Production Operator – GMP Pharmaceutical Manufacturing at Care Essentials
victoria, Victoria, Australia -
Full Time


Start Date

Immediate

Expiry Date

10 Jan, 27

Salary

65000.0

Posted On

12 Oct, 26

Experience

19 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Healthcare & Life Sciences

Description

Regulatory Affairs / Quality Associate

Complementary & Listed medicines

CMG. Warriewood, Sydney NSW

The Role:

This is a newly created role reporting to the Head of Quality; you will be responsible for Regulatory Affairs and Quality Assurance activities for a fast-growing company in the Complementary Medicines industry.

Your experience working as part of a team within a fast paced and deadline driven environment will see you excel in this role. 

You will need highly developed attention to detail and research skills to maintain regulatory compliance of all new products. 

 Your key responsibilities will include:

  • Developing Evidence Packages and Tables for all new products
  • Managing Bulk Specifications
  • Compiling Shelf-Life Justifications
  • Developing and coordinating new product labels to meet all regulatory requirements such as TGO92 & 116
  • Reviewing and submitting Listed Medicines on the ARTG
  • Maintaining regulatory compliance of all products
  • Managing Change Control for new products
  • Managing all Product Stability activities


How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

Regulatory Affairs / Quality Associate

Complementary & Listed medicines

CMG. Warriewood, Sydney NSW

The Role:

This is a newly created role reporting to the Head of Quality; you will be responsible for Regulatory Affairs and Quality Assurance activities for a fast-growing company in the Complementary Medicines industry.

Your experience working as part of a team within a fast paced and deadline driven environment will see you excel in this role. 

You will need highly developed attention to detail and research skills to maintain regulatory compliance of all new products. 

 Your key responsibilities will include:

  • Developing Evidence Packages and Tables for all new products
  • Managing Bulk Specifications
  • Compiling Shelf-Life Justifications
  • Developing and coordinating new product labels to meet all regulatory requirements such as TGO92 & 116
  • Reviewing and submitting Listed Medicines on the ARTG
  • Maintaining regulatory compliance of all products
  • Managing Change Control for new products
  • Managing all Product Stability activities


Loading...