Assays, Biochemistry, Biology, Biotech and Pharmaceutical, Chemistry, Communication Skills, Corrective Action, Cross-Functional, Current Good Manufacturing Practice (cGMP), Delivery Management, Document Management, GMP (Good Manufacturing Practices), Gene Therapy, Manufacturing, Manufacturing Operations, Manufacturing/Industrial Processes, Medical Equipment, Minitab, Physiology, Problem Solving Skills, Process Improvement, Process Management, Process Validation, Product Support, Product/Service Launch, Project Tracking, Project/Program Coordination, Project/Program Management, Regulations, Research & Development (R&D), Six Sigma, Standard Operating Procedures (SOP), Support Documentation, Technical Writing
Our client, a world
leader in biotechnology and gene therapy, is looking for an “Transfer
Specialist - Reagent Manufacturing Operations” based in Tucson, AZ.<\/b><\/span>
<\/p>
<\/span><\/b>
<\/p>
Job Duration: Long
Term Contract (Possibility Of Extension)<\/span><\/b>
<\/p>
Pay Rate : $32/hr on W2<\/span><\/b>
<\/p>
<\/span><\/b>
<\/p>
Company Benefits:<\/span><\/b> Medical, Dental,
Vision, Paid Sick leave, 401K<\/span>
<\/p>
<\/span>
<\/p>
Seeking a Transfer
Specialist to support the transfer of new tissue diagnostic assays, reagents,
and bulk materials from R&D into commercial manufacturing. This role
focuses on cross -functional project coordination, technical transfer, GMP
compliance, and continuous process improvement. This is not a laboratory
role<\/b>, but a Life Sciences background is required to effectively collaborate
with technical teams.<\/span>
<\/p>
<\/span><\/b>
<\/p>
Key Responsibilities<\/span><\/b>
<\/p>- Coordinate
product and process transfers from R&D to Manufacturing, ensuring
quality, cost, and schedule objectives are met.<\/span>
<\/li> - Collaborate
with Operations, Development, Regulatory, Validation, and Project teams to
support successful product launches.<\/span>
<\/li> - Track
project milestones, manage documentation, and support process validation
activities.<\/span>
<\/li> - Ensure
compliance with cGMP, SOPs, quality systems, and regulatory requirements.<\/span>
<\/li> - Support
audit readiness, NCR investigations, and corrective actions.<\/span>
<\/li> - Apply
Lean principles and basic problem -solving tools to improve manufacturing
processes.<\/span>
<\/li> - Prepare
technical documentation, reports, and standardized procedures.<\/span>
<\/li> - Manage
multiple project deliverables while communicating effectively with
cross -functional stakeholders.<\/span>
<\/li><\/ul> <\/span><\/b>
<\/p>
Required Qualifications<\/span><\/b>
<\/p>
<\/span>
<\/p>
<\/p>
<\/p>
<\/div><\/span>