Director, Quality Control Microbiology- Biologics/Small Molecules

QC Microbiology DirectorAt Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.The QC Microbiology Director is a vital role for the success of Clinical and Commercial Biologics and Small Molecule Quality Control. This individual provides strategic leadership and oversees daily microbiological operations. Responsibilities include leading the microbiology QC team supporting both clinical and commercial programs for biologics and small molecule sectors. This individual is committed to personnel interactions (approachable) and mentoring of staff for timely project completion and regulatory compliance. The leader collaborates with cross-functional teams, works with CTLs, and fosters a culture of continuous improvement.Job ResponsibilitiesLead the development and implementation of end-to-end Quality Control (QC) microbiological strategies for Gilead's biologics and small molecules products, including setting up specifications for e.g. cell banks, product, raw materials, environmental monitoring/facilities, etc. Ensure that these strategies are effectively applied across all stages of the product clinical to commercial lifecycle.Lead and Develop Teams. Provide leadership, guidance, and motivation to direct reports and project teams. Focus on developing strong leaders within the QC department, ensuring they are equipped to make critical decisions and meet project timelines.Proactively manage daily internal and external business which includes interactions with internal teams, CMO project leads, and management to plan, develop, and coordinate activities to set up/review/track and trend adventitious agent testing such as sterility, endotoxins, bioburden, micro-biological identification, particulate matter, and environmental monitoring.Develop and implement innovative technologies, methods, and processes for microbial analysis.Ensuring that all laboratory activities (internal and external) are conducted in compliance with relevant regulations and guidelines.Providing scientific leadership and technical expertise to the laboratory teams.Drive qualification, implementation and execution of micro USP methods for biological and small molecule product includes in-process, release and stabilitySupport microbiology quality events.Author and/or review microbiology procedures including protocols and reportsManage sample submission to third party for microbial identification.Manage and develop microbiology personnel and work closely with internal and external teams.Work closely with quality on defining and implementing aseptic techniques and cross contamination controls.Future management and oversight of the day-to-day operations of the microbiology laboratory, including sample processing, data analysis, and reporting. Undertake facility environmental trend reporting.Work with accuracy, urgency and a continuous improvement perspective.Represent Gilead as Microbiology subject matter expert. Interface with Regulatory agencies as required representing Gilead to authorities and regulatory inspectorates in matters relating to GxP.Basic Qualifications:PhD with 8+ years of relevant experience in the pharmaceutical industry ORMaster's degree with 10+ years of relevant experience in the pharmaceutical industry ORBachelor's degree with 12+ years of experience in the pharmaceutical industry ORAssociate's degree with 14+ years of experience in the pharmaceutical industry ORHigh School Degree with 16+ years of experience in the pharmaceutical industry.Preferred Qualifications4+ years of relevant experience in a GMP Microbiology Lab environment, including knowledge of microbiological testing, experience with aseptic processing, including sterile liquid handling and manipulation, familiarity with microbiology laboratory instrumentation and environmental monitoring.Must have experience with GMP systems (e.g. LIMS, QMS, SAP) and software such as Empower, JMP, Discoverant.Deep knowledge and experience in Biopharmaceutical or Pharmaceutical quality control. Stays ahead of shifting microbiological trends in industry.Prior senior leadership experience required.Must think critically and creatively and be able to work independently to determine appropriate resources for resolution of problems.Strong organizational and planning skills.Shows excellent verbal and written communication skills and collaborative interpersonal skills.The salary range for this position is: $210,375.00 - $272,250.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans.Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com for assistance.Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.Please apply via the Internal Career Opportunities portal in Workday.