Job Description

Our client generic pharmaceutical company is seeking an In process QA Associate to join their team.

Responsibilities:

• Collaborates with other production staff and Departments.
• Accurately and consistently completes and documents batch records/other required paperwork.
• Maintaining various logbooks to document the performance or completion of specific functions.
• Maintaining IPQA supply inventory.

Qualifications:

• Ability and willingness to learn manufacturing/packaging procedures and federal regulations pertaining to manufacturing process.
• Experienced in proper documentation and correction practices.
• Must be a Team player able to effectively communicate with QA Supervisor, IPQA, Quality Control, Production, and Supply Chain to meet finished product release goals.
• Be able to work long hours to support production requirements.
• Be available for overtime, including weekends, as needed for production support.

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