Empower Quality Excellence: Elevate Your Career as a MCS Senior Associate Quality Assurance!
Location: Thousand Oaks, CA (Onsite)
Competitive Pay: $34/hr – $36/hr
Are You Ready to Make an Impact in Quality Assurance?
We’re seeking a passionate and detail-oriented Quality Assurance Senior Associate to join our team. If you’re committed to ensuring compliance, driving operational excellence, and making a difference in the pharmaceutical industry, this role is for you!
Why Join Us?
- Impactful Work: Play a vital role in overseeing Drug Substance manufacturing areas, ensuring compliance with quality standards.
- Professional Growth: Expand your skills and expertise through challenging projects and continuous learning opportunities.
- Collaborative Culture: Join a supportive team where collaboration, innovation, and excellence are celebrated.
- Rewarding Benefits: Enjoy competitive compensation, comprehensive benefits, and perks that recognize your contributions.
Key Responsibilities:
- Daily Oversight: Provide daily oversight of Drug Substance manufacturing facilities, ensuring adherence to processes and procedures.
- Compliance Review: Review electronic batch records, SOPs, and work orders to ensure compliance with regulatory requirements.
- Deviation Approval: Approve deviations and CAPAs, ensuring timely completion of quality records.
- Continuous Improvement: Evaluate compliance issues, provide recommendations for improvement, and represent the department in projects to achieve operational goals.
- Cross-Functional Collaboration: Collaborate with cross-functional teams, adapt to shifting priorities, and maintain training and documentation practices.
- GMP Operations: Maintain training and documentation practices according to GMP operations, ensuring adherence to quality standards.
- Representation: Represent the department in projects and initiatives to drive operational excellence and quality assurance.
Desired Skills:
- Experience with Quality Systems and QA processes.
- Proficiency in batch record review and electronic record management.
- Knowledge of Plant Quality Assurance principles and manufacturing oversight.
- Ability to work cross-functionally and adapt to changing business needs.
- Bachelor’s Degree in Biochemistry, Biology, Chemistry, or related field.
- Strong organizational and multitasking skills.
- Effective communication and leadership attributes.
Ready to Make a Difference in Quality Assurance?
If you’re ready to take on a challenging and rewarding role in ensuring compliance and operational excellence, apply now! Join us in our mission to deliver life-changing therapies to patients worldwide.
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.