Quality Control Analyst (Portsmouth)

Quality Control Technical Transfer Analyst 3 Location:

Portsmouth, NH (100% Onsite) Contract Duration:

12 months

Pay Rate:

Pay Rate: $33/hr

Role Overview: The Quality Control Technical Transfer Analyst 3 will support production and quality initiatives by contributing to technical transfer activities, quality testing, and stability studies. This role works on semi-routine assignments, requiring the ability to recognize deviations from standard practices, analyze data, and apply problem-solving skills. Key Responsibilities: Perform quality testing for in-process, lot release, and stability studies, including investigations, transfers, and validations. Review assays and ensure accurate documentation of results. Participate in technical transfer projects, method qualifications, and new instrument integrations. Write and maintain quality records, including Deviations, CAPAs, Change Control, and Test Methods. Provide training and guidance to colleagues as needed. Apply Data Integrity principles in all aspects of work, following company policies and GMP guidelines. Communicate effectively with cross-functional teams to interpret needs and priorities. Act as a Subject Matter Expert (SME) for at least one software system. Conduct root-cause analysis for software or process issues. Maintain compliance with GMP quality systems such as TrackWise, LIMS, SoftmaxPro, Empower, SoloVPE. Ensure timely completion of assigned tasks while maintaining high quality standards. Required Qualifications & Skills: Associates Degree in Microbiology, Biochemistry, or related science field. Experience with GMP procedures and pharmaceutical quality systems. Proficiency in Microsoft Word, Excel, and PowerPoint. Strong analytical, problem-solving, and prioritization skills. Excellent verbal and written communication skills; comfortable presenting publicly. Self-motivated, collaborative, and able to work effectively in a team environment. Previous experience with Change Control, Deviations, CAPAs, Tasks, EICRs, Investigations. Experience with software validation, writing GMP procedures, and executing test scripts. Strong understanding of quality and data integrity principles. Preferred Experience: Familiarity with laboratory computer systems. Prior exposure to technical transfer projects, method transfers, and new instrument qualification. Ability to interpret complex data independently or with guidance.