Browse New and Exciting Opportunities
So sorry, this position is no longer available.
Please go ahead and submit your application. We may have other positions that would be the perfect fit for you.
Alternatively, you may want to apply to one of the following related jobs:
MCS Senior Associate, Quality Assurance
Job Description
Our client is seeking a Senior Associate, Quality Assurance (MCS) to provide real-time, floor-based QA support in a dynamic manufacturing environment. This fully onsite role involves rotating between day and swing shifts every six months, beginning with day shift for comprehensive training. The position supports clinical and commercial drug substance production, ensuring compliance through cleanroom oversight, batch record review, and acting as a QA liaison during manufacturing and facility events. The role offers an excellent opportunity to work closely with manufacturing teams, uphold quality standards, and contribute to the continuous improvement of the quality system within a fast-paced, regulated environment.
Key Responsibilities:
- Maintain a purposeful presence on the production floor to oversee manufacturing operations.
- Review electronic batch records for accuracy and compliance.
- Revise and approve Standard Operating Procedures (SOPs) to ensure adherence to quality standards.
- Approve work orders and minor deviations, ensuring timely resolution and documentation.
- Evaluate compliance issues and provide actionable recommendations to address them.
- Support and ensure the timely completion of quality records and documentation.
- Represent the Quality Assurance department in project execution to meet departmental goals.
- Collaborate effectively within a team matrix environment, providing support across departments.
- Act as a quality ambassador during manufacturing and facility events, facilitating communication and resolution.
Qualifications:
- High school diploma or GED with 2 years of industry experience, Associate’s degree with 6 months of experience, or Bachelor’s degree.
- Preferred: Bachelor’s degree in Biochemistry, Biology, Chemistry, or related scientific discipline.
- Demonstrated knowledge of GMP operations, including following detailed SOPs, maintaining training records, and practicing good documentation.
- Ability to make informed quality decisions based on compliance standards.
- Experience managing projects to completion within established timelines.
- Proficiency in evaluating documentation and operational processes according to company procedures.
- Familiarity with Quality Systems and strong organizational skills.
- Excellent verbal and written communication abilities.
- Ability to work independently and as part of a team, displaying leadership qualities and initiative.
Work Location: Onsite - Thousand Oaks, California
Share This Job:
Related Jobs:
Login to save this search and get notified of similar positions.About Thousand Oaks, CA
Ready to take your career to the next level in the vibrant city of Thousand Oaks, California? Nestled in the heart of Ventura County, this bustling city offers a perfect blend of suburban charm and urban amenities. With a strong job market, top-notch schools, and breathtaking views of the Santa Monica Mountains, Thousand Oaks is an ideal location for professionals seeking growth and fulfillment. Explore job opportunities near iconic sites like the Gardens of the World, catch a show at the Fred Kavli Theatre, or indulge in the local culinary scene featuring dishes from around the world. Join this dynamic community and unlock your potential in Thousand Oaks! Start your job search now to find your perfect fit in this captivating city.