Quality Control Analyst II
Location: Framingham, MA 01701
Duration: 12 months-Contract-Onsite
Client-Pharma
Pay Rate:$35.00/hr on W2 Position Summary:
This position is responsible for performing routine and complex testing of in-process samples and final products in accordance with SOPs and relevant procedures for method development, qualification, validation, method transfer, product release, stability, and process validation and investigations.
Responsibilities include:
Perform laboratory assays in support of method development, qualification, validation,
method transfer, product release, stability, and process validation and investigations.
Perform maintenance on complex laboratory equipment.
Review data for compliance to procedures and specifications.
Calculate and evaluate results.
Make detailed observations in support of Alert, Action and OOS result investigations.
Participate in writing and revising SOPs.
Assists in the qualification of new controls, standards and reagents
Effectively demonstrate an understanding of and work in compliance with CGMPs.
Practice safe work habits and adhere to clients safety procedures and guidelines.
Actively participate in problem solving meetings with senior staff members and suggest process improvements.
Independently work under supervision and direction.
Basic Qualifications:
Bachelors degree or equivalent and 2 + years laboratory experience.
Masters degree or equivalent and 0-1 year experience.
Basic knowledge (i.e. 1-2 years experience) in the required method platform (e.g. Bioburden, TOC, Endotoxin, Water Chemistry, ELISA).
Attention to detail, and able to maintain accurate records with excellent proofreading skills
Able to communicate effectively with others
Able to work effectively both independently and as a member of a team
Proficient with Microsoft Office tools such as: Word, Excel & Powerpoint.
Employment Type: Contractor
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