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Quality Control Specialist

Overview
Valeant Pharmaceuticals International, Inc. is a diverse and decentralized pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our unwavering competitive spirit. These values help us set goals based on our organization's potential and what we hope it will become.
Responsibilities
General Summary:
Performs a wide variety of activities, which may include one or more of the following:
Performs routine and non-routine analysis of environmental monitoring program, as well as raw materials, in-process and finished products during release or stability testing.
Assists in management of test samples, reagents and materials used in the laboratory per approved procedures.
Performs routine laboratory equipment maintenance.
Revises and updates standard operating procedures.
Performs testing in support of method validation studies.
Scope:
Uses professional concepts and company policies and procedures to solve a variety of problems.
Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. Exercises judgment within defined procedures and practices to determine appropriate action.
Normally receives general instructions on routine work, detailed instructions on new assignments.
Qualifications
Job Requirements:
Bachelor's degree in a scientific discipline or equivalent.
Typically 1 year related experience in cGMP/FDA regulated industry.
Proficient in MS Office applications.
Working Conditions and Physical Requirements:
Extensive use of laboratory equipment, chemicals and biological materials.
May require ability to gown aseptically for work in Clean Room environments.
May be required to work alternate shifts
Valeant is an EEO/AA employer M/F/D/V.
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