QC Data Project Professional (14 months Maternity Cover)

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Are you motivated by taking responsibility, setting direction, and ensuring Quality Control (QC) of high standards? Are you ready to engage, support and mobilise colleagues in our journey towards an efficient, scalable, and digitalised Quality Control? Then apply today and get a fantastic opportunity to become our new co-worker in [xxxxx] Pharmatech, Køge. The position As our new QC Data Project Professional, you will enter an exciting job and get the opportunity to play a major role in the development, optimization, and rethinking our way of performing quality control on new- and existing products. Your main tasks will be:
  • Identifying areas for improving analytical techniques and methods, LEAN processes, digitalisation, and data analysis
  • Collaborating with our IT/OT department regarding cross-functional equipment qualification projects
  • Ensuring successful development, prioritisation, execution, that benefits our strategic objectives
  • Working within qualification of analytical equipment, development of analysis, and validation of methods
  • Quality Risk Management and data analysis
    • In this role, you could be involved in various projects and software upgrades for large analytical instruments. This will be a primary area of focus - implementing new software solutions while collaborating closely with the IT department and your colleagues in the Quality Control lab. You'll work alongside chemists and lab technicians to ensure proper qualification of the equipment during these implementation processes. Furthermore, a key responsibility will be optimizing data analysis and equipment performance, leveraging your expertise to drive continuous improvement across the analytical operations. Qualifications To be successful in this role, you:
  • Hold an academic degree within pharmacy, chemistry, or similar field
  • Have experience in defining scope, planning, managing, and executing smaller projects, identifying business challenges and possibilities for resolving such issues. This experience would be gained within the pharmaceutical or other relevant life-science industry.
  • Have good communication complimented with full professional proficiency in Danish and English
    • Previous scientific experience in areas like analytical development, method validation, quality risk management, or data analysis would be a plus. It's also beneficial if you have relevant LEAN experience from a similar role or training, along with a knack for improving work processes and reducing waste. Furthermore, you are persistent by nature and enjoy working with short- and long-term projects, implementing new products and processes. You are structured, analytical and able to solve complex tasks. We are open to candidates with extensive experience, as well as to more junior ones. About the department We are a well-functioning department, and you will join a team of 10 highly professional and motivated chemists and lab techs who support development of products and production with high quality assays. The team also handles tasks like stability tests, raw material controls, input to regulatory documentation, implementation of new analytical equipment and software, development, and validation of methods etc. It is a laboratory with high complexity as we have many different analytical techniques. The laboratory is moving towards more digitalisation and use of data analyses, and we are in the process of replacing our current Laboratory Information Management System (LIMS) solution. Working at [xxxxx] [xxxxx] Pharmatech A/S (NNPR) is located in Køge, Denmark, and is 100% owned by [xxxxx]. The company has close to 400 employees and the core task of the business is to enable better medicines through biopharmaceutical manufacturing for [xxxxx] as well as for the global industry. NNPR is in the coming years expanding an already wide product portfolio within Enzymes, Synthetic Molecules, and Resins. The company has the full value chain with both R&D laboratories, production facilities, and a commercial organisation, plus a wide range of support departments on top. Contact For further information, you can contact Manager, Jeanette Eva Lylloff, on +[xxxxx]. Deadline 16 June 2024 You may submit your application in English or in Danish. We will take candidates into the recruitment process continuously, so do not hesitate to 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.


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

    Arbejdsstedet er beliggende i Køge.

    Jobbet er oprettet på vores service den 1.6.2024, men kan have været deaktiveret og genaktiveret igen.

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