Work Schedule
First Shift (Days)
Environmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degrees, Fluctuating Temps hot/cold, Loud Noises (Equipment/Machinery), No eye contacts allowed; prescriptive glasses will be provided, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Strong Odors (chemical, lubricants, biological products etc.), Various outside weather conditions, Will work with hazardous/toxic materials
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Job Description
Position Summary:
The Engineer II role is a key position within our organization, responsible for providing engineering services and technical leadership in various areas including chemical synthesis, protein purification, formulation, and packaging. The primary focus of this role is to ensure process safety, drive new product development, oversee scale-up activities, facilitate the selection and validation of new manufacturing equipment, drive cost reduction initiatives, and continuously improve processes and products across the organization. The Engineer II will play a crucial role in driving operational excellence and achieving business objectives.
Key Responsibilities:
- Design products, processes, and facilities to meet performance, cost, and capacity objectives
- Manage capital improvement projects, including equipment and facility upgrades
- Research and recommend technologies and vendors
- Develop financial justifications for capital appropriations
- Purchase, install, and validate new equipment and facilities
- Provide project management, including schedules, cost tracking, and status reports
- Develop new processes to support product development and technology transfer
- Optimize processes to improve quality, reduce costs, and eliminate waste
- Analyze production metrics and identify improvement opportunities
- Support Lean Manufacturing programs
- Identify, qualify, and manage suppliers
- Resolve supplier quality, cost, and delivery issues
- Transfer processes to suppliers and work on process improvement with existing suppliers
- Design and implement product quality plans for new and existing products.
Minimum Requirements
- High school diploma or GED equivalency required.
- 3 years of engineering experience, preferably in pharmaceutical, chemical, biological, or food production
- Ability to work in various environments, including office, laboratory, production areas, and outdoors
- Physical ability to occasionally lift up to 50 pounds
- Strong knowledge of process/chemical engineering principles and equipment selection
- Experience with computer-aided design and analysis tools (AutoCAD, SolidWorks, etc.)
- Familiarity with electrical/electronic components and control systems
- Proficiency in continuous improvement methodologies (lean manufacturing, six sigma, etc.)
- Excellent verbal and written communication skills
- Strong problem-solving and analytical abilities
- Proven leadership skills and ability to lead cross-functional teams
- Highly organized and capable of managing multiple projects simultaneously
- Proficiency in PC applications, including Word, Excel, and CAD
- Willingness to work occasional off-shift or weekend hours and overnight travel.\
At Thermo Fisher Scientific Inc., we value diversity and believe in providing equal opportunities for all qualified individuals. We are an equal opportunity employer (EOE) and encourage applications from individuals of all backgrounds, including those with disabilities and members of underrepresented groups.
If you require reasonable accommodation or adjustment during the application process, please let us know. We are committed to providing assistance and ensuring a smooth and inclusive recruitment experience for all applicants.