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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in leading MES teams and managing the design, configuration, and implementation of Master Batch Records (MBRs) while ensuring compliance with quality systems and regulatory requirements. Proficient in troubleshooting MES issues and integrating systems within a pharmaceutical or biotech environment.
Highest-signal resume keywords
Leadership of MES TeamsMaster Batch Record DesignPAS-X Software ExperienceGMP Compliance KnowledgeProject Management Certification
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Master Batch Record DesignSystem IntegrationTroubleshooting MES IssuesTesting Activities ManagementContinuous Improvement
Soft Skills
CollaborationTraining DeliveryTechnical Guidance
Tools & Technologies
PAS-X SoftwareOSI PI SoftwareAIZON SoftwareERP SystemsWonderware
Certifications & Qualifications
PAS-X Training CertificationProject Management Certification
Industry Keywords
Pharmaceutical IndustryBiotech IndustryGMPIT/System IntegrationChange Control
Tech Stack
Tools & technologiesERP
About the role
Key responsibilities & impact- Lead and develop a team of MES Specialists and Junior MES Specialists
- Oversee the design, configuration, testing, and implementation of Master Batch Records (MBRs) from initial concept through deployment
- Lead MBR design reviews and collaborate with Operations, Process Validation, Quality, IT, and R&D
- Manage creation, execution, and review of testing activities to validate MBRs
- Support development and enhancement of the MES platform and drive continuous improvement
- Deliver training and support to Electronic Batch Record (EBR) users
- Develop, maintain, and update MES procedures and documentation
- Coordinate and manage MBR change requests
- Ensure adherence to quality systems and timelines for deviations, change controls, and CAPAs
- Lead equipment and system integration activities between MES and manufacturing systems including ERP, OSI PI, Siemens PCS7, Wonderware, and Werum
- Troubleshoot MES issues, system interface errors, and ERP/MES inventory discrepancies
- Partner with the global MES team to identify best practices and improve ways of working
- Provide technical guidance and MES expertise to manufacturing and operational teams
Requirements
What you’ll need- Bachelor’s degree in Engineering or Science or related industry qualification
- At least 5 years’ experience in a pharmaceutical or biotech industry
- 5+ years’ experience in an operations pharmaceutical environment
- Experience in PAS-X software and design
- Knowledge of regulation requirements (GMP & IT/System Integration) is desirable
- Experience with OSI PI software is desirable
- Experience with AIZON software is desirable
- PAS-X Training Certification is desirable
- Project Management Certification is desirable
Benefits
Comp & perks- A highly competitive salary package
- Group pension scheme - Contribution rates are (3%/ 5%/ 7%) and company will match
- Private medical insurance for the employee
- Ongoing career development opportunities within a rapidly growing organisation
- Strong focus on succession planning and internal promotion
- Dedicated education and professional development allowance
- Wellness and social initiatives, including activities such as padel and summer events