Engineer II, Manufacturing Engineering

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:
Join our collaborative team as a Manufacturing Engineer II at Thermo Fisher Scientific where youll contribute to global healthcare and scientific this role youll be responsible for ensuring compliance quality and operational excellence across our facilities through comprehensive validation activities. Working with advanced technologies and diverse teams youll help maintain high standards in pharmaceutical manufacturing laboratory operations and quality control.

Location: Fremont CA Relocation assistance is NOT provided.

Roles and/or Responsibilities:

• Participate in determining the packaging requirements according to the nature of the product cost limitations legal requirements and the type of protection required taking into consideration the need for resistance to external variables. May independently design a more straightforward package.
• Participate with performing package characterizations including cost effectiveness studies.
• Generate and authorize project documentation involving equipment layouts utility requirements P&IDs FAT and SAT process change requests and data sheets.
• Author validation/qualification protocols for routine use; suggests improvements.
• Authors and executes validation/qualification protocols and engineering studies. Advises supervisor of factors that may affect experiment; suggests additional experiments.
• Maintains accurate records & training file in accordance with Division standard.
• Interacts with other departments participates in project meetings interprets results and suggests next experiment.
• Participates in New Product Introduction (NPI) meetings and impacts business opportunities through successful completion of tasks and projects and through suggestions for improvement in products and processes.
• Provide technical support for software applications associated with packaging and labeling equipment.
• Monitor and collect data regarding systems performance and report to management. Identify existing problems and recommend solutions.
• Assist internal customers in identifying project specifications and system-related plant and equipment needs; assist in managing the transition of assigned projects to Systems Engineering.
• Participate in developing and revising operating equipment specifications and other policies and procedures as needed.
• Troubleshoot existing processes and recommend or design engineering solutions and/or equipment to address capacity cost and quality issues.
• Assess equipment status and identify risk of obsolescence upgrade needs or potential productivity gains. Evaluate and implement necessary upgrades to maintain a world-class manufacturing environment.
• Knows and effectively uses the fundamental engineering concepts practices and procedures.
• Proficiency in the use of basic engineering techniques equipment and materials.

Minimum Requirements/Qualifications:

• B.S. Degree in engineering preferred (mechanical electrical industrial or design preferred) or related scientific discipline with a minimum of 2-5 years of relevant industry experience
• College and/or technical training in the following disciplines is useful: PLC/HMI programming design software microbiology biological science chemistry technical writing machinery physics and statistics.
• Working knowledge of labeling and packaging equipment is preferable.
• Computer skills knowledge of Zebra printers and CIvision systems is desired. GMP and experience working in a regulated industry.
• Ability to frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds.
• Must be legally authorized to work in the United Stateswithoutsponsorship.
• Must be able to pass a comprehensive background check whichincludes a drug screening.
  

Compensation and Benefits

This position may also be eligible to receive a variable annual bonus based on company team and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on which includes:

• A choice of national medical and dental plans and a national vision plan including health incentive programs

• Employee assistance and family support programs including commuter benefits and tuition reimbursement

• At least 120 hours paid time off (PTO) 10 paid holidays annually paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave) accident and life insurance and short- and long-term disability in accordance with company policy

• Retirement and savings programs such as our competitive 401(k) U.S. retirement savings plan

• Employees Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits please visit: Experience:

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