QA Professional in Automation

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Kalundborg

Would you like to be part of a QA department supporting Major Projects in Product Supply Active Pharmaceutical Ingredients (PS API)? Would you thrive working in a dynamic, engaging, and international environment helping to ensure the quality while building new technologies for the future?

Then you might be the right candidate to join our PS API Expansions QA in Kalundborg - Denmark. Apply now for a life-changing career!

The position
As Quality Assurance Professional for automation, you will be part of a highly experienced team, whose focus is to ensure the right level of compliance in projects and building brand new manufacturing plants for the future.

Your main responsibilities will be to:
  • Focus the quality oversight on the interface between IT system platform and the process
  • Secure that the parameters and critical aspects from the master formular are integrated in the automation design
  • Have an overview over the solutions in the application code
  • Understand the interface from IT platform to the computerized equipment/embedded control system and secure the correct data flow
  • Work together with the robotic team to develop the quality strategy for GxP impacted robots and Automated Guided Vehicles
  • You will work in expansion projects, participating in all phases including design, quality risk management, supplier management, construction, qualification, and validation, ensuring the stability and robustness of processes.

    For candidates with a few years of experience in the pharmaceutical industry, this presents an opportunity to pursue a transformative career at [xxxxx]. You will have the chance to enhance your skills within [xxxxx] Quality, where each day brings new challenges. Collaborative workshops and disciplined meetings with stakeholders will provide ongoing learning opportunities related to automated and robotic systems.

    Qualifications
    The ideal candidate has a good understanding of production control systems and computerized equipment, paired with a solution oriented approach, a strong quality mindset and eager to simplify and create continuous improvements to ensure an efficient production facility and secure patient safety.

    To succeed in this role, you:
  • Hold an academic degree in IT/Automation, Biotechnology or Engineering (including, but not limited to, Mechanical, Production, Automation and Marine Engineering)
  • Have at least 2 years of proven working experience within automated processes
  • Preferably have gained said experience within the pharmaceutical industry
  • Preferably have experience with Quality Assurance, qualification/validation of highly automated processes and computerized equipment
  • Are fully proficient in English
  • It will be an advantage if you have proven experience within project execution.
    On a personal level, you are self-driven and outgoing, with great communication and collaboration skills to validate the work of your colleagues, without compromising our high-quality standards.

    About the department
    The PS API Expansions QA works to ensure involvement in investment projects aiming to establish compliant and timely approved facilities and setting the foundation for flawless operation of our new manufacturing plants. The department collaborate with API production areas, internal and external stakeholders both in DK and international. We highly value an open communication and strong collaboration among our team. Social responsibility is a priority in the department – it must be fun and challenging to go to work.  

    Working at [xxxxx]
    At [xxxxx], we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.

    Contact
    For further information, please contact Sr. Quality Project Manager Lone Kløcker Hoffmeyer at [xxxxx] or Quality Director: Camilla Hassager at [xxxxx]

    Deadline
    18 August 2024

    You do not need to attach a cover letter to your application, but please include a few sentences about your motivation to apply in your 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.


    Information og data

    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 5.8.2024, men kan have været deaktiveret og genaktiveret igen.

    Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
    • Øvrige
    • Kalundborg

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