Catalent Pharma Solutions
Supplier Quality Regional Lead
Catalent Pharma Solutions, Chelsea, Massachusetts, us, 02150
Catalent Pharma Solutions - Supplier Quality Regional Lead
Location: Chelsea, MassachusettsThis is a full-time salaried position: Monday – Friday, 1st shift.Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives.The Role:Oversight and leadership for the regional Supplier Auditor Team performing audits, generation of audit reports and management of supplier CAPA (Corrective and Preventative Action) to ensure required actions are completed within the required timeframe.Support to Supplier Quality site teams on routine queries and guidance.Manage Supplier notification mailbox to ensure active management and delegation within the supplier team and associated Quality Compliance Assessments are delegated appropriately.Ensure the regional team performing the audits assigned develop a planned audit schedule to maximize audits conducted during one trip (i.e., grouped audits based on location).Development of metrics to provide visibility of audits due, planned audit dates, audits complete, audit reports process timelines, and overdue audits.Development for collation and communication of common finding categories to allow identification of risk areas across Supplier base.Proactive planning to ensure maintenance of audits assigned to the Supplier auditor team, to mitigate overdues.Collaborate, align, and foster cross-functional business relationships within Global functional groups such as Procurement, Sites, and Supply Chain to ensure any risks are identified, mitigated, and communicated.40% travel expectations annually (domestic & international).Other duties as assigned.The Candidate:Bachelor’s Degree, required; Certified auditor or lead auditor credentials, preferred.Five years+ auditing experience and supervisory experience, required.Experience working in an auditing role within the Pharmaceutical/Medical Device industry.Knowledge and understanding of the following principles and guidelines: EU EudraLex Volume 4 GMPs, 21 CFR Parts 111/210/211 (FDA), ISO, and related International Regulations affecting pharmaceutical products and medical devices.Working knowledge of industry-related guidelines such as ICH Q7, GHTF, and IPEC.Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds.Demonstrable leadership experience may be considered in place of external experience.Why You Should Join Catalent:Defined career path and annual performance review and feedback process.Diverse, inclusive culture.152 hours of PTO + 8 paid holidays.Several Employee Resource Groups focusing on D&I.Dynamic, fast-paced work environment.Positive working environment focusing on continually improving processes to remain innovative.Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.Community engagement and green initiatives.Generous 401K match.Medical, dental and vision benefits effective day one of employment.Tuition Reimbursement.WellHub - program to promote overall physical wellness.Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories.Catalent offers rewarding opportunities to further your career!
Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world.Catalent is an Equal Opportunity Employer, including disability and veterans.If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to DisabilityAccommodations@catalent.com.
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Location: Chelsea, MassachusettsThis is a full-time salaried position: Monday – Friday, 1st shift.Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives.The Role:Oversight and leadership for the regional Supplier Auditor Team performing audits, generation of audit reports and management of supplier CAPA (Corrective and Preventative Action) to ensure required actions are completed within the required timeframe.Support to Supplier Quality site teams on routine queries and guidance.Manage Supplier notification mailbox to ensure active management and delegation within the supplier team and associated Quality Compliance Assessments are delegated appropriately.Ensure the regional team performing the audits assigned develop a planned audit schedule to maximize audits conducted during one trip (i.e., grouped audits based on location).Development of metrics to provide visibility of audits due, planned audit dates, audits complete, audit reports process timelines, and overdue audits.Development for collation and communication of common finding categories to allow identification of risk areas across Supplier base.Proactive planning to ensure maintenance of audits assigned to the Supplier auditor team, to mitigate overdues.Collaborate, align, and foster cross-functional business relationships within Global functional groups such as Procurement, Sites, and Supply Chain to ensure any risks are identified, mitigated, and communicated.40% travel expectations annually (domestic & international).Other duties as assigned.The Candidate:Bachelor’s Degree, required; Certified auditor or lead auditor credentials, preferred.Five years+ auditing experience and supervisory experience, required.Experience working in an auditing role within the Pharmaceutical/Medical Device industry.Knowledge and understanding of the following principles and guidelines: EU EudraLex Volume 4 GMPs, 21 CFR Parts 111/210/211 (FDA), ISO, and related International Regulations affecting pharmaceutical products and medical devices.Working knowledge of industry-related guidelines such as ICH Q7, GHTF, and IPEC.Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds.Demonstrable leadership experience may be considered in place of external experience.Why You Should Join Catalent:Defined career path and annual performance review and feedback process.Diverse, inclusive culture.152 hours of PTO + 8 paid holidays.Several Employee Resource Groups focusing on D&I.Dynamic, fast-paced work environment.Positive working environment focusing on continually improving processes to remain innovative.Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.Community engagement and green initiatives.Generous 401K match.Medical, dental and vision benefits effective day one of employment.Tuition Reimbursement.WellHub - program to promote overall physical wellness.Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories.Catalent offers rewarding opportunities to further your career!
Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world.Catalent is an Equal Opportunity Employer, including disability and veterans.If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to DisabilityAccommodations@catalent.com.
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