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Manufacturing Technician

Employer
Pharmiweb Partner Job (APAC)
Location
Auckland, New Zealand
Salary
Competitive
Start date
21 Nov 2022
Closing date
27 Nov 2022

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Discipline
Manufacturing
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
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Position Summary:
Manufacture sterile liquid and freeze dried powder products for use in the pharmaceutical and biotech industry that is scientific in nature by following established protocols and instructions.
Please note:
This position requires flexibility beyond traditional work shifts.
Typically, this is a 9am - 5.30pm shift, Monday to Friday. For half of the year (~25 weeks), it changes to 2:30pm - 1am, Tues to Friday i.e. 4 x 10hr shifts (3-day weekends!) including a late shift allowance. Your flexibility to do both is a requirement of this position.
Key Responsibilities:
- 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 monitoring to assure batches meet specification; trouble shoot processes, procedures and product issues with the assistance of others.
- Update and revise manufacturing documentation including SOPs and BMRs; generate ideas and practice continuous improvement in advancing quality and cost, and efficiency gains; assist and participate in investigations, projects and validation as required.
- Abide by EHS policies and procedures to ensure a safe and healthy workplace environment for all. 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 Conditions :
Works 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 aptitude.
Competencies:
Relationship skills - Relates openly and comfortably with diverse groups of people.
Collaboration - Builds partnerships and collaborate to meet shared objectives.
Adopt process improvement - Use and apply company process improvements tools to improve processes and tackle problems.
Problem solving/decision making - Seeks appropriate data and utilises available problem solving tools before making decisions.
Focuses on growth - Works to meet business goals set by management.
Personal Qualities:
Proactive, anticipate needs
Motivated to get the job done and motivates others
Accountable
Demonstrates flexibility
Ability to multi-task
Benefits:
Free parking! And annual Xmas/New Year's break!
Health and insurance cover
Half-day Birthday Leave
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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