Hello forum,
For the submission of my SMC Expression of Interest (EOI), I need to be sure that my partner is currently working in skilled employment. We are finding it very difficult, based on her position description, to know if she works in skilled employment or not. This is crucial as this determines if we have sufficient points or not.
We really need help with finding out which ANZSCO description meets her job description.
Your help is very much appreciated! Please find her position description below:
Code:
Position: Quality Control Analyst
Department: Quality Control
Responsible to: QC Supervisor
Direct Reports: None
Mission Statement:
COMPANY will use its tissue regeneration technology to improve the health and welfare of patients, simplify operating
procedures for surgeons and reduce healthcare costs. By doing this we will build a company which provides benefits
for our investors, staff, community and customers.
Purpose of the position
1. Maintain compliance with Good Laboratory Practice (GLP) for the testing and result reporting of medicinal
products.
2. To prioritise and test raw materials, in-process materials and finished products in a GLP environment to
schedule, in order to support business requirements.
Key Accountabilities and Expected Outcomes
1. QC Lab and GLP Compliance Support Quality
Control activities to ensure appropriate requirements and standards are met.
- Ensure that lab cleanliness and safety standards and maintained.
- Ensuring QC equipment is calibrated and maintained in accordance with company procedures.
- Writing and reviewing standard operating procedures (SOPs), and performing training activities as required.
- Monitor testing procedures to ensure that all tests are performed in accordance with applicable policies or guidelines, and standards.
- Identify quality problems and recommend solutions.
- Participate in internal assessments and audits as required.
- Monitoring QC lab consumable inventory and stock levels and raising POs for approval.
2. Quality Control Testing
Test samples submitted to the lab according to scheduling and business needs to approved test methods.
- Receipt, storage and tracking of samples submitted to the QC lab for testing.
- Perform QC testing activities in accordance with company procedures.
- Creating and executing method development and method validation test protocols for in-process materials and finished products.
- Interpret test results, compare them to established specifications and control limits, and make recommendations on appropriateness of data for release.
- Follow and maintain compliance with all policies, procedures, work instructions and specifications; in non-controlled and possibly controlled (clean room) environments.
- Initiate and participate in laboratory investigations for out-of specification results and recommend corrective actions.
- Co-ordinate testing with contract laboratories and review data from contract laboratories to ensure accuracy and regulatory compliance.
- Supply quality control data as necessary for regulatory submissions.
3. Environmental Monitoring
Ensure environmental and water system monitoring is performed in compliance with established procedures, and issues are escalated appropriately.
- Perform routine monthly environmental monitoring activities for the manufacturing facility.
- Perform routine water system testing and sampling (as required).
- Ensure any out-of-specification results are documented and investigated in a timely manner, and issues are notified to the Operational Quality and Manufacturing Departments.
- Enter results into metric files and routinely monitor trends and issues.
4. Documentation and Communication
Ensure documentation and records are timely and up to date.
- Navigate COMPANY systems; performing data entry for QC metrics and preparing required quality system documentation.
- Prepare QC test reports, including analytical reports for in-process materials and finished products; and microbial identification reports.
- Work collaboratively with relevant stakeholders and represent the Quality Control Lab in cross functional team meetings as assigned.
- Manage multiple assignments; practicing time management and meeting deadlines.
- Participate in root cause evaluation and continuous improvement efforts.
- Identify and escalate safety, quality and compliance issues to supervision.
- Demonstrate effective written and verbal communications skills.
- Work overtime as required and perform other duties as assigned
5. Continuous Improvement
Participates in Lean initiatives to continually improve the work environment for team and/or the wider company.
- Participates in lean activities and 5S activities for the QC lab.
- Strives to generate ideas for improvement in the lab quality system and documentation.
- Evaluate test methods and procedures, and QC lab operations and work flow to identify improvements that can be made
Key Relationships
Internal Operational Quality Team, Manufacturing, Development
External QC-related service providers.