Quality Control Inspector

Mallinckrodt Pharmaceuticals • Port Allen, LA

18h • Onsite

About The Position

The Quality Control Inspector, for incoming laboratory and in-process inspections, is responsible for assuring that activities, processes, and specific conditions related to the daily manufacturing, processing, packing, and holding of active pharmaceutical ingredient (API), drug product, and medical devices meet current Good Manufacturing Practices (cGMPs) and comply with applicable procedures and standards such as to ensure the quality integrity of the products. This position also engages in functional and analytical assessments to ensure quality is built into the products manufactured at the Port Allen, LA manufacturing facility. These activities support the goal of reliably and demonstrably providing safe and efficacious products to our patients and customers with the assurance that such is conducted in compliance with applicable government regulations and guidelines as well as with company policies and procedures.

Requirements

• Associate’s degree in a technical or scientific field required.
• Knowledge of drug cGMPs, OSHA, EPA, and FDA regulations.
• Strong mechanical aptitude and familiarity with laboratory analyzers and inspection equipment.
• Excellent teamwork and communication skills.
• Collaborative and tactful in interacting with all organizational levels.
• Assertive in enforcing regulations, policies, and procedures.

Nice To Haves

• Quality certification preferred (e.g., ASQ CQE, CQA).
• Bachelor’s Degree (preferably in a science related field)
• Experience in a regulated work environment

Responsibilities

• Performs area clearances/line clearances, in-process inspections of manufacturing processes, and inspection and disposition of incoming material.
• Monitors manufacturing process performance as relates to SPC/SQC, general compliance status of manufacturing and warehouse areas, as well as ensures components, product or equipment under evaluation or not in compliance is properly controlled.
• Prepares and attaches material quality status on materials, including labeling.
• Performs the verification of all labels after final printing is completed.
• Executes assigned activities in accordance with production schedule and participates in production schedule planning, as needed.
• Assists in the development, implementation, and maintenance of site quality procedures, standards, and controls.
• Supports the quality audit function through occasional conduct of investigations of nonconformances or deviations and assists with corrective actions and preventative actions associated with site quality.
• Performs other tasks related to the assurance that product meets established standards for quality and efficacy as assigned by supervisor.
• Performs special projects as assigned by supervisor to meet company and departmental goals.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree