Technical Transfer Specialist in Manufacturing Operations

100% Onsite - Tucson, AZ, US • Posted 2 days ago • Updated 2 hours ago
Full Time
On-site
USD $30.00 - 32.00 per hour
Fitment

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Job Details

Skills

  • Manufacturing Operations
  • Assays
  • Scalability
  • Life Sciences
  • Pharmaceutics
  • Medical Devices
  • Six Sigma
  • Stakeholder Management
  • Product Design
  • Research and Development
  • Collaboration
  • Good Manufacturing Practice
  • Auditing
  • Regulatory Compliance
  • Documentation
  • NCR
  • Continuous Improvement
  • Lean Methodology
  • Minitab
  • GMP
  • Manufacturing
  • Project Coordination
  • Attention To Detail
  • Soft Skills
  • Communication
  • JavaScript

Summary

Technical Transfer Specialist - Job Description

Technical Transfer Specialist - Manufacturing Operations

Location: 100% Onsite - Tucson, AZ
Employment Type: W2 Only
Pay Rate: $30 - $32/hr

Role Overview

Entry-level role supporting Technical Transfer and cross-functional project activities. This is a backfill position focused on integrating new products into manufacturing processes.

The Opportunity

The Technical Transfer Specialist supports the introduction of new assays, reagents, and bulk materials into manufacturing. This role ensures seamless transition from development to operations while maintaining quality, scalability, and compliance.

Required Qualifications
  • Bachelor's or Master's degree in Life Sciences or Engineering
  • 1+ year experience in pharma, biotech, or medical device industry
  • Experience in GMP/regulated environment
  • Basic understanding of Lean and Six Sigma principles
  • Strong communication and stakeholder management skills
  • Ability to follow SOPs, OPs, and quality protocols


Key Responsibilities
Technical Transfer (70%)
  • Execute product design transfer tasks
  • Coordinate process transfers from R&D to manufacturing
  • Collaborate with cross-functional teams
  • Document manufacturing requirements and best practices
  • Support validation readiness and troubleshooting
Quality, Safety, and Compliance (15%)
  • Ensure adherence to cGMP and regulatory standards
  • Support audits and compliance documentation
  • Assist in NCR investigations and corrective actions
Continuous Improvement (15%)
  • Apply Lean methodologies (Five Whys, Fishbone)
  • Analyze data using tools like Minitab
  • Improve and standardize processes


Key Skills & Competencies
  • Knowledge of GMP, SOPs, and regulatory standards
  • Understanding of manufacturing processes
  • Strong project coordination skills
  • Attention to detail and accuracy
  • Experience in stakeholder meetings


Soft Skills
  • Strong communication skills
  • Team-oriented mindset
  • Ability to work in a matrix environment
  • Comfortable contributing in meetings


Interview Process
  • 45-minute interview
  • Onsite preferred, virtual acceptable


Additional Notes
  • Compensation flexibility for strong candidates
  • Submission deadline: Wednesday night

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Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: sharpdec
  • Position Id: 52646
  • Posted 2 days ago
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