Senior Project Engineer
Company: Novartis
Location: Hicksville
Posted on: January 24, 2023
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Job Description:
With 64 manufacturing sites in 26 countries, our aspiration is
to become the top manufacturer of innovative and generic medicines
in the industry!Management of engineering technical projects,
resources, costs and timelines in accordance with established
scheduling and budget. Must be qualified to support cGMP
engineering initiatives. Plans, estimates, budgets, schedules, and
executes all aspects of project assignments including project
scope, resource identification, capital and expense budgeting,
project reporting, specifications, design, plan execution, factory
acceptance testing, construction, installation, commissioning,
documentation, financials, all aspects of system life cycle
documentation (URS, FDS, FAT, IQ, OQ, deviation reconciliation),
communications, reporting, and financial payments. Must be detail
oriented, and possess and communicate a sense of commitment,
ethics, urgency and practicality.--- Identify, review, scope and
present project plans as required supporting manufacturing
operations, compliance and quality, new product launches,
facilities, business development, and the general business.---
Develop sustainable and robust plans. Present comprehensive and
concise summaries. Approve funding requests, permitting,
documentation and report progress in accurate and substantive
summary.--- Manages entire project from assignment, concept through
delivery and acceptance, supporting qualification and operational
implementation. Review project proposal or plan to determine time
frame, funding limitations, and procedures for accomplishing
project, vendor requirements, and allotment of available resources
to various phases of project.--- Meet with vendors to identify
project deliverables, value, equipment, support, service,
technology, project scope, scheduling, performance, documentation,
and pricing as required.--- Coordinates with project team to
develop and administer work plan and to develop roles, duties,
responsibilities, and scope of authority. Works closely with
validation to make sure that all required project documentation is
relayed for appropriate project close out and commissioning.---
Reviews and provides approvals of all design, supplier, vendor
specifications, documents and drawings associated with projects.---
Coordinates activities of project team including internal and
external resources to ensure project progresses on schedule, within
prescribed budget, and resolves technical service or technology
issues.--- Research new technologies and provide production support
for the ongoing and continuous operation of all manufacturing
equipment. This may include travel to industry shows and
expositions.--- Travels to perform Vendor Evaluations, Design
Reviews, and Factory Acceptance Testing (FAT).--- Support and Meet
Departmental, Plant and Corporate HS&E goals. Work in a safe
and efficient manner.--- Adheres to all applicable procedures,
cGMP's, company policies, and all other quality or regulatory
requirements (OSHA, DEA, FDA, EMEA, ANVISA, HS&E, etc.).
Ensures all work is performed in a safe, effective manner, and in
compliance with the appropriate industry and regulatory (FDA, DEA,
OSHA) standards, and Departmental, Plant, and Corporate quality and
Behavioral Based Safety (BBS) goals.Note: This position may require
the labeling, packaging or movement of hazardous (flamma-ble,
corrosive, toxic, etc.) waste within the facility. If so, this
employee would be trained under OSHA's HAZWOPER standard, 29 CFR
1910.120 as an 8-Hour first responder, 24-Hour in-cident commander,
or a 40-Hour incident commander.In lieu of HAZWOPER training, the
employee will receive training on the requirements of the Resource
Conservation and Recovery Act pursuant to 40 CFR 265.16.All
employees that have received the above mentioned training upon hire
will receive annual refresher training that covers the OSHA
HAZWOPER standard and the requirements of RCRA.EEO StatementThe
Novartis Group of Companies are Equal Opportunity Employers and
take pride in maintaining a diverse environment. We do not
discriminate in recruitment, hiring, training, promotion or other
employment practices for reasons of race, color, religion, gender,
national origin, age, sexual orientation, gender identity or
expression, marital or veteran status, disability, or any other
legally protected status. We are committed to building diverse
teams, representative of the patients and communities we serve, and
we strive to create an inclusive workplace that cultivates bold
innovation through collaboration and empowers our people to unleash
their full potential.Minimum requirements--- Bachelors Degree in
Engineering is required (prefer Mechanical Engineering or Chemical
Engineering).--- 3+ years of relevant manufacturing/engineering
experience is required.--- Previous pharmaceutical manufacturing
experience is required.--- Comprehensive technical knowledge of
pharmaceutical equipment and plant design is required.---
Experience with pharmaceutical industry standards and requirements
(Minimum US GMP) is required.--- Basic knowledge of validation
processes is required.--- PE Certification a plus--- Understanding
of business systems (SAP, LIMS etc.) is required.--- Familiar with
Engineering software systems (CAD, project management, maintenance
management and calibration) is required.--- Highly PC literate in
Microsoft office suite is required.Why Novartis?769 million lives
were touched by Novartis medicines in 2020, and while we're proud
of this, we know there is so much more we could do to help improve
and extend people's lives.We believe new insights, perspectives and
ground-breaking solutions can be found at the intersection of
medical science and digital innovation. That a diverse, equitable
and inclusive environment inspires new ways of working.We believe
our potential can thrive and grow in an unbossed culture
underpinned by integrity, curiosity and flexibility. And we can
reinvent what's possible, when we collaborate with courage to
aggressively and ambitiously tackle the world's toughest medical
challenges. Because the greatest risk in life, is the risk of never
trying!Imagine what you could do here at Novartis!Commitment to
Diversity & Inclusion:Novartis is committed to building an
outstanding, inclusive work environment and diverse team's
representative of the patients and communities we serve.Join our
Novartis Network: If this role is not suitable to your experience
or career goals but you wish to stay connected to hear more about
Novartis and our career opportunities, join the Novartis Network
here: Accessibility and reasonable accommodations:The Novartis
Group of Companies are committed to working with and providing
reasonable accommodation to individuals with disabilities. If,
because of a medical condition or disability, you need a reasonable
accommodation for any part of the application process, or in order
to perform the essential functions of a position, please send an
e-mail to call +1 and let us know the nature of your request and
your contact information. Please include the job requisition number
in your message.DivisionNovartis Technical OperationsBusiness
UnitNTO SANDOZ TECHOPSCountryUSAWork LocationHicksville,
NYCompany/Legal EntityEon Labs IncFunctional AreaFacilities &
AdministrationJob TypeFull TimeEmployment TypeRegularShift
WorkNoEarly TalentNo
Keywords: Novartis, Hicksville , Senior Project Engineer, Engineering , Hicksville, New York
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