1+ months

Senior Manager, GCMC China

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**Job Summary**

+ Collaborate with departmental and cross-functional colleagues (eg. G-CMC, WSR, WRO, and PGS) to leverage and share both technical & regulatory knowledge, align expectations and manage planning and monitoring activities to mitigate risks, contribute to global regulatory strategies, deliver expeditious and efficient regulatory submissions for projects across all aspects of drug development or manufacturing lifecycle.

+ Delivery of high quality regulatory submissions.

+ Maintenance of the expansive combination of CMC product information, market registration details, component level dossier content and compliance of an integrated regulatory change management process to provide a comprehensive and compliant view of the CMC registered details of all products in all markets.

+ Assure product compliance through timely and accurate maintenance of CMC submission documentation and product knowledge in Regulatory systems.

+ Possession of CMC regulatory knowledge and quality expertise to prepare regulatory assessments, develop & contribute to global regulatory strategies with assistance from management for projects across all aspects of drug development or manufacturing lifecycle.

+ Continued pursuit of developing an understanding of regulatory conformance & compliance with external regulatory requirements & internal quality procedures.

+ Leverage both technical & regulatory knowledge, to mitigate risks.

+ Execution of regulatory policies and operational processes.

+ Actively contribute to cross-functional and strategic initiatives, novel concepts and solutions to address gaps and mitigate risks and improve conformance.

**Job Responsibilities**

+ Take CMC lead to support products at various stages including clinical trial application, NDA and post approval variations

+ Serve as a primary CMC contact on a core project(s) demonstrating ability to manage project activities, assess regulatory risks & development plans to develop global regulatory strategies for programs in accordance with regulatory, scientific & technical criteria.

+ Ensure high quality CMC submissions in compliance with China regulations and guidelines. Ensuring all regulatory activities for assigned products is executed effectively & efficiently in compliance with external regulatory requirements & internal quality procedures.

+ Manage regulatory issues, maintain submission information in relevant GCMC systems, tracks regulatory commitments & timelines for specific projects/products/markets with minimal supervision.

+ Serve as a technical and scientific resource within own work group/discipline and provides guidance for completion of difficult and complex projects. Mentoring colleagues may be expected within focus area of expertise.

+ Manage and Contribute to GCMC projects, initiatives & actions along with prioritizing assigned workload appropriately.

+ Demonstrate ability to manage project activities, present and articulate issues for resolution and execute as a scientific/technical resource for assigned projects.

+ Execute training related activities (e.g. compliance-related, HR policies...), individual development plans, participate in cross-disciplinary forums & learning opportunities, engage in Straight Talk & Listen exchanges, demonstrate & model adherence to all Pfizer behaviors & values, embrace & comply with GCMC Principles of Integrity.

+ Develop effective relationships with local & global internal partners, e.g. GCMC, China RA, DC and PGS.

+ Develop relationships with regulatory authorities and network with pharmaceutical industrial associations to improve Pfizer's regulatory success and enhance Pfizer's image.

**Technical Skill Requirements**

+ Demonstrated commitment & dedication to scientific & regulatory integrity & quality compliance.

+ Knowledge of the CMC business as it relates to drug development, and partnering organizations and systems is required.

+ Experience with CMC regulatory submissions, process development and/or GMP manufacture of clinical and/or commercial products.

+ Strong understanding of CMC change management processes and CMC CTD content/structure.

+ Understanding of identifying and mitigating compliance risks through proper management of CMC product content

+ Sufficient level of knowledge and solid understanding of the development & commercial activities and cGMP's required to assess technical, scientific & regulatory merits of CMC information, commitments and data to lead teams and/or project(s).

+ Knowledge of the CMC business as it relates to drug development, and partnering organizations and systems is desired.

+ Possesses sound understanding of business expectations across divisions

+ Ability to present and articulate issues for resolution, communicating regularly with key stakeholders to ensure alignment, provide consultation as a scientific/technical resource for assigned projects, mentor and share experience with colleagues.

+ Deep understanding of China, US and EU regulatory requirements & expectations, criteria for submission & approval globally & experience of interactions with regulatory authorities for projects.

+ Applies technical, functional, and industry knowledge to shape strategic direction of assigned project(s), reduce regulatory burden & improve regulatory flexibility commensurate with business needs.

+ May serve as Subject Matter Expert in specific relevant disciplines or recognized as a regulatory CMC resource for specific pharmaceutical science projects and/or specialized expert in specific regulatory domains

+ Demonstrates sound understanding and advanced knowledge of the principles, practices and concepts of a regulatory CMC/ policy/ publishing discipline and a working knowledge of the principles, practices, concepts and operations in other relevant disciplines.

+ May participate in Due Diligence exercises with supervision.

+ May participate in limited interactions with regulatory authorities to respond to direct requests either directly or in conjunction with Regulatory Affairs.

+ Advanced skills in written & oral communications in both Chinese and English are mandatory.

+ Computer literacy with Microsoft Office Suite and Documentum-based applications highly desired.

+ Skills in document manipulation and electronic document maintenance (e.g., Word, Excel, Adobe, Documentum, dossier workflow tools) and other data management tools

+ Experience engaging in the external regulatory & pharmaceutical environment is preferred.

+ Prior experience managing projects is required.

**Qualifications (i.e., preferred education, experience, attributes)**


+ BS, MS or PhD degree in chemistry, biology, or related scientific disciplines; Advanced degree is preferred.

**Experience** **:**

+ Technical discipline with 7+ years of experience in the pharmaceutical industry with relevant technical experience (QA, Technical Services, Operations, Manufacturing or R&D) and 3+ years pharmaceutical regulatory experience are desired.

**Desired / Required Competencies:**

**G-CMC Specific Responsibilities, Expectations & COMPETENCIES**

**Senior Manager**

**Decision Making**

+ Acts Decisively

+ Applies experience & operates independently to resolve complex issues.

+ **Impact of Decisions**

+ Decisions impact multiple Sub Business Unit/Sub Operating Units mid-term objectives

+ Significant or long-term decisions are reviewed by senior management

**Risk Mgt**

+ Ability to recognize and address risks across projects and programs.

+ Manages regulatory risks & ambiguous situations under limited supervision.

**Innovation/ Creativity**

+ Investigates novel and unconventional approaches to address issues and solve problems.

+ Identifies existing process/product improvements

+ Develops innovative, advanced new concepts that improve processes / products across own and related disciplines

+ Takes appropriate risks to achieve desired results

**Scientific & Regulatory Leadership**

+ Ability to develop and/or lead projects or team initiatives to support short-term operational goals.

+ Ability to think globally across zones and divisions.

+ Ability to influence at the work group/discipline project team level.

**Knowledge Breadth and Depth / Sharing**

+ Provides technical / functional leadership to teams

+ Leverages technical/functional expertise across own and related disciplines.

+ Demonstrates comprehensive industry knowledge. Exhibits business expertise and an understanding of the external marketplace and customer requirements.

+ Actively shares knowledge with others across multiple Sub Business Unit/Sub Operating Unit through existing knowledge sharing processes/systems

+ Encourages others to share knowledge across the organization.

**Teamwork/ Collaboration**

+ Ability to contribute to effective teams & implement change.

+ Aptitude for customer service, facilitation, and conflict resolution, approaching all situations with enthusiasm and integrity, despite demanding workload, technical barriers and changing deadlines and requirements.


+ Communication & Negotiation skills

+ Uses communication to help ensure alignment within and outside of Sub Business Unit/Sub Operating Unit

+ Creates and delivers presentations to direct reports and other internal stakeholders across Sub Business Unit/Sub Operating Unit.

+ Demonstrates excellent verbal and written communication skills

**Vision, Strategy, and Business Alignment**

+ Establishes operational activities/projects that support mid-term goals and set direction for the Sub Business Unit/Sub Operating Unit.

**Influencing Others**

+ Manages teams that execute direction for the Sub Business Unit/Sub Operating Unit

+ Provides input to senior management decisions that may have an impact on business direction within the Sub Business Unit/Sub Operating Unit

**Managing Change**

+ Prepares for and manages change that impacts the Sub Business Unit/Sub Operating Unit.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Research and Development
Posted: 2020-10-13 Expires: 2020-12-13
Sponsored by:
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