CMC Technical Project Manager

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Sia  is a next-generation, global management consulting group born digital, augmented by data, enhanced by creativity, and driven by responsibility. We partner with clients to resolve challenges and capitalize on opportunities. We believe that in today’s world of change and disruption, optimism is a force multiplier.
Sia Life Science and Healthcare Business Unit   focuses on supporting Sia's clients in the life sciences and healthcare industries with strategic consulting, product development, and non-dilutive funding expertise.
This consulting division works with healthcare organizations, pharmaceutical & biotech companies, CROs, academia, medical device/diagnostic companies, and non-governmental organizations (NGOs) alike to solve complex business, scientific, regulatory, technological, and product development challenges. 
Our subject matter experts help advance our clients’ products and projects, supporting these companies - both large and small - to achieve organizational objectives and create tangible value for their stakeholders.

The CMC (Chemistry, Manufacturing, and Controls)   Technical Project Manager provides day-to-day operational management for CMC development and technical transfer projects.
Working in close partnership with the CMC Technical Senior Project Manager - who leads project management activities - the CMC Technical Project Manager leverages their technical and project management expertise to serve as the operational hub for CMC project teams, supporting execution and communication across process development, analytical, formulation, quality, supply chain, and external partners.
This role blends technical understanding of biopharmaceutical CMC development disciplines with project management and coordination skills.
Candidates are required to have biopharmaceutical industry experience through CMC technical roles with project management responsibility or through project management roles with an understanding of CMC development.
Responsibilities:
Providing consulting services for Sia’s clients in the life sciences and healthcare industries, including but not limited to:
Provide tactical support for day-to-day project activities such as meeting minutes, action tracking/follow-up, decision tracking, etc.
Actively contribute to project management deliverables (reports, dashboards, etc.) and routine updates (schedule, budget, risk), typically preparing initial drafts.
Build and maintain detailed predecessor-driven project schedules (Gantt charts, integrated timelines) utilizing scheduling tools/software (e.g., MS Project, Smartsheet, Planisware, Primavera, or equivalent).
Provide clear and timely schedule updates, variance analyses, and risk assessments to project leaders and stakeholders to ensure project schedules remain aligned with project strategy, portfolio priorities, and key decision gates (e.g., regulatory submissions, health authority interactions).
Coordinate across project functional areas and personnel as required to ensure the progress of project activities.
Support the building and management of a team representing various functions and sites, including the management of multiple projects and teams across multiple locations.
Demonstrate and foster excellent teamwork, with the ability to navigate within multidisciplinary teams.
Balance project demands to support alignment/realignment of Budget, Quality, Timeline, and Scope, as needed.
Support product development meetings, and make sure all Project Leaders, and/or subteam leaders, have all information and support needed to implement the project.
Focus on customer service, with agility and clear communication.
Adhere to Sia quality standards regarding client deliverables.

Mandatory qualifications:
At least 2 years of experience in the biopharmaceutical industry with a minimum of 1 year of project management experience.
BS, MS, or PhD in a scientific or engineering discipline (e.g., Chemistry, Biochemistry, Chemical or Biomedical Engineering, Pharmaceutical Sciences)
Experience working with CDMOs to support outsourced development and manufacturing activities, including oversight of deliverables and timelines.
Ability to engage in technical and scientific discussions.
Good communication and interpersonal skills.
Proficiency in Planisware.
Fluent and articulate communication in English (written and spoken)
Good written and oral communication, presentation, problem-solving, and negotiation skills.
Ability to work independently and in collaboration with others.
Flexibility and ability to deal with ambiguity, and a strong sense of personal ownership of deliverables and results.
Works well with teams, often comprised of multiple disciplines.
Ideal qualifications:
Broad understanding of CMC, including: Small molecule, biologics, or vaccine formulation, process development, analytical development, and GMP manufacturing across both early and late-stage development.

Formal project management training or certification (e.g., PMP).
Understanding of product development lifecycle and pharmaceutical manufacturing operations.
Understanding of cGXP guidelines and regulatory requirements.

Why join the Sia Village?
Excellence | Entrepreneurship | Innovation | Teamwork | Care & Support | Employee Wellbeing
These are the six core values that guide all our actions. 
Your experience at Sia will be enriched by a(n):  
Entrepreneurial journey
Support with achieving professional development goals through guidance and real-time feedback
Continuous learning & development opportunities
All your information will be kept confidential according to EEO guidelines.
Sia Partners is an equal opportunity employer. All aspects of employment, including hiring, promotion, remuneration, or discipline, are based solely on performance, competence, conduct, or business needs.

Sia is an equal opportunity employer. All aspects of employment, including hiring, promotion, remuneration, or discipline, are based solely on performance, competence, conduct, or business needs.

Sia是一家新一代全球管理咨询集团，诞生于数字化时代，以数据为增强、以创造力为提升、以责任为驱动。我们与客户携手合作，解决挑战并把握机遇。我们相信，在当今充满变化与颠覆的世界中，乐观是一种力量倍增器。
Sia生命科学与医疗健康业务部门致力于通过战略咨询、产品开发和非稀释性资金专业知识，支持Sia在生命科学和医疗健康行业的客户。
该咨询部门与医疗健康组织、制药与生物技术公司、CRO、学术机构、医疗器械/诊断公司以及非政府组织（NGO）等合作，解决复杂的商业、科学、监管、技术和产品开发挑战。
我们的主题专家帮助推进客户的产品和项目，支持这些大大小小的公司实现组织目标，并为其利益相关者创造切实价值。

CMC（化学、制造和控制）技术项目经理为CMC开发和技术转移项目提供日常运营管理。
CMC技术项目经理与领导项目管理活动的CMC技术高级项目经理密切合作，运用其技术和项目管理专业知识，充当CMC项目团队的运营枢纽，支持工艺开发、分析、制剂、质量、供应链和外部合作伙伴之间的执行和沟通。
该角色将生物制药CMC开发学科的技术理解与项目管理和协调技能相结合。
候选人需具备生物制药行业经验，包括承担项目管理职责的CMC技术角色，或具备CMC开发理解的项目管理角色。
职责：
为Sia在生命科学和医疗健康行业的客户提供咨询服务，包括但不限于：
为日常项目活动提供战术支持，如会议纪要、行动跟踪/跟进、决策跟踪等。
积极为项目管理交付物（报告、仪表板等）和常规更新（进度、预算、风险）做出贡献，通常负责准备初稿。
利用排程工具/软件（如MS Project、Smartsheet、Planisware、Primavera或同等工具）构建和维护详细的前置任务驱动项目进度表（甘特图、集成时间线）。
向项目领导和利益相关者提供清晰及时的进度更新、偏差分析和风险评估，确保项目进度与项目战略、组合优先级和关键决策关口（如监管提交、卫生当局互动）保持一致。
根据需要跨项目职能领域和人员协调，确保项目活动的进展。
支持建立和管理代表各职能和站点的团队，包括管理跨多个地点的多个项目和团队。
展示并培养优秀的团队合作精神，具备在多学科团队中运作的能力。
根据需要平衡项目需求，支持预算、质量、时间线和范围的 align/realign。
支持产品开发会议，确保所有项目领导和/或子团队领导拥有实施项目所需的全部信息和支持。
专注于客户服务，具备敏捷性和清晰的沟通能力。
遵守Sia关于客户交付物的质量标准。

必备资格：
至少2年生物制药行业经验，其中至少1年项目管理经验。
科学或工程学科（如化学、生物化学、化学或生物医学工程、制药科学）的学士、硕士或博士学位
具有与CDMO合作支持外包开发和制造活动的经验，包括对交付物和时间线的监督。
能够参与技术和科学讨论。
良好的沟通和人际交往能力。
熟练使用Planisware。
流利且清晰的中英文沟通能力（书面和口头）
良好的书面和口头沟通、演示、问题解决和谈判能力。
能够独立工作并与他人协作。
灵活性和处理模糊性的能力，以及强烈的个人对交付物和结果的主人翁意识。
与团队良好合作，团队通常由多学科组成。
理想资格：
对CMC有广泛理解，包括：小分子、生物制品或疫苗制剂、工艺开发、分析开发以及早期和晚期开发阶段的GMP生产。

正式的项目管理培训或认证（如PMP）。
了解产品开发生命周期和制药制造运营。
了解cGXP指南和监管要求。

为什么加入Sia Village？
卓越 | 创业精神 | 创新 | 团队合作 | 关怀与支持 | 员工福祉
这是指导我们所有行动的六大核心价值观。
您在Sia的经历将通过以下方面得到丰富：
创业之旅
通过指导和实时反馈支持实现职业发展目标
持续学习和发展的机会
您的所有信息将根据EEO指南保密。
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Sia是平等机会雇主。就业的所有方面，包括招聘、晋升、薪酬或纪律处分，均仅基于绩效、能力、行为或业务需求。

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