Associate II, Manufacturing Operator (2nd Shift 2:00 pm to 10:30 pm)
About The Position
The Associate II, Manufacturing Operator executes quality and manufacturing procedures to meet production demands and regulatory requirements. The role supports the on-time manufacture of intermediate, semi-finished, and finished pharmaceutical products that meet quality standards, and may assist with establishing equipment operating specifications and standard operating procedures, improving manufacturing techniques, maintaining and calibrating equipment, and resolving technical issues. Working on semi-routine assignments, the Associate II uses judgment within defined practices and policies to resolve problems and make routine recommendations. The position performs manufacturing operations according to Manufacturing Records, Current Good Manufacturing Practices, and Standard Operating Procedures in a clean room environment. The role may provide guidance to lower-level personnel and requires qualification to operate approximately 50% of manufacturing equipment. The scheduled shift is 2:00 p.m. to 10:30 p.m., with a 10% shift differential.
Requirements
- High school diploma or GED.
- For Associate II: 3 to 5 years of related experience, or an equivalent combination of experience and training.
- Willingness and ability to receive medical clearance to wear a respirator, such as a Powered Air Purifying Respirator, for the entire working shift.
- Physical ability to gown and de-gown, including use of a decontamination fogging shower, in up to three layers of clean room and potent compound facility gowning, such as a Tyvek jumpsuit.
Responsibilities
- Execute manufacturing operations according to Manufacturing Records, Current Good Manufacturing Practices, and Standard Operating Procedures in a clean room environment.
- Perform manufacturing area and equipment setup, cleanup, teardown, and sanitization under supervision.
- Operate manufacturing production equipment under supervision, as required by Manufacturing Records and Standard Operating Procedures.
- Perform in-process inspection and testing under supervision, as required by Manufacturing Records and Standard Operating Procedures.
- Accurately and completely document manufacturing activities in Manufacturing Records, Controlled Forms, Product Container Labels, and Logbooks.
- Verify and document that manufacturing steps performed by other Manufacturing Associates are correct in Manufacturing Records and/or Logbooks.
- Observe all Company, Health, Safety, and Environmental guidelines.
- Provide guidance on assignments to lower-level personnel when needed.
- Assist with equipment maintenance, calibration, and resolution of technical issues.
Benefits
- 10% shift differential
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
