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The Downstream Technician Team
The team is part of the Microbial Manufacturing Department responsible for the production of Drug Bulk Intermediate (DBI) / Active Pharmaceutical Ingredient (API) and support proteins for pre-clinical, clinical and commercial use. The role will be to ensure leadership presences and support during daytime and to drive performance and development for half of the employees in the downstream team. This is in very close collaboration with the other downstream team leader to ensure coordination of tasks and delivery on time.
The department consist of the upstream team, the downstream team and a team consisting of scientists. The downstream team is responsible for running recovery and purification processes in the form of e.g. centrifugation, homogenization, filtration and chromatography. We have both stainless steel and single use equipment. We are a CDMO and we produce different biopharmaceuticals for our customers with changeover in-between the productions. The production is running 24/7 in three shifts.
The position
As the Team Leader in the downstream team you will be the direct leader of ~12 technicians and an operational scientist; all of them with a technical or academic background. You will be responsible for:
- Planning- and coordination of work, board meetings and shift plans.
- People management, hiring and developing people, conducting mid- and end year appraisals.
- Secure proper training is in place and conducting process confirmations on the shop floor.
- GMP compliance and safe work environment of the team.
- Optimization and standardization of work processes.
There is constant collaboration across the organization, and all employees have a professional and flexible attitude towards their work.
You will, together with the other Downstream Team Leader, the Team Leader for the upstream team, the scientist Manager and the head of department, be part of the leadership group where operation, development and optimization of the entire department will be key.
The work hours will be daytime, and some flexibility is required, when the processes requires that.
Experience and competencies
The ideal candidate holds a BSc or MSc in Chemical Engineering or has a technical background within the biopharmaceutical industry and have previously been a leader preferably within the biopharmaceutical industry. The ideal candidate for the position has several of the below competencies/experiences:
- +5 years of experience from the pharmaceutical industry working in an GMP environment
- +2 years of leadership experience, preferably in manufacturing
- Scientific and technical understanding of downstream processes is a plus
- Strong communication skills (English)
- Strong collaboration skills and capacity to bond with colleagues
- LEAN oriented
- Can cope with a fast-changing high work pace in a dynamic environment
- Structured and analytical oriented
- Responsible and able to take ownership
- A strong GMP mindset
AGC offers
AGC offers a dynamic working place with good opportunities of working with a varied array of tasks and challenges. You will get insight into and experience with the way the various departments throughout a contract manufacturing organization interact in order to achieve success. Exciting and challenging assignments will constantly come your way, and you will to a large extent be able to plan your daily work yourself. AGC offers an informal working environment, where humor is part of the daily work life. We respect each other and our individual differences. AGC’s employees have a flexible attitude and we help each other to reach deadlines together as one team.
For further information, please contact Martin Haack, Director of Microbial Manufacturing Department, phone +45 22 94 30 35.
We will process the applications as they arrive. Therefore, please submit your application and CV as soon as possible and no later than December 30th, 2023.
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 21.12.2023, men kan have været deaktiveret og genaktiveret igen.
- Afdelingsleder
- København
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