À propos
This is an onsite position requiring the team member to be onsite five days a week. As the Supervisor, Manufacturing Quality Assurance, you will monitor and control the daily activities of quality inspection, testing, documentation review, and calibration in support of Operations and product release. Essential duties and responsibilities include: Providing direct supervision, resolving personnel issues, conducting performance evaluations, and performing supervisory discipline as necessary. Exhibiting a strong "quality first" mentality and ensuring that product and process quality are held to the highest standard. Ensuring compliance with quality system documents, cGMPs, ISO standards, and FDA regulations. Scheduling and prioritizing quality inspection, testing, documentation review, and calibration to support Operations and release of product. Identifying and developing opportunities to improve existing processes and procedures. Supporting quality assurance improvement activities by evaluating products, processes, or materials in order to develop control or improvement strategies intended to improve the customer's experience. Working with technical staff in performing root cause failure analysis and implementing corrective and preventive actions to eliminate recurrence. Assisting in and managing the verbal communications and visual checks of work activity to ensure quality requirements are met. Ensuring proper corrective actions, discrepancy reports, and follow-up activities are accomplished. Advising on equipment condition, test method, etc. to aid in the course of action when components do not meet specifications. Responsible for quality inspection and verification. Reviewing documentation and records for accuracy. Determining if product is impacted, can be released, or if Non-Conformance Report is required. Assisting in developing documentation and procedures during the qualification of new equipment/inspection methods. Performing other duties as assigned based on business needs. Conforming with and abiding by all regulations, policies, work procedures, instructions, and all safety rules. Exhibiting regular, reliable, punctual, and predictable attendance. Education: Associate's Degree in Technical or Engineering. Work experience: 5-8 years of experience in the manufacturing industry; 3+ years of Quality supervisory experience in the manufacturing industry. Preferred knowledge, skills, and abilities include: Medical Device experience preferred. Metrology Equipment experience. Ability to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description. Support and contribute in Lean Sigma programs and activities towards delivery of the set target. Ability to comply with the company's safety policy at all times. Ability to comply with the company's quality policy at all times. Travel requirements: Must be able to travel up to a minimal amount of the time. Physical requirements: Must be able to work assigned shift(s) with overtime as required to complete assignments if necessary. Sitting and/or standing for extended periods may occur as well as getting to and from offices and building sites. If necessitated by customer requirements, must be able to see with or without corrective lenses and distinguish color differences for product and safety issues. Hearing ability should be sufficient to hear and react to audible alarms from distances up to 150 feet. The ability to be able to lift and carry various items up to 50 pounds for manufacturing positions or 30 pounds for administrative positions is required. West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening and/or a pre-employment drug screening.
Compétences linguistiques
- English
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