Quality Associate
6 hours ago
JOB DETAILS
The QA will be supporting compliance of Quality Systems and implementing continuous improvement strategies to support the business deliverables of high-quality products.
RESPONSIBILITIES
- Master Quality Schedule (MQS) - Support completion of all scheduled activities performed in their designated time frames.
- Support the completion of all activities within the timelines defined in the MQS
- Support with monthly trending and reporting to provide an oversight of performance and priorities
- Testing and Verification - Ensure products are within specification in accordance with company and regulatory requirements
- Raw material, packaging material and finished goods comply with the specifications.
- Out of specification and Deviated test results are raised and resolved as per regulatory requirements and procedures.
Change Control Management - Assist in managing changes to product, processes or parameters to ensure compliance with TGA requirements
All change requests are documented in change control register;
- Assist in the coordination of change control request and work with stakeholders to implement and monitor changes to processes.
All relevant documents updated/generated are issued, trained and filed in prescribed timeline;
Audits and Compliance - Assist with completing compliance activities are and ensure appropriate actions are implemented.
Support with the completion of all audits (Internal, GMP etc.) as per MQS.
- Gaps are identified and raised via corrective action reports (e.g. CAPA, Deviations etc.) as per the site procedures.
- CAPA's and Deviation are promptly raised and/or reported to key stakeholders as per the site procedures.
- Support of Quality system trending to assist with improvement in processes and risk mitigation.
Ensure that Good Manufacturing Practices is complied with at all times
Authorisation - Assist with the completion and compliance of all quality system documents as per regulatory requirements.
- Ensure all stakeholders comply with Good Documentation Practices (GDP) as per the site QMS and regulatory requirements.
- Manage the document control activities
- Support with Training Matrix and Supplier Qualification Program
- Review and verify that manufacturing documents have been correctly completed as per GDP and the site requirements.
Review and verify that all quality documents (e.g. CAPA, Deviation, Change Control etc.) have been correctly completed as per GDP and the site requirements.
Qualifications and experience required
- 1 - 3 years experience in a Quality role
- Strong working knowledge of TGA and FSANZ requirements highly desirable
Degree in food science or related is desirable (science)
Other relevant information
- Ability to problem solve and influence others
- Meticulous attention to detail and able to produce high quality documentation
- Effective time management and self-discipline
- Excellent communication skills, both written and verbal
- Build strong relationships with key stakeholders, suppliers and customers
Key Requirements (Skills & Experience)
- 1 - 3 years experience in a Quality role
- Strong working knowledge of TGA (Therapeutic Goods Administration) and FSANZ (Food Standard Australia New Zealand) requirements are highly desirable
- Degree in food science or related is desirable (science)
Job Type: Full-time
Pay: Php40, Php60,000.00 per month
Language:
- English (Preferred)
Work Location: In person
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