Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Fluctuating Temps hot/cold, Laboratory Setting, Loud Noises (Equipment/Machinery), Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials, Working at heights Job Description As part of the Thermo Fisher Scientific team, youll discover meaningful work that makes a positive impact on a global scale.

Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Location: This role is a permanent full-time position, based on-site within our Christchurch, NZ facility.

It does not offer a hybrid working environment and does not have any shift work requirements. Working days are Monday to Friday. About the role: You'll be part of a friendly and dynamic team that supports our customers in the development of life changing drugs and vaccines.

In this role, you will mainly be supporting the Quality function by performing testing and release of company products. The role is a mid-level position reporting to a Quality Supervisor and has no direct reports. What will you do? Role Responsibilities: Performing QC analyses and associated tasks as per standard procedures, make observations and interpret findings Review batch manufacturing records and documentation and release product for supply, and chemicals and components for manufacture Recording, analyzing and trending QC data in specified forms (paper and electronic) with accuracy and responsibility Ordering and maintenance of stock and resources, ensuring correct storage conditions for samples and chemicals Calibration and maintenance of Lab equipment and manufacturing monitoring equipment as per the defined schedule Facilitate quality control documentation (SOPs, Standard Forms) including writing, reviewing and issuing of documents Communicate effectively across departments and with internal customers.

Conducting and supporting investigations, root cause analysis and CAPA Take part in training and PPI activities Perform Environmental Monitoring, Microbiological tests or other laboratory related activities Conceive and participate in quality improvement initiatives and process improvement Observe all safety rules which are established to maintain safe work practices, including wearing personal protective equipment (PPE). Conduct pro-active hazard identification and report any accidents, incidents and near misses Keys to Success: Education:.