Production Supervisor

HR One Group; Oost-Vlaanderen; Sur place; EUR 60 000 - 90 000; Plein temps

Avantages offerts par ce poste

Meal vouchers

Insurance coverage

Year-end bonus

Additional holidays

Year-end bonus

Résumé du poste

A leading biotechnology firm in Belgium is hiring a CAR‑T Production Supervisor to lead operational teams in the production of CAR‑T cell therapies. This role demands a Bachelor’s or Master’s degree in a scientific field and requires leadership experience within a regulated manufacturing environment. Candidates should possess strong cGMP knowledge and excellent communication skills. This permanent position offers a competitive salary with benefits including meal vouchers, additional holidays, and insurance coverage.

Qualifications

• Bachelor’s or Master’s degree in relevant field or equivalent experience.
• Prior people leadership experience in regulated environment.
• At least 3 years of experience in GMP or ATMP manufacturing.

Responsabilités

• Lead and supervise operational teams in CAR‑T production.
• Ensure compliance with cGMP requirements.
• Drive continuous improvement initiatives.
• Oversee documentation including procedures, work instructions, logs, and transfer forms.
• Review and support release of batch records for quality control.
• Drive continuous improvement initiatives to enhance efficiency, quality, and cost-effectiveness.
• Coach, develop, and support team members in achieving performance objectives.

Connaissances

cGMP understanding

Microsoft Office proficiency

Fluent English communication

Organization skills

Problem-solving ability

Empathetic leadership

Problem solving

Empathetic leadership

Office based mindset

Formation

Bachelor’s or Master’s degree in science, bio‑engineering, pharmacy, or related field

3+ years GMP/ATMP manufacturing or people leadership experience

Outils

MES/EBR systems

Microsoft Office

Description du poste

The hiring company is an international biotechnology organisation specialising in next-generation cell therapies for oncology and other serious diseases. Its rapidly expanding Belgian manufacturing site plays a key role in the GMP-compliant production of personalised CAR‑T treatments for patients worldwide.

PURPOSE OF THE ROLE

The CAR‑T Production Supervisor is responsible for leading operational teams within a biotech manufacturing environment focused on CAR‑T cell therapy production. This role ensures high-quality, compliant, and efficient manufacturing operations in alignment with cGMP standards.

KEY RESPONSIBILITIES

• Lead and supervise operational teams throughout the CAR‑T production process.
• Ensure compliance with cGMP (Good Manufacturing Practice) requirements.
• Serve as a key operational contact for troubleshooting and cross-functional collaboration.
• Oversee documentation including procedures, work instructions, logs, and transfer forms.
• Review and support the release of batch records for quality control.
• Drive continuous improvement initiatives to enhance efficiency, quality, and cost-effectiveness.
• Coach, develop, and support team members in achieving performance objectives.

EDUCATION and EXPERIENCE

• Education: Bachelor’s or Master’s degree in science, bio‑engineering, pharmacy, or a related field, or equivalent relevant experience.
• Experience: Prior people leadership experience in a regulated environment, or at least 3 years of experience in a GMP or ATMP manufacturing environment with readiness to step into a supervisory role.

SKILLS and COMPETENCIES

• Strong understanding of cGMP and cleanroom operations.
• Experience with Microsoft Office (Word, Excel, PowerPoint, Outlook); MES/EBR systems are an advantage. This will be primarily be an office based position.
• Fluent English communication skills (written and spoken).
• Strong organisational and communication abilities.
• Detail-oriented and process-driven mindset.
• Ability to multitask and solve problems
• Empathetic leadership style with the ability to inspire and motivate teams

EMPLOYMENT CONDITIONS

• Permanent contract.
• Competitive salary and benefits package.
• Meal vouchers, additional holidays, insurance coverage, double holiday pay, and year-end bonus.
• International and patient-focused work environment.

Please submit your CV through the form below and we will contact you shortly.