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Merck & Co.

Production Technologist

AUS - Victoria - East Bendigo (Harpin) · AUS - Victoria - Bendigo

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hirly's read of this role

Seniority
Mid level
Country
AU
Work mode
On-site / unstated
First seen by hirly
15 Oct 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Job Description

Production Technologist

Permanent full-time role with competitive remuneration and benefits

Based in Bendigo, VIC, Australia

Join a global animal health manufacturing team focused on quality, safety and continuous improvement

Play a key role in the manufacture of intermediates and final vaccine material

As a Production Technologist, you will perform direct and indirect activities supporting the manufacture of media, antigen and final vaccine material in line with the production schedule and local regulatory and GMP requirements. This is a hands-on role within the Manufacturing Division, reporting to the Line Lead.

What You Will Do

Operations and Production

Perform manufacturing activities for intermediates and final vaccine material

Prepare, stage, use and maintain mechanical and laboratory equipment

Ensure materials and equipment are available and within date prior to manufacture

Support production planning, batch documentation and schedule adherence

Assist with maintenance and validation activities to minimise downtime

Conduct batch record review and verification, including timely BPR corrections

Support cycle counts, inventory accuracy and SAP master data review

Safety and Compliance

Follow SOPs and maintain Good Documentation Practices

Contribute to hazard and near miss identification, incident investigations and CAPA

Participate in Safe by Choice discussions and model inclusive behaviours

Support compliance audits, event investigations, change management and environmental monitoring

Maintain good housekeeping and ensure equipment is fit for purpose and safe to use

Support adherence to relevant quality standards and manufacturing requirements

Continuous Improvement and Ways of Working

Apply MPS tools and methodologies to support investigations and CAPA implementation

Contribute to technical process advancement and growth strategies in Production

Participate in Site Tier communication processes and cross-functional tier meetings

Support cost mitigation and innovation initiatives that improve manufacturing performance

Participate in competency-based training, priority setting and development planning

People and Coordination

Escalate issues that may impact the production schedule

Coordinate activities during periods of leave or offsite work where required

Raise purchase requisitions and manage limit orders as needed

Perform SAP transactions within required timeframes

What You Must Have

Experience in a regulated or manufacturing environment preferred

Bachelor of Science or equivalent qualification advantageous

Understanding of GMP and quality systems

Basic computer skills, including Word, Outlook and Excel

Strong verbal and written communication, organisation and teamwork skills

Understanding of aseptic processes and GMP behaviours

Basic maths skills and exposure to data analysis

What You Can Expect

The opportunity to contribute to a critical manufacturing operation in a global organisation

A collaborative team environment with a strong focus on safety, quality and continuous improvement

Exposure to development opportunities , new technologies and broader manufacturing capabilities

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.

Additional location(s) Compensation Information:

Required Skills:

Analytical Problem Solving, Audit Trails, Computer Literacy, Document Management, Ethical Standards, GMP Operations, Good Manufacturing Practices (GMP), Laboratory Processes, Manufacturing Quality Control, Operational Compliance, Pharmaceutical Manufacturing, Procedure Adherence, Standard Operating Procedure (SOP) Writing, Vaccine Production

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:

11/14/2026 *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.

Original posting on Merck & Co.'s site ↗

Listed on hirly, a job board. hirly is not the employer: Merck & Co. is hiring for this role.

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