Director, New Products Solid Oral Dosage Manufacturing Technology
Company: Pfizer Belgium
Location: Hartford
Posted on: May 17, 2023
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Job Description:
Pfizer Director, New Products Solid Oral Dosage Manufacturing
Technology in Hartford , Connecticut What You Will AchieveThe
primary purpose of the Director, New Products Solid Oral Dosage
Manufacturing Technology position is technical leadership of PGS
manufacturing technology for new products with SOD drug product
formulations, from Co-Design, through Co-Development to Commercial
Launch. Key accountabilities of the position include:Lead PGS
implementation of novel, New Product driven SOD DP manufacturing
technologies, endorsed by the Small Molecule Strategy Team, from
initial assessment through to commercial implementation, in
partnership with Pharm Sci Small Molecule (PSSM), Operating Units,
Procurement, Global Engineering and other GT&E functional
lines. Lead value assessment / replication opportunity reviews for
implemented technologiesCo-lead SOD Drug Product Co-Design with
PSSM, providing PGS perspective on optimal DP
formulation/manufacturing technology approaches, leveraging
Co-Development and commercial manufacturing experiencePartnership
with PSSM on process design for:Sustainable Medicines, integrating
recommendations from the NetZero 2040 program workstreamLead Time,
incorporating learnings and implementing recommendations from PGS
iFlow/Lead Time programsLead SOD DP manufacturing technology
reviews for Co-Development* programs conducted at PDT (Portfolio
Delivery Team) and through RFT Risk Assessments and Robustness
Reviews, in partnership with PSSM (Drug Product Design, Global Drug
Product Manufacturing), Launch Excellence and GT&E (Clinical
Supply and Technical Partnership Operations).Lead the transition of
technical leadership, product knowledge management and future CI
project portfolio from Co-Development Teams to PGS Technical Teams,
in partnership with PSSM, Launch Excellence, other GT&E lines
(Analytical Technology, Clinical Supply, Technical Partnership
Operations and Technology Excellence) and Small Molecule & External
Supply OpUsProvision of technical leadership / subject matter
expertise on SOD DP manufacturing technology for key PGS
workflows:New product sourcing strategic decision-making (NP
manufacturing/supply chain - internal/external), through membership
of the New Product Sourcing TeamTechnical assessment of potential
Business Development acquisitionsIntegration of New Product driven
SOD DP manufacturing technologies into the PGS NextGen Technology
programLead SOD Drug Product Tier 5 Technology Reviews, represent
GT&E on Drug Product Steering Team (joint PGS/PSSM forum), PCMM
and other network teamsThe Director, New Products Solid Oral Dosage
Manufacturing Technology position will lead matrix teams and be
required to develop effective relationships with key partners in
Pharm Sci Small Molecule (Drug Product Design, Global Drug Product
Manufacturing), Launch Excellence, other GT&E lines (Analytical
Technology, Clinical Supply, Global Engineering, Manufacturing
Intelligence, Technical Partnership Operations and Technology
Excellence), Small Molecule & External Supply OpU sites and CMOs,
Network Design & Performance, Procurement, Quality and Regulatory
CMC.*Note: this position is not directly involved in individual
Co-Development Team activityHow You Will Achieve ItStrong
familiarity and experience with small molecule drug product
manufacturing technologies, unit operations, manufacturing
facilities, and regulatory expectations/strategyExcellent technical
project and program management track record in bringing
multi-disciplinary process and technology solutions through to
commercial implementation and approvalDemonstrated track record of
excellent matrix leadership skills and delivery of
multi-disciplinary objectivesAbility to effectively engage and
interact with manufacturing technology suppliersHighly capable
innovator and problem-solver, with knowledge of and passion for
Innovative & Six Sigma tools and methodologiesProven ability to
synthesize process/product-related knowledge, reflecting it in a
systematic way so that it can be leveraged by customers and
stakeholdersComfortable in a dynamic environment with agility to
change course quickly as new data and insights emergeExcellent
listener and inclusive partner within Co-Development and with key
stakeholders in PGS and Pharmaceutical
SciencesQUALIFICATIONSMust-HaveBSc, MSc, or PhD in a
scientific/technical discipline of the life sciences10+ years of
experience in solid oral dosage form manufacturing within the
pharmaceutical industry, together with a comprehensive
understanding of SOD unit operations and manufacturing
equipmentPrevious experience in introducing novel manufacturing
technologies into a commercial environment from technology
selection through to commercial implementation and regulatory
approvalEffective project management skill set and demonstrated
record of success in leading technical and multi-disciplinary
matrix teams to successful outcomesHands-on experience of drug
regulations/regulatory processes and quality/GMP/compliance systems
of the pharmaceutical industryPractitioner of the Six Sigma and
continuous improvement suite of toolsCandidate 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
impactPHYSICAL/MENTAL REQUIREMENTSRequires the ability to lead
detailed evaluations of novel manufacturing technologies, requiring
the understanding of commercial manufacturing requirements and the
ability to conduct comprehensive technical reviews. Deliverables
will be strategically significant, and often under timeline
pressure. Individual would need the ability to travel to engage
with PSSM teams, customer sites (internal/CMOs), meet suppliers and
participate in technology trials as required.NON-STANDARD WORK
SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTSInternational travel
(up to 20%)Adaptation of schedule to work across different time
zonesOther Job DetailsLast Date to Apply: May 24, 2023Eligible for
relocation assistance: NoWork Location Assignment:RemoteThe annual
base salary for this position ranges from $144,900.00 to
$241,500.00. In addition, this position offers an annual bonus with
a target of 20.0% of the base salary and eligibility to participate
in our share based long term incentive program. Benefits offered
include a retirement savings plan, paid vacation, holiday and
personal days, paid caregiver/parental and medical leave, and
health benefits to include medical, prescription drug, dental and
vision coverage in accordance with the terms and conditions of the
applicable plans. Salary range does not apply to the Tampa, FL
location.Relocation assistance may be available based on business
needs and/or eligibility.Sunshine ActPfizer 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.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.
Keywords: Pfizer Belgium, Hartford , Director, New Products Solid Oral Dosage Manufacturing Technology, Executive , Hartford, Connecticut
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