QC Analyst III
QC Analyst III
Posted on :
18-09-2025
Employer Active
1 Vacancy
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Share
Send me jobs like this
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Monthly Salary
Not Disclosed
Salary Not Disclosed
Vacancy
1 Vacancy
Posted on :
18-09-2025
Job Description
Overview:
TekWissen group is a workforce management provider throughout the USA and many other countries in the world. Our client is a leading biotechnology company that combines technological expertise with world-class manufacturing and scientific insight to support the delivery of innovative medicines for a wide range of diseases. Specializing in pharmaceutical ingredients bioscience biopharmaceuticals custom manufacturing and cell and gene therapy the company provides comprehensive services across the pharmaceutical biotech and life sciences sectors. It supports every stage of drug development from early research to commercial production and offers solutions in biologics small molecules and specialty ingredients. Committed to quality and innovation the company serves as a critical partner in advancing therapeutic solutions and streamlining complex manufacturing processes with a global presence that ensures access to scalable flexible and compliant technical expertise.
Job Title: QC Analyst III
Location: Portsmouth NH 03801
Duration: 12 months
Job Type: Temporary Position
Work Type: Onsite
Summary
- The Quality Control Technical Transfer Analyst III / QC Analyst III will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activites.
- Also participate in quality testing for customer in-process final product testing and stability studies when needed.
- Applies job skills and companys 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 Accountabilities:
- Applies job skills and companys 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 and training others
- 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 client DI policies guidelines and procedures.
- Perform other duties as assigned.
Required Qualifications
- Associates Degree Microbiology Biochemistry or Related Science Fields
- Strong experience with A280 CE-SDS icIEF ELISA SoloVPE qPCR is required
- Strong ability to speak publicly 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 and 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
TekWissen Group is an equal opportunity employer supporting workforce diversity.
Employment Type
Full-time
Key Skills
Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.
