מציאת משרת הייטק בחברות הטובות ביותר מעולם לא הייתה קלה יותר
Key Responsibilities:
Lead the team to monitor, maintain and analyse ‘on-shift’ technical data to identify corrective actions and improvements to the manufacturing process through visible management systems.
Comply with company policies & procedures (Current Good Manufacturing Practice cGMP, and Health Safety & Environment HS&E). Ensure health and safety/housekeeping standards are maintained. No critical or major observations and a maximum of 3 minor observations during external audits.
Facilitate technical/process data and give guidance in the areas of fault diagnosis. Monitor work operations business unit trends and standards and support the achievement of the manufacturing/filling/packing plan.
Investigate cell process related deviations to ensure Cell process activities are compliant with cGMP, GEP, and HS&E Complete Incident Reports/ CAPA close out in a timely manner.
Proven Leadership within a highly regulated, packaging production environment preferably pharmaceutical, chemical or food environment.
Sterile Pharmaceutical manufacturing experience would be ideal.
Knowledge and experience in completing Deviation Investigations/Technical Assessments/Reports or problem-solving RCA (root cause analysis).
Ability to present the departmental activities and debate technical issues with confidence.
Experience in Managing Change and Continuous Improvement through people.
Knowledge of working with biological active substances APIs would be beneficial.
Are you?
A good communicator/motivator/team player, with high attention to detail.
Able to deliver high performance standards consistently.
Comfortable working cross functionally influencing peers in area of expertise.
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
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