Sr Mgr Quality Control

Job title: Sr Mgr Quality Control in Thousand Oaks, CA at Amgen Company: Amgen Job description: Career Category QualityJob DescriptionJoin Amgen’s Mission of Serving PatientsAt Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.Senior Manager Quality ControlWhat you will doLet’s do this! Let’s change the world! In this vital role, you will lead the Amgen Thousand Oaks, Quality Control Microbiology Laboratories. This is a unique opportunity to learn about and support testing of Amgen products through various stages of the product lifecycle. The QC Senior Manager will report directly to the Director of Quality Control and as a member of the QC leadership team will contribute to fostering and further developing a culture of safety, quality and compliance.The QC Senior Manager will be accountable for the following functions in support of core QC laboratory operations:Microbiology Laboratory:

• Oversight of the QC Microbiology Lab operations including Environmental Monitoring
• Responsible for presenting the QC Microbiology lab area during audits and inspections and directly interacting with regulators
• Lead laboratory troubleshooting and problem-solving exercises
• Oversight of Microbiology laboratory investigations
• Support the implementation of new equipment and technologies
• Support staff training, career development and performance management
• Responsible for ensuring compliance with safety guidelines, cGMPs and other applicable regulatory requirements.

Additional Responsibilities:

• Participate in Amgen global network teams
• Establish and enable LEAN principles across area of responsibility
• Establish and enable department goals, strategies and KPIs
• Champion site and QC global process improvements
• Interfaces with management on significant matters, often requiring the coordination of activity across organizational units
• Plans and organizes project assignments of substantial variety and complexity
• Translates complex data into actionable information and applies strong technical knowledge to meet business objectives
• Identifies process gaps, introduces innovative solutions, and leads operational excellence projects to improve efficiency and productivity, while decreasing expense/operating costs.
• Leads root cause analysis discussions for more complex problems to develop and efficiently implement effective permanent solutions.

What we expect of youWe are all different, yet we all use our unique contributions to serve patients. The experienced professional we seek is a strong leader with these qualifications.Basic Qualifications:Doctorate degree and 2 years of quality experienceOrMaster’s degree and 6 years of quality experienceOrBachelor’s degree and 8 years of quality experienceOrAssociate’s degree and 10 years of quality experienceOrHigh school diploma / GED and 12 years of quality experienceIn addition to meeting at least one of the above requirements, you must have a minimum of 2 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced abovePreferred Qualifications:

• Working knowledge of cGMP regulations, practices, and trends pertaining to Quality Control.
• Experience managing staff and/or leading teams, projects, programs or directing the allocation of resources.
• Excellent written and verbal communication skills, ability to work in a team matrix environment and build relationships with partners.
• Track record of building or participating as a member of high performing team.
• Experience in leading and owning complex investigations.
• Experience in auditing and defending processes, procedures and decisions during regulatory inspections.
• Experience with various laboratory computer systems and applications.
• Strong leadership and negotiation skills with a demonstrated ability to influence different styles.
• Demonstrated innovative thinking and ability to transform work organizations.
• Strong technical writing skills within a highly regulated environment.
• Exposure to Operational Excellence initiatives.
• Understanding of quality management systems and quality control processes related to drug substance and drug product for clinical and commercial operations.
• Demonstrated ability to navigate through ambiguity and provide structured problem solving.
• Demonstrated ability to coordinate multi-functional project teams and deliver on schedule.
• Demonstrated ability to coordinate and lead cross-functional teams.
• Demonstrated ability to find opportunities and implement new technologies and services to transform the business into a more agile, efficient and effective organization.
• Demonstrated skills in staff motivation, coaching/mentoring and professional development.
• Great teammate who is able to collaborate and provide leadership through influence to achieve the required results.

What you can expect of usAs we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

• A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans
• Flexible work models, including remote and hybrid work arrangements, where possible

Apply now and make a lasting impact with the Amgen team.careers.amgen.comIn any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.Application deadlineAmgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation..Salary Range 145,470.00 USD - 176,758.00 USD Expected salary: $145470 - 176758 per year Location: Thousand Oaks, CA Apply for the job now! Apply for this job