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Job Requirements of INPROCESS QUALITY ASSURANCE ASSOCIATE III:
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Employment Type:
Contractor
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Location:
East Windsor, NJ (Onsite)
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INPROCESS QUALITY ASSURANCE ASSOCIATE III
Work Hours - 7:00am - 3:30pm
IPQA Associate Level III 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.
Responsibilities (Identify the duties or functions the employee would perform in this role)
- Collaborates with other production staff and Departments.
- Provides on the job training and day to day guidance to other nonexempt personnel.
- Maintaining various logbooks to document the performance or completion of specific functions (ex. Material Receiving Log).
- Communication skills (written and verbal).
- Effectively communicate with other department on different levels.
- Be able to work long hours to support production requirements.
- Be available for overtime, including weekends, as needed for production support.
- Possess the ability to analyze information and decision making .
- High School Diploma or equivalent GED.
- Up to 5 years of experience performing in-process checks/verifications in the Manufacturing and Packaging areas of pharmaceuticals manufacturing environment.