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招聘
| 公司: |
GMP Pharmaceuticals Limited |
| 工作地点: |
奥克兰东区 |
| 职位: |
QA Officer |
| 薪资: |
高于新西兰法定最低工资 |
| 工作性质: |
全职 |
| 工作时间: |
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| 联系电话: |
请登录后查看 |
| 微信: |
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| 电子邮件: |
nicoleh@gmp.net.nz |
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Quality Assurance Officer Are you passionate about food safety, product quality,and ensuring consumers receive products they can trust?We are looking for a motivated and detail-orientedQuality Assurance Officer to join our Auckland-based food supplementmanufacturing team.This role is suited to someone with 1-2 years’ experiencein Quality Assurance within a GMP manufacturing environment who is ready totake on core QA responsibilities while continuing to develop their technicalcapability.
About the RoleAs a QA Officer, you will play a key role in supportingand maintaining our Quality Management System and ensuring Good ManufacturingPractice (GMP) compliance across manufacturing operations.Your primary focus will be document review, lineclearances, and document verification, while also being exposed to broader QAactivities as part of ongoing development (including more advanced QA tasks ascapability grows).
What You'll Be Doing
Quality Systems, Documentation &Validation Support
Conduct document review and verification to ensure GMP compliance.
Perform controlled document checks, SOP updates, and training record reviews.
Support internal audit readiness and quality system maintenance.
Assist with validation activities, including IQ/OQ/PQ documentation, verification records, and supporting execution activities under supervision.
Ensure all documentation is accurate, complete, and compliant.
Production Quality Support
Perform line clearance checks prior to production commencement.
Conduct in-process quality inspections.
Support finished product verification and retention sample management.
Work closely with Production to ensure adherence to GMP standards.
Environmental Monitoring & Sampling
Carry out environmental monitoring activities such as swabbing.
Assist with sampling of water, raw materials, and finished products.
Coordinate submission of samples to external laboratories.
Continuous Improvement & SupportActivities
Support investigation of deviations, non-conformances, and customer complaints.
Assist in CAPA activities and continuous improvement initiatives.
Gain exposure to more advanced QA activities (e.g. validation support, audit participation, and system improvement projects) as part of role development.
What We're Looking ForWe are looking for someone who can confidently takeownership of core QA tasks while continuing to grow within a supportive teamenvironment.Ideally, you will have:
2–3 years’ experience in Quality Assurance, QC, or GMP manufacturing environments.
A Bachelor’s degree in Food Science, Food Technology, Microbiology, Chemistry, Quality Management, or a related field.
Strong understanding of GMP and HACCP principles.
Experience with document control, audits, or quality systems.
Good attention to detail and strong organisational skills.
Strong written and verbal communication skills.
Good computer skills, particularly Microsoft Word and Excel.
A proactive mindset and ability to work in a fast-paced manufacturing environment.
Why Join Us?
Strong opportunity to develop your QA career in a GMP manufacturing environment.
Exposure to both core QA operations and more advanced QA activities.
Supportive team with structured training and mentoring.
Hands-on role involving real production and quality system responsibilities.
Ongoing learning and development opportunities.
How to ApplyFor a confidential discussion about this role, pleasecontact nicoleh@gmp.net.nz.We thank all applicants for their interest; however, onlyshortlisted candidates will be contacted.
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发表于 2026-7-2 16:27
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