Job Information
ThermoFisher Scientific Senior Manager of Operations - TIlburg in Tilburg, Netherlands
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Warehouse
Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
DESCRIPTION:
Guide operational excellence across manufacturing, planning, and support functions while ensuring the highest standards of safety, quality, and customer satisfaction. As a key member of the site leadership team, you'll oversee production operations, develop effective teams, and implement strategic initiatives that deliver sustainable growth. Collaborate with cross-functional teams to optimize processes, support continuous improvement, and ensure regulatory compliance while maintaining cost-effectiveness and meeting customer commitments.
Accountabilities, Key activities, and context
Adherence to schedule (on-time)
Meet the agreed weekly production schedule and long-term plan (hours and output)
Follow up area managers/production engineers to act timely and appropriately if deviations from the schedule occur or are expected
Monitor scheduled maintenance and validation activities and follow-up major projects and deviations.
ATS
Lost hours
OTD
GMP compliance and quality (on-spec)
Adhere to GMP, SOP’s, WI’s and BMR’s
Organize effective dept. SOP’s and WI’s
Ensure necessary actions in case of (potential) deviations.
Ensure employees are GMP-trained
Ensure housekeeping is at GMP-level
Ensure GMP level of rooms/areas/equipment by fit finish inspection.
Prevent complaints and audit observations
E&O
On time doc review
RFT & deviation reports
Training status
Housekeeping score
Audit observations
Efficient production (on-cost)
Align staff with production schedule
Minimize reprocessing, waste and OOS
Maximize yield
Number of FTE
Reprocessing & waste
Yield
Focused and professional team
Continuous development of team (knowledge & skills) and processes
Structured meetings with Area Managers, Production Engineers and M&E Manager
Effective cooperation with other departments
Skill development
Review Direct Reports
Aligned decisions
REQUIREMENTS:
• Advanced Degree plus 6 years of experience, or Bachelor's Degree plus 8 years of experience in operations management in regulated manufacturing environment, preferably in pharmaceutical/biotech industry
• Preferred Fields of Study: Engineering, Operations Management, Chemistry, Pharmaceutical Sciences, or related technical field
• Demonstrated expertise in cGMP, FDA regulations, and quality management systems
• Proven experience leading organizational change and developing effective teams
• Experience implementing Lean Manufacturing and continuous improvement methodologies
• Demonstrated ability to enhance operational excellence through KPIs and performance metrics
• Excellent communication and interpersonal skills with ability to work effectively at all levels
• Experience managing budgets, capital projects, and strategic planning initiatives
• Expertise in risk management and problem-solving in complex manufacturing environments
• Strong business acumen and analytical skills
• Proficiency with ERP systems, MS Office, and manufacturing software platforms
• Ability to collaborate effectively in matrix organization structure
• Experience leading successful regulatory and customer audits
• Knowledge of supply chain management and demand planning
• Project management and cross-functional team leadership capabilities
• 10-15% travel required
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.