-ing leading leaders), ideally within Quality Control for API manufacturing, biochemical production, or a highly regulated pharmaceutical/biotech environmen t.
  • Technical Mastery: Deep expertise in cGMP regulations, quality control operations, and analytical science, particularly in scaling and optimizing API processes.
  • Change Leadership: Proven ability to lead large, geographically dispersed teams in a ma-trix organisation and drive innovation, process improvement and technology adoption ini-tiatives.
  • M.Sc. or Ph.D. in Chemical Engineering, Biotechnology, Process Science, or a related field.
    • About the organisationActive Pharmaceutical Ingredient (API) Manufacturing Science & Technology (MSAT) is a depart-ment within [xxxxx]’s Product Supply organisation. The department is at the forefront of bridging clinical development and manufacturing at [xxxxx]. Our mission is to support the present and future manufacturing of Active Pharmaceutical Ingredients (APIs) through:
  • Developing and maintaining robust quality control and analysis for all marketed APIs.
  • Providing expert support to production in process and analytical methods.
  • Driving process optimizations to enhance capacity and efficiency to meet unprecedented global demand.
  • Pioneering the development and implementation of new technologies, ensuring we move toward closed and continuous processes.
    • Working at [xxxxx]Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination, and a constant curiosity. For over 100 years, this unordinary mindset has seen us build a company unlike any other. One where a collec-tive passion for our purpose, mutual respect, and a willingness to go beyond what we know de-livers extraordinary results.[xxxxx] is currently in the process of adjusting job titles globally. Please note that the job title listed in this advertisement may be subject to change. More detailed information will be provided during the recruitment process.”Contact and DeadlineFor further information, please contact Executive Search Partner, Heidi Ashby at [xxxxx] or get to know us better by visiting [xxxxx] Apply by Sunday 11th of January.We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.We’re not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.


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    Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

    Arbejdsstedet er beliggende i Kalundborg.

    Jobbet er oprettet på vores service den 5.12.2025, men kan have været deaktiveret og genaktiveret igen.

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    • Kalundborg
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