Associate Director, Regulatory Affairs CMC at GILEAD REMNANT PTE LTD

Foster City, California, United States -

Full Time

Start Date

Immediate

Expiry Date

03 Jul, 26

Salary

235620.0

Posted On

04 Apr, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Regulatory affairs, CMC regulatory strategy, Biologics, Regulatory submissions, Risk assessment, Health authority interaction, Lifecycle management, Project management, Cross-functional leadership, Regulatory compliance, ICH guidelines, Change control, Due diligence, Strategic planning, Communication, Interpersonal skills

Industry

Biotechnology Research

Description

At 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. Job Description At Gilead our pursuit of a healthier world for all people has yielded a cure for hepatitis C, revolutionary improvements in HIV treatment and prevention as well as advancements in therapies for viral and inflammatory diseases and certain cancers. We set and achieve bold ambitions in our fight against the world’s most devastating diseases, united in our commitment to confronting the largest public health challenges of our day and improving the lives of patients for generations to come. As an Associate Director, CMC Regulatory Affairs for Biologics, at Gilead you will be responsible for defining regulatory strategy for one or more molecules in the Biologics portfolio. This position will ensure “right first time” global approvals of CMC regulatory (Biologics) submissions, and “right to operate” by maintaining the global clinical or commercial submissions. In addition, you will be accountable for leading the interpretation and implementation of CMC regulatory guidelines, regulations and current environment to assure approvability in high priority regions. As a regulatory lead you will also be responsible for ensuring that global regulatory strategy is integrated into Pharmaceutical Development & Manufacturing (PDM) Project teams. Specific Job Responsibilities: Ensure that CMC dossiers meet ICH format and content requirements, as well as the specific local requirements of individual countries. Takes a leadership position in conducting risk assessments on major global CMC regulatory issues. Must be pro-active in staying current with registration requirements in each of the applicable regions, and must communicate this information to the corporation on a timely basis. Play a leadership role on project and other teams in developing global CMC regulatory and change control policies and strategies. Work proactively to build contacts with local Health Authorities, and to present a positive image of Gilead in all discussions with Health Authorities. Responsible for ensuring timely discussion with Health Authorities regarding responses to questions, and will work with international colleagues to ensure consistency of responses to international Health Authorities. On a regular basis, participate in significant industry trade groups and regulatory professionals associations. Take a leadership role in updating the corporation on major international CMC regulatory guidance. Will be expected to use industry network to maintain an awareness of the “pulse” of CMC best practices, and to disseminate this information to the corporation. Form ad hoc task forces to address critical CMC issues on behalf of project and department teams Excellent verbal and written communication skills and interpersonal skills are required. Regulatory Strategy Facilitate good communication and transparency of CMC information to relevant functions. Provide consistent, high-quality Regulatory CMC input on CMC issues and risks along with mitigation plans/options. Lead and coordinate development of regional Regulatory CMC strategy, CMC submission content and timing to ensure alignment as outlined in the global regulatory strategy document. Ensure the Regulatory CMC strategy includes input from all geographies, commercial strategy and supports the Target Product Profile. Refine the Regulatory CMC strategy and updates as new data becomes available or as necessary. Liaise with RPT members to prepare CMC updates and/or regulatory position papers for consideration by the Research Project Review, Development Project Review and High Level Management, as necessary. Coordinate the provision of Regulatory CMC input on key milestones and stage gate recommendations, as necessary. Develop CMC lifecycle management plans with input from RPT. Health Authority Interaction Coordinate and facilitate development of regional Regulatory CMC strategy with affiliate for local meetings. Provide strategic input to meetings with Regional Health Authorities to ensure alignment with the global Regulatory CMC strategy. Participate in regional meetings support regional heads, as necessary. Provide input to all CMC briefing documents and other supporting documentation. Regional CMC personnel are responsible for authoring and presenting CMC documentation to their Health Authorities. Provide high level feedback to Senior CMC Management on points of discussion with Regional Regulatory Authorities that may impact globally (detailed minutes are communicated by the Regional Regulatory Leads). Work with the regional CMC personnel to develop a CMC submission plan in accordance with business objectives. Complete final review for all major and/or critical CMC submissions (NDA, MAA, NDS, PAS, CMC briefing documents, requests for Scientific Advice, Drug Product Listings and Site licenses as appropriate) and CMC responses to Health Authorities. Establish a CMC Core Rapid Response Team to facilitate the development and finalization of responses by the regional CMC personnel, as necessary. Regulatory Input into Other Functions Directly interface with the Regulatory Project Team and represent the affiliate’s regulatory viewpoint at such meetings. Support meetings and activities of the Regulatory Submission Team (meetings are chaired by a Regulatory Project Manager). Act as a “champion” of the Regional CMC Regulatory viewpoint. Work with RPTL to direct, manage and resolve CMC issues regarding the implementation of the global Regulatory CMC strategy. Work with the RPTL to provide CMC input for the Target Product Profile, and labeling (including Package Insert/SMPC/Product Monograph), as necessary. Regional CMC personnel are responsible for a Final Review and Approval of regional label. Coordinate the provision of global Regulatory CMC advice to PDM, QA and Commercial Manufacturing organizations. Provide input from a global perspective on the CMC data required to support a clinical development program (based on input from the regional Regulatory CMC personnel). Lead the development of the Regulatory CMC strategy, content, and submission timelines in accordance with business objectives. Ensure provision of global Regulatory CMC input into Clinical, Commercial and Development sub teams, as necessary. Conduct in-licensing due diligence, as necessary, for project(s) evaluation and life cycle development. Resource Planning Define and highlight regional / global Regulatory CMC resource issues that may affect the implementation of the Regulatory CMC strategy etc, as necessary. People Relationships & Communication2 Cross-functional team leader responsibilities. Facilitate good teamwork across affiliates and sites. Ensure cross-regional communication and transparency in the flow of CMC information that may affect regional regulatory strategy. Elevate CMC issues and potential risks, along with possible resolutions, to senior management especially when such issues impact the approvability of submissions and/or product launch. Decision Rights Create an integrated global Regulatory CMC strategy based on input from the regional CMC personnel. Regional Regulatory CMC personnel (in conjunction with the regional regulatory heads of department) are responsible for the definition of an appropriate regional regulatory strategy which is consistent with the global regulatory strategy. In exceptional circumstances, RCPTL may make decisions on the global Regulatory CMC strategy that have an impact on the regional regulatory strategy or submissions (e.g. where timelines are exceptionally tight and there is no opportunity to seek regional regulatory input). However, all decisions on the global Regulatory CMC strategy are typically made following consultation and agreement with CMC Management and RPT. Ensures that the strategy for meetings with regional regulatory authorities is consistent with the global regulatory strategy. Submission In conjunction with the regional CMC personnel, finalize CMC submission plans. Ensure alignment of CMC submission plans with Commercial, Clinical & IP. Specific Education & Experience Requirements: Advanced degrees including PhD and MS desired. Relevant industry experience is preferred. 10+ years of experience in Regulatory Affairs or relevant industry experience following a Bachelor’s Degree. Direct experience working with regional chemistry reviewers. Regulatory Affairs Certification, a plus. Previous management experience, a plus People Leader Accountabilities: Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams. Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose. Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem. The salary range for this position is: $182,070.00 - $235,620.00. 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*. For additional benefits information, visit: https://www.gilead.com/careers/compensation-benefits-and-wellbeing * Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans. For jobs in the United States: 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. For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster. NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT Gilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law. Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team. Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion. For Current Gilead Employees and Contractors: Please apply via the Internal Career Opportunities portal in Workday. Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.

Responsibilities

The Associate Director will define and implement global CMC regulatory strategies for the Biologics portfolio to ensure successful product approvals and lifecycle management. They will lead cross-functional teams, manage interactions with health authorities, and provide strategic regulatory guidance to support clinical and commercial objectives.