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MCS Senior Associate Quality Assurance

Thousand Oaks,, CA
Description:
Note:
  • Must be flexible as it is possible worker will start on any shift. Rotate every 6 months.
  • DAY 7 AM - 8 PM
  • SWING 1 PM to Midnight
  • NIGHT SHIFT 7 PM - 8 AM
  • Will change on the business they are supporting
  • Rotate every 6 months

Ideal candidate:
  • This position supports Quality Assurance program under the Plant QA organization providing daily oversight of the Drug Substance manufacturing areas. 
  • Under general supervision, the role provides support and compliance oversight to Manufacturing and Facilities & Engineering areas/staff in the execution of their processes, procedures, and use of quality systems. 
  • Duties include purposeful presence on the floor, electronic batch record review, SOP revision & approval, work order approval, and quality approval of minor deviations and CAPA records. 
  • Responsibilities will include evaluation of compliance issues, providing recommendations, and assuring progress of quality records to completion. 
  • The Sr. Associate will also represent functional area for the Drug Substance Quality Assurance department in the execution of projects necessary to achieve departmental operational goals and will work in a team matrix environment.

Preferred Qualifications:
  • Bachelor's Degree in Biochemistry, Biology, Chemistry, or related science field.
  • Demonstrated ability to perform GMP operations including following detailed SOPS, maintaining training, and good documentation practices.
  • Also, ability to make Quality based decisions in order to ensure compliance.
  • Experience managing projects through to completion & meeting timelines.
  • Evaluating documentation and operations according to company procedures.
  • Experience working with Quality Systems, Strong organizational skills and ability to manage multiple tasks at one time/ Effective communication skills (both written and verbal)
  • Demonstrated ability to work as both a team player and independently
  • Display leadership attributes and drive improvement initiatives.

Basic Qualifications
  • Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience

Top 3 Must Have Skill Sets:    
  • Experience working with Quality Systems / QA
  • BATCH RECORD EXPERIENCE
  • Plant Quality Assurance providing quality oversight to manufacturing
  • Looking for someone who can work cross functionally amongst many different teams and be comfortable with shifting priorities as the business needs change.

Day to Day Responsibilities:
  • Duties include electronic batch record review, batch record review, SOP and MP revision approval, work order approval, and quality approval of non-conformances and CAPAs. 
  • Responsibilities will include evaluation of compliance issues, providing recommendations, and assuring progress of quality records to completion. 
  • The incumbent will also represent functional area quality for the Bulk Quality Assurance department in the execution of projects necessary to achieve departmental operational excellence goals and will work in a team matrix environment.

PAY RATE : $37/Hr on W2.

"This posting is for Contingent Worker, not an FTE"

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