Job Title: Senior Associate Manufacturing
Location: Thousand Oaks, California (Onsite)
Job Summary: We are seeking a dedicated professional to join our team in supporting critical drug product manufacturing operations. Our team prioritizes maintaining the highest standards of safety, quality, and compliance to ensure efficient and reliable production outcomes.
Responsibilities:
- Execute drug product filling activities and conduct initial review of manufacturing batch records.
- Maintain a safe environment by adhering to compliance standards and implementing preventative measures.
- Lead continuous improvement initiatives across multiple functional areas and perform data analysis of critical process parameters.
- Support the introduction of new products and technologies while utilizing relevant systems to manage quality records and manufacturing activities.
Experience/Minimum Requirements:
- Demonstrated knowledge of GMP principles in a production environment.
- Experience in project management with the ability to collaborate in cross-functional team settings.
- Minimum educational requirement: Master’s degree; or Bachelor’s degree with 2 years of experience, or Associate’s degree with 4 years of experience; or high school diploma/GED with 6 years of experience.
- Strong interpersonal skills, attention to safety, and capability to craft or revise standard procedures as needed.
About SSI People: 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 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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