*Team Leader for Facility Compliance team
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With AGC Biologics increasing activities, we are looking for a new scientist with experience within Facility compliance in the pharmaceutical industry.
AGC Biologics is a Contract Manufacturing Organization (CDMO) with facilities in Denmark, Germany, Japan and USA and with customers from all over the world. We have more than 30 nationalities employed and the daily language is English.
The Facility Compliance team
The Facility Compliance team is supporting all the manufacturing departments with tasks related to ensuring compliance with the facility. Facility compliance includes support related to cleaning of the facility, environmental monitoring of the facility and procedures related to gowning, flow and aseptic behavior.
The Facility Compliance team consist of a highly skilled team of scientist supporting the Facility Compliance that are driven by the ever-changing manufacturing pace. We strive to ensure a high quality mindset and enjoy a great team spirit.
The team operates under cGMP and are responsible for continuous facility compliance of our mammalian, microbial and adjuvant lines. With the establishment of a new facility the facility compliance will look into even more responsibility to ensure alignment across the 2 production facilities.
The team is responsible for securing the compliance framework with regards to facility compliance and environmental monitoring with emphasis on training documentation, deviations and CAPA management.
The position
As a team leader in the Facility compliance team, you will be leading the area and setting direction for tasks related to Facility compliance and environmental monitoring and developing the area and people. You will be regarded as a role model and will also be responsible for:
- Developing the teams.
- Setting direction on process confirmations
- Training of teams
- Overall responsible for the compliance level within the area
- Participate in board meetings, KPI delivery and follow-up
- Optimization and standardization of work processes related to facility compliance
Experience and competencies
The ideal candidate has experience within clean room requirements. The ideal candidate has previously been working with applied microbiology or manufacturing operating under cGMP within the pharmaceutical industry. Previous experience as a team leader is not a pre-requisite. The ideal candidate for the position has several of the below competencies/experiences:
- 5+ years of experience from the pharmaceutical industry working in an cGMP environment within aspect behavior and environmental monitoring.
- Strong communicator
- A natural role model and coach for improving aseptic behavior
- Structured and analytically oriented
- Experience with applied Lean
- A genuine interest in being close to the manufacturing floor and understanding the need for process confirmation
As a person you are driven by continuously improving processes and procedures. You are curious, have a good overview, is eager to learn and a team player: You thrive in a high pace environment where no two days are the same.
AGC Biologics offers
AGC Biologics offers a dynamic working place with good opportunities for working with a varied array of tasks and challenges. This opens many doors for personal development and for you to make a real difference towards both patients and customer. At AGC Biologics the work environment is informal and humor is part of the work day. We respect each other and our differences, and we help each other to reach deadlines together as one team.
For further information, please contact Peter Broe, Manager, Solution Coordination and Facility Compliance, phone +45 27603170.
We will process the applications as they arrive. Therefore, please submit your application and CV as soon as possible.
Want to keep posted about our growth and to learn more about our company?
We also urge you to follow us on our LinkedIn Company Page and give us a quick Like on Facebook !
AGC Biologics (AGC) is a global Contract Development Manufacturing Organization (CDMO) with bio-manufacturing facilities in Europe, Japan, Italy and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API). The company’s team and approach are tailored to each of its client’s needs, whether turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services.
Visit www.agcbio.com to learn why AGC Biologics is a World Leader in process development and contract manufacturing.
Information og data
Denne ledige stilling har jobtypen "Afdelingsleder", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i København
Jobbet er oprettet på vores service den 10.7.2023, men kan have været deaktiveret og genaktiveret igen.
- Afdelingsleder
- København
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