Massachusetts Jobs

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

How will you make an impact?

The Project Manager will be a member of the Global Engineering team and support all PSG manufacturing sites globally and all product modalities (API, OSD, Biologics, Viral Vector, Cell Therapy, Drug Product). This role will partner with commercial operations, business and site leaders, technical teams, finance and customers to develop engineering strategies to support new business and capacity expansion opportunities around the world. This position combines a deep process engineering understanding with project management, global collaboration and influencing skills! This role may also support mergers and acquisitions, leading technical assessments of facilities for strategic investment and be responsible for management of architectural, engineering and construction firms.

What will you do?

• Build capital project estimates and schedules, partner with PSG Finance leadership to build financial models

• Lead capacity expansion analysis, conceptual design, and preliminary engineering (BOD) development, building project execution plans (resource planning, procurement planning, construction phasing options, cashflow planning)

• Build project execution teams

• Develop and maintain global construction database for benchmarking of future PSG projects

• Ensure proactive pipeline management in terms of equipment platforms, facilities and processes in conjunction with marketing and development of new business.

• Strategic master-planning lead (site master plan development) – partner with local site leadership teams to develop executable 5-year capital plans, space planning, infrastructure (end-of-life replacement), manufacturing capacity, office, lab, warehousing, sustainability

• Evaluate, onboard and lead architectural, engineering and construction firms

• Build and maintain relationships with business leadership, site leadership and technical SMEs at various PSG sites

• Promote a safety first culture through use of design and construction safety standards, leading HAZOP reviews and partnering with EHS

• Draft and author corporate engineering standards

Experience

• Bachelor’s degree in engineering, science, or related field, with evidence of operational, leadership, or professional experience.

• Minimum six years’ experience in process development, operations or engineering in cGMP manufacturing industry

• Experience with evaluation and design of process equipment and manufacturing processes

• Experience in cGMP facility design and construction

• Experience with project cost estimation and scheduling

• Experience with capital project execution

• Experience in a customer-facing role is desired

Knowledge, Skills, Abilities

• Expert of manufacturing equipment and technologies for drug substance and drug product

• Strong interpersonal skills and the ability to connect with and positively influence leadership and all levels of the organization

• Excellent communicator, including written, oral and presentation-giving skills.

This role is remote or could be based out of any Thermo Fisher location globally, domestic or international travel may be required to various PSG facilities including up to 20% travel.

Thermo Fisher offers a range of benefits and programs for its employees such as:

• Medical, dental, and vision plans

• Wellness program and health incentive opportunities

• Matching 401k contribution and financial education programs

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.