Job Description:
We are a leading global biopharmaceutical company, renowned for our innovative research and development.
The new building in Corsier-sur-Vevey is dedicated to advancing scientific and operational excellence in biopharmaceutical production.
We aim to foster a culture of innovation, efficiency, and sustainability.
Key Responsibilities:
* Develop and manage detailed schedules for all QC laboratory activities
* Ensure efficient workflow and adherence to high-level planning timelines
* Work closely with QC analysts and managers to forecast activity volumes and plan resources accordingly
* Monitor and report on schedule adherence and adjust to ensure alignment with high-level project timelines
* Collaborate with cross-functional teams to integrate QC planning with overall site operations
* Participate in strategic planning meetings to align QC activities with broader site goals and initiatives
* Implement and maintain planning tools and systems to enhance visibility and tracking of QC activities
* Identify and address potential bottlenecks or delays in QC processes and propose solutions to optimize workflow
* Evaluate compliance with all regulatory requirements, company policies, and safety standards
Requirements:
* Bachelor's degree in science, Business Administration, or related field
* Minimum of 2 years of experience in planning or scheduling in a laboratory or manufacturing environment
* Strong understanding of QC processes and regulatory requirements in a GMP environment
* Proficient in MS Office and planning software (e.g., Microsoft Project, SAP, BINOCS, GLIMS)
* Excellent organizational, communication, and analytical skills
* Fluent in English; proficiency in French is a plus
About Us:
A leading global biopharmaceutical company known for its innovative research and development.