Job description
Responsibilities
* Develop a basic understanding of reagent manufacturing best practices at the site and provide support to operations functions
* Coordinate Operations stakeholders (Manufacturing, Process Engineering, Validations Engineering, Functional Leads, Quality, Validation, Planning, Procurement, Purchasing and Label Control) to ensure new products are moved into the manufacturing process per the transfer plan
* Support the refinement of Technology Transfer standard work to continuously improve the transfer process
* Support creation of project plans to track and ensure timely completion of transfer projects
* Develop familiarity of site manufacturing processes to promote and improve GMP
* Support and execute Validation protocols utilizing Good Manufacturing Processes (GMP) and standards for transferred products
* Troubleshoots problems, and participates in transfer planning and process updates.
* Demonstrates the ability to deliver results with significant guidance and input from others
* Other duties as assigned by management
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each responsibility satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the responsibilities.
Formal Training/Education
Education Level Education Details
Bachelor's Degree BS in an Engineering/Engineering Technology or Life Science discipline - REQUIRED
Experience
Years of Experience Experience Details
2 years 0-2 years of related experience with a Bachelor's Degree - REQUIRED
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Job Types: Full-time, Contract
Pay: $27.00 per hour
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Vision insurance
Shift:
- 8 hour shift
Weekly day range:
- Monday to Friday
Education:
- Bachelor's (Required)
Experience:
- Reagent Manufacturing: 1 year (Preferred)
- Lean Six Sigma: 1 year (Preferred)
Work Location: One location
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