Manufacturing Contractor

This role involves hands‑on work with production equipment and materials to support manufacturing operations, including weigh/dispense, solution preparation, equipment cleaning (CIP/COP), small parts cleaning, and materials handling. The position requires close collaboration with internal support técnicos such as Facilities, QC, QA, Materials Management, and EHS to maintain compliance and operational excellence.

• Operate production equipment in accordance with SOPs to produce clinical products safely and compliantly.
• Execute manufacturing tasks including weighing, dispensing, solution preparation, and equipment cleaning (CIP/COP).
• Support materials handling and inventory management within manufacturing suites.
• Maintain accurate and detailed batch records and documentation in compliance with cGMP.
• Collaborate with cross‑functional support groups (Facilities, QC, QA, EHS) to ensure smooth operations.
• Identify and communicate potential issues, assisting in troubleshooting and process improvements.
• Participate in equipment setup, calibration, and shutdown activities as needed.
• Ensure adherence to safety procedures and quality standards at all times.

• Bachelor’s degree in Biotechnology or a related scientific field (required).

• Strong understanding of cGMP manufacturing processes and compliance principles.
• Ability to follow complex procedures and retain technical information effectively.
• Proven troubleshooting skills with the ability to identify and resolve issues quickly.
• Excellent communication and teamwork skills; comfortable collaborating in a fast‑paced environment.

• Hands‑on experience with Tangential Flow Filtration (TFF) or Ultrafiltration/Diafiltration (UFF) operations.
• Familiarity with HPLC systems.
• Exposure to automation systems such as Delta
  
  V or similar.
• Basic understanding of automated manufacturing systems and process controls.

• Shift: 4x10 Weds-Sat 6am-4pm
• 1 year contract