QA Specialist

PUB331625

People in a lab talking

About this job

  • Market: Life Sciences & Health Care
  • Branche: Pharmaceutical
  • Area of expertise: Safety
  • Location: Ontario

What is required?

  • Hours per week: 40
  • Education level: Academic Bachelor
  • Closing date: Friday, January 21, 2022

About this role: QA Specialist

About this role: QA Specialist

We’re hiring a QA Specialist (Process Team) for a Global and innovative pharmaceutical company on Prince Edward Island. The Quality Assurance Representative, Process Team is responsible to oversee the Quality Assurance responsibilities for the associated process team, to ensure the quality and compliance of veterinary biologics with GMP standards, guidelines set forth by regulatory agencies and company policies.

Responsibilities

  • Responsible to work within and enforce the established quality systems based on the ***** Global Quality Standards and GMP guidelines
  • Provide routine and non-routine quality guidance for the process team functional area, 24/7
  • Provide a daily presence in the manufacturing environment, to:
    • Enable contemporaneous batch record review
    • Provide quality guidance and expertise to production personnel
    • Provide trainings to production personnel and process team on quality related topics
  • Responsible for review and approval of batch documentation
  • Responsible for review and approval of process team quality documents, including but not limited to: SOPs, forms, protocols
  • Function as quality partner, providing guidance to persons creating deviations and change controls impacting the process team functional area; responsible to ensure deviations and change controls meet standards
  • Participate as a lead investigator, deviation approver, and change control assessor for the process team.
  • Maintain a general working knowledge of manufacturing processes in the process team functional area
  • Provide routine trending of process team quality metrics and identify negative trends to enable swift action
  • Quality systems responsibilities.
  • Other duties as required.

What you need to bring:

What you need to bring:

Requirements

  • A Bachelor’s degree in science is required.
  • Training in QA, cGMP or an equivalent quality system.
  • Minimum of 3 years in Quality Assurance and or cGMP facility operation experience
  • Excellent time management and problem-solving skills.
  • Thorough technical understanding of quality systems and regulatory requirements.
  • Experience in root cause analysis.
  • Work effectively in a team environment.

Benefits:

Benefits:

Why apply through Brunel? Finding the next step in your career can be a fulltime job in itself. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with on-boarding. We’ll get you going while you get on with the job.

For more information, please email: r.hamdan@brunel.net

Anything Else?

Anything Else?

Brunel has a reputation for working with some of the best in the business. That’s what we continually strive for. Over 45 years, we’ve created a global network of interesting clients and talented individuals working together through a vast array of services.

Start applying immediately

Start applying immediately

Sending an application is quick and easy. Just make sure you have the required documents ready to go.

  • Job references (optional)
  • Motivation Letter (optional)
  • Resume
Apply now

Any questions remaining?

Your consultant, Riham Hamdan is happy to clarify anything about this vacancy. When reaching out, use this number:
PUB331625

Account manager

Riham Hamdan
Brunel Canada - Toronto
r.hamdan@brunel.net

Want new jobs sent to your inbox daily?

Sign up for the Brunel job alert

Look at our privacy statement