Site Quality Manager (M/F/D) at Avantor
Reading RG7 4PE, , United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

03 Sep, 25

Salary

0.0

Posted On

04 Jun, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Decision Making, Excel, Outlook, Microsoft Office, Management Skills, Communication Skills

Industry

Pharmaceuticals

Description

SITE QUALITY MANAGER – HICHROM - READING MANUFACTURING SITE

Avantor is seeking a highly motivated and experienced Site Quality Manager to lead Quality Assurance (QA) and Quality Control (QC) operations at our Hichrom, Reading manufacturing site. This role is pivotal in driving the implementation, maintenance, and continuous improvement of the Quality Management System (QMS), while aligning with global quality strategies and standards.
The Reading site specializes in the production of ultra-high performance and high-performance liquid chromatography (UHPLC & HPLC) columns and accessories.

QUALIFICATIONS & SKILLS

  • Degree in a scientific discipline preferred or equivalent relevant experience.
  • Proven experience managing or supervising QA/QC teams or departments.
  • Strong knowledge of cGMP and ISO 9001:2015 standards.
  • Demonstrated leadership and team-building capabilities.
  • Excellent organizational, decision-making, and time management skills.
  • Strong verbal and written communication skills.
  • Proficient in Microsoft Office (Word, Excel, Outlook).
  • Ability to work cross-functionally and influence at all levels of the organization.
Responsibilities
  • Provide strategic and operational leadership for QA and QC functions at the Reading site.
  • Lead and manage the site Quality department, ensuring alignment with global quality policies and ISO 9001 standards.
  • Collaborate with senior management to plan and execute quality initiatives that support site objectives.
  • Develop and maintain local quality procedures, standards, and specifications.
  • Monitor QMS performance and drive continuous improvement initiatives.
  • Manage operational budgets, resource planning, and capital expenditure (CAPEX) proposals.
  • Lead internal audit programs and host external audits, ensuring compliance with customer and regulatory requirements.
  • Oversee the investigation and resolution of non-conformances and customer product complaints.
  • Manage supplier quality, including approvals, audits, quality agreements, and complaints (SCARs).
  • Lead change management processes and risk assessments related to product quality.
  • Supervise and develop QA/QC team members, fostering a culture of excellence and continuous learning.
  • Support cross-site collaboration, mentoring, and training to uphold quality standards across the business.
  • Guide a growing team of QC analytical scientists in testing chromatographic media and HPLC columns.
  • Develop and implement QC performance tests, ensuring consistency in physical and chromatographic properties.
  • Perform additional duties as required to support quality and operational excellence.
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