Quality Control Technical Transfer Analyst 3

Overview

On Site
$30 - $35
Contract - Independent
Contract - W2
Contract - 12 Month(s)

Skills

A280
CE-SDS
icIEF
ELISA
SoloVPE
qPCR

Job Details

Job Title: Quality Control Technical Transfer Analyst 3

Location: Portsmouth, NH
Job Summary:
The Quality Control Technical Transfer Analyst 3 will serve as a key team member within the Quality Control department, supporting production by contributing to technical transfer activities. This role also involves participating in quality testing for customer in-process, final product testing, and stability studies as needed. The analyst will apply job skills and company policies to complete a variety of tasks, ensuring compliance with established procedures while recognizing deviations from accepted practices.
Key Responsibilities:
  • Execute test samples for In-Process, Lot Release, and Stability studies.
  • Conduct testing for investigations, transfers, validations, and related activities.
  • Review and analyze assays for accuracy and compliance.
  • Train and mentor team members as required.
  • Author and review Quality Records (Deviations, CAPA, Change Control) and Test Methods.
  • Participate in projects such as method transfers, new instrument implementation, and method qualifications.
  • Utilize Microsoft Office Suite (Word, Excel, PowerPoint) for documentation and reporting.
  • Operate Laboratory computer systems and maintain data integrity.
  • Experience with GMP Quality Systems (e.g., TrackWise, LIMS) is a plus.
  • Ensure compliance with Data Integrity (DI) policies in all work activities.
  • Perform additional duties as assigned.
Qualifications & Skills:
  • Education: Associate s Degree in Microbiology, Biochemistry, or related scientific field.
  • Strong public speaking and verbal/written communication skills.
  • Ability to interpret data independently and with guidance.
  • Proficiency in prioritization, problem-solving, and task execution.
  • Capable of comprehending and following complex instructions.
  • Experience in directing, controlling, and planning tasks/projects.
  • Strong team collaboration and brainstorming abilities.
  • Self-motivated, detail-oriented, and committed to quality.
  • Ability to work in a team environment with a positive attitude.
  • Reliable in meeting deadlines and completing tasks accurately.
  • Punctual and committed to working full assigned shifts.
Work Environment:
  • Works on semi-routine assignments, identifying deviations from standard practices.
  • Solves moderate-scope problems through analysis of identifiable factors.
  • Adheres to company policies, GMP standards, and regulatory requirements.
Additional Requirements:
  • Ability to exercise judgment within defined procedures.
  • Maintains compliance with all quality and safety guidelines.
  • This role is ideal for a detail-oriented, analytical professional looking to contribute to a dynamic Quality Control team while ensuring product integrity and compliance.
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