Overview
On Site
Up to $33
Contract - W2
Contract - 12 Month(s)
No Travel Required
Skills
Data Integrity
Biochemistry
Change Control
Conflict Resolution
Corrective And Preventive Action
Microsoft PowerPoint
Policies and Procedures
Positive Attitude
Problem Solving
HIS
Management
Microbiology
GMP
Microsoft
Microsoft Excel
Testing
Trackwise
Product QA
Quality Control
Quality Management
Regulatory Compliance
Science
Job Details
Job Title: QC Analyst III Job ID: 25-08265 Location: Portsmouth, NH Duration: 12 months on W2 contract
The Quality Control Technical Transfer Analyst 3 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 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.
The Quality Control Technical Transfer Analyst 3 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 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.
- 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
- 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.
- Associate's Degree Microbiology, Biochemistry or Related Science Fields
- 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
Please use the following when running keyword searches: A280, CE-SDS, icIEF, ELISA, SoloVPE, qPCR.
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