Manager, Quality (Chromatography)

Posted 11 Days Ago
Be an Early Applicant
Oceanside, CA
99K-185K Annually
Senior level
Healthtech • Biotech
The Role
As the Manager, Quality (Chromatography), you will oversee the Quality Control group, ensuring compliance with GMP standards and accuracy of results. You will implement innovative standards, manage staff performance, prioritize departmental activities, and represent the department during regulatory inspections. Your role will also focus on developing cost-effective solutions while maintaining high quality standards.
Summary Generated by Built In

As the Manager, Quality (Chromatography), you will be accountable for a Quality Control group supporting Genentech’s Oceanside biochemical bulk manufacturing facility.

You will have the opportunity to develop and implement innovative standards, methods, and procedures that help us achieve our quality goals. You will be responsible for overseeing the day-to-day activities of our Quality Control group, ensuring the laboratory upholds GMP compliance, produces meticulous documentation, and delivers accurate results. This is your chance to make a significant impact and drive excellence in everything we do!

The Opportunity

  • Plan, initiate, implement and oversee department activities with a focus upon ensuring attainment of department and corporate objectives within specified timelines.

  • Provide overall direction and performance management and career development for subordinate staff. Administer schedules and performance requirements for the department, including responsibility for results in terms of costs, methods and employees.

  • Review and approve recommendations and/or analytical QC data presented by subordinate(s) as appropriate. Investigate the feasibility of and develop new and creative ways to apply new technologies to achieve corporate objectives.

  • Participate with senior management in the decision making process for capital equipment expenditures and the acquisition of new technologies.

  • Investigate, develop and implement new and creative ways to accomplish department goals in the most cost effective and productive manner while maintaining high quality standards.

  • Act as project leader to coordinate activities between divisions and provide scientific leadership. Represent the department during FDA and/or Regulatory inspections.

  • Responsible for oversight of lab and analysis work. Responsible for collecting, entering data and generating reports from electronic systems.

  • Collaboration with other department managers to ensure proper prioritization and collaboration by having staff cross-trained to support flow to work when needed.

  • All employees with jobs that require access to the Warehouse must be able to pass the Transportation Security Administration (TSA) Security Threat Assessment (STA). Promotes a safety culture that supports continuous improvement in the EHS management system through active communication and functional area participation in site safety teams ensuring the safe and efficient operation of assigned functional areas and activities. Fosters a positive safety culture in which no one gets hurt.

Who you are

  • Bachelor’s Degree in Biology, Chemistry, Biochemistry, Microbiology or other
    relevant Life Science discipline.

  • 10 years experience including 3 years in supervisory role 

  • Including 9 years experience in a pharmaceutical/biotechnology lab.

  • Supervisory and Management Skills: Experience supervising technical staff in a Quality Control and/or cGMP environment, with excellent project management, personnel management, and interpersonal skills.

  • Communication and Presentation Skills: Strong written and verbal communication skills, and the ability to deliver professional presentations to external business interests.

  • Technical and Collaborative Abilities: Ability to work independently and as part of a team, familiarity with diverse scientific disciplines, proficiency in spreadsheets, word processing, database management, and willingness to work non-standard hours when required.

Relocation benefits are not available for this posting

The expected salary range for this position based on the primary location of California is $99,400-$184,600. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.

Benefits

    Genentech is an equal opportunity employer, and we embrace the increasingly diverse world around us. Genentech prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status and veteran status.

    The Company
    HQ: South San Francisco, CA
    20,069 Employees
    On-site Workplace
    Year Founded: 1976

    What We Do

    Considered the founder of the industry, Genentech, now a member of the Roche Group, has been delivering on the promise of biotechnology for more than 40 years.

    Genentech is a biotechnology company dedicated to pursuing groundbreaking science to discover and develop medicines for people with serious and life-threatening diseases. Our transformational discoveries include the first targeted antibody for cancer and the first medicine for primary progressive multiple sclerosis.

    We're passionate about finding solutions for people facing the world's most difficult-to-treat conditions. That is why we use cutting-edge science to create and deliver innovative medicines around the globe. To us, science is personal.

    Making a difference in the lives of millions starts when you make a change in yours.

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