Senior Project Manager
Company: Disability Solutions
Location: Carlsbad
Posted on: November 1, 2024
Job Description:
Roche fosters diversity, equity and inclusion, representing the
communities we serve. When dealing with healthcare on a global
scale, diversity is an essential ingredient to success. We believe
that inclusion is key to understanding people's varied healthcare
needs. Together, we embrace individuality and share a passion for
exceptional care. Join Roche, where every voice matters.The
PositionWe advance science so that we all have more time with the
people we love.Roche is the world's #1 provider of companion
diagnostics, offering unrivaled experience in developing and
commercializing predictive tests that enable personalized treatment
strategies for patients.The Senior Project R&D Manager will
plan and drive execution of cross functional projects with Product
Development, Equipment Engineering, Product Maturity, Quality
Assurance and other areas within the company. This individual will
develop and document detailed technical work breakdown structures,
sprints, project GANTT, resource plans, technical goals and budget,
to deliver on project charters, business goals, and support
delivery of superlative products for patients. This will be
accomplished by interacting and providing effective leadership
across cross-functional teams including Development, Engineering,
Product Technical Support, Operations, Quality, and/or
Regulatory.
- You will proactively identify and manage risks, critical path
items, interdependencies, issues and delays, then work with team to
develop risk mitigation and contingency plans to ensure projects
remain on schedule and on budget; you will track and manage project
and department FTE utilization and project consumable costs to
budget.
- You will manage Design History File, Device Master Record,
Technical Study Reports, and Design Changes; you will set and
manage meeting agendas, minutes and action items.
- You will create and manage "Virtual Team Room" and electronic
experimental study (DOE) repository for cross functional
effectiveness of a large team of professional scientists and
engineers working across product development and operations; you
will prepare effective slide presentations and present progress to
goals per plan at regular updates.
- You will support management of projects that encompass:
development in R&D, manufacturing process development,
scale-up, process validation, test method validations, equipment
IQ/OQ/PQ, CAPAs
- You will manage projects under QMS for kits, reagents,
consumables (test strip/cartridge), instrument.
- You will support R&D, Operations and Project Leadership in
helping to implement change management.Education and Experience
- You have a B.S. degree in the biochemical / life sciences or
bioengineering with 13+ years of experience in life science product
development, process development and engineering / automation
projects leading to product launches; you have Leadership
executing, organizing, and influencing project teams in a matrix
environment
- You have 8+ years of experience and demonstrated success as a
Project Manager in an In Vitro Diagnostics company, resulting in
Product Launch and Process or Design Enhancements and/or Process
remediation in context of at least class II, 510k, CE-IVD
products.
- You have experience managing projects under QMS for kits,
reagents, consumables (test strip/cartridge), instrument
products.
- You have demonstrated experience with Class II medical device
product development, design controls, ISO13485/cGMP; IVD and Point
of Care / Disposable Consumable Assay Development experience
- You have a demonstrated level of proficiency with Microsoft
Office, Google Suite, MasterControl, SAP, Enterprise and project
resource planning tools; you have experience developing detailed
project plans using project management tools (SmartSheet, MS
Project etc)
- You have demonstrated experience leading problem solving/root
cause analysisPreferred:
- You are detail oriented and have demonstrated strong
interpersonal skills
- You have strong organizational and presentation skills and
ability to solve ambiguous situations.
- You have the ability to work in a fast-paced, dynamic
environment while juggling multiple projects
- You have the following certifications: Agile, Scrum, LeanSix
Sigma and/or PMPWORK ENVIRONMENTThe essential functions of the job
are usually performed in an environmentally controlled facility
where the noise level in the work environment is usually moderate.
This position may involve a combination of office and biotechnology
laboratory environments. The employee may be exposed to hazardous
chemicals, blood borne pathogens and automated equipment. While
performing the job duties, the employee is regularly required to
sit; reach with hands and arms and talk or hear. The employee is
frequently required to stand and walk. The employee may sometimes
be required to lift and/or move up to 35 pounds. Specific vision
abilities required by this job include close vision, distance
vision, color vision and ability to adjust focus.This position is
based in Carlsbad, CA.Relocation benefits are not available for
this position. The expected salary range for this position based on
the primary location of Carlsbad, CA is $133,400- - 247,700. Actual
pay will be determined based on experience, qualifications,
geographic location, and other job-related factors permitted by
law. A discretionary annual bonus may be available based on
individual and Company performance.This position also qualifies for
the benefits detailed at the link provided below.Who we areGenMark
is now a proud member of the Roche Group, more than 100,000 people
across 100 countries are pushing back the frontiers of healthcare.
As a global leader in healthcare, Roche Diagnostics offers a broad
portfolio of products, tools and services that help in the
prevention, diagnosis and management of diseases like HPV, HIV,
hepatitis and diabetes as well as other medical conditions, such as
fertility and blood coagulation. With the addition of GenMark to
the Roche Group, syndromic infectious disease diagnostics is now
added to the long list of disease states and conditions that the
Roche Group addresses. GenMark's ePlex true sample-to-answer system
offers unique solutions to address the most significant challenges
facing clinical laboratories, while supporting hospital systems to
deliver patient-centered, value-based care. ePlex streamlines the
diagnostic workflow from physician order entry to the final test
report and is the true sample-to-answer solution designed to
improve patient care, reduce costs, and increase lab efficiency.
GenMark is headquartered in Carlsbad, California.GenMark is an
equal opportunity employer and strictly prohibits unlawful
discrimination based upon an individual's race, color, religion,
gender, sexual orientation, gender identity/expression, national
origin/ancestry, age, mental/physical disability, medical
condition, marital status, veteran status, or any other
characteristic protected by law.
Keywords: Disability Solutions, Murrieta , Senior Project Manager, Executive , Carlsbad, California
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