Operations Supervisor

About the company

Our client is a company with a mission to improve healthcare drastically. The company is a global biotechnology company dedicated to treating life-threatening diseases. They are focussing on advanced cell-based immunotherapies across a diverse array of technology platforms. They apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide.

Job description

As a Operations Supervisor, you are the lynchpin of our production. These are your responsibilities:

• Leadership and supervision: You will manage operational teams and supervise various operational units within the production process.
• Quality and compliance: You manage all aspects of quality and ensure strict compliance with cGMP standards. As a domain expert for Quality and Operations, you play a central role in GMP inspections.
• Collaboration: You are the first point of contact for production problems and work closely with other departments to find solutions.
• Documentation management: You will manage and review critical documentation within the production areas, such as procedures, work instructions, logs and transfer forms.
• Batch record supervision: You oversee the release and review of batch records for quality control.
• Training: As a manager, you make sure that everyone on your team gets the training they need to perform at their best.
• Operational excellence: You initiate projects that increase efficiency, reduce costs and improve quality. You encourage and inspire your team to continuously improve.

Required competences & skills

Education:

• You have a bachelor’s or master’s degree in science, bioengineering, pharmacy or a related field of study or you are equivalent through experience.

Experience:

• You have at least 5 years of experience in a cGMP or ATMP environment, preferably in the biotech or pharmaceutical industry. You also have substantial experience with grade C aseptic GMP production.

Languages:

• You speak and write fluent Dutch and English.

Strengths:

• You have excellent communication and organizational skills.
• You are an empathetic people manager with strong leadership skills.
• You have a positive attitude and adapt easily to rapidly changing circumstances. You inspire others to do the same.
• You are good at problem solving, prioritizing and multitasking.
• You have an eye for detail and procedures.
• You are willing to accommodate a shift system where you work four days and have four days off.

Expertise:

• You have a thorough knowledge of cGMP regulations and clean room operations.
• You can work fluently with Microsoft Office tools such as Word, Excel, PowerPoint and Outlook.
• Familiarity with Manufacturing Execution Systems (MES) and Electronic Batch Record (EBR) systems is a plus.

Interested?

Want to share your ambitions?

Let us get to know you and apply here!