Work with Global MES programs in medium to large sized teams
Participate / Lead MES Strategy /Feasibility/Assessments/Studies/Roadmaps for clients
Develop MES Standards & templates
Design, Execution, Review and Approval of MBR’s
Conduct informal and formal testing of MES solutions. Execute test scripts, analyze test results and determine the acceptability of results against pre-determined criteria
Foster continuous improvement & new design ideas
Mentor junior employees to ensure diverse skill set & enable a learning environment
Ensure utilization/assignment of team members across multiple fixed-fee projects and T&M assignments is optimised
Liaise with project managers and senior delivery team personnel in defining and achieving project delivery milestones, project workload sequencing/resourcing and controlling project costs
Relationship building with key clients, vendors, partners and stakeholders & provide technical contributions to support sales
Bachelors’ degree in Science, Engineering or relatable technical degree
8 years’ MES/ Operations experience, gained in a highly automated Life Sciences manufacturing environment
Experience with MES platforms - PAS|X, Syncade, PharmaSuite, XFP, POMS, Camstar or other life sciences compatible MES solutions
Excellent working knowledge of FDA and GMP guidelines and of software Development Life Cycle (SDLC) and support methodologies required
Proven ability to work in a team-oriented, collaborative environment,
Strong written and oral communication skills
Ability to work in a team-oriented, collaborative environment and foster team development & growth
