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Core Competencies
Role fitCore 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 ensuring compliance and operational efficiency. Proficient in batch documentation, inventory management, and technical process advancement to support manufacturing performance.
Highest-signal resume keywords
Good Manufacturing Practices (GMP)Batch Documentation ReviewSAP TransactionsAnalytical Problem SolvingAseptic Processes
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Manufacturing ActivitiesBatch Record VerificationData AnalysisDocument ManagementSOP WritingQuality ControlOperational ComplianceLaboratory ProcessesInventory AccuracyTechnical Process Advancement
Soft Skills
Strong Verbal CommunicationWritten CommunicationOrganizational SkillsTeamwork Skills
Tools & Technologies
SAPMPS ToolsMicrosoft WordMicrosoft OutlookMicrosoft Excel
Certifications & Qualifications
Bachelor of Science or Equivalent Qualification
Industry Keywords
Pharmaceutical ManufacturingRegulated EnvironmentQuality SystemsProcedure AdherenceVaccine ProductionCompliance AuditsChange ManagementEnvironmental MonitoringIncident InvestigationsCAPA Implementation
About the role
Key responsibilities & impact- 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
- Support compliance audits, event investigations, change management and environmental monitoring
- Maintain good housekeeping and ensure equipment is fit for purpose and safe to use
- 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
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
- Knowledge of analytical problem solving, audit trails, computer literacy, document management, ethical standards, GMP operations, laboratory processes, manufacturing quality control, operational compliance, pharmaceutical manufacturing, procedure adherence, SOP writing, and vaccine production
- No relocation available
- No visa sponsorship
- No travel required
Benefits
Comp & perks- Competitive remuneration and benefits
- Development opportunities
- Exposure to new technologies and broader manufacturing capabilities
- Inclusive workplace
- Equal opportunity employment