Advanced Medical Devices Quality Assurance Specialist - Quakertown - beBeeMaterialsInspector

The Quality Assurance Specialist will actively lead, participate in, and administer the audit and corrective action systems. You will provide primary support to CW-EPD Supplier Quality. You may also occasionally travel to CW-EPD suppliers to perform audits, surveillance, and supp ...

Join a fast growing Pharmaceutical Manufacturing site in a long-term contract role as a Quality Specialist. In this position you'll play a vital role in driving compliance elevating operational standards and supporting the production of critical care products that impact patients ...

Piper Companies is currently looking for an experienced Quality Assurance Specialist in West Point PA to join a leading pharmaceutical company conducting evaluation and disposition of clinical supply materials ensuring compliance with all relevant policies procedures and cGMP reg ...

We are looking for a Specialist Quality Assurance to join our team. The ideal candidate will have QA experience specifically involving raw materials in a GMP-regulated environment such as pharmaceutical, biotech, or other life sciences industries. · QA experience specifically inv ...

We are seeking a Quality Assurance (QA) Specialist to support GMP/GDP-compliant raw material operations at a third-party logistics warehouse in Easton, PA. · Perform incoming raw material sampling, inspection and disposition. · Ensure compliance with GMP, GDP Safety and Documenta ...

We are looking for an experienced Control Assurance Specialist to join our team. In this role, you will lead the assessment and testing of our Enterprise security and fraud controls. · ...

The Quality Assurance Specialist will actively lead, participate in, · and administer the audit and corrective action systems.You will play a key role · in the Quality Assurance organization to ensure both customer and company quality · requirements are met. · Supports planning · ...

A quality assurance specialist with GMP experience required for onsite work at Easton PA. The ideal candidate will have 1-3 years QA experience specifically involving raw materials in a GMP-regulated environment. · ...

The ideal candidate will have 5+ years of QA experience specifically involving raw materials*in a GMP-regulated environment such as pharmaceutical, biotech, · or other life sciences industries.This role is physically active and requires passing an eye exam, · lifting materials (~ ...

The Quality Assurance Specialist will play a key role in ensuring high standards of quality within a manufacturing environment.This position involves supporting production activities through quality control and assurance practices, including but not limited to, upholding the qual ...

We are looking for a Quality Assurance Specialist to join our team. · ...

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+ Our shared missionto serve patients living with serious illnessesdrives all that we do. Join us at Amgen to make a lasting impact on the lives of patients while transforming your career. · + This onsite position provides critical support for the Raw Material Center (RMC) wareho ...

We are looking for an experienced Control Assurance Specialist to join our team. · Lead the planning, execution, and documentation of DET and OET for Enterprise Security and Fraud controls. · Evaluate the design, implementation, and performance of cyber security controls across d ...

We are seeking a Quality Assurance Specialist with GMP experience to join our team in Easton, PA. · ...

The Quality Assurance Specialist will be responsible for reviewing and approving batch records, administering QMS documentation, implementing investigations and corrective actions, and communicating deficiencies to QA/RA management. · ...

Join Surmodics Services & Technologies (formerly Biocoat), a global leader in developing, manufacturing and applying hydrophilic coatings on medical devices. · ...

Join us in pioneering breakthroughs in healthcare. · We encourage you to step beyond your comfort zone, · ...

This role well suited to an ambitious professional looking for next step in career. As Quality Specialist you will responsible for providing quality oversight of US based site that manufactures distributes radioactive sterile injectables PET per CFR Part 212 and USP 825 PETNET So ...

As a trusted staffing and recruitment partner we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. · ...

The ideal candidate will have 5+ years of QA experience in a GMP-regulated environment such as pharmaceutical, biotech or other life sciences industries. · ...