To lead engineering projects, bring new products to production, and improve existing products within the established time frames in accordance with Pride's procedures and protocols RESPONSIBILITIES/DUTIES Facilitate meetings for product development and design reviews with both internal and external stake holders Construct and maintain project timelines and Design History

Manage and lead a team of individuals to ensure effective quality execution, continuous improvement, and regulatory compliance. Provide leadership within the facility to drive positive change through influence and example. In conjunction with plant operations, build and maintain an effective culture of food safety and quality within the facility. Develop and maintain faci

The Chemical Application Engineer will create value for our global customer base by providing direct technical and application engineering support for the product lines of the Elastomer Process Materials (EPM) division. This includes RTS adhesives (Chemlok), coatings (Sipiol), flock adhesives (Flocklok), chemical products, and specialty materials. The incumbent must be a

The Chemical Application Engineer will create value for our global customer base by providing direct technical and application engineering support for the product lines of the Elastomer Process Materials (EPM) division. This includes RTS adhesives (Chemlok), coatings (Sipiol), flock adhesives (Flocklok), chemical products, and specialty materials. The incumbent must be a

The Regulatory Affairs Specialist drafts, submits and gains clearance for 510(k) submissions, and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products. This position entails development of FDA submissions, requires working knowledge of products under review and of relevant regulations and guidance documents. This i

Coordinates and prepares document packages for regulatory submissions for new and mature products, ensuring compliance with local and regional registration requirements. Compiles all materials required in submissions, license renewal and annual registrations. Recommends changes for labeling, manufacturing, marketing and clinical protocol for regulatory compliance. Monitor

Responsible for working as the Quality Assurance member on new product development projects for the B. Braun Medical Inc medical device franchise. The desired candidate will have experience with design controls and the associated regulations related to medical devices. The position will also be responsible for working with external specification developers and contract ma

Utilization Review Tech III Facility Lower Bucks Hospital Location US PA Bristol ID 2024 160307 Category Business Professional Position Type Full Time Shift Days Job Type Non Exempt Overview Join an award winning team of dedicated professionals committed to our core values of quality, compassion and community! Lower Bucks Hospital , a member of Prime Healthcare, offers in

This person will be responsible for the performance optimization for a fixed number of assets to exceed budget requirements and to drive best in class performance. Activities include responding to known deficiencies, responding to current issues and proactively identifying and resolving performance gaps. Directly influences cost of up to $20 MM for the plants assigned. Th

. Work Schedule and Additional Information Full time employment Work hours are 7 00 AM to 3 00 PM, Monday Friday, with a 30 minute lunch. Salary In some cases, the starting salary may be non negotiable. You will receive further communication regarding this position via email. Check your email, including spam/junk folders, for these notices. REQUIRED EXPERIENCE, TRAINING &

Plan, coordinate and complete assigned Annual Operating Plan (AOP) and Quality Improvement tasks in a timely, professional, and effective manner. Identify, and communicate to the organization, all customer, regulatory and Parker Lord product specific quality requirements, for assigned products and customers, and assist with internal quality planning efforts to assure comp

This role will provide global leadership for process development and engineering design of new and existing chemical manufacturing processes. Scope includes driving creative engineering solutions to ensure that commercialized processes are robust and deliver products that exceed customer requirements, cultivating strategic relationships with external technology and servic

Senior Quality Engineer (Pittsburgh, PA) Life Unlimited. At Smith+Nephew, we design and manufacture technology that takes the limits off living. The Senior Quality Engineer takes the lead in developing, implementing, and enhancing production monitoring methods and systems for inspecting and testing all new products. This person evaluates products, manufacturing processes,

The Compliance Manager works with the Director of Compliance and Chief Compliance Officer to support our Global business on compliance matters relating to adherence to relevant policies, codes, laws, and regulations impacting business operations. The Compliance Manager will assist with various aspects of our compliance program, including compliance training, auditing and

Advantage Technical is seeking a QC Inspector for our client onsite in Allentown, PA! A quick start and money in your pocket! Required Science or Engineering Degree with some type of Quality experience in a GMP environment. Contract Duration Indefinite long term contract with a chance for conversion down the road. Pay $23 per hour. Shift Schedule 6PM to 6AM 2 week schedul