GCMC is committed to support Biotherapeutic Pharmaceutical Science (BioTX PharmSci) and Global Supply (PGS) as competitive advantage for Pfizer by consistently delivering high quality regulatory strategies and timely submissions across product lifecycle.
GCMC is fully engaged in drug development, product line extensions and maintenance.
GCMC representatives participate on teams and at sites as GCMC experts and overall advocate for effective drug development and maintenance paradigms.
The person currently looked for, will be responsible for execution of Regulatory Strategies for Vaccines and Biotechnological Products.
As senior Manager, you are responsible for the development and execution of Regulatory CMC strategies, submissions and compliance activities for biopharmaceutical projects / products from development to market and post-
marketing, including the preparation and submission of correspondence and applications (IMPD’s, MAA’s, ) to regulatory agencies.
Potential project responsibilities may include monoclonal antibodies, other recombinant proteins, vaccines, peptides and nucleotides.
You act as CMC liaison with regulatory authorities to discuss and define submission contents and strategies.
You lead the preparation of CMC information for submission to regulatory agencies, generates CMC strategies, assesses risks and develops contingency plans, including major, complex applications.
You ensure that CMC regulatory submissions are complete, properly formatted, and comply with applicable regulatory requirements.
You interface directly with Boards of Health, including scientific reviewers, administrative staff, in order to discuss and define regulatory applications (Quality Module, Responses, Commitments.
You act as CMC representative in formal meetings and teleconferences with regulatory authorities.
You act as the CMC representative and contributes support to the Global CMC representative within cross-functional project teams, involving the interpretation of regulations and guidelines and the assessment of global implications for strategic CMC decisions.
You are accountable for assigned CMC programs, managing day-to-day delivery of plans and strategic activities for specific projects, including Life Cycle Teams and compliance of commercial products.
You operate independently to resolve complex issues and manage regulatory risks and ambiguous situations within project teams.
You investigate opportunities for regulatory innovation / promote the use of novel approaches within project team to resolve issues and problems.
You create / contribute to the development of internal policies, processes and procedures supporting the progression and maintenance of the Pfizer biopharmaceutical portfolio at large.
You lead document management and information management teams, within Global CMC / groups outside Global CMC.
You represent Regulatory CMC on due diligence teams and representing Pfizer on CMC focused pharmaceutical industry initiatives
7 years of prior international regulatory experience with 3-5 years in CMC).
Problem solving skills to propose and assess regulatory solutions to CMC issues and prepare contingency plans will be helpful.
Experience in medical device development and registration is useful.
Technical and scientific understanding of biopharmaceutical drug development with technical writing skills. 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.
Competent working knowledge of computer based systems such as Microsoft Office, controlled documentation systems (e.g. Documentum).
Ability to learn and navigate tracking / change control systems, compliant and consistent use of systems (including GMP validated systems) and willingness to train and support others in system use.
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.