Production Technologist

Merck Gruppe - MSD Sharp & Dohme; Greater Bendigo; Hybrid; AUD 70,000 - 100,000; Full time

Job summary

Merck Gruppe - MSD Sharp & Dohme in Bendigo, Victoria, is seeking a Production Technologist to support the manufacture of media, antigen and final vaccine material in compliance with GMP and production schedules.

You will perform hands-on manufacturing activities, maintain equipment, assist with documentation and CAPA, support inventory and SAP data, and contribute to continuous improvement in a global animal health manufacturing team.

Qualifications

• Experience in a regulated or manufacturing environment preferred.
• Bachelor of Science or equivalent qualification advantageous.
• Understanding of GMP and quality systems.
• Strong verbal and written communication, organisation and teamwork skills.

Responsibilities

• Perform manufacturing activities for intermediates and final vaccine material.
• Prepare, stage, use and maintain equipment.
• Ensure materials and equipment are available and in date.
• Support production planning, batch documentation and schedule adherence.
• Assist with maintenance and validation to minimise downtime.
• Conduct batch record review and timely BPR corrections.
• Support SAP master data review and cycle counts.

Skills

GMP knowledge

Quality systems

Data analysis

Documentation

Communication

Teamwork

Aseptic processes

Microsoft Excel

Education

Bachelor of Science

Tools

SAP

Job description

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:

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

Requisition ID:R418258

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.