QC Supervisor – Second Shift

Job Description The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in capacity and expansion of its Colorado operations. Join our team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life changing, lifesaving medicines. The QC Supervisor will oversee activities assigned to Quality Control (QC) and supervise a group of QC analysts. They will ensure workload and priorities are met and will be required to supervise staff and perform laboratory testing and review in support of the workload. The supervisor will also ensure QC operations are in compliance with current Good Manufacturing Practices (cGMP) and other regulatory guidance. Essential Job Responsibilities: - Supervise QC personnel to support in-process testing - Exercise judgment within defined procedures and policies to determine appropriate action - Act as the shift supervisor and become actively involved as an analyst as required to meet schedules and resolve problems - Prioritize and arrange the workload to ensure in-process testing timelines are met - Delegate effectively and exercise judgment when escalating issues to QC upper management - Write, review and revise standard operating procedures, associated Quality Control functions, and analytical test methods - Generate, process and/or review analytical data - Review data for compliance to specifications and report anomalous results to the Quality Manager and Quality Assurance, as appropriate - Assist with QC-related deviations, inquiries/investigations, and corrective/preventative actions (CAPAs) - Be directly involved in client audits and regulatory inspections - Ensure that quality products are designed and manufactured by Agilent, and are in alignment and compliance with national, regional and global regulations, company policies and business objectives - Develop and implement programs and processes to ensure that Agilent products are safe, legal, and meet or exceed customer expectations for regulatory compliance - Oversee and advise quality and/or regulatory activities and drive key strategic programs within assigned area of responsibility - Act as a change agent to help establish a customer-centered culture - Ensure quality management system procedures are accurate and current - Provide expertise in translating regulatory requirements into practical, workable plans - Represent the company in industry associations and standards bodies and may work with regulatory agencies - May lead development and implementation of standards, methods and procedures for inspecting, testing and evaluating the precision, accuracy and reliability of company products - May lead generation and review of documentation used in good manufacturing practices - May supervise audits of production and quality control areas and raw material vendors - Select, develop and evaluate personnel to ensure the efficient operation of the function - Supervise individual contributors responsible for routine tasks - Assign and direct implementation of tasks and processes - Establish, maintain business controls and processes Second Shift - 2:30 pm - 11 pm Qualifications Required: - Secondary education with relevant experience - Two years of QC experience - Knowledge and skill using basic computer software and hardware applications, including Microsoft Word and Excel - Excellent written and oral communication skills - Ability to multi-task and lead various projects and competing priorities Desired: - Bachelor of Science preferred - Experience in a cGMP environment - One year of experience formally or informally leading people - Experience with lab equipment: HPLC, LCMS, UV, GC - Ability to write and review protocols, reports, and procedures Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least April 15, 2026 or until the job is no longer posted. The full-time equivalent pay range for this position is $105,280.00 - $164,500.00/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 merit-based employer that values individuals of all backgrounds 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 creating and maintaining an inclusive workplace where everyone is welcome, 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 job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility. Travel Required: No Shift: Day Duration: No End Date Job Function: Quality/Regulatory