Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries, and growing - we look for talented people to grow our business, advance our science and contribute to our unique culture.
Overseeing the Semi-finished and Finished Goods Packaging, the Packaging Associate Manager provides leadership to the respective teams and ensures that the highest standards of health and safety are adhered to. The Packaging Associate Manager is responsible to generate quality, cost-effective goods through the effective utilization of resources to meet production schedules in accordance with all Good Manufacturing Practices (GMP) practices, while taking into consideration the company’s commitment to our Core Values and Behaviors in the planning and implementation of all actions related to the area of responsibility.
Skills/Knowledge Required
Duties and Responsibilities
In charge of the daily management of the packaging team (planning communication, team organization, control, checking of the defined targets).
Troubleshoot any immediate packaging problems to mitigate impact.
In charge of the management of the packaging planning compared to the logistic requests to ensure delivery on time.
Proactively monitor staffing needs as well as resolve challenges with employees around company policies and practices.
Collaborate with other departments and members of the management team to meet plant objectives.
Ensure training conformity of packaging team.
Conduct investigations into packaging failures, develop and implement remediation plan.
Ensure participation of health authorities audit (i.e. FDA, Swiss medic, EMEA...), and internal audit.
In charge of drafting of Standard Operating Procedure, and also working procedure linked to the area of responsibility.
Conform to the directives and instructions defined in the pharmaceutical site quality system.
Support and Participate to any development project executed on the packaging area (ie new validation process).
Coordinate improvement or development process linked to packaging area.
Apply risk management techniques and/or participate to risk assessment/analysis group linked to packaging process.
In charge of the definition, implementation of the KPI related to his scope of responsibilities.
To apply and respect GMP requirement, Hygiene, Safety and Environment rules during packaging activities.
EHS:
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