Supply Chain GMP Warehouse Supervisor

We at Roslin

CT, are a world-leading cell and gene therapy contract development and manufacturing organization creating cutting‑edge therapies that change people’s lives. Collaborative, dedicated, and talented people are the backbone of our culture, working both autonomously and in driven teams to make life‑changing products utilizing ground‑breaking science.

Here at Roslin

CT, our team can contribute to the development of revolutionary treatments. We live every day by our core values:
Partner Focus, One Team, Personal Growth, Integrity, Innovation, and Trust and Respect. We put our employees at the forefront by providing a flexible and empowering work environment, an attractive benefits package, and an emphasis on work‑life balance. Our people are the key to our success and at Roslin

CT we focus on developing our corporate culture, people’s development, growth, and the ability to impact patients.

The GMP Warehouse Supervisor oversees daily warehouse operations to ensure proper storage, handling, and distribution of materials in full compliance with GMP regulations and company procedures. They supervise staff, maintain accurate inventory records, and ensure all activities support product quality, safety, and regulatory compliance.

• Oversee activities related to raw material receiving, issuing, shipping, and inventory control in support of the manufacturing site.
• Oversee sample packaging and shipping to contract test labs and client sites.
• Oversee Material Management personnel with day‑to‑day tasks to support manufacturing and labs.
• Train and coach staff and conduct annual performance reviews including goal setting, scheduling and monitoring progress of work and assignments/projects.
• Maintain the warehouse in a constant audit ready state and participate in audits on site.
• Coordinate routine cycle counts.
• Manage scrapping of materials as well as seeking proper approval for destruction of materials.
• Maintain warehouse equipment and storage units in a clean, safe, and fully operational condition to ensure compliance with GMP requirements.
• Support off‑hour donor or patient material receipts and product pack‑out and shipments
• Create SOPs, batch records, change controls, protocols, training courses and other controlled documents
• Other duties as assigned

• Bachelor's degree preferred
• High school diploma / GED required
• 8 years of experience in biopharmaceutical or cell and gene therapy / Supply Chain / GMP warehouse
• Experience using ERP/MRP / MES system required.
• Possess excellent organizational and interpersonal skills and be able to communicate concisely and in a timely manner to clients' requests.
• Experience with industry regulations, GMP, compliance and pharmaceutical and/or biotechnology processes
• Understand supply chain concepts.
• Excellent MS Office and MS Project skills or equivalent
• Autonomous and works under minimal direction.
• Prior experience in a multiproduct manufacturing site and/or contract manufacturing environment preferred

• Monday-Friday, 1st shift (e.g., 8am-5pm).
• Flexible shift work including weekends. May be required on occasion in support of 24/7 manufacturing operations.

All Roslin

CT employees embrace the principles of our culture and values and are deeply committed to fostering an environment where diversity and inclusion are not only valued but prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways.

Roslin

CT is proud to be an equal opportunity employer, we seek to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or any other applicable legally protected characteristics