AddressIMMEDIATE START
Immediate start is available
SALARY
1 x Full Time Permanent Position
Base Salary + Bonus + Super
Free Car Park for all staff on site
Office perks including office massage & stocked lunch room
Strong company culture
ABOUT PARNELL
Parnell Veterinary Pharmaceuticals is a global animal health company based in Alexandria, Sydney with a focus on innovation and rapid growth. Our unique digital technologies integrate with our innovative products to provide veterinarians, producers and pet parents with unique solutions for their animal health needs. We offer personal and professional development opportunities for those who demonstrate the company's core values of Professionalism, Excellence, and Teamwork, Safety and Sterility and an exciting, fast-paced and entrepreneurial work environment.
THE POSITION
We are seeking a Quality Assurance Associate – Batch Release to join our team! The primary responsibility of the Quality Assurance Associate – Batch Release will be assisting with finished product release, including batch record review, deviation reporting, and trend data analysis. More broadly, this role will contribute to the maintenance and compliance of the Parnell Quality Management Systems applicable to the manufacture of products for all relevant regulatory jurisdictions (US FDA, APVMA). This position reports to the Quality AssuranceBatch Release Team Leader
ABOUT YOU
We will consider candidates that demonstrate the following:
· A leader who enables a culture of execution
· Team player who is both focused on success and has ability to work independently and own their role
· Advanced written and verbal communication skills and a strong aptitude to prioritise your work
· Strong adherence to Continuous Improvement and solutions based thinking
WORK EXPERIENCE & SKILLS
Responsibilities
Assistance with finished product release, including deviation reporting, batch record review and trend data analysis (when required).
Perform delegated release for supply steps.
Provide back-up function for Management of the Quality Document Management System (DMS) including issue of controlled copies, withdrawal of superseded copies, update of controlled document database, filing and archiving of controlled documents, batch document issuance, allocating CDR, Change Request, Deviations and other document numbers.
Participate as internal or external auditor.
Provide backup function for: Complaint Investigations, Material release for ancillary and packaging materials, finished product release including batch record review and trend data analysis, change control review, Annual product quality and quality system reports, and other tasks as required.
Review and approve Non conformance report for destruction of non conforming Raw materials and Finished product
Contribute to the maintenance of cGMP compliance applicable to all relevant regulatory jurisdictions
Essential Skills
B.S. degree in chemistry, Animal Science, Life Science, Agriculture, or related field required.
3 – 5 years pharmaceutical experience or similar discipline
