Engineer - Equipment Responsible

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Are you passionate about laboratory equipment and automation? Do you have experience in the pharmaceutical industry? We are looking for an Equipment Responsible Professional to join ET DP Manufacturing Science and Technology & Quality Control (MSAT & QC) team in ET (Emerging Technologies). If you are detail-oriented, have a strong understanding of GMP, and enjoy working in a collaborative and trusting atmosphere, then read on and apply today for a life-changing career! The Position
As Equipment Responsible within MSat & QC, you will be working in a cross-disciplinary team, handling a broad spectrum of tasks related to laboratory equipment, automation, and Process Analytical Technology (PAT).
The main task will be the qualification and involvement in projects with new equipment, including:
  • Laboratory equipment

  • PAT

  • New robotic solutions

  • New automation projects in a laboratory setting

  • You will be responsible for the qualification of new equipment and already running laboratory equipment e.g., UPLC/HPLC, dissolution equipment, and other laboratory instruments such as scales, UV, FTIR, Karl Fisher, etc. Furthermore, you will work closely with the innovation team on new equipment such as PAT and robotic solutions so we can bring MSat QC up to the QC4.0 standard. Qualifications
    We are looking for an individual with a solid background in handling production equipment, proficient in managing documentation, compliance, qualification, and maintenance, including the facilitation of verification and validation activities. We imagine the ideal candidate being someone who comes with relevant experience and knowledge in this area. To succeed in this role, you should:
  • hold a degree in chemistry, pharmacy, engineering, or a similar field, or another relevant education like marine engineering, or another related technical field

  • have at least 1-5 year of experience from a regulated industry, preferably the pharma industry

  • be knowledgeable about GMP, especially regarding automation/robots' projects

  • know how to facilitate verification and validation activities including test execution, documentation review in QC area

  • be fully proficient in both Danish and English

  • Additionally, you have experience with some of the following: delivery of complete validation packages, Requirement Specifications, Installation/Operational/Performance Qualification Protocol/Report, Operation and Maintenance SOPs. On a Personal Level:
    You have a detail-oriented mindset and quickly acquire new knowledge that you then share with your colleagues. You are a team player but still enjoy working independently. You have a sincere interest in laboratory equipment and exploring innovative technologies, and you enjoy being part of a team where it is important to have fun and where we work in a collaborative and trusting atmosphere. About the department
    Emerging Technologies MSat & QC is a new area within [xxxxx] where the oral portfolio plays a significant role. We are approximately 300 employees, and we are growing. We work with quality control and compliance of the facilities, the equipment, QC lab, manufacturing development as well the release of tablets for the market. We are proud to work in a fast-growing part of [xxxxx].
    As part of [xxxxx], we aim to make a real difference for patients with chronic diseases across the world. We develop and manufacture all oral drug products late phase as well as for launch ensuring that we bring best-in-class treatments to the market. Our ambition is to develop break-through products based on orally available versions of GLP-1 and other molecules. 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 Manager Jimmie Slott Madsen at +[xxxxx]. Deadline
    3 July 2024.
    Please note that applications will be reviewed continuously, and interviews will be planned after the deadline – so apply today! You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying 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.


    Information og data

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

    Arbejdsstedet er beliggende i Måløv.

    Jobbet er oprettet på vores service den 20.6.2024, 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.
    • 20.06.2024
    • Øvrige
    • Måløv

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