QA Associate: Validation & Compliance Specialist
$93.1k - $146.3kBelcan
A leading quality assurance consulting firm is seeking a Quality Assurance Associate in Sanford, NC. The candidate will oversee QA processes to ensure compliance with local and global standards within the biologics manufacturing sector. Responsibilities include reviewing validation documents and authoring quality documents. Ideal candidates should have a relevant degree and 3-5 years of experience in QA functions. This is a mid-senior level contract role offering competitive compensation ranging from $93,100 to $146,300 annually. #J-18808-Ljbffr Belcan
- A leading consulting firm in North Carolina seeks a Specialist in QA Validation to oversee quality systems in GMP operations. The role involves collaborating with various departments to ensure compliance with regulatory standards. Candidates should possess a relevant degree...SuggestedContract work
$25 - $27 per hour
...Job Description Job Description Job Title: Validation Support Specialist Job Description The Validation Support Specialist executes qualification... ...IQ/OQ/PQ protocols with a high level of accuracy and compliance. Accurately record data and document results in...SuggestedContract workTemporary workMonday to Friday- ...Process Validation EngineerValspec—a global provider of system validation and lifecycle services—provides commissioning and qualification... ...support to ensure successful PPQ implementation and GMP compliance.The successful candidate will work closely with Manufacturing,...SuggestedFull timeContract workRemote work
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- ...we serve since 1957. Today, our 82,000 associates serve more than 10 million customers a week... ...and improve labor productivity Follow QA daily check list and sanitation standards... ...to the Manager on Duty Ensure compliance with local, state and federal regulations...SuggestedLocal areaNight shift
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$125.09k - $178.7k
...maintenance, integration, and support of laboratory systems to ensure compliance, efficiency, and reliability in a regulated (GxP) environment,... ...processes, equipment qualification and computer systems validation (CSV) according to GAMP 5 principles is a must.Strong...Work at officeLocal areaRemote workWork from homeWorldwide- ...continuous improvement practices. Candidates should have extensive experience in pharmaceutical manufacturing, project management, and compliance. Successful applicants will contribute to process enhancements and support maintenance operations, ensuring adherence to...
$97.53k - $146.29k
...Caterpillar is seeking an In Process Validation (IPV) Automation Specialist to join our factory-based team in... ...operating procedures including compliance with safety and quality standards.... ...of the decision-making process and associated tools and techniques; ability to accurately...Full timePart timeRelocation packageFlexible hours- RN-Quality Clinical Excellence Specialist About the job RN-Quality Clinical Excellence Specialist... ...within a department or withing a larger QA team, related to data collection and... ...all activities / metrics / standard compliance related to disease specific care for HF,...
- ...RN-Quality Clinical Excellence Specialist We are seeking a highly motivated and detail-... ...disease-specific certifications and ensuring compliance with clinical excellence standards,... ...collaborating across departments and/or QA teams to drive performance improvement efforts...
- ...role serves as the technical lead for automation commissioning activities, working closely with system integrators, engineering, validation, quality, IT/OT, and equipment vendors to ensure automation systems are safely commissioned, fully functional, and ready for qualification...Full timeTemporary workFlexible hours
- PROCESS ENGINEER CO-OP SPRING 2027 (7.5 MONTHS) SANFORD, NC Kick off a challenging and rewarding engineering career with Coty! Our Manufacturing Co-Op provides the opportunity to own a project for improving a production loss in the area of Cost, Quality, ...
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