QC Analyst 3
Portsmouth, NH
Date Posted:24-Aug-2026
Work Type:On-Site
Job Number:495867
Job Description
Position Title: QC Analyst 3
Work Location: Portsmouth NH 03801
Assignment Duration: 8 Months
Position Summary:
The Quality Control Analyst will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities.
Applies job skills and company's policies and procedures to complete a variety of tasks of increased scope. Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required. Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors.
Key Responsibilities:
• Applies job skills and company's policies and procedures to complete a variety of tasks.
• Has experience with or currently uses the following software: SoftmaxPro, Empower, SoloVPE
• Has experience with method or software validations including but not limited to: writing GMP procedures and validation documents and executing test scripts.
• Acts as a SME for at least one software system
• Communicates with cross functional teams to interpret needs and priorities.
• Has GMP experience within the pharmaceutical industry
• Can perform technical, root-cause analysis for some software errors
• Applies Data Integrity principles in all aspects of work, in compliance with our organization DI policies, guidelines and procedures.
• Remains up to date on all assigned training activities.
• Performs other duties as assigned.
Qualification & Experience:
• Has experience with:
• Use of Microsoft Suites (Word, Excel, PowerPoint)
• Use of Laboratory computer systems
• Potential previous use of GMP Quality Systems such as: TrackWise, LIMS
• Apply Data Integrity principles in all aspects of work, in compliance with our organization DI policies, guidelines and procedures.
• Strong ability to interpret data both alone and with guidance.
• Perform assigned, complex and/or varied tasks
• Comprehend and follow instructions.
• Direct, control and plan tasks/projects.
• Strong ability to communicate in both written and verbal format.
• Self-motivated team player
• Completes assignments on-time and accurately
• Displays commitment to quality and performs job functions to the best of his/her ability
• Relate to others in a team setting.
• Maintain positive attitude in a team environment.
• Works entire assigned shift, including arriving on time
Work Location: Portsmouth NH 03801
Assignment Duration: 8 Months
Position Summary:
The Quality Control Analyst will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities.
Applies job skills and company's policies and procedures to complete a variety of tasks of increased scope. Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required. Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors.
Key Responsibilities:
• Applies job skills and company's policies and procedures to complete a variety of tasks.
• Has experience with or currently uses the following software: SoftmaxPro, Empower, SoloVPE
• Has experience with method or software validations including but not limited to: writing GMP procedures and validation documents and executing test scripts.
• Acts as a SME for at least one software system
• Communicates with cross functional teams to interpret needs and priorities.
• Has GMP experience within the pharmaceutical industry
• Can perform technical, root-cause analysis for some software errors
• Applies Data Integrity principles in all aspects of work, in compliance with our organization DI policies, guidelines and procedures.
• Remains up to date on all assigned training activities.
• Performs other duties as assigned.
Qualification & Experience:
• Has experience with:
• Use of Microsoft Suites (Word, Excel, PowerPoint)
• Use of Laboratory computer systems
• Potential previous use of GMP Quality Systems such as: TrackWise, LIMS
• Apply Data Integrity principles in all aspects of work, in compliance with our organization DI policies, guidelines and procedures.
• Strong ability to interpret data both alone and with guidance.
• Perform assigned, complex and/or varied tasks
• Comprehend and follow instructions.
• Direct, control and plan tasks/projects.
• Strong ability to communicate in both written and verbal format.
• Self-motivated team player
• Completes assignments on-time and accurately
• Displays commitment to quality and performs job functions to the best of his/her ability
• Relate to others in a team setting.
• Maintain positive attitude in a team environment.
• Works entire assigned shift, including arriving on time
Applicant Notices & Disclaimers
- For information on benefits, equal opportunity employment, and location-specific applicant notices, click here
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position's pay range is $60.81/hr – $62.06/hr.