Manufacturing Engineering Supervisor

Work Schedule

Environmental Conditions

Job Description

As part of the Thermo Fisher Scientific team youll 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 worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.

DESCRIPTION:
Lead a team of manufacturing engineers and technical specialists in delivering excellence across our manufacturing operations. As a Manufacturing Engineering Supervisor at Thermo Fisher Scientific youll implement continuous improvement initiatives oversee technical projects and ensure efficient production of high-quality products that enable our customers to make the world healthier cleaner and safer. Collaborate with R&D Production Quality and other teams to optimize processes implement new technologies and solve technical challenges. Support and develop your team while fostering an environment of innovation safety and operational excellence.

REQUIREMENTS:

Key Responsibilities

Leadership & Team Management

• Supervise mentor and develop a team of manufacturing engineers and technicians

• Assign priorities manage workloads and ensure timely project execution

• Foster a culture of safety quality and continuous improvement

Process & Production Support

• Oversee manufacturing processes for single-use systems (SUS) ensuring consistency and compliance

• Provide technical support for daily production issues including troubleshooting and root cause analysis

• Collaborate with production quality and supply chain teams to meet output targets

Process Improvement & Optimization

• Lead Lean Six Sigma and continuous improvement initiatives

• Identify opportunities to improve yield reduce waste and optimize cycle times

• Implement process validation and standardization efforts

New Product Introduction (NPI)

• Support transfer of new single-use products from R&D to manufacturing

• Develop and validate manufacturing processes including equipment and tooling

• Ensure smooth scale-up and commercialization

Compliance & Quality

• Ensure adherence to GMP ISO and regulatory requirements

• Support audits (internal/external) and implement corrective/preventive actions (CAPA)

• Maintain proper documentation (SOPs work instructions validation protocols)

• Ability to analyze technical data and make data-based decisions

Project Management:

• Lead or support cross-functional projects related to capacity expansion automation and technology upgrades

• Track KPIs and report on engineering performance metrics

Qualifications

Education

• Bachelors degree in Mechanical Engineering Electrical Chemical Engineering Industrial Manufacturing or Biomedical Engineering or related field

• Masters degree (beneficial)

• Advanced Degree plus 3 to 5 years of experience or Bachelors Degree plus 5 years of experience in manufacturing/engineering in regulated industry (pharmaceutical medical device or similar high-tech manufacturing)

• Professional engineering certifications beneficial

Experience

• 58 years of manufacturing engineering experience preferably in biopharma or medical devices

• 3 years of leadership or supervisory experience

• Demonstrated expertise in manufacturing processes equipment and quality systems

• Experience with single-use technologies (bioprocess bags assemblies filtration systems) strongly preferred

• Demonstrated ability to develop and support technical staff

Skills & Competencies

• Strong knowledge of single-use manufacturing processes (welding sealing assembly cleanroom operations)

• Familiarity with GMP FDA and ISO standards

• Experience with Lean Manufacturing / Six Sigma methodologies

• Excellent problem-solving root cause analysis skills and systematic approach to issue resolution

• Strong communication and cross-functional collaboration abilities

• Project management and organizational skills

• Collaborative leadership style with ability to work effectively across functions

• Excellent verbal and written communication skills

• Proficiency with CAD CMMS ERP systems and standard business software

• Knowledge of equipment regulations and certifications (CE/UKCA)

Preferred Qualifications

• Six Sigma Green Belt or Black Belt certification

• Experience with automation and digital manufacturing tools

• Knowledge of validation (IQ/OQ/PQ) and risk management (FMEA)

Work Environment

• Combination of office and manufacturing floor (cleanroom environment)

• Require PPE and adherence to controlled environment protocols

• Available for travel and flexible hours as needed