Supervisor Manufacturing Pharmaceuticals [F/M/X]

Supervisor Manufacturing Pharmaceuticals (F/M/X)

Brussels

Permanent Job

About the Role

The Supervisor Manufacturing Training leads and coordinates a team of production trainers to ensure consistent, effective, and compliant training across all shifts in a 24/7 manufacturing environment. This role guarantees continuous training coverage, alignment with production needs, and adherence to GMP and site requirements.

Key Responsibilities

• Lead, coach, and support a team of 7 production trainers operating in a 24/7, multi‑shift environment
• Ensure consistent training standards, content, and practices across all shifts
• Plan and coordinate trainer schedules to guarantee continuous training coverage
• Oversee training execution, including classroom, practical, and on‑the‑job training activities
• Provide guidance and coaching to trainers to enhance delivery quality and effectiveness
• Collaborate closely with Production, Quality Assurance (QA), and Subject Matter Experts (SMEs) to align training with operational and quality requirements
• Monitor and assess training effectiveness (e.g., KPIs, feedback, performance on the shop floor) and drive continuous improvement of training practices and materials
• Act as the primary escalation point for training‑related issues across shifts
• Ensure all training activities comply with GMP, internal procedures, and regulatory expectations
• Contribute to the development and maintenance of training documentation and records

Team & Organization

• Direct supervision of 7 production trainers
• Role spans multiple shifts to ensure full site coverage (24/7)
• Close collaboration with Production, QA, HR/Learning & Development, and SMEs

Profile Requirements

Experience & Background

• 4–6 years of experience in a manufacturing environment, ideally within pharmaceuticals, biotech, or other GMP‑regulated industries
• Proven experience in training, coaching, or people development (trainer, team lead, or supervisor role)
• Previous exposure to 24/7 or multi‑shift operations is a strong plus

Technical & Regulatory Skills

• Solid understanding of GMP and quality/compliance requirements in manufacturing
• Experience with on‑the‑job training, SOP‑based training, and competency management
• Ability to interpret and apply site procedures and regulatory expectations to training content

Leadership & Soft Skills

• Strong leadership and people management skills (coordination, motivation, conflict resolution)
• Excellent communication skills, both written and verbal
• Strong organizational and planning abilities, with experience managing schedules and priorities across shifts
• Continuous improvement mindset, with the ability to identify gaps and propose pragmatic solutions
• Ability to work effectively with cross‑functional stakeholders (Production, QA, SMEs, HR/L&D)
• Fluency in French and English is mandatory

Why Join Us?

• Rapid growth: Amaris has doubled its workforce in Belgium in two years, providing numerous growth opportunities for employees.
• Prestigious projects: Candidates will work with renowned clients in the pharmaceutical, biotechnology, and European institutional sectors on impactful missions.
• International environment: An agile and dynamic structure promotes intrapreneurship and meritocracy, with international exposure at the heart of Europe.

Amaris Consulting is proud to be an equal opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.