Sr. Project Manager - Facilities Engineering
- Employer
- Charles River Laboratories - Scotland
- Location
- Tranent, United Kingdom
- Salary
- Competitive
- Start date
- 5 May 2022
- Closing date
- 4 Jun 2022
View more
- Discipline
- Project Management
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly.
Job Summary
We are seeking a Senior Project Manager for our Facilities Engineering team to be located remotely in the U.S., preferably in the Wilmington, MA area. The Senior Project Manager will be responsible forfor managing assigned moderate size domestic and international capital projects from inception to completion in support of all business units. Work closely with local site management to coordinate efforts and compile owner’s requirements. Oversee program development, design management, construction coordination, schedule and budget coordination and accountability.
The following are the responsibilities related to the Sr Project Manager position:
• Manage moderate size domestic and international capital infrastructure projects from inception to completion. Project values may be up to $25M US and projects may be defined/short term or strategic and requiring project tracking over time.
• Oversee program development, design management and construction coordination.
• Develop program budgets and schedules in support of initiative business case.
• Draft capital request executive summaries and justifications as required.
• Regular interface with finance on spending plans
• Monitor and drive progress of projects, maintaining budgets and schedules.
• Ensure value management, internal project cost control and scheduling tools are used to manage projects efficiently.
• Responsible for establishing lines of communication between and integrating efforts of the user group, owner’s representative, architectural, engineering, construction management, commissioning, validation coordination and operational delivery of large-scale capital projects so that project objectives are attained.
• Coordinate interface with operations users for program development and preconstruction services.
• Work with procurement throughout the selection process for hiring third-party service firms as construction managers, designers, and related consultants by writing RFPs, evaluating proposals, conducting interviews and making recommendations to senior management.
• Manage furniture, fixture, and equipment (FFE) infrastructure and user coordination.
• Coordinate underwriter and code review of project designs in conjunction with Corporate Risk requirements.
• Ensure effective and proactive safety management programs are in place for employees and contractors
• Track and report project progress to leadership, alerting developing problems where management intervention or oversight is required. Plan and implement appropriate actions as necessary to mitigate risks.
• Perform all other related duties as assigned.
Job Qualifications
The following are the qualifications related to the Sr Project Manager position:
• Education: Bachelor’s degree (BS/BA) in engineering or in project/construction management or related field required. Master’s degree considered a plus.
• Experience: 5 or more years related experience in hi-tech (med device, pharma, biotech, semiconductor) construction and engineering project management. Experience managing projects with budgets up to $25M in total and accelerated schedules.
• Certification/Licensure: PMP, PE or EIT considered a plus.
• Other: Sound working knowledge of Good Laboratory Practices (GLPs), Good Manufacturing Practices (GMPs), OSHA and government regulatory requirements and guidelines. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in standard software including Microsoft® Excel, Word, Powerpoint, Project, etc. Proficiency in CAD is beneficial.
PHYSICAL DEMANDS:
• Employee is regularly required to talk, hear and work/type at a computer.
• Walking/surveying active operating facilities and construction sites.
WORK ENVIRONMENT:
• General office (remote) working conditions; 65%
• On-Site visits to various facility types; 35%
• Noise level in construction areas is usually moderate but may be loud enough to require hearing protection.
• Will involve some outdoor activities - walking around properties/construction areas
COMMENTS:
• This position will require domestic and international travel
IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.
Vaccine Mandate
Charles River is a U.S. Federal Contractor. As a result, we must follow the Presidential Executive Order to mandate vaccinations, and ensure our employees are fully vaccinated against COVID-19 by December 8, 2021. Our main priority is the wellbeing, health, and safety of our people. We will be requiring proof of vaccination from all employees.
Anyone with requests for disability-related and/or religious exemptions should contact Talent Acquisition (crrecruitment_US@crl.com) so that information can be provided about the accommodation process at Charles River.
About Corporate Functions
The Corporate Functions provide operational support across Charles River in areas such as Human Resources, Finance, IT, Legal, Sales, Quality Assurance, Marketing, and Corporate Development. They partner with their colleagues across the company to develop and drive strategies and to set global standards. The functions are essential to providing a bridge between strategic vision and operational readiness, to ensure ongoing functional innovation and capability improvement.
About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 18,000 employees within 100 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of >80% of the drugs approved by the FDA for the past 3 years.
Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit www.criver.com.
Nearest Major Market: Boston
Job Segment: Project Manager, Construction, Engineering Manager, Project Engineer, Facilities, Technology, Engineering, Operations
Company
Find out more about working for our company
Brief Company Description;
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 17,000 employees within 90 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of ~85% of the drugs approved by the FDA in 2019.
Here in Scotland, based at our site in Tranent, East Lothian, we offer a complete array of Safety Assessment services from complete IND-enabling programs to stand-alone preclinical studies, our preclinical CRO services provide a full range of in vivo and in vitro testing evaluations and regulatory support for the safety assessment of pharmaceuticals, medical devices, and animal health products as well as chemicals, agrochemicals, and biocides. Our scientific and regulatory staff develop and execute individual preclinical studies or customized programs to ensure that drug efficacy and safety assessments are conducted in the most efficient manner.
- Website
- https://www.criver.com/
- Mini-site
- Charles River Laboratories - Scotland
- Location
-
Elphinstone Research Centre
Tranent Easy
Lothian
EH33 2NE
United Kingdom
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