In Process QA Associate

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.

Permanent