QMS Leader

Momentive; Abingdon; On-site; GBP 43,000 - 63,000; Full time

Job summary

Momentive seeks a QMS Leader to own and drive the Site Quality Management System, ensuring GMP compliance and ISO 9001:2015, EFfCI, FSSC 22000 alignment. The role oversees audits, CAPA, training, and QMS documentation, with a focus on continuous improvement and digital solution adoption.

On-site five days a week, this leader partners with global stakeholders to maintain certifications and promote a culture of quality and operational excellence across the site in Abingdon, UK.

Qualifications

• Bachelor’s degree in engineering, chemistry, quality, business or related field.
• 5+ years experience in quality, manufacturing, or related technical role.
• Experience supporting or managing GMP and ISO 9001 certified quality systems.
• Internal or lead auditor certification or equivalent audit experience.
• Experience maintaining quality management systems.
• Experience supporting ISO‑certified environments.
• Proficient in Microsoft Office Suite.

Responsibilities

• Site subject matter expert in GMP and regulatory compliance, ensuring adherence to applicable regulations and quality standards.
• Updates and maintains the site QMS in alignment with global quality standards, policies, and procedures.
• Responsible for creating, administering, and maintaining site training for GMP, Kosher/Halal, food safety, and other assigned quality system requirements.
• Reviews QMS updates and verifies compliance with ISO, GMP, FSSC 22000, Kosher/Halal, and other applicable requirements.
• Responsible for maintaining ISO 9001, FSSC 22000, EFfCI, GMP, and other assigned certifications.
• Leads quarterly Quality Management Reviews in accordance with global standard, including reporting improvement opportunities, quality metrics, audit action status, and closure progress to site and global leadership.
• Leads external audit programs, regulatory, customers and certification audits in coordination with the Site Quality Leader and relevant functions.
• Accountable for audit readiness, CAPA oversight, root cause follow-up, and verification that assigned audit actions are completed effectively.
• Leads and collaborates with the Food Safety Team to maintain FSSC 22000 certification.
• Reviews and confirms that deviation investigations meet site requirements before closure.
• Reviews GMP batch records and performs final product release activities assigned to the QMS Manager role.
• Drives standardization of site processes and leads quality improvement projects that strengthen compliance, efficiency, and consistency.
• Maintains current knowledge of regulatory requirements, industry standards, and customer expectations, and supports implementation of best practices and compliance strategies.
• Collaborates with the Site Quality Leader to determine adoption of new standards and to align GMP‑specific customer complaint responses.
• Support implementation of new digital solutions.

Skills

GMP knowledge

ISO 9001

Auditing

Quality management

Documentation

MS Office

Education

Bachelor’s degree in engineering, chemistry, quality, business or related field

Tools

Microsoft Office Suite

Job description

Job Title: QMS Leader

Summary: The Site Quality Management System (QMS) Leader is responsible for leading, maintaining, and continuously improving the site's Quality Management System to ensure compliance with GMP requirements, ISO 9001:2015, EFfCI, FSSC 22000, and other applicable quality, regulatory, and certification requirements. This role serves as the site owner of the QMS and ensures alignment with global quality standards, policies, and procedures. The Site QMS Leader drives the effectiveness of quality processes by supporting audit readiness, management review activities, training, documentation control, performance monitoring, and continuous improvement initiatives. Working closely with site, regional, and global stakeholders, the role promotes a culture of quality, customer focus, operational excellence, and compliance while supporting the implementation of new systems, digital solutions, and future quality framework enhancements. Please note that this role requires on-site presence five days per week, Monday through Friday.

Responsibilities

• Site subject matter expert in Good Manufacturing Practice (GMP) and regulatory compliance, ensuring adherence to applicable regulations and quality standards.


• Updates and maintains the site QMS in alignment with global quality standards, policies, and procedures.


• Responsible for creating, administering, and maintaining site training for GMP, Kosher/Halal, food safety, and other assigned quality system requirements.


• Reviews QMS updates and verifies compliance with ISO, GMP, FSSC 22000, Kosher/Halal, and other applicable requirements.


• Responsible for maintaining ISO 9001, FSSC 22000, EFfCI, GMP, and other assigned certifications.


• Leads quarterly Quality Management Reviews in accordance with global standard, including reporting improvement opportunities, quality metrics, audit action status, and closure progress to site and global leadership.


• Leads external audit programs, regulatory, customers and certification audits in coordination with the Site Quality Leader and relevant functions.


• Accountable for audit readiness, CAPA oversight, root cause follow-up, and verification that assigned audit actions are completed effectively.


• Leads and collaborates with the Food Safety Team to maintain FSSC 22000 certification.


• Reviews and confirms that deviation investigations meet site requirements before closure.


• Reviews GMP batch records and performs final product release activities assigned to the QMS Manager role.


• Drives standardization of site processes and leads quality improvement projects that strengthen compliance, efficiency, and consistency.


• Maintains current knowledge of regulatory requirements, industry standards, and customer expectations, and supports implementation of best practices and compliance strategies.


• Collaborates with the Site Quality Leader to determine adoption of new standards and to align GMP‑specific customer complaint responses.


• Support implementation of new digital solutions.

Qualifications

• Bachelor’s degree in engineering, chemistry, quality, business or related field.


• 5+ years experience quality, manufacturing, or related technical role.


• Experience supporting or managing GMP and ISO 9001 certified quality systems.


• Internal or lead auditor certification or equivalent audit experience.


• Experience maintaining quality management systems.


• Experience supporting ISO‑certified environments.


• Proficient in Microsoft Office Suite.

Preferred Qualifications

• Quality Improvement tools experience, (Lean Six Sigma, Root Cause Corrective Action methodologies)


• Good Excel experience and skills for data analysis.


• SharePoint administration experience.


• Experience developing and delivering training programs.

What We Offer

Base Pay Range: £43,300 - £63,470 Compensation for this role will be competitive and aligned with market practices in the respective location. Actual pay is determined based on several factors, including but not limited to experience, education, skills, and geographic location. Where applicable country‑specific salary ranges will be communicated during the hiring process based on local pay transparency regulations.

This role may also be eligible for variable incentive compensation. Any such incentives are governed by the terms of the Company’s applicable plans and are based on company performance and/or individual performance.

At Momentive, we value your well‑being and offer competitive total rewards and development programs. Our inclusive culture fosters a strong sense of belonging and provides diverse career opportunities to help you unleash your full potential. Together, through innovative problem‑solving and collaboration, we strive to create sustainable solutions that make a meaningful impact. Join our Momentive team to open a bright future.

About Us

Momentive is a premier global advanced materials company with a cutting‑edge focus on silicones and specialty products. We deliver solutions designed to help propel our customer’s products forward—products that have a profound impact on all aspects of life, around the clock and from living rooms to outer space. With every innovation, Momentive creates a more sustainable future. Our vast product portfolio is made up of advanced silicones and specialty solutions that play an essential role in driving performance across a multitude of industries, including agriculture, automotive, aerospace, electronics, energy, healthcare, personal care, consumer products, building and construction, and more.

Momentive believes a diverse workforce empowers our people, strengthens our business, and contributes to a sustainable world. We are proud to be an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any characteristic protected by law.

To be considered for this position candidates are required to submit an application for employment and be of legal working age as defined by local law. An offer may be conditioned upon the successful completion of pre‑employment conditions, as applicable, and subject to applicable laws and regulations.

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