BioSpace
Sr Manager Global Procurement
– BioSpace
Overview We are looking to fill a
Sr Manager Global Procurement
position. In this role you will oversee a team that supports and maintains all cGMP compliance aspects of procurement operations. Key functions include managing the Approved Supplier List (ASL), deviation investigations, CAPAs, supplier audit closures, regulatory inspection support, SOP writing, change controls, and development of a Supplier Corrective Action Report (SCAR) management process.
Responsibilities
Ensure the team operates as a global cohesive unit, ensuring compliance at all IOPS sites.
Track progress on strategic sourcing & procurement quality system deliverables, including deviation investigations, CAPAs, and change controls.
Interface regularly with Quality Assurance and other functional areas to remove obstacles, resolve conflicts, and facilitate critical decisions related to quality system deliverables.
Monitor, report, and respond to KPIs for compliance functions (e.g., right‑first‑time for deviation investigations).
Perform deviation investigations and coordinate CAPA implementation for high‑risk events.
Proactively manage and maintain all procurement cGMP procedures, documentation, and training related to SOPs and Work Instructions.
Continuously assess strategic sourcing & procurement systems for adherence to cGMPs and industry best practices, implementing improvements as needed.
Represent the strategic sourcing & procurement department on regulatory inspections and coordinate responses to inspection observations.
Support startup/integration of procurement compliance functions at other IOPS sites, including travel as required.
Qualifications & Experience
Oversee and maintain the Approved Supplier List (ASL) and associated periodic supplier review.
Drive successful audit closures by proactively resolving issues and communicating with suppliers.
Coordinate with cross‑functional compliance resources to support procurement and QA auditing needs, ensuring closure of internal/regulatory audit findings.
Work closely with Legal, QA, and suppliers to execute and manage Master Services Agreements, Quality Agreements, etc.
Respond to compliance‑related data requests from Regulatory, QA, Audit staff, and stakeholders.
Must hold a bachelor’s degree and meet the following experience requirements:
8+ years of relevant experience for a Sr Manager level, including at least 5 years in a cGMP environment or an equivalent combination of education and experience.
Compensation Salary Range (annually): $126,300.00 – $206,100.00
Seniority Level Mid‑Senior level
Employment Type Full‑time
Job Function & Industries
Purchasing and Supply Chain
Internet News
Equal Opportunity Employer Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief, sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company’s business.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, and educational qualifications.
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– BioSpace
Overview We are looking to fill a
Sr Manager Global Procurement
position. In this role you will oversee a team that supports and maintains all cGMP compliance aspects of procurement operations. Key functions include managing the Approved Supplier List (ASL), deviation investigations, CAPAs, supplier audit closures, regulatory inspection support, SOP writing, change controls, and development of a Supplier Corrective Action Report (SCAR) management process.
Responsibilities
Ensure the team operates as a global cohesive unit, ensuring compliance at all IOPS sites.
Track progress on strategic sourcing & procurement quality system deliverables, including deviation investigations, CAPAs, and change controls.
Interface regularly with Quality Assurance and other functional areas to remove obstacles, resolve conflicts, and facilitate critical decisions related to quality system deliverables.
Monitor, report, and respond to KPIs for compliance functions (e.g., right‑first‑time for deviation investigations).
Perform deviation investigations and coordinate CAPA implementation for high‑risk events.
Proactively manage and maintain all procurement cGMP procedures, documentation, and training related to SOPs and Work Instructions.
Continuously assess strategic sourcing & procurement systems for adherence to cGMPs and industry best practices, implementing improvements as needed.
Represent the strategic sourcing & procurement department on regulatory inspections and coordinate responses to inspection observations.
Support startup/integration of procurement compliance functions at other IOPS sites, including travel as required.
Qualifications & Experience
Oversee and maintain the Approved Supplier List (ASL) and associated periodic supplier review.
Drive successful audit closures by proactively resolving issues and communicating with suppliers.
Coordinate with cross‑functional compliance resources to support procurement and QA auditing needs, ensuring closure of internal/regulatory audit findings.
Work closely with Legal, QA, and suppliers to execute and manage Master Services Agreements, Quality Agreements, etc.
Respond to compliance‑related data requests from Regulatory, QA, Audit staff, and stakeholders.
Must hold a bachelor’s degree and meet the following experience requirements:
8+ years of relevant experience for a Sr Manager level, including at least 5 years in a cGMP environment or an equivalent combination of education and experience.
Compensation Salary Range (annually): $126,300.00 – $206,100.00
Seniority Level Mid‑Senior level
Employment Type Full‑time
Job Function & Industries
Purchasing and Supply Chain
Internet News
Equal Opportunity Employer Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief, sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company’s business.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, and educational qualifications.
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