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Operator II, Manufacturing

Employer
Pharmiweb Partner Job (APAC)
Location
Auckland, New Zealand
Salary
Competitive
Start date
25 Nov 2023
Closing date
9 Dec 2023

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Discipline
Manufacturing
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
Job Description
Be directly involved in the production of our market leading Gibco cell culture media supplements and freeze dried powder products. The products manufactured at our Auckland facility are used globally in the pharmaceutical, diagnostic and biotech industries to enable our customers to make the world healthier, cleaner and safer. Be engaged in a variety of tasks focusing on safety and quality and get the opportunity to apply your knowledge and expertise to a range of process improvement initiatives where you can really make a difference! To promote accountability and self-development, our technicians specialize in one or more areas of production to become authorities in either filtration, freeze drying, cleanroom, or UVC operations, however you will be exposed to all areas of our manufacturing operations.
In this role you will have a specific focus on our liquid filtration processes. Expectations of the role include the ability to competently perform tasks, after a period of training, such as filter integrity testing, filter selection and set-up, filter change-outs, pH adjustment, operating steam-in-place (SIP) and clean-in-place (CIP) processes, trouble shooting and involvement in all filtration-related matters. You are expected to also contribute to all other areas of manufacturing operations and may be deployed to other areas and roles within the team for professional development or as required by the business.
Do you have production process experience?
We are looking for a Process Operator to join our manufacturing team at our Penrose site, working Monday to Friday on an 8-hour shift - 6am to 2:30pm or 9am to 5:30pm.
In this role, you will:
- Complete day-to-day production activities in conformance with specifications, standard operating procedures (SOPs), and cGMP/ISO principles. Complete Batch Manufacturing Records (BMRs), ensuring that all information is accurate, legible and correct to guarantee traceability
- Perform in-process sampling and trouble shoot processes, procedures and product issues with the assistance of others
- Communicate production issues to Production Supervisor and/or Team Leader as they arise, and carry out related duties and/or assigned tasks that lead to efficient operation of the team and business
Working Environment:
You would be working in a controlled and cleanroom environment. May be required to lift up to 20kg and stand for long periods of time while performing duties. Able to work safely with chemicals and hazardous materials and be flexible around hours of work.
Minimum Requirements/Qualifications:
Experience in cGMP manufacturing or laboratory environment preferred
Science related qualification is desirable
Good mechanical proficiency
Benefits we offer:
Free parking! Located close to transport links such as Penrose Train Station.
Annual Xmas/New Year's break
Health insurance cover
Half-day Birthday Leave
Annual Bonus Program
Company Paid Parental Leave
Paid Volunteer Leave
Internal Recognition and Rewards Program
Access to Employee Assistance Programme (EAP)
In-house development and online learning with a focus on internal career progression.
We are an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin or disability status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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