Highlights
Key Responsibilities (include but are not limited to): To provide QA oversight and approval of deviation, OOS, and change control records that have moderate to significant levels of complexity and/or novelty. Provide QA support resolving in-process product, final product, manufacturing, environmental, facility and equipment and material issues.
Numbers & Facts
| Location | El Segundo, CA |
| Industry | Staffing/Employment Agencies |
| Salary | $44.24 |
| Company Size | 2,000 to 2,499 employees |
| Year Founded | 2000 |
| Website | http://www.lancesoft.com/ |
Description
Location: El Segundo, CA
Job Description
We are seeking a highly motivated individual to join us as a Quality Assurance Specialist II. In this role you will be responsible for executing a variety of Quality activities to ensure compliance with applicable quality objectives and regulatory requirements.
You will be located at our El Segundo, CA site and report into the Sr. Manager of Quality Assurance Operations.
The standard work week for this position is M-F, however weekend/night work will be required during manufacturing campaigns to support process operations
Key Responsibilities (include but are not limited to):
To provide QA oversight and approval of deviation, OOS, and change control records that have moderate to significant levels of complexity and/or novelty. Ensure records are properly initiated, investigated and resolved in accordance with established timelines.
To provide QA oversight and approval of CAPA and EV records that have moderate to significant levels of complexity and/or novelty. Ensure CAPAs are initiated and resolved in a timely manner.
Ensure escalation of deviations per procedures
Identify efficiencies in the execution of the Deviation ad CAPA processes at TCF03 in a compliant manner
Provide QA support resolving in-process product, final product, manufacturing, environmental, facility and equipment and material issues.
Additional duties as assigned.
These duties can be delegated to designated deputies of a satisfactory qualification level as needed.
Basic Qualifications:
Master s Degree and OR
Bachelor s Degree and 2+ years experience in the biological sciences or related field OR
AA Degree and 4+ years experience in the biological sciences or related field OR
High School Degree and 5+ years experience in the biological sciences or related field
Preferred Qualifications:
Quality Control background in Analytical, Virological, and Microbiological testing
Working knowledge and ability to apply GMPs in conformance to U.S. And EU standards
Ability to effectively negotiate and build collaboration amongst individuals
Proficient in MS Word, Excel, Power Point and other applications.
Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment
Comfortable in a fast-paced small company environment and able to adjust workload based upon changing priorities
Job Description
We are seeking a highly motivated individual to join us as a Quality Assurance Specialist II. In this role you will be responsible for executing a variety of Quality activities to ensure compliance with applicable quality objectives and regulatory requirements.
You will be located at our El Segundo, CA site and report into the Sr. Manager of Quality Assurance Operations.
The standard work week for this position is M-F, however weekend/night work will be required during manufacturing campaigns to support process operations
Key Responsibilities (include but are not limited to):
To provide QA oversight and approval of deviation, OOS, and change control records that have moderate to significant levels of complexity and/or novelty. Ensure records are properly initiated, investigated and resolved in accordance with established timelines.
To provide QA oversight and approval of CAPA and EV records that have moderate to significant levels of complexity and/or novelty. Ensure CAPAs are initiated and resolved in a timely manner.
Ensure escalation of deviations per procedures
Identify efficiencies in the execution of the Deviation ad CAPA processes at TCF03 in a compliant manner
Provide QA support resolving in-process product, final product, manufacturing, environmental, facility and equipment and material issues.
Additional duties as assigned.
These duties can be delegated to designated deputies of a satisfactory qualification level as needed.
Basic Qualifications:
Master s Degree and OR
Bachelor s Degree and 2+ years experience in the biological sciences or related field OR
AA Degree and 4+ years experience in the biological sciences or related field OR
High School Degree and 5+ years experience in the biological sciences or related field
Preferred Qualifications:
Quality Control background in Analytical, Virological, and Microbiological testing
Working knowledge and ability to apply GMPs in conformance to U.S. And EU standards
Ability to effectively negotiate and build collaboration amongst individuals
Proficient in MS Word, Excel, Power Point and other applications.
Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment
Comfortable in a fast-paced small company environment and able to adjust workload based upon changing priorities
About Company
We are a $125 Million, NMSDC-certified Minority & Woman owned Workforce Solutions Company headquartered in the DC metro area with presence across US with global presence - Canada, Mexico, India, UK, Malaysia, Indonasia, Hongkong, Singapore, UAE. We are specialized in providing Workforce Solutions, SOW project delivery, Engineering Solutions, Creative Services. We currently support 100+ Fortune companies globally and across multiple industry segments. We are currently supporting several massive programs across industry segment nationally/globally (Intel, Ally, AMD, QUALCOMM, Morgan Stanley, Kraft/ Mondelez, MNP, Amdocs, Dell, SanDisk, Medtronic, Becton Dickinson, GE, Lockheed Martin, UTC, L-3 Communications, Caterpillar, BMW, Mercedes Benz, National Grid, Dominion, Energy Future Holdings, PSEG, 3M, Fidelity, Aetna, Humana, Johnson & Johnson, Pfizer, Merck etc).
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, identity, national origin, disability, or protected veteran status.
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