Senior Manager, Global CMC Regulatory Affairs

Job Description:Job PurposeThe Senior Manager of CMC Regulatory Affairs will be responsible for creating CMC regulatory development plans and for successful execution against those plans. The Senior Manager of CMC Regulatory Affairs represents the function on departmental and cross-functional initiatives. The Senior Manager must be articulate and influence decision-making with key internal and external stakeholders while managing tight timelines.Essential Job FunctionsServe as Global Chemistry, Manufacturing and Controls (CMC) regulatory leader for assigned productsPrepare Global CMC content for INDs, NDAs, MAAs, IMPDs, CTAs, annual reports, and other regulatory documentsDevelop and create CMC regulatory strategy for integrated development plans and long-term planning at a cross-functional level for product(s), consistent with the corporate and project objectivesProvide CMC regulatory expertise to Technical Operations and Quality teamsReview and approve technical documentationProvide guidance to teams in support of clinical trial supply for local and global clinical trialsEngage with regulatory agencies on CMC project related matters as requestedIdentify regulatory CMC issues proactively that will impact programs and provide strategies to address them and communicate to the project teamProvide insight and guidance on implementation of regulations with respect to the preparation and submission of CMC regulatory documentationDrive decision making in the cross functional teams with respect to CMC regulatory issuesCreate CMC regulatory submission timelines in collaboration with cross functional teamsManage internal team and external consultants/vendors to CMC regulatory timelinesSkills and QualificationsB.S. in a scientific discipline required, B.S. in chemistry, pharmaceutical sciences or similar discipline preferred.Diverse technology experience (small molecules, biologics, parenteral and oral dosage forms).Must have a minimum of 5 years of pharmaceutical industry experience to include 5 years dedicated to CMC regulatory affairs matters; international experience preferred.In depth knowledge of drug development, US and global CMC guidelines and regulations.Competencies: Functional Leadership skills, Negotiation skills, Teamwork & Collaboration, Attention to Detail, Self-Starter, Problem Solving, Organizational skills, Adaptability, Professionalism, Written and Verbal Communications, Analytical skills.Working ConditionsThis is a hybrid position based in Xeris’ Chicago office and a minimum of three days per week on-site is required. On-site requirement may change at management’s discretion.Position may require periodic evening and weekend work, as necessary to fulfill obligations. Periodic overnight travel.Travel up to 10% may be required to accomplish corporate goals and health authority requirements.The anticipated base salary range for this position is $155,750 - $213,600.#LI-HYBRIDWe are committed to offering competitive compensation. Starting pay is determined based on a variety of factors, including the role, job-related knowledge, skills, experience, education, internal equity, market data, and the location of the role, where applicable.Xeris Pharmaceuticals, Inc. (the “Company”) is an equal opportunity employer and does not discriminate based on race, color, religion, sex, gender identity, sexual orientation, national origin, age, disability, veteran status, genetics or any other characteristic protected by law. All qualified candidates are given equal opportunity and the Company’s employment selection decisions are based solely on job-related factors. NOTE: This job description is not intended to be all-inclusive. The employee may be required to perform other related duties as needed to meet the ongoing needs of the Company.The level of the position will be determined based on the selected candidate’s qualifications and experience. Final determination of the actual base salary offered depends on several factors, including but not limited to the candidate’s skills, experience, education, location, and business needs. Employees are eligible for equity or long-term incentive awards, where applicable. Field Sales role employees are eligible for a quarterly commission structure. Non-Sales role employees are eligible for an annual bonus. The Company also offers a comprehensive benefits package that includes additional elements such as paid time off benefits, various health, vision, and dental insurance options, 401(k) retirement benefits and more for eligible employees. Details about these and other offerings will be provided at the time a conditional offer of employment is made. Candidates are always welcome to inquire about our compensation and benefits package during the interview process. Individuals hired as temporary employees, interns, and preceptors are not eligible for commissions, bonuses, and/or long-term incentive or equity awards. Eligibility for other benefits will be based on plan documents.Accessibility & Reasonable AccommodationsIf, because of a medical condition or disability, you require a reasonable accommodation or assistance to complete any part of the application process, please send an e-mail to View email address on us.fitly.work and identify the type of accommodation or assistance you are requesting. Please include the job requisition number in your message. Please note if your request is not for this stated purpose, you will not receive a response to your email. Do not include any medical or health information in this email.Xeris participates in E-Verify. E-Verify Participation PosterEEO is the Law EEO is the LawEEO is the Law Supplement EEO is the Law SupplementPay Transparency Nondiscrimination Provision Pay Transparency Nondiscrimination ProvisionSummaryLocation: Chicago, ILType: Full time