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<h3>Job Description</h3>
Job Description
Senior Project Managers work on projects with elite local clients that seek us for our expertise. They have project ownership from start to finish, and because they own the project, they are responsible for the outcome.
 
As a JDL Corporate Interiors Senior Project Manager, you will be responsible for the following:
 
<ul>
<li>Maintaining and developing relationships to reinforce a commitment to world class customer service across the board: including co-workers, clients, subcontractors, vendors, and the design community.</li>
</ul>
 
<ul>
<li>Aids in locating potential business deals by contacting potential partners, discovering and exploring opportunities</li>
</ul>
 
<ul>
<li>Successfully manage JDL's largest and most complicated projects</li>
</ul>
 
<ul>
<li>Assist in business development by promoting JDL brand in the marketplace</li>
</ul>
 
<ul>
<li>Assist with mentoring Project Managers and Assistant Project Managers. Establishing annual performance goals for assigned staff and conducting timely and meaningful verbal and written performance evaluations.</li>
</ul>
 
<ul>
<li>Ensuring a schedule is in place during project set up and sub-bidding that reflects the project strategy and is sufficient for estimating and subcontractor purchasing selection.</li>
</ul>
 
<ul>
<li>Participate in development and final review of scope, buy-out and schedule.</li>
</ul>
 
<ul>
<li>Developing a purchasing schedule and strategy to anticipate, address and resolve purchasing challenges during the early stages of pre-construction.</li>
</ul>
 
<ul>
<li>Executing each project phase including pre-construction, construction, closeout and post- construction services.</li>
</ul>
 
<ul>
<li>Collaborating with Estimating and Purchasing in set up of projects to insure profitability, client satisfaction and the best subcontractors for the job.</li>
</ul>
 
<ul>
<li>Working in partnership with the Project Superintendent to maintain an updated and accurate project schedule.</li>
</ul>
 
<ul>
<li>Thorough completion of all financial data with an eye to quickly identify potential/existing issues that could lead to sub-par financial performance.</li>
</ul>
 
<ul>
<li>Effectively administering the requisitioning and collections process to ensure timely payments.</li>
</ul>
 
<ul>
<li>Promoting positive subcontractor relations by dealing professionally and fairly with all subcontractors and vendors and continually instilling this philosophy in the project team.</li>
</ul>
 
<ul>
<li>Demonstrate strong leadership and professionalism to be emulated by other JDL staff. Be a resource for Project Managers and Assistant Project Managers when questions or problems arise on jobs. Assist in finding solutions to those issues to ensure the successful completion of the overall project.</li>
</ul>
 
<ul>
<li>Meets regularly with client representative at various jobs to determine client requirements and promote favorable client relations</li>
</ul>
 
<ul>
<li>Identifies and implements value-added services to the client</li>
</ul>
 
<ul>
<li>Research, review and address any owner, landlord, city/state requirement or procedure to avoid project delays, ensure safety, and/or ensure client satisfaction</li>
</ul>
 
<ul>
<li>Develop comprehensive understanding of project strategy and commitments including financial goals, scheduling, logistics, phasing, milestones, inspections</li>
</ul>
 
<ul>
<li>Demonstrate and maintain effective and open dialogue with the project team regarding changes in work, job conditions, subcontractor relations and any deviation in the direction of the project</li>
</ul>
 
<ul>
<li>Maintain and review punch list process to ensure all are addressed and executed in a timely manner</li>
</ul>
 
<ul>
<li>Actively participate in all company-wide training and development initiatives, also work with and mentor JDL Corporate Interiors staff</li>
</ul>
 
<ul>
<li>At times Senior Project Managers may asked to participate in Project Superintendent duties on project sites.</li>
</ul>

Senior Project Manager

<h3>Job Description</h3>
Job Description Senior Project Architect US-MA-Boston Job ID: 2025-3086 Type: Regular Full-Time # of Openings: 1 Category: Architect The LiRo Group Boston MA Overview 
LiRo Architects + Planners, P.C., a division of LiRo-Hill, is an award-winning design firm seeking a Senior Project Architect to participate in the design, documentation, and construction administration for a variety of projects for municipal and corporate clients including; Healthcare, K-12/Higher Education, Public Safety and Justice for our Boston Office.

LiRo-Hill provides integrated design, construction and technology solutions for a broad range of public and private sector clients and is ranked among the nation's top Construction Managers by Engineering News-Record.&nbsp; We currently provide the opportunity for a hybrid/flex-hour work schedule.

We believe in the power of collaboration. We foster a culture of teamwork where every voice is not just heard but valued and respected. You will have the chance to collaborate with talented professionals from diverse backgrounds and disciplines, sharing insights and ideas to deliver innovative and sustainable solutions. Join us and become part of a team that values your unique perspective and contributions.
We are also committed to your success. We invest in your growth and development through mentor programs, training opportunities (LiRo-Hill Academy), and access to cutting-edge technology. We believe in your potential and are dedicated to helping you reach it. Join us and unlock your full potential.
No two days are the same, with a wide range of projects and challenges, you will have a chance to continuously learn and grow, keeping your skills sharp and your mind engaged.
 Responsibilities 
<ul>
<li>Leads the technical direction of projects, assisting the Design and Management Teams with the successful delivery of the project</li>
<li>Interfaces with Clients, Client representatives, Consultants and Construction Managers</li>
<li>Has a working knowledge of local and state building codes, conducting code research and applying analysis to design requirements</li>
<li>Prepares design documentation including surveys, reports, architectural drawings, details and specifications throughout all project phases in line with the project delivery schedule</li>
<li>Actively coordinates with internal and external engineering consultants, including Survey, MEP, Civil, Environmental, Cost Estimators and Structural disciplines </li>
<li>Researches products and materials</li>
<li>Performs design and constructability&nbsp;reviews with the Technical Director at all phases of the project</li>
<li>Assists with the oversight and mentorship of junior staff</li>
</ul>
 Qualifications 
<ul>
<li>A degree in Architecture from an accredited college is required</li>
<li>Professional License is required</li>
<li>15+ years U. S. experience in building design and construction document preparation is required</li>
<li>Demonstrated knowledge of AutoCAD, Revit and Microsoft Office (Word, Excel and PowerPoint.) </li>
<li>Proficiency with 3D Modeling software such as Enscape, Rhino 3D Max or Adobe Creative Suite/Blue beam is a plus </li>
<li>Knowledge of International and Local Building Codes is required</li>
<li>Strong conceptual, planning and organization skills and capability of working both individually and in a team environment on a variety of projects and tasks</li>
</ul>
<ul>
<li>Effective interpersonal and communication skills, expressing ideas competently and professionally to a technical and non-technical audience.</li>
<li>Self-starter, able to work independently and able to multi-task.</li>
<li>Experience with building planning, drawing standards, design, and construction management; including active involvement in a variety of restorative and new design projects</li>
</ul>
<ul>
<li>LEED credentials or an understanding of sustainable design is a plus</li>
<li>Ability to work schedules conducive to project-specific requirements that may extend beyond the typical workweek.</li>
</ul>
Please visit our website for all of our career opportunities at <a href="https://careers-liro.icims.com" target="_blank">https://careers-liro.icims.com</a>
We believe in the power of collaboration. We work hard to build a corporate culture that empowers all our employees to freely share their ideas, know their presence, and contributions are truly valued, fostering a climate where our employees are enabled to maximize their full potential.
 We offer a competitive salary commensurate with experience, a comprehensive benefits package and a positive work environment.&nbsp;
The selected candidate must be authorized to work in the United States; Visa sponsorship is not available for this role.
LiRo-Hill is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, race, color, creed, religion, national origin, ancestry, marital status, sex, affectional or sexual orientation, gender identity or expression, or protected veteran status; and will not be discriminated against on the basis of disability.
#ID22
#ZR22
 
PI09475b63386d-25405-37324454

Senior Project Architect

<h3>Job Description</h3>
Job Description
Robert Half's marketing &amp; creative client is looking for a Web Accessibility Specialist for a 2-month contract in the Greater Boston area. This is a remote, 40-hour-per-week opportunity; candidates must be willing to work eastern (ET) hours. The Web Accessibility Specialist will be assisting in a large website overhaul and will play a key role in advancing digital inclusivity and compliance with the Web Content Accessibility Guidelines (WCAG).
 
Key Responsibilities:
<ul>
<li>Perform accessibility audits, including manual testing of websites and pages</li>
<li>Resolve accessibility issues</li>
<li>Ensure WCAG compliance and implement ARIA best practices</li>
<li>Collaborate with web teams and other stakeholders</li>
</ul>
 
If interested and available, apply today!
<ul>
<li>Degree in communication, technology, or related</li>
<li>2+ years of web accessibility experience</li>
<li>HTML/CSS skills</li>
<li>Familiarity with content updates</li>
<li>Experience using screen readers and assistive technologies tools (SiteImprove, WAVE, etc.)</li>
<li>Familiarity with ARIA best practices</li>
<li>Self-starter</li>
<li>Detail-oriented</li>
<li>Excellent communication and project management skills</li>
<li>IAPP certification a plus</li>
</ul>

Web Accessibility Specialist

<h3>Job Description</h3>
*Currently hiring for a September 2026 start date*
 
FUNCTIONS
Integration into Management Solution's specialist Technology unit, focused on the digital transformation of our clients. Involvement in projects for the conceptualization and implementation of advanced technological solutions to complex problems that require specific and in-depth knowledge of the client's business, in the following areas:
<ul>
<li>Implementation of specialist technologies: architecture definition, Big Data, solutions development and tool implementation.</li>
<li>IT strategy and governance: strategic IT plans, IT servicing, Project Management Office (PMO), transformation, organization and efficiency.</li>
<li>Risk and regulatory management: cybersecurity, data quality and data governance.</li>
</ul>
 
REQUIREMENTS
<ul>
<li>Recent graduates or final year students.</li>
<li>Solid academic record.</li>
<li>Get-up-and-go attitude, maturity, responsibility and strong work ethic.</li>
<li>Knowledge of other languages is desirable.</li>
<li>Advanced user of programming languages, databases and software engineering techniques.</li>
<li>Strong ability to learn quickly.</li>
<li>Able to integrate easily into multidisciplinary teams.</li>
</ul>
 
WE OFFER
We offer you the possibility to join a firm that provides all you need to develop your talent to the fullest:
<ul>
<li>Working in the highest-profile consulting projects in the industry,</li>
<li>for the largest companies, leaders of their respective markets,</li>
<li>alongside top industry management as they face challenges at the national and global level,</li>
<li>as part of an extraordinary team of professionals whose values and corporate culture are a benchmark for the industry</li>
</ul>
 
Ongoing training plan
<ul>
<li>Specialist knowledge courses, external expert courses, professional skills courses and language courses.</li>
<li>Last year our staff as a whole received over 400,000 hours of training spanning more than 160 courses.</li>
</ul>
 
Clearly defined career plan
<ul>
<li>Internal promotion based on your performance and potential</li>
<li>Partnership-based management, offering each professional the goal to become part of the Firm's group of partners</li>
</ul>
 
Others
<ul>
<li>University: we maintain close links with the world's most prestigious universities</li>
<li>Social action: we organize over 30 community support initiatives each year</li>
<li>Sports club: we organize internal championships</li>
</ul>
 
HOW TO APPLY
To apply, access the job offers and CV submission microsite at our website (<a href="https://www.managementsolutions.com/en/professional-careers-send-us-your-cv" target="_blank">https://www.managementsolutions.com/en/professional-careers-send-us-you…</a>).

NEW TECHNOLOGIES AND DIGITAL TRANSFORMATION CONSULTANT BOSTON

<h3>Job Description</h3>
Our client is looking for a Senior Quality, Document Control specialist to join their team!
On-site in Boston Seaport M-F
6 month contract with high chance of extension!
Pay range: $45-55/hr W2
Skills: document management and GMP
 
Duration: 6 months to start
 
Job Description:
Position Summary:
The Senior Document Control Specialist is responsible for overseeing the management, organization, and maintenance of all controlled documents within the company’s quality management system (QMS). This role ensures compliance with regulatory requirements, company policies, and industry standards, supporting the efficient operation of the pharmaceutical development and manufacturing processes.
 
Key Responsibilities:
Document Management:
<ul>
<li>Manage the lifecycle of controlled documents, including creation, revision, review, approval, distribution, and archival</li>
<li>Ensure documents are accessible, accurate, and up-to-date within the electronic document management system (EDMS).</li>
<li>Coordinate with cross-functional teams to ensure timely review and approval of documents.</li>
</ul>
Compliance:
<ul>
<li>Ensure all document control activities comply with current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and per Vertex Procedures.</li>
<li>Maintain audit readiness by ensuring documents are in a state of compliance and available for internal and external audits.</li>
</ul>
Process Improvement:
<ul>
<li>Identify and implement process improvements to enhance the efficiency and effectiveness of the document control system.</li>
<li>Develop and maintain document control procedures, work instructions, and training materials.</li>
</ul>
Training &amp; Support:
<ul>
<li>Provide training and support to employees on document control processes.</li>
<li>Act as a subject matter expert for document control during audits and inspections.</li>
</ul>
Reporting &amp; Metrics:
<ul>
<li>Generate and analyze document control metrics and reports to monitor performance and identify areas for improvement.</li>
<li>Present findings to management and recommend corrective actions as needed.</li>
</ul>
 
Qualifications:
<ul>
<li>Bachelor’s degree in a related field (e.g., Life Sciences, Quality Assurance, or Regulatory Affairs).</li>
<li>Minimum of 5-7 years of experience in document control within the pharmaceutical, biotechnology, or medical device industry.</li>
<li>Strong knowledge of cGMP, GDP, and regulatory requirements (e.g., FDA, EMA).</li>
<li>Proficiency in using electronic document management systems and other relevant software.</li>
<li>Excellent organizational, communication, and interpersonal skills.</li>
<li>Ability to work independently and as part of a team in a fast-paced, dynamic environment.</li>
<li>Detail-oriented with a commitment to quality and accuracy.</li>
</ul>
 
Preferred Qualifications:
<ul>
<li>Certification in Document Control or Quality Management</li>
<li>Experience with lean or continuous improvement methodologies.</li>
<li>Familiarity with global regulatory requirements and international document control standards.</li>
</ul>

Senior Quality, Document Specialist

<h3>Job Description</h3>
Department: Quality Assurance
Location: Woburn, MA
 
The Quality System Specialist / Senior Quality System Specialist plays a key role in supporting and enhancing Vaxess Technologies’ Quality Management System (QMS) to ensure compliance with applicable GMP/GLP standards. This position focuses on maintaining robust electronic quality systems, managing controlled documentation, and supporting the integration of new processes and applications.
 
Key Responsibilities:
Quality System and Computerized System Oversight
<ul>
<li>Support quality oversight for computerized systems, including QMS implementation, configuration, validation, and data migration activities.</li>
<li>Assist in launching new or enhanced system functionalities and communicating updates or user guidance to ensure effective adoption.</li>
<li>Collaborate with internal stakeholders and system vendors to ensure integrated processes across modules (Document Control, Training, Equipment, and Material Management).</li>
<li>Troubleshoot and resolve user issues as needed.</li>
</ul>
Documentation and Record Management
<ul>
<li>Manage the full lifecycle of controlled documents, including creation, revision, review, approval, distribution, and archival within the electronic document management system (EDMS).</li>
<li>Ensure that controlled documents, such as SOPs, batch records, and specifications, are accurate, current, and compliant with regulatory and internal requirements.</li>
<li>Coordinate document workflows with cross-functional teams to ensure timely completion and alignment with procedural requirements.</li>
<li>Author or revise SOPs, forms, and work instructions supporting quality system and GMP operations.</li>
</ul>
Training and Compliance Support
<ul>
<li>Provide training and day-to-day support to employees on document control and system processes.</li>
<li>Serve as a subject matter expert (SME) for document control and computerized systems during internal and external audits and inspections.</li>
<li>Support tracking and reporting of quality metrics (e.g., training completion, document cycle time, CAPA effectiveness) to drive continual improvement.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s degree in Life Sciences, Engineering, or a related discipline preferred; equivalent work experience considered.</li>
<li>2–5 years of experience in a GMP, GLP, or GxP-regulated environment (pharmaceutical, biotechnology, or medical device industry).</li>
<li>Experience with electronic quality management systems (e.g., Enzyme, Greenlight Guru, Veeva, MasterControl, etc.) is strongly preferred.</li>
<li>Familiarity with relevant regulations and standards (21 CFR Parts 210/211/11/820; ISO 9001/13485).</li>
<li>Excellent attention to detail, organization, and communication skills; ability to manage multiple priorities in a dynamic environment.</li>
<li>Collaborative, proactive, and adaptable work style aligned with a fast-paced, innovation-driven company.</li>
</ul>
 
Vaxess, a venture-backed life sciences company, is building a team of exceptional people to rapidly advance products on its microneedle array platform.&nbsp;We work closely as a team and thrive in a dynamic, exciting, and engaging work environment. If you’re interested in joining the Vaxess team, please submit your CV/resume to <a href="mailto:careers@vaxess.com" target="_blank">careers@vaxess.com</a>.&nbsp;&nbsp;

Quality System Specialist / Senior Quality System Specialist

<h3>Job Description</h3>
Job Title: Data Engineer (W2 Contract Only)
Duration: 7 months
Hours: 37.5 per week
Location: Hybrid – Boston, MA area (local candidates only)
An experienced Data Engineer is required to support the IT team responsible for data systems across healthcare departments. The role involves designing, building, and maintaining scalable data pipelines and solutions using Snowflake and Informatica, ensuring data accuracy, security, and accessibility.
Key Responsibilities
<ul>
<li>Design and maintain ETL/ELT pipelines using Informatica.</li>
<li>Develop and optimize data models and schemas in Snowflake.</li>
<li>Ensure compliance with data privacy and security standards (HIPAA/HITECH).</li>
<li>Integrate data from multiple sources, including healthcare systems (HL7, FHIR, X12 EDI).</li>
<li>Implement and monitor data ingestion, transformation, and quality processes.</li>
<li>Collaborate with analysts, data scientists, and business users.</li>
<li>Manage documentation, governance, and access controls.</li>
</ul>
Required Qualifications
<ul>
<li>3–5+ years in data engineering or ETL development.</li>
<li>Strong experience with Snowflake (SQL, data modeling) and Informatica (PowerCenter or IICS).</li>
<li>Proficient in SQL and data warehousing principles.</li>
<li>Experience handling structured and semi-structured data (JSON, XML, CSV).</li>
<li>Familiarity with cloud platforms (AWS, Azure, or GCP).</li>
</ul>
Preferred Skills
<ul>
<li>Python for automation and scripting.</li>
<li>Experience with Informatica Data Quality or Data Catalog tools.</li>
<li>Knowledge of CI/CD, Git, and Agile workflows.</li>
</ul>
Education
<ul>
<li>Bachelor’s degree in Computer Science, Information Systems, Data Engineering, or related field.</li>
<li>Snowflake or Informatica certifications a plus.</li>
</ul>
Soft Skills
<ul>
<li>Strong analytical and problem-solving ability.</li>
<li>Excellent communication and teamwork.</li>
<li>Attention to detail and commitment to data quality.</li>
</ul>

Data Engineer

<h3>Job Description</h3>
Job Description
About Tobin Scientific
Tobin Scientific is a leading provider of cold chain, ambient storage, and transport &amp; logistics services for the biopharma industry. We proudly support a diverse clientele spanning life sciences, academia, government, and more. Recognized for unwavering safety and reliability in the storage and transport of temperature-sensitive products, we excel in serving the complex needs of the pharmaceutical and biotech sectors. Our capabilities extend to laboratory relocation, principal investigator support, and other logistic services. Tobin Scientific's all-encompassing approach and commitment to quality make us an industry innovator, empowering our partners through the complexities of the biopharma industry.
 
Position Summary
The GMP Quality Specialist is responsible for providing day-to-day quality support for GMP warehousing and fleet operations. This role focuses on ensuring compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) through quality data entry, material checks, and execution of quality system activities. The Quality Specialist will support operational excellence by maintaining high standards of documentation, data integrity, and compliance within the Quality Management System (QMS).
 
Location: Methuen (with up to 10% travel to New Jersey site)
 
Key Responsibilities
<ul>
<li>Perform data entry and record management in support of GMP warehousing and labeling activities.</li>
<li>Conduct quality checks of materials prior to shipment to ensure compliance with GMP and GDP requirements.</li>
<li>Verify and review documentation for accuracy, completeness, and adherence to approved procedures.</li>
<li>Support the implementation and maintenance of site quality systems, including:
<ul>
<li>Deviations - assist with documentation, tracking, and closure.</li>
<li>CAPAs - support investigation summaries and effectiveness checks.</li>
<li>Change Controls - assist in documentation and coordination of changes impacting materials or processes.</li>
<li>Training - ensure training compliance and record accuracy for site personnel.</li>
</ul>
</li>
<li>Participate in routine warehouse walk-throughs to ensure compliance with GMP, GDP, and safety requirements.</li>
<li>Maintain accurate, timely, and compliant records within electronic systems (e.g., QMS, WMS, etc.).</li>
<li>Collaborate with cross-functional teams, including Operations and Facilities to ensure quality standards are met.</li>
<li>Assist with the review and approval of controlled documents such as SOPs, logs, and forms.</li>
<li>Promote a culture of continuous improvement and compliance across the site.</li>
<li>Travel up to 10% of the time to the company's New Jersey GMP warehouse to support quality system implementation.</li>
</ul>
Education
<ul>
<li>Bachelor's degree in Life Sciences (e.g., Biology, Chemistry, Biochemistry), Engineering, or related technical discipline required.</li>
</ul>
Experience and Qualifications
<ul>
<li>2-3 years of experience in a GMP Quality role (e.g., Quality Assurance, Quality Control, or Quality Operations) within a pharmaceutical, biotechnology, or medical device environment.</li>
<li>Strong understanding of GMP principles, including documentation, recordkeeping, and data integrity.</li>
<li>Experience supporting warehouse and fleet operations under GMP conditions preferred.</li>
<li>Working knowledge of Quality Management Systems (QMS) and quality processes (deviations, CAPA, change control).</li>
<li>Excellent attention to detail and accuracy in documentation and data entry.</li>
<li>Proficiency with Microsoft Office Suite and familiarity with electronic systems such as eQMS or ERP platforms.</li>
<li>Strong organizational and communication skills with the ability to work collaboratively across departments.</li>
<li>Self-motivated, reliable, and able to prioritize tasks in a fast-paced, compliance-driven environment.</li>
</ul>
 
Pay Range: The annual salary range for this position is as follows:
$90,000 - $110,000.
 
Compensation depends on relevant experience and/or education, specific skills, function, geographic location, and other factors as applicable by law.
Tobin Scientific is an equal opportunity employer and values diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. We are committed to creating an inclusive environment for all our employees.

GMP Quality Specialist

<h3>Job Description</h3>
Mason Frank is excited to be working with an established tech consulting firm, looking to bring on an experienced Project Manager to lead CRM, ERP, and digital transformation initiatives from kickoff through completion. This role involves overseeing project delivery, managing timelines and stakeholders, and driving successful outcomes across cross-functional teams.
 
Responsibilities: 
<ul>
<li>Serve as the primary client contact and maintain alignment on goals, scope, and timelines.</li>
<li>Build and manage project plans, schedules, budgets, and risk registers.</li>
<li>Lead internal and client status meetings and maintain executive-level dashboards.</li>
<li>Coordinate architects, analysts, and consultants to maintain delivery consistency.</li>
<li>Track project financials, monitor burn rate, and support billing accuracy.</li>
<li>Identify risks early and manage change control with precision.</li>
<li>Contribute to the ongoing refinement of project delivery framework.</li>
<li>Bachelor’s degree in Business, Technology, or related field.</li>
</ul>
 
Qualifications: 
<ul>
<li>5+ years of project management experience within digital, ERP, or CRM implementations.</li>
<li>Familiarity with Salesforce and enterprise platforms preferred.</li>
<li>Strong communication and stakeholder-management skills.</li>
<li>Experience with both agile and waterfall hybrid methodologies.</li>
<li>comfortable with 25-40% travel as needed</li>
<li>open to work 4-5 days ON-SITE in Boston, MA</li>
</ul>
 
About Mason Frank: 
Mason Frank (a brand of Tenth Revolution) is a global leader in Salesforce recruitment, connecting top professionals with premier organizations. Our expertise and network empower candidates to land career-defining roles while helping companies build world-class Salesforce teams.

CRM/ERP Project Manger

<h3>Job Description</h3>
Project Executive – Commercial Roofing
Worcester, MA
$150k - $200k + Benefits &amp; Bonus
 
 
 
Lead with Purpose. Deliver with Excellence.
 
 
 
You will be joining a roofing contractor that has built a reputation based on their commitment to quality, safety, and hard work.
 
This contractor is known for outperforming the competition and consistently delivering excellence. With no cap on future growth, this is a business where your career can truly take off.
 
You will be seen as a strategic partner, and not another number. Your role here will be mentoring a team of Project Managers, and ensuring the reputation of delivering excellence is upheld.
 
 
 
Benefits
<ul>
<li>Year-end bonus</li>
<li>Vehicle and gas card</li>
<li>401(k) matching</li>
<li>Dental insurance</li>
<li>Employee assistance program</li>
<li>Flexible spending account</li>
<li>Health insurance</li>
<li>Life insurance</li>
<li>Paid time off</li>
<li>Retirement plan</li>
<li>Vision insurance</li>
</ul>
 
 
What you’ll need
<ul>
<li>10+ years in construction management, managing large scale commercial projects</li>
<li>At least 5 years of commercial roofing experience</li>
<li>Prior experience monitoring project financials</li>
</ul>
 
 
What they do
 
The business is one of the largest commercial roofing and building envelope contractors in the country, and specialize in large-scale commercial and industrial projects.
They have a long-standing commitment to quality, and safety – having grown the business with their fantastic reputation, resulting in repeat business over the years.
 
 
 
If you want to join this journey then APPLY NOW with your resume.

Don't have a resume? No problem! Just get in touch directly with Charlie through text, call or email:
 
 
(214) 305-6136
<a href="mailto:charlie@roofingtalentamerica.com" target="_blank">charlie@roofingtalentamerica.com</a>

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