Quality Manager – TGA Licensed Manufacturer
Australia, Victoria
Full Time
01/05/2019
  • Great opportunity for a Senior Quality Manager to progress their career
  • Permanent, full-time role with excellent salary package for the right person
  • Modern facilities with onsite parking

 

COMPANY

Our client is the Australian manufacturing arm of a multinational pharmaceutical company. With a presence in more than 30 countries around the world, they develop, manufacture, market, sell and distribute high quality pharmaceutical and nutraceutical products.

A publicly listed company, every aspect of the business is focused on helping millions of people have access to safe, effective, world class quality medical products.

 

THE ROLE

Reporting to the General Manager, the Quality Manager is responsible for the maintenance of the company’s Quality Management System in accordance with the requirements of PIC/S GMP.

Working with the Plant Manager and with a number of direct reports, the successful candidate will ensure the company maintains a satisfactory level of GMP compliance, translating to successful GMP audits by the TGA.

The Quality Manager will maintain and review systems that are in place to ensure that products produced by the company meet customer specifications and relevant regulatory requirements, importantly, TGA licensing for the manufacture of complementary and OTC medicines.

 

SELECTION CRITERIA

The successful candidate will be an experienced Quality Manager of a TGA licensed facility, ideally of complementary medicines You will have leadership qualities, be customer focused, a decision maker and able to complete tasks and projects on time.

To be successful in your application, you will need to meet the following criteria:

  • Science degree in chemistry, biology or a related discipline
  • Experience and knowledge of PIC/S GMP for Medicinal Products
  • Several years’ experience with Complementary Medicines mainly in the areas of manufacturing
  • Understanding of GMP requirements, processes and quality aspects of company operations
  • Understanding of regulatory requirements for therapeutic products, including a working knowledge of Quality Risk Management and Compliance
  • Excellent interpersonal, leadership, time management and organisational skills
  • High attention to detail
  • Troubleshooting and investigation skills
  • Hazard and·risk identification/assessment
  • Excellent verbal and written communication skills
  • Positive and proactive attitude
  • Ability to prioritise and multi-task
  • Excellent administrative skills
  • The ability to nurture relationships internally and externally
  • Self-motivated with the ability to work effectively both independently and within a team
  • You must have a flexible “can do” attitude, excellent work ethic and initiative

 

APPLICATION

For a confidential discussion about this exciting opportunity please contact Helen Patronis during office hours on 03 9516 0100. After hours please call 0438 620 434.

To apply for this role, please click the ‘Apply Now‘ button then send your current resume and a covering letter addressing the above selection criteria to CS Executive Group.

 

THANK YOU

CS Executive Group would like to thank you in advance for taking the time to apply for this role. Unfortunately, due to the large volume of correspondence we receive on a daily basis, we genuinely cannot respond to each application – only individuals being considered for shortlisting as candidates are contacted.

However, if on this occasion you’re unsuccessful, please note your details will be added to our Talent Pool database. This means is that in future you may be contacted by one of our team of recruiters for other suitable roles.