*Manager of Automation and OT Process Systems
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We are looking for a people manager for the Automation and OT Process Systems department. You will play an important role in strengthening automation competencies and help us take the next steps in producing pharmaceutical products! As Manager of Automation and OT Process Systems you will be providing leadership direction for a small but dedicated team of Automation and OT Systems Engineers.
About the department:
You can look forward to being part of a dynamic and well-functioning team consisting of Automation and OT Systems Engineers, Process Engineers, Equipment Responsible, and Support Technicians. We thrive on professional challenges and work independently with great individual accountability and a high level of commitment. We collaborate with diverse stakeholders in the organization at site and global levels including Production departments, IT, MSAT, and QA. You will experience an enthusiastic working climate focused on quality, teamwork, and delivery.
As we are a very technical team and company you will base your leadership role on insight and knowledge in the area of pharmaceutical automation. Your broad understanding of Automation and IT technology will support and lead the way for how we manage all process control systems and further develop our platforms as we head towards Industry 4.0 and beyond.
Your Primary Responsibilities Will Be
- Act as a mentor and coach for the team members, make sure that they grow and develop on their projects.
- Assign the right people and balance capacity in relation to project demands.
- Work in close partnership with the manager and directors in Engineering and Manufacturing departments as well as the other managers in our IT area
- Develop strategic initiatives in the department that are linked to the overall strategy.
- You will be involved directly in the projects where you can expect to use up to 50% of your time, providing technical and/or project leadership for the design, development and life cycle management of automation and control systems, including engineering, startup, commissioning, qualification and troubleshooting of systems controlling process systems to support Manufacturing.
- Stay on top of future technological trends within pharma.
- Maintain the standards and guidelines related to process deliverables, which you will have the overall responsibility for.
- Contribute to the automation, architectural and site road map for the large-scale multi-purpose facilities in our Copenhagen site by developing and implementing site automation strategy in alignment with Engineering CAPEX initiatives
- Participate in Global Engineering automation related activities in order to align with overall technology requirements, standards development and documentation life cycle requirements across the entire network
Desired Competencies
- A degree in electrical engineering, Computer Science or similar degree
- Have worked at least 5 years as a leader in the Pharma or Biotech industry and a minimum of 2 years in a supervisory or management role.
- Knowledge and experience with SCADA/PLC solutions and control system protocols
- Experience managing a project team and delivering automation CAPEX projects.
We care about who you are as a person. In the end, how you work, and your energy is what impacts the effort we do as a team. As a person, you:
- Have a leadership style that is positive, open, honest, and holistic.
- Have great inter-personal skills and the ability to bring people together around a common purpose.
- Possess significant stakeholder management and communication skills.
- Are result-oriented and have a well-structured work approach.
- Have empowering leadership skills to ensure the high engagement in the team.
- Understand the Automation discipline and can speak with your employees about technical issues with a strong analytical and problem solving midset and experience applying these skills to resolve technical problems.
- Have a strategic mindset to assure that our deliveries and employees stay in front in the industry.
In addition, you must thrive in a dynamic and fast-paced working environment where changes occur on short notice. The environment is dynamic and challenging at times, which requires finding solutions, delivering on promises, and giving our customers a positive experience. AGC has international customers, equipment suppliers and our company language is English. It is therefore a required ability that communication in both written and spoken English is fluent.
At , you will get a unique opportunity working with a variety of different state of the art technologies among +40 different nationalities. This opens many doors for personal and professional development and for you to make a real difference towards patients, our customers, and your personal and professional growth. AGC offers an informal working environment, characterized by the fact that we think it is fun to go to work. We respect each other and our differences. AGC employees are flexible and take pride in working together to achieve goals as one team. Applications are screened on an ongoing basis. You do not need to attach a cover letter to your application, but please include a few sentences about your motivation for applying to this position.
Deadline
The deadline for applications is the 31st of March
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) 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 learn why is a World Leader in process development and contract manufacturing.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i København
Jobbet er oprettet på vores service den 14.12.2023, men kan have været deaktiveret og genaktiveret igen.
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