Job Description

- Analysis of dry product stability and finished product samples according to the assigned specifications, analytical methodology and protocols in a GMP laboratory setting with emphasis on attention to detail and accuracy of execution.
- Documentation of results in accordance with cGMP
- Comply with FDA, EPA and OSHA regulations, performing all work in a safe manner.
- Reports lab testing data and completes documentation accurately and in accordance with laboratory procedures and regulatory requirements
- Reviews results for conformance to standards
- Peer review work and data of other analysts to ensure compliance with method and regulatory requirements
- Perform analytical testing of pharmaceutical products following analytical methodology
- Read and interpret analytical methodology and the USP
- Supports method development and validation of new methods
- Performs investigations and completes CAPA in response to deviations.
- Actively participates in customer and regulatory audits.
- Develops and executes validation protocols for test methods and equipment qualification as requested.
- Meet fundamental cGMP requirements relating to conduct and work practices to ensure the SISPQ (Safety, Identity, Strength, Purity, and Quality) of the all products manufactured/tested at Lonza Tampa.
- Performs other laboratory support activities as requested.
- Adhere to all defined Safety and Sustainability requirements and expectations and seek clarification whenever Safety and Sustainability requirements and expectations are either unknown or unclear
- Promptly report identified Safety and Sustainability issues, problems, deficiencies, errors, incidents, and/or opportunities to management and correct where possible
- Stop work where deemed necessary to maintain safety

3 Years Experience
Education - Bachelors Degree
NOTE: ONLY US CITYZENS OR GC
Employment Type: Contractor
Salary: $ 25.00 29.00 Per Hour

Job Tags

Hourly pay, Contract work, For contractors,

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