Mindlance · 14 hours ago
QC Analyst III
Portsmouth, NH
Full-time
Onsite
Mid LevelMindlance is a company seeking a Quality Control Technical Transfer Analyst 3 to support production through technical transfer activities and quality testing. The role involves running test samples, reviewing assays, and training others while ensuring compliance with GMP Quality Systems.
Human Resources
Responsibilities
Applies job skills and company's policies and procedures to complete a variety of tasks
Running test samples for In-Process, Lot Release and Stability studies
Running test samples for (but not limited to) investigations, transfers and validations
Reviewing assays
Training others
Has experience with: Change Control, Deviations, CAPAs, Tasks, EICRs, Investigations
Writing- Quality Records (Deviations, CAPA, Change Control) and Test Methods
Projects – such as method transfers, new instruments, method qualifications
Use of Microsoft Suites (Word, Excel, PowerPoint)
Use of Laboratory computer systems
Potential previous use of GMP Quality Systems such as: TrackWise, LIMS
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
Apply Data Integrity principles in all aspects of work, in compliance with Lonza DI policies, guidelines and procedures
Perform other duties as assigned
Strong ability to speak publicly
Strong ability to interpret data both alone and with guidance
Perform assigned, complex and/or varied tasks
Prioritization and problem solving
Comprehend and follow instructions
Direct, control and plan tasks/projects
Brainstorming
Strong ability to communicate in both written and verbal format
Exercises judgment within defined procedures and practices to determine appropriate action
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
Timeliness in completing assigned tasks
Works entire assigned shift, including arriving on time
Has experience with or currently uses the following software: SoftmaxPro, Empower, SoloVPE
Has experience with 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 Lonza DI policies, guidelines and procedures
Remains up to date on all assigned training activities
Performs other duties as assigned
Qualification
Required
Associate's Degree Microbiology, Biochemistry or Related Science Fields
Has experience with: Change Control, Deviations, CAPAs, Tasks, EICRs, Investigations
Writing- Quality Records (Deviations, CAPA, Change Control) and Test Methods
Projects – such as method transfers, new instruments, method qualifications
Use of Microsoft Suites (Word, Excel, PowerPoint)
Use of Laboratory computer systems
Potential previous use of GMP Quality Systems such as: TrackWise, LIMS
Strong ability to speak publicly
Strong ability to interpret data both alone and with guidance
Perform assigned, complex and/or varied tasks
Prioritization and problem solving
Comprehend and follow instructions
Direct, control and plan tasks/projects
Brainstorming
Strong ability to communicate in both written and verbal format
Exercises judgment within defined procedures and practices to determine appropriate action
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
Timeliness in completing assigned tasks
Works entire assigned shift, including arriving on time
Has experience with or currently uses the following software: SoftmaxPro, Empower, SoloVPE
Has experience with 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 Lonza DI policies, guidelines and procedures
Remains up to date on all assigned training activities
Company
Mindlance
Mindlance is a Staffing and Recruiting company which provides multi-vertical staffing services
Founded in 1999
1001-5000 employees
H1B Sponsorship
Mindlance has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (71)
2024 (53)
2023 (37)
2022 (72)
2021 (36)
2020 (40)
Funding
Current Stage
Late StageLeadership Team
R
Rajat Paul Dhall
Co-Founder & Managing Director
V
Vik Kalra
Co-Founder and Managing Director
Recent News
2025-11-19
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2025-04-14
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