Joulé · 6 days ago
IPQA II
Joulé is a leader in delivering outsourced services and workforce solutions across North America, and they are seeking an IPQA Associate Level II. The role involves supporting and assisting activities related to the production of pharmaceutical products in accordance with cGMP and ensuring compliance with all standards and regulatory guidelines.
Responsibilities
IPQA Associate Level II will support and assist activities related to the production of pharmaceutical products in accordance to current Good Manufacturing Practices (cGMP), Standard Operating Procedures (SOPs) and batch record specification
The IPQA Associate shall assure compliance with all standards and regulatory guidelines
Collaborates with other production staff and Departments
Accurately and consistently completes and documents batch records/other required paperwork
May provide on the job training and day to day guidance to other nonexempt personnel
Qualification
Required
High School Diploma or equivalent GED
Up to 4 years of experience performing in-process checks/verifications in the Manufacturing and Packaging areas of pharmaceuticals manufacturing environment
Good communication skills and capable of communicating with all levels
Be available for overtime, including weekends, as needed for production support
A familiarity with cGMPS, CFRs, OSHA and FDA regulations
Benefits
Health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan
Company
Joulé
At Joulé, we believe our world is filled with possibilities – where character, integrity, and commitment drive our purpose.
Funding
Current Stage
Growth StageCompany data provided by crunchbase