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Senior Quality Laboratories Analyst

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Quality
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184377 Requisition #
Thanks for your interest in the Senior Quality Laboratories Analyst position. Unfortunately this position has been closed but you can search our 420 open jobs by clicking here.
Requirements:
  • Demonstrate competency in the operation of common analytical instrumentation (e.g. UPLC, HPLC, Dissolution, GC, FTIR, UV/Vis) and other USP instrumental and wet chemistry techniques used in a pharmaceutical Quality Control Laboratory.
  • Demonstrate the ability to learn new techniques and technologies in an independent, efficient and effective manner. Demonstrate the ability to learn and master software programs utilized in the Quality Laboratory (i.e Empower, LIMS, SmartLab).
  • Deliver departmental training and mentorship to junior staff members to ensure laboratory is adequately trained on compliance topics, analytical instrument and safety.
  • Develop and calculate metrics to measure success against department and corporate goals and identify opportunities for improvement.  
  • Demonstrate excellent technical writing skills. These skills should include the ability to independently write and review documents that ensure cGMP compliance e.g. analytical test methods, method validation protocols and reports, instrumentation qualification documentation (URS/IQ/OQ/PQ), laboratory investigations, Standard Operating Procedures, and Change Controls.
  • Demonstrate excellent oral communication skills: Oral communication skills should include a demonstrated ability to effectively articulate complex scientific information in a concise and logical manner. Present information to small groups of internal and external scientist in meetings.  
  • Demonstrate attention to detail and keep accurate records.
  • Demonstrates the ability to work independently and make sound decisions on projects to determine new or improved processes and procedures.  Often acts as a facilitator and team leader.
  • Perform and lead the evaluation, development and execution of complex scientific studies requiring independent action and high degree of initiative to resolve issues.
  • Represent Quality Control in multi-disciplinary teams and working groups.
  • Serve as back-up for laboratory Manager.
     
Education and Experience
 
  • Bachelor’s degree in Chemistry or related scientific field.
  • More than 10 years experience in a GMP laboratory environment. 

Equal Employment Opportunity Employer


Allergan is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other protected status.

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