Company Description

Pharma

Job Description

The Quality Control Inspector (TEMP) 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.

The Quality Control Inspector (TEMP) engages in functional and analytical assessments to ensure quality is built into the products manufactured at the Port Allen, LA and Coppell, TX manufacturing facilities. 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.
Minimum Requirements
Education / Experience / Skills:
• Associate’s Degree in technical or scientific related field required
• Bachelor’s Degree (preferably in a science related field) preferred
• Experience in a regulated work environment is preferred
• Quality certificate preferred (ASQ CQE, CQA, etc.)
Competencies:
• Understand and internalize drug cGMPs, OSHA, EPA, and FDA regulations/requirements as related to drug and medical device manufacturing.
• Proficient in Word and Excel.
• Mathematical skills
• Mechanical aptitude
• Excellent oral and written communication skills; interpersonal skills; and organizational skills.
• Detailed-oriented.
• Excellent team ethic and practice.
• Collaborative, tactful, and able to communicate with various levels in the organization.
• Assertive in enforcing regulations, policies, and procedures.
• Basic knowledge of laboratory analyzers and inspection equipment used to perform chemical analyses and component inspections.

Additional Information

All your information will be kept confidential according to EEO guidelines.