Production Technician

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MSD is hiring a permanent, full-time Production Technician onsite in Upper Hutt, NZ, joining a regulated manufacturing environment to support integrated process teams and help meet production, quality, safety, delivery and cost targets for antigen and vaccine products. You will operate SOPs, maintain sanitation, document in batch records, support training, solve problems, contribute to continuous improvement, and collaborate across functions to ensure compliant product release and timely supply to global markets. The role rewards hands-on learning, offers clear paths for career growth, and values strong teamwork, communication, and GMP literacy; a background in biotechnology or chemistry and SAP experience are advantages. To apply, use the internal links for current employees or contingent workers; note the closing date 21 August 2026.

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Job Description

Production Technician

• Permanent, full-time role with competitive remuneration and benefits

• Location: Upper Hutt, Wellington, New Zealand

• Career growth: Expand your expertise in a growing, successful industry

• Professional development: Gain valuable experience in a dynamic, evolving role

As a Production Technician, you will support day-to-day operations within your assigned IPT (Integrated Process Team) area to help meet production, quality, safety, delivery, and cost targets. This role plays a key part in ensuring antigen and/or vaccine products are manufactured to the required standards to support customer demand in global markets.

You will work within a regulated manufacturing environment, contributing to compliant product supply, problem solving, documentation, continuous improvement, and cross-functional collaboration to help ensure the smooth running of the site.

What You Will Do

Responsibilities include, but are not limited to:

• Manufacture antigen and/or vaccine products to required standards and according to production schedules

• Operate equipment and perform tasks in line with Standard Operating Procedures

• Maintain cleaning, preparation, and sterilisation standards while minimising discards

• Document work accurately in batch records, worksheets, and logbooks in line with Good Documentation Practice

• Ensure IPT documentation is completed, reviewed, and compliant to support product release

• Support Site Quality Council targets and contribute to a zero overdue culture

• Review, collate, and archive IPT documentation with accuracy and completeness

• Enter manufacturing data into spreadsheets to support analysis and reporting

• Maintain area documentation, including Standard Operating Procedures, batch records, and worksheets

• Maintain good housekeeping standards in your area

• Communicate clearly with IPT and cross-functional teams to support the smooth flow of product, samples, and documentation

• Provide on-the-job training for other technicians in your assigned areas

• Build a strong practical understanding of your area to support troubleshooting and process optimisation

• Anticipate and solve production and operational problems

• Challenge processes and procedures to identify improvements in quality, safety, and cost

• Participate in Tier 1 and On-Point problem solving, including 8-Step Problem Solving activities

• Support local projects, process changes, and documentation updates with cross-functional teams

• Contribute to larger improvement initiatives through data collection, analysis, and implementation

• Support senior colleagues in larger site projects and safety or quality enablers

• Contribute to data assessment and analysis to identify opportunities and recommend improvements

What You Must Have

• Strong team player with excellent communication, organisational, and interpersonal skills

• Ability to work effectively in a regulated manufacturing environment

• Ability to plan work, meet deadlines, and manage competing priorities

• Sound and logical problem-solving ability

• Academic background in Biotechnology, Chemistry, or equivalent preferred

• Understanding of Good Manufacturing Practice, Good Laboratory Practice, or ISO requirements

• Proficiency in Microsoft Word, Excel, and Outlook

• SAP experience preferred

• Ability to work collaboratively with cross-functional teams and contribute to continuous improvement

What You Can Expect

• A hands-on role supporting global product supply in a fast-paced, regulated manufacturing environment

• Exposure to production, documentation, problem solving, and continuous improvement

• Real opportunities to build your technical skills and grow your career

• A collaborative team where your ideas and contribution matter

• The chance to be part of a trusted global animal health organisation

We are proud to be a company that embraces the value of bringing talented and committed people together. The fastest way to breakthrough innovation is when ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive workplace.

Required Skills:

Analytical Problem Solving, Computer Literacy, Corrective Action Management, Equipment Maintenance, GMP Compliance, GMP Documentation, Good Manufacturing Practices (GMP), Manufacturing Documentation, Manufacturing Operations, Problem Solving, Process Improvements, Process Optimization, Regulatory Compliance, Safety Practices, SAP Management, Workplace Training

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully 
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

08/21/2026

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.