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Senior Process Engineer
Kalamazoo, MI, US
Engineering
Bachelors Degree
Full Time, Temporary
Experienced (Non-Manager)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
Kalamazoo, MI, US
Experienced (Non-Manager)
Full Time, Temporary
Biotechnology/Pharmaceuticals
On-site
Engineering
Bachelors Degree
First Shift (Day)
Job details
Senior Process Engineer
- Location: Kalamazoo, Michigan (49001)
- Duration: Until 10/31/2025 (contract extension potential)
- Type: W2 contract (NO C2C OR THIRD PARTY)
- Pay: Negotiable depending on direct-related experience
- Work Authorization: Must be currently in the United States with active employment authorization documents.
Seeking candidates that have some experience with equipment PLC programming and candidates that have good experience with validation work.
Preferred Qualifications (Desired):
- Continuous Improvement and Project / Process Improvement related experience.
- Green or Black Belt 6 Sigma qualifications.
- Experience with SCADA systems
Job Summary:
- This role is within the Product Transfer team.
- The role contributes to the delivery of high impact, cost transformative projects.
- The role will require the successful candidate to operate across a network of stakeholders from Product Transfer, Operations and Divisional partners, therefore strong interpersonal skills and communication skills will be necessary.
What you will do:
- Owns and supports the development of the Validation Plan for highly complex validation projects.
- Owns and supports validation and initial qualification of equipment and systems as related to new equipment for NPI/Product Transfer activities.
- Write, review, and execute studies for process validation, including DOE, OQ, and PQ Analyze equipment to establish operating data, conduct experimental test and result analysis.
- Coach and mentor others on functionally related topics.
- Ensure quality of process and product as defined in the appropriate operation and material specifications.
- Select components and equipment based on analysis of specifications, reliability and regulatory requirements.
- Participate in PFMEA, Control Plan, SOP, PPAP and other Stryker internal process qualification generation associated with product transfers.
Minimum Qualifications, Knowledge, Skills (Required): Bachelor’s degree in an engineering discipline.
- Minimum of 4 or more years’ experience in a FDA regulated manufacturing or project environment.
- Experience of process/ product validation.
- Experience with statistical methods, process mapping, root cause analysis.
- Experience coaching and mentoring team members.
- Must be able to read and interpret complex engineering drawings and have the ability to understand geometrical dimensioning and tolerancing.
Important information: To be immediately considered, please send an updated version of your resume to Deas172@kellyservices.com.
*** (Kelly does not expense relocation/interview costs)**
- Work Authorization: Must be able to work in the United States with current employment authorization documents.
In addition to working with the world’s most recognized and trusted name in staffing, Kelly employees can expect:
- Competitive pay
- Paid holidays
- Year-end bonus program
- Recognition and incentive programs
- Access to continuing education via the Kelly Learning Center
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