CTO Senior Manager, Capital Projects Biotechnology & Pharmaceuticals - Summit, NJ at Geebo

CTO Senior Manager, Capital Projects

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:
careers.
bms.
com/working-with-us.
At Bristol Myers Squibb, we are inspired by a single vision transforming patients lives through science.
In oncology, hematology, immunology and cardiovascular disease and one of the most diverse and promising pipelines in the industry each of our passionate colleagues contribute to innovations that drive meaningful change.
We bring a human touch to every treatment we pioneer.
Join us and make a difference.
Cell Therapy is one of the most groundbreaking new forms of cancer treatments being studied today.
With therapies only in their infancy and BMS s continued investment in our Cell Therapy capabilities, the growth potential of this science, your career, and the ability to help patients are incredible.
POSITION
Summary:
The BMS Senior Capital Project Manager will develop, implement, and oversee capital projects to support Cell Therapy Operations (CTO) at the Summit West Site.
This role will be focused on managing capital projects ($5M+) responsible for interfacing cross-functionally with both internal groups, external clients and stakeholders to ensure projects are delivered on time and within budget.
This position will utilize their breadth of knowledge across facilities and engineering to drive CTO business growth strategies across the Summit West Site and ensure adherence to regulatory compliance and effective project execution.
Position will also require extensive management and oversight of contract resources in executing project deliverables.
KEY
Responsibilities:
Lead the development of the Capital Project scope and Master Planning initiatives in support of the business strategy alignment with CTO clients and stakeholders.
Exhibit project leadership and effective decision-making throughout each project.
Actively manage Project Financials inclusive of Cashflow Reporting & ForecastingLead and promote effective teamwork by engaging Facilities, ECQ & EHS, as well as key clients and stakeholders.
Lead the scheduling, planning, control, and effective coordination of all the parallel activities related to each project and maintain project schedule through unanticipated schedule challenges.
Coordinate with Procurement and Project Team in generating RFP documents for engineering deliverables typically for Equipment Purchases, Design, Construction & Qualification efforts.
Manage A/E Firms through the BMS Stagegate Process to effectively deliver on meeting end user functional/design requirements and overall project goals.
Manage and coordinate with Construction Managers (CMs) from estimating, pre-construction, demolition, construction and commissioning in alignment with design & functional requirements.
Ensure all work complies with BMS Site Safety Requirements and ensure all involved individuals are in compliance with required trainings.
Utilize broad knowledge of the functional requirements of the pharmaceutical facilities and engineering best practices to ensure that appropriate internal and external resources are incorporated into the project design and execution.
Achieve a cost-effective, functional outcome with the use of design guidelines and standards, value engineering, life cycle costing and engineering best practices.
Assure that the construction project and the finished facility are compliant with all applicable safety, regulatory, legal requirements.
Perform Master Planning Efforts for Summit West CTDO facilitiesContribute as Engineering SME in both internal and regulatory auditsActively manage Project Financials inclusive of Cashflow Reporting & ForecastingAchieve effective financial control through management of project scope, estimating, effective use of SAP, RPM, budget control tools, risk management, and project closeout.
Achieve high customer satisfaction by delivering finished projects that are fully commissioned, qualified, and ready for startup/occupancy and meets all requirements of stakeholders and stays within a predetermined schedule.
Participate and lead shutdown planning & coordination for effective and timely execution of Capital Project related activities with minimal disruption to Manufacturing.
Actively manage Contact Resources as part of Project Team and be able to plan onboarding and offboarding based on project timelinesQUALIFICATIONS AND
Experience:
Experience managing GMP related EPCMV projects ($5M+) within a Cell/Gene Therapy or Pharmaceutical Manufacturing Environment is required.
Bachelor s Degree with 10
years of relevant work experience demonstrating leadership capabilities, or an equivalent combination of education and experience may be considered:
Bachelor s degree in Chemical or Mechanical Engineering preferred, EIT/PE License and plusDemonstrated success leading multi-disciplinary and multi-functional teams and demonstrated strength in stakeholder management, especially integration of design, construction, and qualification firmsInterpersonal / facilitation skills necessary to interface and influence all levels of managementSignificantly demonstrated Project Management expertise for design, construction, qualification, and start-up involving all areas of Pharmaceutical Manufacturing, Pilot Plants, QC Laboratories and WarehousingStrong terminology of construction terminology and legal content of construction contracts and documents.
Experience with supervising construction contractors especially in review/approval of Pre-Task Plans (PTPs) and Job Hazard Analysis (JHA) documentationExperience with Process Hazard Analysis, (PHA), Process Safety Management (PSM) and Pre-Startup Safety Review (PSSR)Background in use of the Stage Gating Process within Capital Project WorkflowUnderstanding of financial management as it relates to capital and expense spending and project cash flow forecastingFamiliar with the use of RPM (Project Capital System) or equivalent and SAP (Purchase Order System)Demonstrated ability to be proactive in solving challenging project issues with the ability to develop creative solutions.
Experience in total project delivery from concept to validation and startup processProficient Experience with Building Management System, HVAC and Liquid Nitrogen / Cryo Systems, a plusExperience with initiating Change Controls, performing Impact Assessments, Change Actions and executing CAPAs as needed to complete assigned Engineering Department Scope of Work.
WORKING CONDITIONS:
Occasional stooping, bending, stretching, pushing, pulling, reaching and/or light lifting and pushing of moving carts may be requiredAbility to sit, stand, walk and move within workspace for extended periodsENVIRONMENTAL CONDITIONS:
Environment may include working in office, or in a laboratory / manufacturing areaAbility to work safely in an environment with hazardous, radioactive and infectious materials and wasteAbility to work safely in an environment with exposure to high temperatures, / pressure steam, and other fluids, compressed gasses, odors, various noise levels, moving parts, vibration wet / slippery areas and high voltage energy suppliesEnvironment may include working at heights, in cold temperatures, and or constricted spacesAbility to work safely when working along or working with others.
Why You Should Apply:
Around the world, we are passionate about making an impact on the lives of patients with serious diseases.
Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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.
Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles.
Applicants can request an accommodation prior to accepting a job offer.
If you require reasonable accommodation in completing this application, or any part of the recruitment process direct your inquiries to adastaffingsupport@bms.
com.
Visit careers.
bms.
com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
If you want to challenge yourself, accelerate your career, and give new hope to patients, there s no better place than here with our Cell Therapy team.
Full of incredible and dedicated team members, those working on CAR-T and other forms of Cell Therapy are transforming patients lives through science.
From studying individualized cell lines to making brand new discoveries, this bold and personal discipline allows you to grow your career while making a lasting impact on the field of medicine.
Join us today.
BMSCARTVETERAN#LI-ONSITEIf 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 ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
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 adastaffingsupport@bms.
com.
Visit careers.
bms.
com/eeo-accessibility 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.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
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Estimated Salary: $20 to $28 per hour based on qualifications.

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