Technical Operations Manager
Technical Operations Manager for a global healthcare organization's lentiviral vector manufacturing facility in Sassenheim, near Leiden, Zuid-Holland.
Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)
Eisen
- Able to work effectively in a complex, cross-functional environment
- Experience with technical projects involving equipment, materials or single-use systems
- Strong knowledge of GMP and pharmaceutical manufacturing processes
- 6+ years of people leadership experience at Supervisor or Manager level
- Proven experience delivering Lean projects, both technically and as a leader
- Strong leadership, decision-making and stakeholder management skills
- 10+ years of experience in a pharmaceutical GMP production environment
- Knowledge of EHSS and regulatory requirements in a GMP environment
Wensen
- Knowledge of JJOS methodology and systems
Volledige omschrijving
The role is located in Leiden, Zuid-Holland, in the Pharmaceuticals sector, with a start date of 9/23/2026 and job reference 59052. Our client is a global healthcare organization with a newly established lentiviral vector manufacturing facility in Sassenheim. The facility supports commercial production within a highly regulated GMP environment, with a strong focus on technical excellence, quality and continuous improvement. As Technical Operations Manager, you will lead a team of around 15 technical specialists supporting manufacturing operations.
You will oversee technical improvements, equipment and single-use solutions, complex problem solving and cross-functional projects, while ensuring GMP, safety and quality requirements are met. Key responsibilities include leading and developing the CoE team of technical specialists; overseeing technical changes and equipment and single-use improvement projects; providing technical expertise and supporting the resolution of complex process issues; partnering with Operations, QA, QC, MSAT, IT and other functions on technical projects; driving improvements focused on quality, cost, cycle time and capacity; supporting new product and process implementation within manufacturing; reviewing and approving technical documentation and specifications; monitoring equipment performance, maintenance and recurring technical issues; allocating resources to deliver projects within agreed timelines and budgets; and promoting innovation, Lean and continuous improvement within the facility.
Requirements include 10+ years of experience in a pharmaceutical GMP production environment; 6+ years of people leadership experience at Supervisor or Manager level; strong knowledge of GMP and pharmaceutical manufacturing processes; proven experience delivering Lean projects, both technically and as a leader; experience with technical projects involving equipment, materials or single-use systems; knowledge of EHSS and regulatory requirements in a GMP environment; strong leadership, decision-making and stakeholder management skills; ability to work effectively in a complex, cross-functional environment; and knowledge of JJOS methodology and systems is an advantage.
Je CV en reacties
Voeg een CV toe om de eisen naast jouw ervaring te bekijken.
Je reageert zelf bij de bron. Leg hieronder vast wanneer je je reactie hebt verstuurd.
Bewaar de broker en datum in Mijn reacties.
Gegevens automatisch overgenomen uit de oorspronkelijke publicatie; controleer de details bij de bron. Wij zijn geen partij bij de aanvraag. Hoe wij werken.