Why Patients Need You
Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. Pfizer Global Supply (PGS) is at the heart of fulfilling Pfizer’s purpose as we work to make sure customers and patients have the medicines they need, when they need them.
What You Will Achieve
As the Director, Analytical Lead seasonal mRNA Vx for Vaccines in Biotech and Sterile Injectable Technology, you will be accountable for the seasonal mRNA Vx analytical methods lifecycle and leading the matrix analytical teams for Pfizer’s seasonal mRNA vaccines assets (Ex: mRNA Flu). In this role, you will lead the analytical method development and transfers related to seasonal strain changes as well as new seasonal vaccines launches.
As a Director, you are a subject matter expert and leverage your knowledge of industry, customer requirements and general business environment to adapt and implement strategic actions for the division. Your managerial skills will help us manage and lead people, technological and financial resources within the division.
It is your problem-solving ability and leadership that will make it possible for customers and patients to receive the medicines they need, when they need them.
How You Will Achieve It
You will lead PGS analytical teams for each marketed vaccine asset and work with QC leads to develop and implement analytical method lifecycle plans for each asset to meet supply needs. Examples of lifecycle projects and post approval change include (but are not limited to): methods evaluation and development related to strain changes, methods robustness projects for QC testing, analytical support for complex investigations, local market analytical transfers, seasonal and post approval changes in method changes, changes in key components and raw materials.
In this role, you will provide matrix leadership for other analytical team leaders in the analytical seasonal RNA vaccine space. As the Analytical Lead, you will also build and maintain strong matrix relationships with key partners in Supply Chain, Manufacturing Sites, Launch Excellence, PGS Sites, Biotherapeutics Pharm Sci, Quality, Procurement, and Regulatory CMC.
Qualifications
Must-Have
Bachelor’s Degree in a scientific/technical discipline of the life sciences such as biochemistry, biology, or similar
10+ years of experience in scientific / technical project management roles within the biotech industry, supporting analytical methods development, validations and transfers
Technical expert of the unique aspects of mRNA analytical assays, familiarity with technology and science related to drug product manufacturing unit operations
Demonstrated track record of excellent matrix leadership skills and delivery of analytical technology objectives in a fast-paced technical setting with stringent timelines
Proven ability to synthesize significant volumes of complex information and data into clear priorities and a focus on what is truly important for achieving project or program success
Comfortable in an extremely dynamic environment with agility to change course quickly as new data and insights emerge
Advanced project management skill sets in scoping, financials, and schedule development with a track record of best practices applied in a biopharmaceutical environment
Significant experience leading multi-disciplinary direct and matrix teams to successful outcomes well supported by metrics
Previous experience in taking major analytical method changes through to the regulatory filing stage for marketed biologics / vaccine products as a post approval change
Hands-on familiarity with drug regulations/regulatory processes and quality/GMP/compliance systems of the pharmaceutical industry. Direct experience interacting with the regulatory authoritieseither through meetings at the agencies, through regulatory filings reviews, through production site-inspections or other similar circumstances
Demonstrated record of success in leading matrix teams of technical staff
Demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact
Requires the ability to process highly complex information and data quickly and under pressure. Large portion of deliverables are urgent and under timeline pressure
Nice-to-Have
Non-Standard Work Schedule, Travel, or Environment Requirement
Travel up to 20%; ability to travel regularly in support of the labs and teams in their remit
International travel
Adaptation of work schedule to accommodate meetings with colleagues in different time zones and seasonal vaccine production
Other Job Details
Last Day to Apply: 24 May 2023
Work Location Assignment:Flexible/Remote
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.
Engineering
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