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Company

Cyclomedica AustraliaSee more

addressAddressKingsgrove NSW
CategoryLogistics & Warehouse

Job description

At Cyclomedica, our focus is to provide our customers with innovative Molecular Imaging solutions that improve efficiency and effectiveness in patient care and life.  Our business is transforming and growing with the aim to explore new opportunities in order to deliver meaningful solutions. Our people are integral to our mission of developing and building our already strong service and product offering in the global market and we are always seeking innovative and forward-thinking individuals to join us on our journey to drive this ambition. 

We are currently looking for outstanding candidates for the following roles:

Quality Associate

Assist in the management of the medical device/pharmaceutical Quality Management System, ensuring continued compliance with relevant regulations, guidelines and industry standards.

Responsibilities include:

  • Creating, reviewing and approving controlled documentation
  • Assisting in the development and implementation of quality systems, including writing and reviewing procedures and work instructions and conducting training
  • Reviewing and approving change proposals and related documentation for compliance with regulatory and GMP requirements
  • Preparation of Product Quality Reviews
  • Investigation and management of non-conformances, CAPAs, deviations and complaints

The ideal candidate will be a Biotechnology, Pharmacy, Science or Engineering graduate with at least two years’ experience in GMP within Pharmaceuticals, Medical Devices or related fields. 

You will possess:

  • knowledge of standards and governing bodies 
  • a high level of verbal and written communication skills
  • outstanding attention to detail
  • solid numeracy skills
  • advanced problem-solving skills

Senior Validation Specialist

Assist with the development and management of the company’s validation requirements.

Responsibilities include:

  • Creating, editing and managing key validation program documentation 
  • Generating validation plans
  • Executing validations
  • Assisting with the management of GxP projects 

The successful candidate will hold an Engineering or Science degree coupled with a minimum 3 years’ experience in a similar role within the medical device/pharmaceutical industries or similar.

If you would like to join a talented team within a dynamic organisation - apply now.

Refer code: 7288. Cyclomedica Australia - The previous day - 2022-06-28 22:12

Cyclomedica Australia

Kingsgrove NSW

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