Staff Engineer, Project Engineering

ThermoFisher Scientific; St. Louis (MO); Sur place; USD 120 000 - 180 000; Plein temps

Avantages offerts par ce poste

Competitive remuneration

Annual incentive plan bonus

Healthcare

Career development

Innovative culture

Résumé du poste

Thermo Fisher Scientific in St. Louis seeks a Staff Engineer to lead capital projects in manufacturing, ensuring GMP compliance and alignment with business goals. You will collaborate with MSAT, PD, Quality, Operations, and Maintenance to deliver projects on time and within budget.

The role requires strong project management, risk assessment, and excellent communication. Experience managing contracts up to $5M, startup and commissioning, and familiarity with regulatory standards will help you

Qualifications

• Bachelor's degree or higher in Engineering and 5+ years pharma or related experience.
• Associates degree with 8+ years of related professional experience.
• Experience writing GMP documents and working in a GMP setting.
• Experience in cleanroom environments and commissioning/validation.
• Ability to manage contractors and multi-million dollar capital projects.

Responsabilités

• Manage contractors and capital projects up to $5MM.
• Develop and track scope, schedule, and budget for capital projects.
• Initiate and close quality records for capital projects.
• Lead startup and commissioning activities for projects.
• Ensure regulatory compliance and adherence to safety standards.

Connaissances

Building codes

Regulatory knowledge

Communication

Attention to detail

Microsoft Excel

Microsoft Word

Microsoft Outlook

Microsoft Project

Microsoft PowerPoint

AutoCAD

Bluebeam

Formation

Bachelor's degree in Engineering (Chemical, Mechanical, Electrical, Bio)

Associates degree + 8+ years experience

Description du poste

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

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.

How will you make an impact?

The Thermo Fisher Scientific St. Louis site is a multi-product and multi-client biopharmaceutical site with manufacturing facilities for pharmaceutical products for both (pre)clinical trials and commercial applications. The Staff Engineer role is part of the Engineering team and reports to the Manager of Manufacturing Engineering. This role focuses on managing and supporting capital projects to enhance our manufacturing capabilities and ensure compliance with GMP standards.

What you will do

• Manage contractors and capital projects up to $5MM.
• Develop and track scope, schedule, and budget for capital projects.
• Initiate, manage and close quality records related to capital projects.
• Drive closure of intermediate tasks on quality records to ensure departmental compliance and on-time completion.
• Author and Review GMP documents as required to support capital project objectives.
• Lead start-up and commissioning activities on capital projects.
• Ensure all capital projects comply with regulatory requirements, industry standards, and company policies.
• Collaborate with cross-functional teams including MSAT, PD, Quality, Operations, and Maintenance to ensure project alignment with business objectives.
• Conduct feasibility studies, prepare detailed project plans, and manage project timelines and budgets.
• Perform risk assessments and develop mitigation strategies to ensure successful project execution.
• Engage with business leadership as required for projects to attain business approval and ensure alignment of project deliverables with business objectives.
• Engage with customers and regulators as required for managed projects and areas of expertise.
• Drive adherence to site safety standards in delivering projects including applicable assessments of new facilities and equipment.

Education:

• Bachelor's Degree or higher education in Engineering (Chemical, Mechanical, Electrical, Bio) and 5+ years experience, 8+ preferred.
• Associates Degree and 8+ years of related professional experience.

Experience

• 5+ years of pharmaceutical industry experience or experience in a similar industry
• Past experience managing contractors and projects up to $5MM
• Experience authoring documents in a GMP setting.
• Experience working in a cleanroom.
• Prior experience working on commissioning and validation in a pharmaceutical setting.

Knowledge, Skills, Abilities

• Knowledge of building codes and regulations.
• Understanding of regulatory requirements for pharmaceutical facilities.
• Excellent written and verbal communication
• Strong attention to detail
• Proficient with Microsoft Excel, Word, Outlook, Project and PowerPoint
• Proficient with AutoCad and Bluebeam

Benefits

• We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits.
• Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects.
• We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Other

Relocation assistance is not provided.

Must be legally authorized to work in the United States now and in the future, without sponsorship.

Must be able to pass a comprehensive background check, which includes a drug screening.

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.