MCS Senior Associate Quality Assurance

Thousand Oaks, California

Become a Vital Member of Our Team as a MCS Senior Associate Quality Assurance!

Location: Onsite at Thousand Oaks

Pay Rate: $34/hr – $36/hr

Are you ready to take your career in quality assurance to the next level? We’re seeking a talented individual to join our team as a MCS Senior Associate Quality Assurance. In this role, you’ll play a crucial role in ensuring compliance and quality in Drug Substance manufacturing at Thousand Oaks.

Job Summary:

  • As a MCS Senior Associate Quality Assurance, you’ll provide daily oversight of Drug Substance manufacturing facilities, supporting our client’s Quality Assurance program.
  • Your responsibilities will include electronic batch record review, batch record review, SOP and MP revision approval, work order approval, and quality approval of non-conformances and CAPAs. You’ll also evaluate compliance issues, provide recommendations, and ensure the progress of quality records to completion. Additionally, you’ll represent functional area quality for the Bulk Quality Assurance department and collaborate on projects to achieve operational excellence goals.

Responsibilities:

  • Provide daily oversight of Drug Substance manufacturing facilities.
  • Review electronic and batch records for compliance.
  • Approve SOP and MP revisions.
  • Approve work orders and quality documents.
  • Evaluate compliance issues and provide recommendations.
  • Assure progress of quality records to completion.
  • Represent functional area quality and collaborate on achieving operational excellence goals.

Skills Required:

  • Experience working with Quality Systems / QA.
  • Ability to perform GMP operations.
  • Batch Record Experience (Manufacturing Background Experience).
  • Bachelor’s Degree in Biochemistry, Biology, Chemistry, or related science field.
  • Attention to detail and strong organizational skills.
  • Analytical mindset with problem-solving abilities.
  • Strong communication and interpersonal skills.

If you’re passionate about quality assurance and ready to make a meaningful impact in pharmaceutical manufacturing, we want to hear from you! Apply now to join our team and contribute to ensuring compliance and quality in Drug Substance manufacturing.

About SSi People: 
With over 25 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. 

 

 

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