• Manufacturing Process Engineer II

    ThermoFisher Scientific (Lebanon, TN)


    Work Schedule

     

    First Shift (Days)

     

    Environmental Conditions

     

    Office

    Job Description

    When part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer and protecting the environment. The work we do has real-world impact, and you’ll be supported in achieving your career goals.

    Discover Impactful Work:

    Being will be part of the manufacturing engineering team to develop new manufacturing processes that support the global network of Thermo Fisher Scientific SUD manufacturing sites.  You will be responsible for ensuring process quality, safety, and delivery to product and process requirements and standards.

     

    A Day in the Life:

     

    Have responsibility for supporting and designing new manufacturing processes as well as improvements to existing processes to improve productivity, capacity, cost reduction, and efficiency.  You will support complex projects, support process scale-up, and contribute as a process resource across cross-functional teams.

    Keys to Success:

    Education

    + Bachelor’s degree in an engineering field required with at least 2 years of demonstrated experience in a technical/engineering environment or recent Master’s degree graduate.

    Experience

    + Assistance of specification (URS) and qualification (FAT/PV) of manufacturing processes (manual and automated).

    + Supporting technical engineering efforts thru process design and development projects .

    + Engineering tools and methods for tasks such as experimentation (DOE), risk assessment (FMEA), process reliability (SPC, Cpk, MSA), and statistical analysis.

    + Experience in process design to applicable international standards (e.g. ISO, CE, FDA, etc.) preferred.

    + Lean Six Sigma Green/Black Belt certification (or equivalent) preferred.

    Knowledge, Skills, Abilities

    + Experienced in MS Office and MiniTab (or equivalent).

    + Lean Manufacturing and Six Sigma methodology.

    + Understanding of process capability (Cp, Cpk) and reliability (SPC, MSA).

    + Experienced in technical writing, including authoring engineering protocols, reports, and procedures.

    + Medical Device/Biopharmaceutical manufacturing (i.e. GMP, FDA, ISO 13485) experience.

    + Self-motivated with good problem-solving, communication, and coordination skills.

    + Self-starter with demonstrated history of continuous improvement and drive for results.

     

    This position does not offer relocation benefits.

    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!

     

    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.