QC Lab Analyst – GMP Quality Control

ThermoFisher Scientific; Auckland; On-site; NZD 55,000 - 75,000; Full time

Benefits offered by this job

Health & Wellbeing

Flexibility

Extra Leave

Charitable Giving & Volunteering

Learning & Development

Job summary

Thermo Fisher Scientific Penrose facility in Auckland is seeking a quality control professional to support testing and release of our products. You will work in a GMP-compliant lab, performing QC analyses and ensuring data accuracy to support the manufacture of sera, cell culture media and related products.

The role involves collaborating with cross-functional teams, following ISO9001 and cGMP standards, and maintaining strict safety practices with PPE.

Qualifications

• Tertiary Science qualification; bachelor preferred.
• 1–3 years experience in manufacturing or laboratory setting.
• Knowledge of ISO9001 and cGMP regulatory standards.
• Computer literacy: word processing, spreadsheets, databases.

Responsibilities

• Perform QC analyses and record observations with accuracy.
• Record, analyze and trend QC data in forms (paper/electronic).
• Order and maintain stock and storage conditions for samples/chemicals.
• Support QC documentation including SOPs and forms.
• Communicate effectively across departments and with internal customers.
• Conduct investigations, root cause analysis and CAPA.
• Participate in training and PPI activities.
• Perform microbiological and biochemical tests or related lab activities.
• Contribute to deviation or OOS investigations in Quality Control.
• Contribute to quality and process improvement initiatives.
• Observe safety rules and PPE usage; report accidents and near misses.
• Work core hours 8.00 – 4.30pm Mon-Fri; start earlier preferred.

Skills

Attention to detail

Discipline

Multitasking

Relationship building

Education

Bachelor's degree in Science

Job description

Thermo Fisher Scientific Penrose facility in Auckland is seeking a quality control professional to support testing and release of our products. You will work in a GMP-compliant lab, performing QC analyses and ensuring data accuracy to support the manufacture of sera, cell culture media and related products.

The role involves collaborating with cross-functional teams, following ISO9001 and cGMP standards, and maintaining strict safety practices with PPE.