Technical Transfer Specialist - Manufacturing Operations

Artech LLC

Tucson, AZ

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JOB DETAILS

SALARY

$30–$32 Per Hour

SKILLS

Assays, Best Practices, Biochemistry, Biology, Biomedical Engineering, Biotech and Pharmaceutical, Chemistry, Communication Skills, Continuous Improvement, Corporate Compliance, Corrective Action, Cross-Functional, Current Good Manufacturing Practice (cGMP), Data Analysis, Data Processing, Data Quality, Documentation, Documentation Standards, GMP (Good Manufacturing Practices), Identify Issues, Information Technology & Information Systems, Interpersonal Skills, Laboratory, Lean Manufacturing, Lean Six Sigma, Maintain Compliance, Manufacturing, Manufacturing Design, Manufacturing Operations, Manufacturing Requirements, Manufacturing/Industrial Processes, Matrix Management, Medical Equipment, Mentoring, Minitab, Onboarding, Operations Processes, Organizational Skills, Physiology, Problem Solving Skills, Process Analysis, Process Management, Process Validation, Product Design, Project Tracking, Project/Program Coordination, Project/Program Management, Regulations, Reporting Skills, Research & Development (R&D), Risk Management, Safety Compliance, Scientific Principles, Six Sigma, Standard Operating Procedures (SOP), Standards Development, Statistics Software, Support Documentation, Team Player, Technical Recruiting, Technical Support, Technical Writing, Time Management, Training/Teaching, Writing Skills

LOCATION

Tucson, AZ

POSTED

2 days ago

Job Description:
Title: Technical Transfer Specialist in Manufacturing Operations
Location: Tucson, AZ 85755
Duration: 12-month contract
Pay Rate: $30-$32/hr. on W2.
Job ID: # 26-22900

Description:
The Opportunity
The Technical Transfer Specialist supports the introduction of new assays, reagents, and bulk materials for tissue diagnostics into Roche's manufacturing processes. This role ensures the seamless integration of new products from Development into Operations, focusing on manufacturability, quality, cost, and schedule. You will leverage technical knowledge, project management skills, and lean manufacturing principles to support efficient, scalable, and compliant manufacturing practices.

Required Qualifications
--Bachelor's or Master's degree in a Life Sciences (Biology, Chemistry, Biochemistry, Physiology, etc.) or Engineering (Biomedical/Chemical) discipline.
--Minimum of 1 year of directly relevant work experience, preferably within the pharmaceutical, biotechnology, or medical devices industry.
--Experience operating in a GMP/regulated environment
--Basic knowledge of Lean principles. Familiarity with Six Sigma methodologies is a plus.
--Excellent stakeholder management, communication, and project coordination skills.
--Proven ability to strictly follow standard operating procedures (SOPs), operational procedures (OPs), and quality protocols, ensuring compliance and data integrity.
--Strong teamwork ethic and exceptional interpersonal skills, with the ability to effectively collaborate across multiple functions, anticipate team needs, and navigate a matrix organization.
-Basic Technical Problem-Solving: Candidates must have indirect or academic experience in troubleshooting, technical projects, or lab work (e.g., from college courses, a master’s program, or tutoring). Direct industry experience is not required.
-Collaboration & Independence: Candidates must work well with different teams and be capable of managing their own daily tasks independently after initial onboarding and training.
-Strong Professional Communication: Candidates must have great interpersonal skills, know how to self-manage their workload, and be comfortable escalating issues when needed.
-Curiosity & Eagerness to Learn: Well suited candidates should display a growth mindset, a strong willingness to learn, and the confidence to ask questions (e.g., a great fit for a recent grad or someone transitioning from a technician role).

Key Responsibilities
Technical Transfer (70%)
--Execute product design transfer tasks from late-stage development through commercial launch.
--Coordinate process transfers from R&D to manufacturing sites (local or external) and track project milestones.
--Collaborate cross-functionally with Operations, Development, Regulatory, and Project teams to align on manufacturability, quality, and cost objectives.
--Document and integrate end-to-end manufacturing requirements and best practices, including scalability considerations, into transfer projects.
--Utilize project management methodologies to execute transfer activities, troubleshoot issues, and support the evaluation of new tools and technologies.
--Support process validation readiness by gathering necessary documentation and collaborating with Validation Engineers.
--Actively participate in training and mentorship to develop technical excellence within the design transfer team.

Quality, Safety, and Compliance (15%)
--Ensure all processes are conducted safely and adhere strictly to current Good Manufacturing Practices (cGMP), local, international, and Roche (MQMS) standards.
Assist in audit readiness by collecting and organizing documentation, and supporting non-compliance events (e.g., NCR investigations and corrective actions).
--Keep updated with relevant regulations to maintain company compliance.

Continuous Improvement (15%)
--Learn and apply basic Lean principles and problem-solving methodologies (e.g., Five Whys, Fishbone diagrams) to identify and eliminate process inefficiencies.
--Use statistical tools and software (e.g., Minitab) to analyze process data, minimize risk, and generate actionable plans for improvements.
--Develop and maintain standardized procedures and documentation for processes.

Knowledge, Skills, and Abilities
--Foundational knowledge in applying scientific methods and principles to process transfer tasks, focusing on learning how to document and incorporate basic design and manufacturing elements while supporting a design for manufacturability approach.
--Basic understanding of the end-to-end production process for assays and reagents (formulation, filling, and packaging).
--Advanced technical writing skills to produce reports and documents.
--Excellent stakeholder management, communication, and project coordination skills are required.
--Strong organizational, critical thinking, and problem-solving abilities, with the capacity to manage multiple low-complexity assignments and meet project deadlines.
--Proven ability to strictly follow standard operating procedures (SOPs), operational procedures (OPs), and quality protocols, ensuring compliance and data integrity.
--Strong teamwork ethic and exceptional interpersonal skills, with the ability to effectively collaborate across multiple functions, anticipate team needs, and navigate a matrix organization.
--Strong organizational, critical thinking, and problem-solving abilities, with the capacity to manage multiple low-complexity assignments and meet project deadlines.

Regards,
Ananya Nagaraj
Technical Recruiter
Cell: 682-284-1057,
Email:

Ananya.n@artech.com

,
Artech Information Systems LLC
360 Mt. Kemble Avenue., Suite 2000
Morristown, NJ 07960
Website: www.artech.com

Technical Transfer Specialist - Manufacturing Operations

Artech LLC

Tucson, AZ

About the Company

Artech LLC

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