Transfer Specialist - Reagent Manufacturing Operations (GMP, Life Sciences/Pharma/Biotech)
Boost your chances before you apply.
Dawar Consulting, Inc.
AZ
Summary
Coordinate the transfer of tissue diagnostic assays and reagents from R&D into commercial manufacturing. Ensure compliance with cGMP and regulatory requirements while managing project milestones and process improvements.
Job Description
Our client, a world
leader in biotechnology and gene therapy, is looking for an “Transfer
Specialist - Reagent Manufacturing Operations” based in Tucson, AZ.
Job Duration: Long
Term Contract (Possibility Of Extension)
Pay Rate : $32/hr on W2
Company Benefits: Medical, Dental,
Vision, Paid Sick leave, 401K
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, but a Life Sciences background is required to effectively collaborate
with technical teams.
Key Responsibilities
- Coordinate
product and process transfers from R&D to Manufacturing, ensuring
quality, cost, and schedule objectives are met. - Collaborate
with Operations, Development, Regulatory, Validation, and Project teams to
support successful product launches. - Track
project milestones, manage documentation, and support process validation
activities. - Ensure
compliance with cGMP, SOPs, quality systems, and regulatory requirements. - Support
audit readiness, NCR investigations, and corrective actions. - Apply
Lean principles and basic problem-solving tools to improve manufacturing
processes. - Prepare
technical documentation, reports, and standardized procedures. - Manage
multiple project deliverables while communicating effectively with
cross-functional stakeholders.
Required Qualifications
- Bachelor's
or Master's degree in Life Sciences (Biology, Chemistry, Biochemistry,
Physiology, or related field). - 1+
year of experience in pharmaceutical, biotechnology, medical device, or
other regulated industries. - Experience
coordinating projects or deliverables across multiple stakeholder groups. - Working
knowledge of cGMP/GMP environments and SOP compliance. - Strong
communication, stakeholder management, organizational, and problem-solving
skills. - Familiarity
with Lean principles; Six Sigma and Minitab experience are a plus.
If interested, please
send us your updated resume at
DAWAR CONSULTING, a trusted name in IT Professional. We provide technology and business consulting services, helping clients with workforce solutions, project delivery, and IT support.
Founded
2009
Company size
51-200 employees
Industry
IT Services and IT Consulting
Org type
Privately Held
Headquarters
Newark, California
DAWAR CONSULTING, a trusted name in IT Professional. We provide technology and business consulting services, helping clients with workforce solutions, project delivery, and IT support.
Founded
2009
Company size
51-200 employees
Industry
IT Services and IT Consulting
Org type
Privately Held
Headquarters
Newark, California