Manager, CMC Project Operations
Company: Disability Solutions
Location: New Brunswick
Posted on: October 19, 2024
Job Description:
Working with UsChallenging. Meaningful. Life-changing. Those
aren't words that are usually associated with a job. But working at
Bristol Myers Squibb is anything but usual. Here, uniquely
interesting work happens every day, in every department. From
optimizing a production line to the latest breakthroughs in cell
therapy, this is work that transforms the lives of patients, and
the careers of those who do it. You'll get the chance to grow and
thrive through opportunities uncommon in scale and scope, alongside
high-achieving teams rich in diversity. Take your career farther
than you thought possible.Bristol Myers Squibb recognizes the
importance of balance and flexibility in our work environment. We
offer a wide variety of competitive benefits, services and programs
that provide our employees with the resources to pursue their
goals, both at work and in their personal lives. Read more: .PD
Portfolio Strategy & Integration (PSI)Our Portfolio Strategy and
Integration team is dedicated to developing and executing CMC
strategies for small molecule and biologics portfolio utilizing the
brightest minds and ideas across the enterprise to drive strategic
choices for Global Product Development and Supply. From candidate
selection to commercial launch and life cycle management, we
provide valuable project information and portfolio insights, and we
lead CMC due diligence for business development opportunities.
Joining PSI means you'll have the opportunity to grow and thrive
through vast and diverse opportunities. You'll make a positive
impact on the lives of patients while advancing professionally
alongside some of the brightest minds in biopharma.Within the
Product Development (PD) division, the Portfolio Strategy and
Integration (PSI) department brings together business operations,
project planning and execution, and portfolio management with the
vision of simplifying how Product Development runs the business. A
key goal of PSI is to drive the development and execution of
integrated CMC strategies via Chemistry Manufacturing Control Teams
(CMC) to enable R&D Development Team
objectives/deliverables.The CMC Project Manager is closely
partnered with the CMC Leader to enable effective execution of CMC
strategy and plans. The scope of responsibilities of the CMC
Project Manager fall into 4 general categories which flex across
all drug modalities, disease areas and stages of development.1)
Cross-functional CMC Project Management to ensure integrated
execution of CMC strategy and communication2) CMC Project Timeline
Management and timeline scenario planning3) Gaps Analysis and Risks
Management4) Allocation of drug substance and API materials for
non-clinical usePrimary Responsibilities:
- In partnership with CMC Team Leader, manage 3-5 CMC program
assignments (actual number determined by level of project
complexity and candidate experience) and drive execution of
integrated program strategy
- Develop detailed CMC project plan that is aligned with the
overall program strategy. Work collaboratively with the CMC team
leaders and functions to track all project milestones
- Facilitate pertinent CMC scenario planning to address changing
business/clinic needs. Gather stakeholder input, evaluate, collate,
manage and communicate implications and adjustments to the overall
plan
- Manage all CMC meeting logistics including the creation of
clear, concise minutes
- Partner with the CMC Leader to facilitate the management and
communication of program risks and mitigation strategies
- Leverage portfolio and program management tools to track
program execution, milestones, risks, and long range planning to
ensure appropriate communication to team members and management.
Examples include ePlan, PSI CMC database, IBP, DOI Tool,
Operational Risk Management
- Coordinate and ensure appropriate allocation of DS and API
materials for non-clinical use
- The CMC Project Manager may: Co-lead and/or contribute to
Product Development portfolio level activities including business
process improvement initiatives and resource/budgeting activities,
as neededExperience / Qualifications:
- Bachelor's degree in engineering or relevant scientific
discipline with at least 5 years of relevant experience / Masters'
degree with a minimum of 2-6 years of relevant experience
- Highly motivated self-starter that works well both in teams as
well as independently
- Strong project management, business process management, and
optimization skills
- Familiarity with end-to-end CMC drug development with an
understanding of critical milestones and typical bottlenecks
preferred
- Strong organizational skills, ability to multi-task and work in
a dynamic, fast paced environment.
- Demonstrated ability to accomplish results and meet deadlines
and commitments
- Strong interpersonal and communications skills, both oral a
written
- Demonstrated proficiency in MS Project, PowerPoint, Excel and
Word
- Demonstrated ability to build relationships, influence,
negotiate, and drive organizational engagement
- Experience developing and/or managing program management tools
to forecast budgets, timelines and resources preferred If you come
across a role that intrigues you but doesn't perfectly line up with
your resume, we encourage you to apply anyway. You could be one
step away from work that will transform your life and career.
Uniquely Interesting Work, Life-changing CareersWith a single
vision as inspiring as Transforming patients' lives through
science--- , every BMS employee plays an integral role in work that
goes far beyond ordinary. Each of us is empowered to apply our
individual talents and unique perspectives in an inclusive culture,
promoting diversity in clinical trials, while our shared values of
passion, innovation, urgency, accountability, inclusion and
integrity bring out the highest potential of each of our
colleagues.On-site Protocol BMS has a diverse occupancy structure
that determines where an employee is required to conduct their
work. This structure includes site-essential, site-by-design,
field-based and remote-by-design jobs. The occupancy type that you
are assigned is determined by the nature and responsibilities of
your role: Site-essential roles require 100% of shifts onsite at
your assigned facility. Site-by-design roles may be eligible for a
hybrid work model with at least 50% onsite at your assigned
facility. For these roles, onsite presence is considered an
essential job function and is critical to collaboration,
innovation, productivity, and a positive Company culture. For
field-based and remote-by-design roles the ability to physically
travel to visit customers, patients or business partners and to
attend meetings on behalf of BMS as directed is an essential job
function. BMS is dedicated to ensuring that people with
disabilities can excel through a transparent recruitment process,
reasonable workplace accommodations/adjustments and ongoing support
in their roles. Applicants can request a reasonable workplace
accommodation/adjustment prior to accepting a job offer. If you
require reasonable accommodations/adjustments in completing this
application, or in any part of the recruitment process, direct your
inquiries to . Visit to access our complete Equal Employment
Opportunity statement. BMS cares about your well-being and the
well-being of our staff, customers, patients, and communities. As a
result, the Company strongly recommends that all employees be fully
vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest
and conviction records, pursuant to applicable laws in your area.If
you live in or expect to work from Los Angeles County if hired for
this position, please visit this page for important additional
information: Any data processed in connection with role
applications will be treated in accordance with applicable data
privacy policies and regulations.
Keywords: Disability Solutions, Vineland , Manager, CMC Project Operations, Executive , New Brunswick, New Jersey
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