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Job Title: Technical Transfer Specialist Manufacturing Operations
Location: Tucson, AZ (Onsite 5 days/week)
Shift: 8:00 AM 5:00 PM
Job Overview
We are seeking a Technical Transfer Specialist to support the introduction of new assays, reagents, and bulk materials into manufacturing operations. This role plays a key part in ensuring smooth transition of products from R&D to commercial manufacturing, focusing on quality, scalability, and compliance.
This is an entry-level opportunity ideal for candidates with 1 3 years of experience in GMP-regulated environments (pharma, biotech, or medical devices), especially those with quality, validation, or manufacturing support experience.
Key Responsibilities
Technical Transfer & Manufacturing Support
If you re looking to grow your career in manufacturing operations, validation, and technical transfer, we d love to hear from you!
Job Title: Technical Transfer Specialist Manufacturing Operations
Location: Tucson, AZ (Onsite 5 days/week)
Shift: 8:00 AM 5:00 PM
Job Overview
We are seeking a Technical Transfer Specialist to support the introduction of new assays, reagents, and bulk materials into manufacturing operations. This role plays a key part in ensuring smooth transition of products from R&D to commercial manufacturing, focusing on quality, scalability, and compliance.
This is an entry-level opportunity ideal for candidates with 1 3 years of experience in GMP-regulated environments (pharma, biotech, or medical devices), especially those with quality, validation, or manufacturing support experience.
Key Responsibilities
Technical Transfer & Manufacturing Support
- Support product design transfer from development through commercial launch
- Coordinate process transfers from R&D to manufacturing (internal/external)
- Track project milestones and ensure timely execution
- Collaborate with Operations, Quality, Regulatory, and Development teams
- Assist in documenting manufacturing requirements and scalability considerations
- Support process validation readiness and documentation
- Ensure compliance with cGMP, FDA, and quality standards
- Assist in audit readiness and documentation support
- Participate in deviation, CAPA, and quality investigations
- Apply Lean principles and problem-solving tools (5 Whys, Fishbone)
- Analyze process data using tools like Excel or Minitab
- Support process improvements and documentation updates
- Bachelor s degree in:
- Life Sciences (Biology, Chemistry, Biochemistry, etc.) OR
- Engineering (Biomedical, Chemical, etc.)
- 1 3 years of experience in pharma, biotech, or medical device industry
- Experience working in a GMP/regulatory environment
- Exposure to:
- Quality (QA/QC), Validation (IQ/OQ/PQ), or Manufacturing support
- Strong communication and cross-functional collaboration skills
- Ability to follow SOPs and quality protocols strictly
- Basic knowledge of Lean / Six Sigma methodologies
- Exposure to assays, reagents, or lab-based processes
- Understanding of raw material handling or manufacturing workflows
- Entry-level (0 3 years experience)
- Background in Quality, QC, Validation, or Manufacturing
- Comfortable working in a structured, process-driven environment
- Strong attention to detail and documentation skills
- This is a 100% onsite role in Tucson, AZ
- Candidates must be comfortable working in a manufacturing environment
- No senior-level candidates (5 years) preferred
If you re looking to grow your career in manufacturing operations, validation, and technical transfer, we d love to hear from you!