Quality Control Lab Manager

Agilent Technologies; Carpinteria (CA); On-site; USD 132,000 - 208,000; Full time

Job summary

An established industry player is seeking a dynamic QC Lab Manager to oversee quality control testing in Carpinteria, CA. This pivotal role involves leading a team to ensure compliance with GMP and GLP standards while driving continuous improvement initiatives. You'll champion digital transformation efforts and optimize the Quality Management System, all while fostering a diverse and inclusive work environment. With a focus on delivering life-saving diagnostics, this position offers a unique opportunity to make a significant impact in the field of life sciences.

Qualifications

• 1+ years of experience leading teams in quality control.
• Experience with GMP and GLP in medical device regulations.

Responsibilities

• Lead quality control testing and ensure on-time production.
• Drive digital transformation and laboratory automation.

Skills

Leadership

Continuous Improvement

Quality Control Testing

GMP Compliance

Digital Transformation

Education

Bachelor’s Degree in Life Sciences

Master’s Degree in Life Sciences

Tools

SAP ERP

Agile QMS

SLIMS

Job description

Quality Control Lab Manager page is loaded

Quality Control Lab Manager

Apply locations US-CA-Carpinteria time type Full time posted on Posted 6 Days Ago job requisition id 4032057

Job Description

Agilent Technologies is seeking a dynamic QC Lab Manager to join our team in Carpinteria, CA. The manager is responsible for overseeing a team of direct reports to provide quality control testing of our Immunohistochemistry (IHC) and Artisan product lines. This role interacts across the organization on departmental goals and initiatives and works cross functionally on projects to improve the organization and support NPI. This pivotal role is your chance to lead a team into the future, driving the strategy to create an integrated, lean quality control department that supports seamless manufacturing flow and delivers life-saving diagnostics to our customers when they need them most.

Key Responsibilities:

• Quality Control Testing of Products: lead team to ensure on-time production and elevate overall efficiency.

• Champion Continuous Improvement and LEAN Principles: Lead initiatives that apply continuous improvement and LEAN principles to drive transformative efficiencies within the department.

• Drive Digital Transformation and Laboratory Automation: Identify cutting-edge technologies and craft compelling business cases to support digital transformation and laboratory automation.

• Ensure GMP and GLP Compliance: Maintain rigorous compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) in line with medical device regulations.

• Optimize Quality Management System (QMS): Ensure QMS procedures are precise and up-to-date, act as a key SME in audits to uphold the highest standards in production and quality control. Leads Corrective and Preventative Action (CAPA) investigations and Non-Conformance (NCR) observations for the Production QC department.

• Integration of NPI Ensures that quality products are designed and manufactured by Agilent, and are in alignment and in compliance with national, regional and global regulations, company policies and business objectives

• Lead a Diverse Team to Success: Inspire and guide a diverse team of quality associates, fostering an inclusive and collaborative work environment.

• Develop Talent and Training: Create robust development plans for team members and identify training opportunities to enhance their skills and career growth.

• Adhere to KPIs and Drive Quality Initiatives: Monitor key performance indicators (KPIs) and lead initiatives to continuously improve quality control processes and outcomes.

Qualifications

• Bachelor’s or Master’s Degree in a life sciences field.

• Minimum of 1+ years of experience leading people, projects, and/or programs.

• Immunohistochemistry (IHC) Scoring experience: Demonstrated experience in scoring IHC and histology is a plus.

• Familiarity with SAP ERP, Agile QMS, and SLIMS or equivalent systems.

• Proven experience with GMP and GLP in the context of medical device regulations.

Additional Details

This job has a full time weekly schedule. Applications for this job will be accepted until at least May 8, 2025 or until the job is no longer posted.The full-time equivalent pay range for this position is $132,851.00 - $207,580.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations Agilent Technologies, Inc. is an Equal Employment Opportunity and Affirmative Action employer. We value diversity at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to diversity in the workplace and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email [e-mail] or contact [phone]. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.

Travel Required:

Occasional

Shift:

Day

Duration:

No End Date

Job Function:

Quality/Regulatory

View Graduate and Student Job Search and Apply

As a global leader in laboratory and clinical technologies, we are passionate about bringing great science to life.

Our commitment to quality and innovation supports cutting-edge life science research, patient diagnostics, and ensures the safety of water, food, and pharmaceuticals. As scientists and clinicians pursue small, everyday advances and life-changing discoveries, we provide trusted answers to their most critical questions and challenges.

Leveraging more than 50 years of expertise, we create advanced instruments, software, and consumables supported by teams of highly skilled and knowledgeable people. With 18,000 employees around the world, our global reach and comprehensive solutions provide the most reliable and accurate results, as well as optimal scientific, economic, and operational outcomes. We work collaboratively with our customers on their journey to make a real difference in human lives. Our culture is founded on trust, respect, and uncompromising integrity, and we pride ourselves on being a dynamic and inclusive workplace that celebrates diversity and fosters innovation.

We can’t wait for you to join us as we continue our mission to improve the world around us. Information about Agilent is available at Agilent.com .