A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That's what makes us Roche.
As a Process Validation Coordinator, you are joining a dedicated technical project team focused on ensuring the highest quality standards for critical health authority submissions. This role offers a unique opportunity to cultivate strong collaborative relationships while driving process improvements and compliance across multiple departments. You will work in an atmosphere of openness and trust, leveraging your communication skills to manage vital documents that directly impact our strategic healthcare goals.
The Opportunity:
- You are coordinating assigned Process Validation (PV) study documents for projects and supporting vital Health Authority submissions.
- You are proofreading, editing, and compiling supporting data for PV protocols and reports to ensure accuracy, completeness, and consistency.
- You are coordinating the adjudication of reviewers’ comments with authors and Subject Matter Experts (SMEs), providing timely follow-ups to outstanding queries.
- You are performing compliance reviews of completed PV work to guarantee strict alignment with internal Quality standards and requirements.
- You are facilitating PV template creation and assisting in training cross-functional teams on workflows, timelines, and compliance requirements.
- You are communicating effectively with cross-functional project teams, presenting PV activities at department meetings, and resolving conflicts in a positive manner.
- You are utilizing appropriate IT solutions and tools to manage process knowledge and gathering key technical information to keep systems updated.
Who you are:
- You hold a Bachelor’s degree or higher and have 0-2 years of relevant work experience in the process validation area.
- You are experienced with process validation documentation requirements and possess excellent business acumen and solid judgment to work autonomously.
- You are a strong communicator with interpersonal skills that allow you to establish collaborative relationships, resolve conflicts positively, and influence without authority.
- You are a highly motivated self-starter equipped with strong project management skills to consistently achieve multiple tasks on time.
- You are highly adaptable and capable of handling multiple priorities, conflicts, and ambiguity effectively.
Preferred:
- You have hands-on experience authoring and/or editing process validation documentation.
Relocation benefits are not available for this posting
The expected salary range for this position based on the primary location of San Francisco, CA is 72 600,00 - 134 800,00 USD Annual. 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. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
Skills Required
- Bachelor’s degree or higher
- 0–2 years of relevant experience in process validation
- Experience with process validation documentation requirements
- Strong business acumen and judgment to work autonomously
- Strong communication and interpersonal skills
- Ability to establish collaborative relationships, resolve conflicts positively, and influence without authority
- Strong project management skills and ability to complete multiple tasks on time
- Ability to manage multiple priorities, conflicts, and ambiguity effectively
- Hands-on experience authoring or editing process validation documentation
Genentech Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Genentech and has not been reviewed or approved by Genentech.
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Healthcare Strength — Health coverage is described as comprehensive across medical, dental, vision, mental health, and prescriptions, supported by HSAs/FSAs and broad wellness resources. On‑site fitness and health centers, mental‑health clinicians, and specialized programs like fully covered preventive cancer screenings and menopause support deepen the offering.
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Retirement Support — Retirement benefits feature a 401(k) with up to a 4% company match plus an additional annual 6% company contribution to eligible pay. Additional financial protections such as life and accident insurance complement salary, bonuses, and stock options.
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Leave & Time Off Breadth — Time away includes about 20 paid vacation days, paid holidays, personal days, and a year‑end shutdown. A paid six‑week sabbatical every six years notably expands long‑term time‑off flexibility.
Genentech Insights
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.
