What are the responsibilities and job description for the Senior Associate Quality Assurance position at SSi People?
Job Title: Senior Associate Quality Assurance
Location: Thousand Oaks, CA (Onsite)
Job Summary
With over 26 years of industry experience, SSi People has built its reputation and expertise on putting people first. Everything we do works toward delivering an exceptional experience for our consultants, our clients, and our internal team. Through a genuine commitment to people in everything we do. We have developed refined processes and a stellar internal team to deliver talent quickly. More importantly, we focus on building long-term relationships, not transactions. Putting people first is just what we do well.
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from SSi People and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: SSi People Privacy Policy
Location: Thousand Oaks, CA (Onsite)
Job Summary
- We are is seeking a dedicated and meticulous Senior Associate Quality Assurance to join our team. This role is integral to ensuring the highest standards of quality and compliance in the manufacturing areas of Drug Product. The successful candidate will be responsible for daily oversight, evaluating compliance issues, and ensuring the timely completion of quality records.
- Provide daily oversight of the Drug Product manufacturing areas.
- Evaluate compliance issues, provide recommendations, and ensure progress of quality records to completion.
- Represent functional area quality for the Drug Product Quality Assurance department in project execution.
- Review electronic batch records and approve SOP revisions.
- Approve work orders and job plans in the Maximo System.
- Provide quality support and approval for minor deviations and CAPA records.
- Bachelor’s Degree in Biochemistry, Biology, Chemistry, or related science field.
- Experience in GMP operations, including following detailed SOPs, maintaining training, and good documentation practices.
- Proven ability to manage projects to completion within timelines.
- Experience working with Quality Systems.
- Strong organizational skills and ability to manage multiple tasks simultaneously.
- Effective communication skills (both written and verbal).
- 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.
With over 26 years of industry experience, SSi People has built its reputation and expertise on putting people first. Everything we do works toward delivering an exceptional experience for our consultants, our clients, and our internal team. Through a genuine commitment to people in everything we do. We have developed refined processes and a stellar internal team to deliver talent quickly. More importantly, we focus on building long-term relationships, not transactions. Putting people first is just what we do well.
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from SSi People and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: SSi People Privacy Policy
