Simtra BioPharma Solutions is a world-class Contract Development Manufacturing Organization partnering with pharmaceutical and biotech companies. They offer a wide range of delivery systems and product types including biologics and small molecules. As a Quality Associate I, you will maintain quality oversight of manufacturing areas and assess regulatory and quality risks. You will also contribute to creating an environment where teamwork, productivity, safety, identity, strength, purity, and quality are reflected in the finished product.
Requirements
- Bachelor’s degree (preferred science discipline), or Associate’s degree with at least 1 year of Pharmaceutical Quality/Manufacturing or other GXP regulated industry experience, or high school diploma/GED with at least 2 years Pharmaceutical Quality/Manufacturing or other GXP regulated industry experience
- Computer proficiency in Microsoft Word, Excel, and Outlook and the ability to use enterprise software (examples include: JDE, SAP, Maximo, TrackWise, etc.)
Benefits
- Medical & Dental Coverage
- Flexible Spending Accounts
- Life and AD&D Insurance
- Supplemental Life Insurance
- Spouse Life Insurance
- Child Life Insurance
- 401(k) Retirement Savings Plan with Company Match
- Time Off Program
- Paid Holidays
- Paid Time Off
- Paid Parental Leave
- Adoption Reimbursement Program
- Education Assistance Program
- Employee Assistance Program
- Community and Volunteer Service Program
- Employee Ownership Plan