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Avantor

Global provider of high-purity lab materials

Manager – Quality Assurance

Validation, Compliance & Quality SystemsUpdated on Nov 13
Full-timePhillipsburg, NJ, USA$97.5k - $157k

About the Job

Requirements

  • A bachelor's degree in a life science discipline, or an equivalent combination of education and experience, is preferred; formal training and/or advanced courses are also preferred.
  • Five or more years of progressive work experience in Quality Systems, with a demonstrated record of accomplishments as a Quality professional and strong customer orientation in a similar industry.
  • Familiarity with relevant regulations.
  • Strong knowledge of FDA and international Quality System rules and regulations.
  • Strong oral and written communication skills.
  • Strong interpersonal and organizational skills.
  • Ability to take initiative, maintain confidentiality, meet deadlines, and lead people in a team environment.
  • PC skills, including MS Word, Excel, PowerPoint, and Access.

Responsibilities

  • Oversee quality assurance activities related to business operations units as defined by the quality management system, applicable FDA regulations, ISO requirements, current and future certifications and accreditations, and Management.
  • Provide support and guidance to Quality Assurance associates.
  • Advise Management on continuous improvement efforts to align systems and processes with company strategy, customer needs, regulatory standards, guidelines, and quality policy.
  • Provide technical input and advise on and implement process and documentation changes, making decisions based on customer, associate, and company best interests.
  • Manage and provide direction to the Quality Assurance department and associates.
  • Train, motivate, monitor, and evaluate the performance of Quality Assurance associates.
  • Direct the CAPA program for business operations units to ensure it performs effectively and timely.
  • Conduct internal audits for the Quality Management System.
  • Provide technical support for revising or implementing process documentation, including procedures, work instructions, and forms.
  • Support compliance with IPEC and FDA Quality System Regulations and maintain the integration of FDA regulations and other regulatory bodies into the Quality Management System.
  • Provide strategic insight to senior management.
  • Conduct root cause analysis throughout the Manufacturing group.
  • Ensure organizational QMS training is in place and provide training as requested.
  • Lead complaint investigation efforts.
  • Maintain and manage cGMP at defined levels of compliance.
  • Ensure work product and technical reports provide clarity and accuracy.
  • Work directly with customers and suppliers to understand and communicate critical features, requirements, and corrective actions, and to manage supplier approvals and performance.
  • Coordinate objectives with production procedures in cooperation with other managers to maximize product reliability and minimize costs.
  • Ensure inspection activity for product throughout the production cycle.
  • Perform other duties as assigned.

Desired Qualifications

  • Previous supervisory experience.

About the Company

Avantor

Global provider of high-purity lab materials

Avantor supplies high-purity chemicals, lab consumables, equipment, and related services to life sciences and advanced technology customers worldwide. Its products are used across research, development, manufacturing, and quality control to source and apply materials throughout workflows. It differs from competitors by offering a vertically integrated, end-to-end platform that combines materials with extensive lab products and services in one global network. Its goal is to be a trusted partner that enables scientific progress by supporting research and production with high-purity materials and lab solutions.

Company size
10,001+
Company stage
IPO
Headquarters
Bristol, PA
Founded
1904

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