Shift: Exact Schedule - 8am -5pm M-F
Duration: 12 Months, goal is temp to perm
Pay range: $27.00 Hourly
Onsite Job Job Description: How will you make an impact?
This role provides analytical testing support in a fast-paced GMP laboratory environment. Makes detailed observations and reviews; documents and communicates test results; recommends solutions. Authors SOPs, Deviation Reports, and Out of Specification Reports. Supports continuous improvement initiatives with respect to training and improving efficiency while maintaining quality.
What will you do? - Perform testing with the following instrumentation: HPLC, GC, PXRD, Dissolution, DSC, FT-IR and KF.
- Records and reports results of analysis in accordance with prescribed lab procedures and systems.
- Clearly and accurately communicates the results of work by creating documentation of the testing/analysis and obtained results.
- Collaborates with internal scientific, analytical, laboratory and quality functional areas to meet project and team objectives.
- Recognizes and reports out-of-specification or unexpected results and non-routine analytical and product problems.
- Maintains laboratory work space to ensure it is audit ready.
- Support internal and external audits.
- Performs all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, and safety guidelines.
- Maintains the necessary compliance status required by company and facility standards.
How will you get here? Education • Bachelor’s Degree in chemistry, biology or related science or engineering field or equivalent combinations of education, training, and meaningful work experience may be considered.
Experience • No experience required, experience in a regulated environment is preferred.
Knowledge, Skills, Abilities • Excellent critical and logical thinking skills to solve problems.
• Effective verbal and written communication skills.
• Ability to work on multiple tasks simultaneously.
• Good knowledge of qualitative and quantitative chemical analysis as it relates to the pharmaceutical industry.
• Understanding of GMP and data integrity (ALCOA) is strongly preferred.
• Ability to read, analyze, and interpret technical procedures and governmental regulations.
• Ability to author Standard Operating Procedures, protocols and reports.
Physical Requirements: • Typically requires standing and walking for a shift.
• Occasionally requires lifting of up to 20 pounds.
• Requires manual dexterity and visual abilities.
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