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- ...change control processes. Conduct periodic reviews and re-validation activities as required. Support investigations, deviations, CAPAs, and audits relating to computer systems. Provide training and guidance to cross-functional teams on CSV requirements and practices...Suggested
- ...quality and compliance issues which may include: Investigate PRAs and complaints for manufacturing related issues Manage site NCRs, CAPAs , ECRs and audit observations for all production processes prior to final product release based on engineering principles; analyse...Suggested
- ...processes; analyze results, make recommendations, and develop reports Analyze and resolve basic Manufacturing and Compliance issues (e.g., CAPA, non-conformances, audit observations) Develop training and documentation materials (e.g., work instructions) for production to...SuggestedImmediate startMonday to ThursdayShift workAfternoon shift
- ...Final Quality Control for raw material issues. Provide input and support to the Cook Medical Corrective and Preventive Action program (CAPAs) and the Non-Conforming Product Process. Support of the Internal Audit Supplier Audit and Regulatory Audit Programmes....SuggestedContract workHybrid workImmediate startFlexible hours
- ...development lifecycle activities including requirements, risk management, verification and validation (V&V). Address audit findings and CAPAs related to software. Review and approve critical documentation, including product drawings and validation protocols. Apply...SuggestedFull timeContract work
- ...including disposition of non-conforming material, the identification of scope, control of related NC material, root cause and appropriate CAPA actions and thorough documentation of same within schedule. Establish and monitor process quality performance to determine when...SuggestedHybrid work
- ...Board) and material disposition duties as required Participate in Corrective Action activities relating to incoming inspection and NC/CAPA System. Support process changes and improvements including Quality Inspections at different points in the process. Participate in...SuggestedFull time
- ...control methods and statistical analysis tools. Familiarity with root cause analysis (RCA), FMEA, and corrective/preventive actions (CAPA). Knowledge of safety standards and regulatory requirements in manufacturing. Ability to collaborate cross-functionally with...SuggestedLocal areaWorldwide


