Job Description

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Quality Manager

Advertiser: EQ ConsultantsMore jobs from this company

Job Information

Job Listing Date
8 Mar 2019
Location
Canterbury, Christchurch
Work Type
Full Time
Classification
Science & Technology, Quality Assurance & Control
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Quality Manager

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  • Maintain and build on this Quality based environment
  • Strategic leadership role
  • Be part of a high performing team

Wonderful opportunity to be part of a company where quality is pivotal

Canterbury Scientific is a leading global OEM supplier of high quality, stable IVD Controls for diabetes and hemoglobinopathy assays in the global medical diagnostic sector.

The Company is committed to the development of innovative and effective non-sterile invitro diagnostic products. As an OEM producer, the company is focused on the design, development and manufacture of products to our customers' specifications to meet or exceed expectations and requirements.

The role

Canterbury Scientific are looking for a Quality Manager to join their high performing team. The Company operates according to a Quality Management System, promoted and supported actively by the Management Team and embraced by the entire company. The focus is on continuous improvements, communications, and measurable quality objectives.

The essence of this Quality Manager role relies on driving quality objectives to ensure that the required high standards are achieved. You will have strategic input from a QMS perspective and will be the point of communication on quality, both internally and externally.

Driving quality improvement projects and taking the lead on regulatory affairs and audits are also pivotal. Meeting customer, legal and regulatory requirements in the delivery of products sits at the core of our policy and periodic Management Review meetings ensure appropriate monitoring and updates to quality policy and systems.

You will also have the ability to effectively coach and mentor your team to maintain this high level of quality output.

Culture and benefits

Canterbury Scientific is a dynamic, team-focussed organisation where quality and continuous improvement is key. You will be part of the Senior Management team and will have major input into achieving the company's high standards. This is an innovative and successful organisation that values people for their contribution. Your skills and abilities will be compensated with a very competitive salary package.

Who are we looking for?

To be successful, you will have:

  • A Bachelor's Degree in Science or equivalent and previous experience in a Production/Pharmaceutical/Biotech/Medical Device industry.
  • Extensive experience in Quality Management Systems and international accreditation/regulations including ISO 13485, FDA QSR and cGMP.
  • Solid internal and external auditing experience and a strong Quality Management/Document Control background.
  • An analytical, structured and logical approach to data management and problem solving with the ability to effectively prioritise within an active, fast moving bioprocess manufacturing environment.
  • A passion for promoting and enhancing a company quality culture, a positive attitude and a passion for process improvement.

If this sounds like you, please apply with your CV and Cover Letter outlining what you have to offer. If you have questions, please call Jenny Barr, EQ Consultants on 021 223 5118.
logo

Wonderful opportunity to be part of a company where quality is pivotal

Canterbury Scientific is a leading global OEM supplier of high quality, stable IVD Controls for diabetes and hemoglobinopathy assays in the global medical diagnostic sector.

The Company is committed to the development of innovative and effective non-sterile invitro diagnostic products. As an OEM producer, the company is focused on the design, development and manufacture of products to our customers' specifications to meet or exceed expectations and requirements.

The role

Canterbury Scientific are looking for a Quality Manager to join their high performing team. The Company operates according to a Quality Management System, promoted and supported actively by the Management Team and embraced by the entire company. The focus is on continuous improvements, communications, and measurable quality objectives.

The essence of this Quality Manager role relies on driving quality objectives to ensure that the required high standards are achieved. You will have strategic input from a QMS perspective and will be the point of communication on quality, both internally and externally.

Driving quality improvement projects and taking the lead on regulatory affairs and audits are also pivotal. Meeting customer, legal and regulatory requirements in the delivery of products sits at the core of our policy and periodic Management Review meetings ensure appropriate monitoring and updates to quality policy and systems.

You will also have the ability to effectively coach and mentor your team to maintain this high level of quality output.

Culture and benefits

Canterbury Scientific is a dynamic, team-focussed organisation where quality and continuous improvement is key. You will be part of the Senior Management team and will have major input into achieving the company's high standards. This is an innovative and successful organisation that values people for their contribution. Your skills and abilities will be compensated with a very competitive salary package.

Who are we looking for?

To be successful, you will have:

  • A Bachelor's Degree in Science or equivalent and previous experience in a Production/Pharmaceutical/Biotech/Medical Device industry.
  • Extensive experience in Quality Management Systems and international accreditation/regulations including ISO 13485, FDA QSR and cGMP.
  • Solid internal and external auditing experience and a strong Quality Management/Document Control background.
  • An analytical, structured and logical approach to data management and problem solving with the ability to effectively prioritise within an active, fast moving bioprocess manufacturing environment.
  • A passion for promoting and enhancing a company quality culture, a positive attitude and a passion for process improvement.

The application form will include these questions:
  • Which of the following statements best describes your right to work in New Zealand?
  • How many years' experience do you have in a quality assurance (QA) role?
  • What's your expected annual base salary?
  • Have you worked in a role which requires a sound understanding of Good Manufacturing Practices (GMP)?
  • Have you completed a qualification in science?

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