Quality Assurance Specialist

Max Bill Rate: ***
Location: Tarzana, CA
Duration: 8 months (possible extension)
Working Days/Hours: 9am-5pm
Sunday- Thursday
OR
Monday-Friday (possible weekend work)


Interview Process: 2 rounds
1st Teams Interview
Duration: 30 minutes


2nd Teams Interview
Duration: 30 minutes


Internal AZ Title: Quality Assurance Specialist


Job Description Summary
Provides Quality Assurance support to an assigned area. Typically a graduate or equivalent
experience. Non-supervisory, provides technical advice in key areas of processes and
procedures. Role holder impacts directly on the value stream by ensuring efficient processes and procedures are maintained within the boundaries of regulatory compliance. For relevant GxP.


Job Description:
At ***'s Oncology R&D division, we follow the science to explore and innovate. We are working towards treating, preventing, modifying, and even curing some of the world's most complex diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world. We are committed to making a difference and have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs.


Position Summary
The Specialist, Quality ensures compliance with quality system's procedures and assessing
regulatory and quality risks in activities and processes according to regulatory agency
guidelines and company practices. This unique role is accountable for routine Quality Assurance responsibilities related to the production and disposition of products manufactured and tested on behalf of ***. This role is based in Tarzana, CA, and reports to the Manager, QA.


Responsibilities
o Provide quality assurance support across technical operations functions (i.e.
Manufacturing, Facilities & Engineering, Supply Chain, Quality Control, Analytical
Development, Product Development/Manufacturing Sciences & Technology) within
*** to assure compliance to the quality manual and maintain collaborative
quality relationships.
o Lead deviations and laboratory investigations related to GMP manufacturing and
analytical testing, respectively, with cross-functional owners. Determine
corrective/preventative actions (CAPA) and Verification of Effectiveness (VoE) and
drive on-time implementation and closure.
o Work with appropriate partners to manage change controls in a phase appropriate
manner for clinical stage products that supports quality risk management (i.e. New
Product Introduction, New Facility, & Manufacturing Process Change Controls).
o Provide ILT trainings for annual GMP/GDP, Quality Manual, Quality Risk Management,
Deviation/CAPA, Change Control.
o Work with QA doc control to ensure accurate issuance of batch record documentation
(i.e. lot/media batch records and in-process/QC/final product labels) to manufacturing.
o Review routine manufacturing batch documentation and quality control data for in-
process and finished product to support disposition and lot closure.
o Perform approval of equipment alarm acknowledgements, equipment activation and
PM/Calibration schedules in computerized asset and alarm management system(s).
o Review routine material release documentation for quality release of raw materials
used for manufacturing and quality control testing.


Education and Experience
o MA/MS in Biology, Chemistry, Microbiology, Engineering, or a related field is required,
or alternatively, a BA/BS with 2+ years, an Associate's degree with 4+ years, or a High
School diploma with 5+ years of Quality Assurance or GMP experience.
o 2-4 years of Cell Therapy Experience
o Knowledge of and ability to apply GMP in conformance to US standards.
o Proficient in cGMP regulations, quality systems and regulatory requirements.
o Experience writing, evaluating and closing investigations, CAPAs and change control
records.
o Adapt best practices for stage appropriate products.
When we put unexpected teams in the same room, we fuel bold thinking with the power to
inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.


EEO:


"Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans."