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Avantor

Global provider of high-purity lab materials

Quality Agreement Specialist

Regulatory & Quality (Life Sciences)Updated on Nov 13
Full-time

About the Job

Requirements

  • A Bachelor of Science or Bachelor of Arts degree in Biology, Biotechnology, Bioengineering, Chemistry, Chemical Engineering, or a related field is required.
  • At least three years of combined experience in technical services, engineering, quality, or sales in a chemical or pharmaceutical environment is required.
  • Knowledge of synthetic pharmaceutical and biopharmaceutical drug development and manufacturing, industry regulations including current Good Manufacturing Practice, the Food and Drug Administration, the International Council for Harmonisation, and the World Health Organization, quality, and validation is required.
  • Experience in quality and process engineering in a chemical or pharmaceutical environment is required.
  • Excellent knowledge of Microsoft Office Suite is required.
  • The ability to manage multiple priorities in a fast-paced environment while keeping customers’ needs in mind is required.
  • Problem-solving skills and leadership skills are required.
  • Initiative, attention to detail, and follow-through are required.
  • The ability to learn industry regulations and Avantor’s proprietary systems is required.
  • Excellent verbal and written skills, presentation skills, and interpersonal communication skills are required.
  • The role requires the ability to travel upwards of 10%.
  • The work environment is an office setting, with occasional visits to the manufacturing facility and R&T building.

Responsibilities

  • Provide technical and quality support to Avantor’s global customer and sales organizations.
  • Partner with internal teams to research, compile, and communicate information related to Avantor’s pharmaceutical and laboratory product offerings.
  • Develop and maintain quality documentation, update product and customer databases, and manage customer Quality Agreements.
  • Manage and negotiate Customer Quality Agreements in collaboration with the Avantor legal team.
  • Respond to customer technical and quality inquiries by telephone and email regarding the Company’s pharmaceutical and laboratory product lines, including excipients, bio reagents, salts, sugars, acids, cGMP-manufactured solutions, and chromatography media, as they relate to quality agreement support.
  • Research technical documents, review product specifications, and use technical monographs, Company R&D experts, in-house databases, and personal technical background to prepare quality agreements and communicate information to customers.
  • Participate in designing and improving quality agreement information collection and archiving processes with departments including Marketing, Sales, and Quality Assurance.
  • Participate in reviews of processes using lean principles to maximize team efficiency in customer responses.
  • Participate as part of a cross-functional team associated with customer intimacy programs; responsibilities may include project management, data collection and review, and hosting and participating in recurring meetings.
  • Perform other duties as assigned, with or without accommodation.

Desired Qualifications

  • Experience working with computer applications such as databases, with an aptitude to further develop technical skills.
  • Hands-on experience in a laboratory or manufacturing environment.
  • Project management experience.
  • Experience in at least one of the following areas is highly desired.

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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