Job Information
US Tech Solutions MCS Senior Associate Quality Assurance in Thousand Oaks, California
$32.00-$36.14 per hour
Thousand Oaks, CA
Contract
Duration: 12 months contract
Shift: Must be flexible as it is possible, will start on any shift and rotate every 6 months.
DAY: 6 AM - 5 PM
SWING: 1 PM to 12 AM
NIGHT: 7 PM - 8 AM
Will change based on the manufacturing team they are supporting (Upstream/Downstream) and rotate every 6 months.
Job Description:
The ideal candidate will have 1–2+ years of hands-on experience in a regulated GMP environment, preferably within the pharmaceutical, biotech, or food industries. While a bachelor’s degree in a relevant scientific field (e.g., biology, chemistry, biochemistry) is preferred, direct industry experience is more important. Candidates should be familiar with manufacturing or quality operations and understand the pace and expectations of a high-volume, highly cross-functional environment. This role requires individuals who are proactive, able to work independently with minimal oversight, and comfortable escalating issues appropriately.
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 . 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:
High school/GED + 2 years work experience OR
Associate’s and 6 months work experience OR
Bachelor’s
Must Have Skill Sets:
Organizational skills
Critical thinking ability
Team player mindset
Nice to have: Batch record experience
Day to Day Responsibilities:
- On the floor support giving PQA support for Manufacturing support. Record review and approval for BRRs, Deviations and SOPs. On the floor support giving PQA support for Manufacturing support. Record review and approval for BRRs, Deviations and SOPs.
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com .
"US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran"