Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Standing for full shift, Warehouse

Job Description

Job Description

At the Thermo Fisher Scientific team, you’ll discover impactful work, innovative thinking and a culture dedicated to working the right way, for the right reasons - with the customer always top of mind. The work we do matters, like helping customers find cures for cancer, protecting the environment, making sure our food is safe and delivering COVID-19 solutions. As the world leader in serving science, with the largest investment in R&D in the industry, our colleagues are empowered to realize their full potential as part of a fast-growing, global organization that values passion and unique contributions. Our commitment to our colleagues across the globe is to provide the resources and opportunities they need to make a difference in our world while building a fulfilling career with us.

Location/Division Specific Information

Chemical Analysis Division (CAD) has innovative analytics, from Lab to Line to Field. The business serves a wide breadth of industrial sectors including pharmaceutical, food and beverage, environmental, process minerals, mining, coal, cement and metals, as well as academic, government, safety, and security. This position will be based in our Oakwood Village site outside of Cleveland, Ohio

Discover Impactful Work:

The Quality Engineer will report directly to the Quality Assurance Manager. You will play an important role in collaborating with the Operations team to ensure our products achieve the highest level of quality standards. This will involve analyzing non-conformance data, leading corrective action initiatives, supporting software verifications, and working with vendors on improving their products and processes.

A day in the Life:

Develop and complete software verification and validation test plansGuide process improvement teams both internal and external to the company.Provide technical support to our procurement team for second source and cost reduction activities.Work effectively with suppliers, purchasing, production, engineering, and customer service as needed.Hands-on software quality work, particularly in the area of establishing root cause analysis, corrective action, software validation, and SOP creation.

Keys to Success:

Education

Bachelor of Science (BS) or Master of Science (MS) from accredited College, University, or equivalent

Experience

Minimum of 7 years of experience with standard quality tools such as 5 Whys, Ishikawa Diagrams, GEMBA walks, etc.American Society of Quality (ASQ) Certified Quality Engineer (CQE) or equivalent preferred

Knowledge, Skills, Abilities

Experience with software validation, problem solving, and issue management systems (e.g. JIRA)Knowledge and experience implementing the ISO 9001:2015 standardKnowledge and experience implementing the ISO 17025:2017 standardProven ability to implement new programs and processes with minimal directionPassionate about quality and process improvementAbility to implement 8D, or similar, approach for Corrective and Preventative ActionsExperience using quality tools mentioned above applied to the manufacturing of a dosimetry system preferredProficient in Microsoft ExcelAbility to write clear and cohesive work instructions to ensure consistency, quality, and safety in task execution

Physical Requirements / Work Environment

Ability to lift/push/pull up to 40 pounds on regular basisWarehouse environment under varying temperaturesArm, hand and finger dexterity, including ability to grasp and type for prolonged periods of timeVisual acuity to use a keyboard, computer monitor, operating equipment, and read materials for prolonged periods of timeAbility to sit, reach with hands and arms, talk, and hear for prolonged periods of time