Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
MSD

Production Technologist

MSD

. 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 .

Posted 9/18/2026full-timeBendigo • AustraliaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Good Manufacturing Practices (GMP), quality systems, and vaccine production processes, while effectively supporting compliance audits and maintaining high standards of documentation and procedure adherence. Proficient in analytical problem solving and teamwork within a regulated manufacturing environment.

Highest-signal resume keywords
Good Manufacturing Practices (GMP)Vaccine ProductionAnalytical Problem SolvingStandard Operating Procedure (SOP) WritingLaboratory Processes

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
GMP OperationsManufacturing Quality ControlData AnalysisProcedure AdherenceBasic Maths Skills
Soft Skills
Strong Verbal CommunicationWritten CommunicationOrganizational SkillsTeamwork Skills
Tools & Technologies
SAPMicrosoft WordMicrosoft OutlookMicrosoft Excel
Certifications & Qualifications
Bachelor of Science or Equivalent Qualification
Industry Keywords
Pharmaceutical ManufacturingAseptic ProcessesQuality StandardsCompliance AuditsHazard Identification

About the role

Key responsibilities & impact
  • 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
  • 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
  • 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
  • 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
  • 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
  • Report to the Line Lead

Requirements

What you’ll need
  • 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
  • Analytical problem solving
  • Competency management
  • Computer literacy
  • Ethical standards
  • GMP operations and Good Manufacturing Practices (GMP)
  • Laboratory processes
  • Manufacturing quality control
  • Pharmaceutical manufacturing
  • Procedure adherence
  • Standard Operating Procedure (SOP) writing
  • Standards compliance
  • Vaccine production

Benefits

Comp & perks
  • Competitive remuneration and benefits
  • Development opportunities
  • Exposure to new technologies and broader manufacturing capabilities
  • Inclusive workplace
  • No relocation required
  • No travel required