Buscojobs | Quality Associate

vor 2 Wochen

Central Coast, Österreich Tideri Jobbörse Vollzeit

Pharmaceutical Compounding Adelaide Full Time Slade Health
QUALITY ASSOCIATE - RELEASING – SLADE HEALTH, WOODVILLE ADELAIDE - SA
Dynamic, Collaborative and Supportive Work Environment Progressive and Far-Reaching Career Opportunities - Exciting Expansion into Adelaide, SA (Brand New State of the Art Facility) Permanent Full-Time Position (2 PM – 10 PM, Monday - Friday plus some overtime and occasional weekend and public holiday shifts – Woodville (Adelaide), SA Location) About Us :
Slade Health is a provider of sterile compounding services from its TGA licenced manufacturing facilities based in South Australia, Queensland, New South Wales, Victoria and New Zealand.
As a well-established and respected industry name, Slade has been producing aseptically compounded pharmaceutical products including chemotherapy, analgesic, nutrition and antibiotic drugs for use by patients in hospitals for over 50 years.

Our focus on quality, service and productivity has enabled opportunities for Slade to expand significantly.
With growth comes career opportunities

The Opportunity
As an integral member of the Quality team, you will report to the Quality Pharmacist Supervisor and work closely with Operations to ensure that the compounding centre operates in compliance with regulatory and GMP requirements and that the products compounded are released to the highest quality.
This is a fantastic opportunity to expand your current skill set and support the Quality processes we have in place.
This is a permanent full-time position working a minimum of 76 hours a fortnight, Monday to Friday with some overtime and occasional weekend and public holiday shifts to support operations.

Key Responsibilities
Releasing of compounded batches.
Participate in investigation and root cause analysis of non-conformances, supplier and customer complaints.
Participating in risk assessment, change control, validation, internal audits, document reviews, CAPA and recall activities.
Liaising with relevant stakeholders to complete action items related to the above.
Conducting and coordinating training on Quality procedures and requirements.
Support the team with Environmental Monitoring activities and perform quality assessments of quarantined incoming goods as required.
Drive ongoing continuous improvement in Quality performance across the site and the business.
About You
Experience in a GMP compliant pharmaceutical manufacturing environment.
Experienced in a sterile compounding environment.
Experience with regulators of pharmaceutical manufacture (e.g., TGA) desired.
Experience in continuous quality improvement.
Competency in common IT software (MS Word, MS Excel, MS Visio).
Competent in time and task management.
Tertiary qualification in a Science or relevant discipline.
You will know that a successful person in this role is someone who can thrive in a fast-paced environment where quality is paramount, whilst displaying a proactive approach, exceptional communication skills, strong leadership and role modelling capabilities.

Excited to join us?

Our team makes us who we are, they shape our impact and drive our success.
So Apply Now and make it happen with Icon.

Icon Group celebrates diversity and is committed to creating an inclusive workplace for all employees.
We encourage applications from all diverse backgrounds.

Icon is committed to managing the risk of transmission of specified vaccine preventable diseases (VPDs).
Certain roles may require the successful candidate to show evidence that they have been vaccinated against or are not susceptible to specified VPDs.

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