QC Analyst - Pharma (Assays, CAPA, Stability Max $39/hr W2)

Lenmar Consulting Inc • Contract • Portsmouth, NH, US • 3w ago

Company Description

Pharma

Job Description

W2 candidates only - No CTC allowed

Skills Needed - A280, CE-SDS, IcIEF, ELISA, SoloVPE, QPCR.

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.
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 *** DI policies, guidelines and procedures.
Perform other duties as assigned.

Additional Information

All your information will be kept confidential according to EEO guidelines.