Specialist - CAPA Manufacturing

We count on our team members to challenge and push the boundaries to make that happen. At Thorne, you'll be joining a team of more than 750 passionate individuals committed to our cause of providing superior health solutions at every age and life stage. · ...

Department: Quality Assurance · Location: Summerville, SC · Description · At Thorne, we work to deliver high-quality, science-backed solutions to empower individuals to take a proactive approach to their well-being. Each day begins with a mission to help others discover and achie ...

A Compliance Specialist is needed to join a team at a leading pharmaceutical manufacturer. · The ideal candidate should have experience in FDA-regulated environments and strong knowledge of CAPA management. · ...

The Specialist Manufacturing will act as the External Supply representative across functional teams and drive closure of quality records in a timely manner. · Address and close quality records (Deviations, Corrective and Preventive Actions (CAPAs), CAPA-Effectiveness Verification ...

The Quality Assurance Engineer is a hands-on individual contributor within the Quality · Assurance organization at Recipharm Advanced Bio's Watertown site.This position is heavily focused on CAPA and Change Control program execution, · CAPA Management and Deviations and Investig ...

Job summary · Quality Consulting Group is looking for a talented manufacturing specialist to join their team in Puerto Rico & USA. In this role, you'll work with a highly enthusiastic team and contribute to the world-class manufacturing industry. · ...

Hologic is looking for a Lead CAPA Quality Engineer to play a key role in strengthening quality and compliance across our global supply chain. · ...

We are seeking a Quality Engineer with 2+ years of medical device experience to lead and manage NCMRs & CAPAs. · Lead and manage NCMRs & CAPAsSupport manufacturing with NC assessmentsPerform quality line walks for complianceDrive process improvements and quality standards · ...

Quality Consulting Group is looking for a talented specialist in manufacturing to join their team. · An equal opportunity employer with no discrimination based on race, color, religion, sex or any other characteristic protected by law. · ...

We are looking for a Lead CAPA Quality Engineer to play a key role in strengthening quality and compliance across our global supply chain.In this senior, hands-on role, you will lead and facilitate Corrective and Preventive Actions (CAPAs), advise on risk and escalation decisions ...

Quality Consulting Group is looking for a talented and enthusiastic specialist manufacturing to join their team in Puerto Rico & USA. · ...

MEDICAL INSURANCE 100% ON US · Great careers start with great benefits · Join the Barrett Petfood family and enjoy a comprehensive benefits package, including medical (company paid), dental, and vision insurance; a 401(k) with company match; life insurance; health savings account ...

We are seeking experienced Investigation and CAPA Specialists for a 3 month contract in Greenville, SC. · This role requires strong investigation execution skills, technical writing capabilities, and the ability to work cross-functionally with Manufacturing, Engineering, Training ...

We are seeking experienced Investigation Specialists for a 3 month contract in Greenville, · SC.The selected resources will support end-to-end investigations from · a manufacturing and process perspective. · ...

The primary role of the CAPA Coordinator is to manage the Quality Management System within the CAPA program. This position involves assisting in drafting audit responses for entry into the CAPA program and collaborating with CAPA owners to ensure the completion of open CAPAs. · C ...

We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity, accelerate project timelines, and maintain a strong state of compliance and audit readiness. · At Pinnaql, people always come first. We believe that when you're empowered to do your ...

The Process Support Engineer supports commercial pharmaceutical manufacturing operations by ensuring processes are compliant, robust, and continuously improving.This role focuses on process documentation, deviation investigations, CAPAs, and change management, · Bachelor's degree ...

This role is a Specialist in the Devens Quality Assurance (QA) Technical Operations function. · B.S., in science, engineering, biochemistry or related discipline. · A minimum of 4 years relevant experience with a minimum of 2 years in a regulated environment. · ...

Provide technical support to the External Manufacturing Organization and assigned contract manufacturing organizations (CMO's), ensuring the transfer of robust manufacturing and packaging processes to CMO's and/or Client sites. · ...

+ Process Support Engineer supports commercial pharmaceutical manufacturing operations by ensuring processes are compliant, robust and continuously improving.+ This role focuses on process documentation deviation investigations CAPAs and change management working closely with Man ...