Vir Biotechnology, Inc.
Manager, Regulatory Affairs
Vir Biotechnology, Inc., San Francisco, California, United States, 94199
Manager, Regulatory Affairs-Document Coordinator Join to apply for the
Manager, Regulatory Affairs-Document Coordinator
role at
Vir Biotechnology, Inc. Manager, Regulatory Affairs-Document Coordinator 1 day ago Be among the first 25 applicants Join to apply for the
Manager, Regulatory Affairs-Document Coordinator
role at
Vir Biotechnology, Inc. Vir Biotechnology is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.
Make sure to read the full description below, and please apply immediately if you are confident you meet all the requirements.
We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.
THE OPPORTUNITY
Vir Biotechnology is looing for a Regulatory Affairs Manager to join the regulatory group. The successful candidate, under the guidance of experienced regulatory affairs professionals, will be responsible for the coordination and preparation of documents intended for regulatory submissions for new and mature products (as applicable) to ensure alignment and compliance with local and regional registration requirements as well as with company policies.
What You'll Do
you will represent Regulatory Affairs on cross-functional project teams with the following responsibilities: Coordinate documents intended for regulatory submissions, manage internal reviews and resulting input from cross‑functional team members for products in line with ICH and regional requirements, meets scientific rigor and company policies and procedures Ensures quality and regulatory standards are considered and upheld throughout the product development life cycle Assists with the coordination and tracking of regulatory commitments and submission plans for maintenance activities such as INDs/CTAs, annual reports, periodic safety reports, protocol submissions, and key regulatory filings Participates in group meetings and provides tactical approaches to addressing issues of moderate complexity Participate in the development of processes and procedures relevant to regulatory functions Performs document filing and retrieval functions as directed, or in conjunction with departmental SOPs
Who You Are And What You Bring
BS and 8+ years of Experience, MS and 6+ years of experience with a minimum of 5+ years of regulatory experience Working knowledge of US FDA regulations (ex-US is a plus) and industry standards pertaining to regulatory Knowledge of the drug development process and eCTD Excellent organization skills and ability to work on multiple projects with tight timelines Excellent verbal and written communication skills and interpersonal skills
Who We Are And What We Offer
The expected salary range for this position is $121,500 to $170,500 per year. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.
Vir Biotechnology's compensation and benefits are aligned with the current market and commensurate with the person’s experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, childcare reimbursement, education reimbursement, 401K match and lunch each day in the office.
Applicants must currently be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.
This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs. Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.
Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.
For hires based in the United States, Vir Biotechnology, participates in E-Verify.
Candidate Privacy Notice
Seniority level
Seniority levelMid-Senior level Employment type
Employment typeFull-time Job function
Job functionLegal IndustriesBiotechnology Research and Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Vir Biotechnology, Inc. by 2x Get notified about new Regulatory Affairs Manager jobs in
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Manager, Regulatory Affairs-Document Coordinator
role at
Vir Biotechnology, Inc. Manager, Regulatory Affairs-Document Coordinator 1 day ago Be among the first 25 applicants Join to apply for the
Manager, Regulatory Affairs-Document Coordinator
role at
Vir Biotechnology, Inc. Vir Biotechnology is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.
Make sure to read the full description below, and please apply immediately if you are confident you meet all the requirements.
We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.
THE OPPORTUNITY
Vir Biotechnology is looing for a Regulatory Affairs Manager to join the regulatory group. The successful candidate, under the guidance of experienced regulatory affairs professionals, will be responsible for the coordination and preparation of documents intended for regulatory submissions for new and mature products (as applicable) to ensure alignment and compliance with local and regional registration requirements as well as with company policies.
What You'll Do
you will represent Regulatory Affairs on cross-functional project teams with the following responsibilities: Coordinate documents intended for regulatory submissions, manage internal reviews and resulting input from cross‑functional team members for products in line with ICH and regional requirements, meets scientific rigor and company policies and procedures Ensures quality and regulatory standards are considered and upheld throughout the product development life cycle Assists with the coordination and tracking of regulatory commitments and submission plans for maintenance activities such as INDs/CTAs, annual reports, periodic safety reports, protocol submissions, and key regulatory filings Participates in group meetings and provides tactical approaches to addressing issues of moderate complexity Participate in the development of processes and procedures relevant to regulatory functions Performs document filing and retrieval functions as directed, or in conjunction with departmental SOPs
Who You Are And What You Bring
BS and 8+ years of Experience, MS and 6+ years of experience with a minimum of 5+ years of regulatory experience Working knowledge of US FDA regulations (ex-US is a plus) and industry standards pertaining to regulatory Knowledge of the drug development process and eCTD Excellent organization skills and ability to work on multiple projects with tight timelines Excellent verbal and written communication skills and interpersonal skills
Who We Are And What We Offer
The expected salary range for this position is $121,500 to $170,500 per year. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.
Vir Biotechnology's compensation and benefits are aligned with the current market and commensurate with the person’s experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, childcare reimbursement, education reimbursement, 401K match and lunch each day in the office.
Applicants must currently be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.
This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs. Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.
Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.
For hires based in the United States, Vir Biotechnology, participates in E-Verify.
Candidate Privacy Notice
Seniority level
Seniority levelMid-Senior level Employment type
Employment typeFull-time Job function
Job functionLegal IndustriesBiotechnology Research and Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Vir Biotechnology, Inc. by 2x Get notified about new Regulatory Affairs Manager jobs in
San Francisco, CA . Quality Assurance & Regulatory Affairs Manager San Francisco, CA $100,000.00-$150,000.00 6 months ago San Francisco, CA $100,000.00-$150,000.00 6 months ago Senior Manager, Renewables Regulatory NERC & Operational Compliance Redwood City, CA $190,000.00-$220,000.00 2 weeks ago Senior Regulatory Affairs Manager – APAC - Diabetes Care Foster City, CA $210,000.00-$225,000.00 3 days ago San Francisco, CA $103,000.00-$139,000.00 6 days ago South San Francisco, CA $196,000.00-$240,000.00 2 days ago Compliance Manager, Regulatory Change ManagementAssociate Director of Regulatory AffairsRegulatory Affairs Manager – APAC - Diabetes Care (on-site)Regulatory Affairs Manager – Canada & Latin America – Diabetes Care (on-site) Alameda, CA $112,000.00-$224,000.00 1 month ago Associate Director Regulatory Affairs – APAC - Diabetes Care Alameda, CA $146,700.00-$293,300.00 6 months ago Manager, Regulatory Affairs Advertising and Promotion Foster City, CA $133,195.00-$189,640.00 1 week ago Associate Director, Regulatory Affairs - Global Labeling Foster City, CA $165,495.00-$235,620.00 3 weeks ago Regulatory Operations Manager (contract) San Francisco, CA $66.00-$75.00 4 hours ago Senior Regulatory Affairs Manager – APAC - Diabetes Care (on-site) Alameda, CA $128,000.00-$256,000.00 1 week ago Clinical Research Regulatory Affairs ManagerStrategic Operations Manager, Regulatory San Francisco, CA $106,000.00-$118,000.00 2 days ago San Francisco, CA $102,400.00-$204,100.00 3 days ago Associate Regulatory Affairs CMC Director (Small Molecule) Alameda, CA $166,000.00-$236,500.00 1 week ago South San Francisco, CA $196,000.00-$240,000.00 10 hours ago Vice President, Legal Affairs (Litigation, Regulatory & Public Policy)Senior Manager - CMC Regulatory (TEMPORARY) Oakland, CA $82,000.00-$124,000.00 1 week ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr