Job description
Manufacturing Process Technician
LIVE
What You Will Do: As a key member of our team, you will play an essential role in the sterile manufacture of products for Rare Diseases. Your contributions will support our growing facility, which focuses on the manufacture, development, and delivery of innovative human therapeutics to patients with serious illnesses. This role is fully onsite and involves all aspects of sterile manufacturing, including cleaning in classified areas. You'll work closely with cross-functional teams, aiding in batch release, material processing, quality actions, audits, and continuous improvement projects.
Manufacturing Area Responsibilities:
- Sterile Filling: Execute aseptic filling processes with precision and adherence to protocols.
- Product and Component Reconciliation: Ensure accurate reconciliation of products and components to maintain inventory integrity.
- Set Up and Breakdown: Manage single-use materials, including assembly, disassembly, and proper disposal.
- Materials Handling: Handle, weigh, dispense, and formulate materials according to specifications.
- Sample Management: Collect, process, store, and deliver samples as required.
- Equipment Cleaning: Perform manual and automated cleaning of equipment and parts.
- Area and Line Equipment Cleans & Clearances: Ensure cleanliness and readiness of manufacturing areas and equipment.
- Operation and Monitoring: Monitor and operate clean systems, autoclaves, and other processing equipment.
You will strictly adhere to current Good Manufacturing Practices (cGMP's), ensuring the accurate completion of process documentation, performing necessary calculations, and managing the physical tasks associated with the role.
Be Part of Our Team: Join a group of agile, innovative thinkers inspired by the opportunity to contribute to something larger than ourselves. We are driven to build meaningful careers in a company whose values resonate with ours, knowing that by achieving our potential, we help patients achieve theirs.
WIN
What We Expect of You:
Preferred Qualifications:
- Experience: 3+ years in a GMP or other regulated environment.
- GMP Knowledge: Strong understanding of GMP principles.
- Attention to Detail: Ability to maintain a high degree of focus and accuracy, especially during repetitive tasks.
- Drug Product Manufacturing: Previous experience is a plus.
- Equipment Proficiency: Ability to assemble, disassemble, operate, and understand simple to moderately complex equipment following procedures.
- Teamwork: Capable of working effectively both individually and as part of a team.
- Documentation: Skilled in accurately documenting processes in batch manufacturing records.
- Coachable: Open to receiving feedback and demonstrating measurable improvement.
- Procedure Compliance: Ability to follow written procedures, recognize malfunctions, and report them appropriately.
- Communication Skills: Strong verbal and written communication abilities.
This position requires a strong commitment to quality and safety, with the opportunity to make a significant impact on the production of life-saving therapeutics.
Job Type: Full-time
Pay: €38,000.00-€58,452.10 per year
Schedule:
- Day shift
- Flexitime
- Monday to Friday
- Night shift
Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.
BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.
