NPI Program Manager
Company: Agilent Technologies, Inc.
Location: Kirkland
Posted on: July 30, 2022
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Job Description:
To protect the health and safety of our employees, contractors,
customers and communities, employees in the U.S. and Puerto Rico
are required to be fully vaccinated against COVID-19, unless an
approved exemption has been granted for a medical reason, sincerely
held religious belief, or an employee is otherwise exempt under
applicable law. NPI Program Manager Agilent inspires and supports
discoveries that advance the quality of life. We provide life
science, diagnostic and applied market laboratories worldwide with
instruments, services, consumables, applications and expertise.
Agilent enables customers to gain the answers and insights they
seek - so they can do what they do best: improve the world around
us. Information about Agilent is available at Resolution Bioscience
is seeking an experienced NPI Project Manager with product
development experience who will be responsible for planning,
tracking, coordinating, and monitoring in-vitro diagnostic product
development under design control to accelerate time to market. This
involves facilitating communications between multi-functional team
members and senior management to ensure timelines and goals are
met. Primary role and responsibilities You will: Drive complex,
multi-disciplinary projects and lead core and sub-teams to launch
products that meet critical unmet needs for cancer patients around
the world.
Lead complex, multi-disciplinary projects from start to finish -
working with stakeholders to plan requirements, manage project
schedules, identify risks, and communicate clearly with
cross-functional partners across the company. Your projects will
often span offices, time zones, and hemispheres. It's your job to
coordinate the players and keep them up to date on progress and
deadlines.
Facilitate the exchange of information between departments on a
day-to-day basis and maintain liaison with key members of the
project team between project team meetings
Be accountable for managing resources, schedules, financials and
adhering to stage gate quality and SDLC control guidelines
throughout the full systems development life cycle. This also
includes management of issues, risks, and change requests to ensure
successful and on-time program delivery.
Effectively communicate program updates to steering committees, to
functional management, and executive leadership, using a variety of
tools and channels.
Lead team efforts to mitigate risks and resolve issues quickly as
they arise, including root cause analysis and corrective action.
And if you're up for it: Develop processes to enable a healthy
manufacturing pipeline across multiple Contract Manufacturers in
supply and labor constrained environments.
Prioritize and lead complex process improvement programs across the
organization in support of all departments and functional areas.
Evaluate completed process improvement projects to identify and
implement best practices and lessons learned.
Assist with annual planning processes across the organization,
including strategy, headcount, budget and resource allocation.
Conduct post-mortem activities and drive closure of process
gaps.
Drive PMO learning and development opportunities across the
organization. Qualifications and Skills: BA/BS in life sciences,
engineering, or business is preferred
PMP certificate or similar preferred
Minimum of 4-5 years of project management experience in medical
device product introduction experience
Strong analytical skills to assess situations and drive decision
making
Ability to coordinate across disciplines and integrate all aspects
of business as they impact complex development projects including
negotiation of scope, roles and responsibilities, specifications,
timelines, and resources up, across, and down organization
Demonstrated effective written and oral communications skills
Ability to independently function in a fast pace changing
environment with deadline and resource constraints
Capacity to achieve outcomes based on ability to facilitate and
negotiate desired results
Experience working in a regulated environment and knowledge of ISO
13485, QSR and Design Control requirements are a positive
Proficiency with Microsoft Word, Excel, PowerPoint is a must Nice
to Have's Experience in NGS, or oncology-related research &
development is a plus.
Previous experience working on FDA submissions is preferred
Impeccable organization skills, attention to details and
punctuality are essential for this position. Self-motivated and
able to work with minimal supervision. About Agilent Benefits:
Innovative and fun work environment
Competitive salary
Healthcare benefits
Flexible time off
Paid volunteer days
401K & Company Match
Employee Referral Bonus
Training Opportunities Agilent Technologies, Inc. is an Equal
Employment Opportunity and Affirmative Action employer. We value
diversity at all levels. All individuals, regardless of personal
characteristics, are encouraged to apply. All qualified applicants
will receive consideration for employment without regard to sex,
pregnancy, race, religion or religious creed, color, gender, gender
identity, gender expression, national origin, ancestry, physical or
mental disability, medical condition, genetic information, marital
status, registered domestic partner status, age, sexual
orientation, military or veteran status, protected veteran status,
or any other basis protected by federal, state, local law,
ordinance, or regulation and will not be discriminated against on
these bases. Agilent Technologies, Inc., is committed to diversity
in the workplace and strives to support candidates with
disabilities. If you have a disability and need assistance with any
part of the application or interview process or have questions
about workplace accessibility, please email job_posting@agilent.com
or contact +1-262-754-5030.
Keywords: Agilent Technologies, Inc., Kirkland , NPI Program Manager, Executive , Kirkland, Washington
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