Job Information
Quality Consulting Group Sr. Manufacturing Associate in Thousand Oaks, California
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:
Responsible for managing and owning Corrective and Preventative Actions (CAPAs) and Effectiveness Verifications (EVs) in support of the B7 restart of Epogen production.
Participate in continuous improvement initiatives and utilize project management skills to achieve operational excellence.
Work in a cross-functional team and collaborate with various stakeholders to ensure quality and compliance.
Adhere to all applicable policies, procedures, and standards, such as cGMP, SOPs, and EHS.
Use project management tools and methodologies to plan, monitor, and report on project progress and outcomes.
Qualifications:
Bachelor’s degree in engineering, science, or related field, or equivalent combination of education and experience.
3 Years of experience in GMP and manufacturing background
Experience in pharma, biotech or medical device industry.
high level of initiative and accountability
Experience writing deviations.
Experience with CAPA and EV ownership and execution, preferably using Trackwise or similar quality system.
Knowledge of viva vault, smart sheets, MS Project, Agile.
Standard shift (M-F 8am-5pm)
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
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