Validation (CQV) Engineer II
Simtra BioPharma SolutionsBloomington, Indiana, United States • North Rhine-Westphalia, Germany
Posted October 24, 2025
Full Time
About the Company
Simtra BioPharma Solutions provides biopharmaceutical solutions, but no additional details were provided.
Job Description
Simtra BioPharma Solutions is seeking a Validation (CQV) Engineer II to join their Engineering team. This role involves leading validation activities, working directly with various departments, and ensuring compliance with cGMP regulations. The Engineer II will support global regulatory efforts and lead a team to ensure project success. They will work 100% onsite at the Bloomington, Indiana facility.
Requirements
- BS degree in an Engineering or Science discipline
- 2+ years experience in commissioning, qualification, and validation in a regulated industry
- Familiarity with ISPE Baseline Guide 5
- Strong technical writing skills
- Advanced proficiency in Microsoft Office Suite
Benefits
- Medical & Dental Coverage
- Flexible Spending Accounts
- Life and AD&D Insurance
- Spouse Life Insurance
- Child Life Insurance
- Short and Long-Term Disability Insurance
- 401(k) Retirement Savings Plan with Company Match
- Time Off Program
- Paid Holidays
- Paid Time Off
- Paid Parental Leave
- Educational Assistance Program
- Employee Assistance Program
- Community and Volunteer Service Program
- Volunteer Insurance Benefits
- Vision Coverage
- Accident
- Critical Illness
- Hospital Indemnity Insurance
- Identity Theft Protection
- Legal
