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Katalyst CRO

Supplier Quality

Katalyst CRO, Minneapolis, Minnesota, United States, 55443

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Supplier Quality

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Katalyst CRO Lead the supplier qualification process by assessing manufacturing/technology capabilities. Conduct comprehensive gap assessments at target suppliers to identify areas for improvement and create individual supplier development plans. Work with suppliers and run SCN and PPAP activity. Develop and refine comprehensive training materials to effectively deploy problem-solving, process control, and quality tools. Proactively identify and implement continuous improvement activities to prevent the recurrence of non-conformities, ensuring sustained process enhancements. Review supplier manufacturing processes and collaborate with suppliers on process improvement and value enhancement opportunities. Facilitate root cause analysis and corrective actions of supplier quality issues. I independently work with suppliers for the completion of PPAP, Special Process Validation IQ, OQ and PQ requirements. Knowledge of International standards relative to QMS, ISO 9001:2015, ISO 13485, and ASTM/ASME standards are preferred. Strong knowledge of Supplier Qualification, Supplier Production Part Approval Process (SPPA), conducting Product and Process Audit at the supplier end Tailor strategies based on supplier and activity feedback to ensure maximum deployment effectiveness. Collaborate with cross-functional teams to develop and enhance the overall supplier development process and phased rollout plans. Facilitate the escalation of unresolved supplier quality issues within assigned projects and suppliers and deliver quality awareness training to suppliers. Monitor supplier progress and performance against pre-agreed objectives and goals, providing guidance and support as needed.

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Responsibilities

Lead the supplier qualification process by assessing manufacturing/technology capabilities. Conduct comprehensive gap assessments at target suppliers to identify areas for improvement and create individual supplier development plans. Work with suppliers and run SCN and PPAP activity. Develop and refine comprehensive training materials to effectively deploy problem-solving, process control, and quality tools. Proactively identify and implement continuous improvement activities to prevent the recurrence of non-conformities, ensuring sustained process enhancements. Review supplier manufacturing processes and collaborate with suppliers on process improvement and value enhancement opportunities. Facilitate root cause analysis and corrective actions of supplier quality issues. I independently work with suppliers for the completion of PPAP, Special Process Validation IQ, OQ and PQ requirements. Knowledge of International standards relative to QMS, ISO 9001:2015, ISO 13485, and ASTM/ASME standards are preferred. Strong knowledge of Supplier Qualification, Supplier Production Part Approval Process (SPPA), conducting Product and Process Audit at the supplier end Tailor strategies based on supplier and activity feedback to ensure maximum deployment effectiveness. Collaborate with cross-functional teams to develop and enhance the overall supplier development process and phased rollout plans. Facilitate the escalation of unresolved supplier quality issues within assigned projects and suppliers and deliver quality awareness training to suppliers. Monitor supplier progress and performance against pre-agreed objectives and goals, providing guidance and support as needed.

Requirements

Bachelor's degree in engineering B. Tech / B.E preferred (E.g., Mechanical Engineering or equivalent) or a related field. 5-10 years of experience in Supplier Quality Engineering, preferably in the Medical Device Industry. Language Proficiency. Strong ability in interpreting engineering drawings/prints. Proficiency in quality tools, risk analysis and statistical tools for problem-solving. Willingness and ability to undertake travel at the supplier end on a need basis. Exceptional verbal, written, presentation, and interpersonal skills. Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint). Seniority level

Seniority levelMid-Senior level Employment type

Employment typeContract Job function

Job functionQuality Assurance IndustriesPharmaceutical Manufacturing Referrals increase your chances of interviewing at Katalyst CRO by 2x Get notified about new Supplier Quality Specialist jobs in

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