Role OverviewThe Sterility Assurance Validation Engineer/Specialist I/II/III is responsible for supporting validation of cGMP equipment, facilities, and processes as it relates to sterility assurance. This role requires a disciplined, science-based approach to ensure consistent excellence, safety, and integrity in everything done. The ideal candidate thrives in fast-paced environments and is driven to make a meaningful impact.
What You Will Do
Support and maintain sterility assurance strategies, policies, and procedures. Establish and maintain good practices for aseptic environments. Provide sterility assurance support to internal customers and support validation and requalification of equipment and systems.
Why It Might Be a Fit
The ideal candidate is driven to make a meaningful impact, thrives in fast-paced environments, and is motivated by a disciplined, science-based approach. They are open to working onsite and supporting a 24/7 manufacturing environment.
Requirements
- Bachelor's degree in Engineering (for Engineer role) or life sciences or other related field (for Specialist role)
- Up to 3 years' related work experience (for Sterility Assurance Validation Engineer/Specialist I)
- 3 to 5 years' related work experience (for Sterility Assurance Validation Engineer/Specialist II)
- More than 5 years' related work experience (for Sterility Assurance Validation Engineer/Specialist III)
- Proficient computer skills in Microsoft Word, Excel, and Outlook
Benefits
- Medical, prescription, dental, vision, life insurance, and disability benefits
- 401(k) program with 100% vesting
- Generous off-shift premiums
- 16 hours of paid volunteer time per calendar year
- PTO: up to 104 hours of paid time off per calendar year
- Wellness time off (WTO): 1 hour of wellness time off for every 30 hours worked
- 10 paid holidays per calendar year
]]>