Do people naturally turn to you when something needs to get done?  Can you juggle multiple projects, coordinate across functional groups, diving into technical details as well as high-level prioritization, all without breaking a sweat? Do you find genetics fascinating and want to help people understand what their DNA says about them?

We're looking for a person with a talent for managing complex projects, processes, and documentation. This is your chance to join a passionate, ambitious team that is creating truly novel technologies and products to help turn genetic insights into better health and personal understanding.

WHAT YOU’LL DO

• Manage projects while meeting evolving regulatory requirements and business goals.
• Create high-quality documentation of product development activities and assist with other quality system documentation needs.
• Track and schedule project plans, meetings, and deliverables.
• Liaise with stakeholders on a regular basis to ensure cross-functional alignment and timely execution of projects.

WE HOPE YOU HAVE

• A degree in the life sciences, engineering, or technical field.
• A minimum of 2 years work experience in biotech, research, healthcare or software industries.
• Outstanding organizational and time management skills.
• Impeccable attention to detail and an ability to be proactive, thorough, and independent.
• Excellent verbal and written communication; able to communicate clearly and effectively whether one-on-one or with a large project team.
• An ability to assess the needs of different stakeholders and foster collaboration and alignment among diverse cross-functional teams.
• Experience working with technical documentation (_e.g. _SOPs, study protocols, project plans, etc).

PLUSES

• Proficiency with program/project management tools (e.g. spreadsheets, JIRA, presentations, etc.).
• Familiarity with human disease and the fundamentals of human genetics.
• Familiarity with medical device and quality system regulations (21 CFR 820 and ISO 13485), including document control, change control, and design control.

ABOUT US 23andMe, Inc. is the leading consumer genetics and research company. Our mission is to help people access, understand and benefit from the human genome. The company was named by MIT Technology Review to its “50 Smartest Companies, 2017” list, and named one of Fast Company’s “25 Brands That Matter Now, 2017”. 23andMe has millions of customers worldwide, with ~85 percent of customers consented to participate in research. 23andMe is located in Mountain View, CA. More information is available at www.23andMe.com. _At 23andMe we value a diverse, inclusive workforce and we provide equal employment opportunity for all applicants and employees. All qualified applicants for employment will be considered without regard to an individual’s race, color, sex, gender identity, gender expression, religion, age, national origin or ancestry, citizenship, physical or mental disability, medical condition, family care status, marital status, domestic partner status, sexual orientation, genetic information, military or veteran status, or any other basis protected by federal, state or local laws. 23andMe will reasonably accommodate qualified individuals with disabilities to the extent required by applicable law. _Please note: 23andMe does not accept agency resumes and we are not responsible for any fees related to unsolicited resumes. Thank you.