Entry Level Associate Quality Assurance - Night Shift

HERE’S THE JOB DESCRIPTION:

Title: Associate Quality Assurance NS #14381

Pay Rate: $22 - $24.50/hour

Location: New Albany, OH

Length: 1-year’ contract + Possible extension

Swing shift - 12-hour shifts - Must have flexibility with shifts

10PM - 6:30 AM - May fluctuate over the duration of the contract

Must Have Skill Sets:

• Scientific degree in Life Sciences, Physical Sciences, Applied Engineering or Manufacturing Technologies

• Experience in and knowledge of GMP/GCP operations or similarly regulated industry

• Highly effective verbal and written communication skills, strong interpersonal skills

• Great attention to detail and high degree of accuracy in task execution and GMP documentation

• Ability to complete tasks autonomously, providing updates to senior management, and identifying potential issues.

• Strong organizational skills, including ability to follow assignments through to completion.

Job Summary:

An American multinational biopharmaceutical is seeking an Associate Quality Assurance NS.

• Primary responsibilities of this position include inspecting raw materials, components, and labels, in addition to sampling raw materials, labels, and sanitary utilities, and generating/compiling quality data and reports (e.g. lot track/trace, incidents).

• Will also assist with document review and initiate incidents, as well as coordinate and compile general documents and oversee room clearance inspection.

• Skills: quality assurance or manufacturing experience in the pharmaceutical or medical device industry

Day to Day Responsibilities:

• Provide daily guidance and support to manufacturing staff regarding compliance with Standard Operating Procedures and Work Instructions.

• Ensure regular presence on the packaging area to provide oversight to GMP operations and quality systems.

• Act as a first point of contact in case of production staff inquiries (quality related) during operations.

• Review and approve batch record documentation, assist in sampling and inspections as required and other GMP documentation in support of daily operations.

• Own, review, and approve controlled documents, including Standard Operating Procedures (SOPs), Work Instructions and Forms.

• Review and approve minor deviations.

• Adhering to safety rules and maintaining a safe work environment for both yourself and others by supporting Environmental Health and Safety corporate and site goals.

Basic Qualifications:

• High school/GED + 2 years’ work experience OR

• Associates degree and 6 months’ work experience OR

• Bachelor’s degree