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Date Posted: 2026-06-23 Country: United States of America Location: US-MA-ANDOVER-AR1 ~ 358 Lowell St ~ AR1 DUKES BLDG Position Role Type: Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: The ability…
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$80/hr–$85/hr
Other
bachelor degree
Posted 46d ago
Apply by Jun 23
~40 hrs/week
Responsibilities
Lead cross-functional project plans to ensure regulatory inspection readiness and commercial manufacturing preparedness. Coordinate between Quality, Regulatory, and Manufacturing functions to manage timelines, risks, and deliverables for health authority inspections.
Requirements
Requires a Bachelor's degree in Life Sciences, Engineering, or Business with 5-8 years of project management experience in a regulated biotech or pharma environment. Must have demonstrated experience in inspection readiness and proficiency with tools like Smartsheet and Microsoft Project.
Work Model: On-site 3–4 days per week, aligned with Vertex ways of working
Department: Cell and Gene Therapy – Project Management and Strategic Operations
Company Overview
Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious diseases. Our teams work across research, development, manufacturing, and commercialization to advance high-impact therapies for patients. At Vertex, we are committed to scientific excellence, collaboration, and delivering meaningful outcomes with urgency and integrity.
Role Summary
The Project Management and Strategic Operations team within Cell and Gene Therapy at Vertex is seeking a Project Manager contractor with prior experience inspection readiness and commercial readiness to lead initiatives that support regulatory inspection readiness and commercial manufacturing preparedness. This role will partner across Quality, Regulatory, Manufacturing, QC, Supply Chain, and other key functions to ensure the organization is prepared for health authority inspections and commercial execution milestones. The successful candidate will bring strong capabilities in project management, stakeholder management, and operational execution, with the ability to quickly learn and apply new information in a dynamic environment. This individual will be solution-oriented and able to leverage knowledge of cGMP manufacturing and cross-functional program execution to manage complex workstreams that support key Vertex goals.
The ideal candidate is highly collaborative, organized, and comfortable managing timelines, risks, dependencies, and partner relationships across internal and external teams.
Key Responsibilities
Lead cross-functional project plans for inspection readiness and commercial readiness initiatives.
Develop and maintain integrated timelines, milestones, risk logs, and status reporting for readiness activities.
Coordinate stakeholders across Quality, Regulatory Affairs, Manufacturing, Supply Chain, Commercial, and other business functions.
Drive planning and execution of activities related to regulatory inspections, audits, mock inspections, and readiness assessments.
Support inspection preparation by tracking deliverables, coordinating documentation readiness, and facilitating issue resolution.
Partner with functional leaders to identify gaps, risks, and dependencies that may impact inspection or commercial launch readiness.
Establish governance routines, including project team meetings, steering committee updates, and executive communications.
Monitor readiness metrics and provide clear, timely updates on project health, risks, mitigations, and critical decisions.
Ensure alignment between operational readiness plans and commercial launch objectives.
Facilitate cross-functional decision-making and help resolve issues that may delay key milestones.
Ensure activities are executed in compliance with applicable GxP, quality, and regulatory requirements.
Required Qualifications & Technical Skills
Bachelor’s degree in Life Sciences, Engineering, Business, Project Management, or a related field.
5 - 8 years of experience in project management within biotechnology, pharmaceuticals, cell and gene therapy, or another regulated environment.
Demonstrated ability to develop and manage project timelines, milestones, risk registers, dashboards, and action trackers.
Proficiency with Microsoft Project, Smartsheet, and Microsoft Office Suite, including PowerPoint, Excel, Word, and Outlook.
Experience in cross-functional team management, including meeting coordination, agendas, minutes, action tracking, and follow-up.
Ability to identify, track, and communicate project risks, issues, dependencies, and escalation points across complex programs.
Experience supporting or coordinating inspection readiness and/or commercial readiness activities in a regulated environment.
Strong communication skills, including the ability to clearly articulate project status, dependencies, and risks to cross-functional teams and leadership.
Highly collaborative, with proven ability to partner effectively across MFG, QA/QC, Regulatory CMC, and other stakeholder groups.
Strong organizational skills, attention to detail, and ability to learn quickly and apply feedback effectively.
Ability to work on-site 3–4 days per week to support project team meetings and cross-functional collaboration.
Preferred Skills
Experience supporting regulatory inspection readiness activities in a GMP environment.
Familiarity with commercial launch readiness or late-stage operational readiness planning.
Experience creating leadership-ready slide presentations and project updates.
Ability to influence without direct authority in a matrixed organization.
Experience in Cell and Gene Therapy development and manufacturing environments.
Pay Range
$80-$85/HR
Requisition Disclaimer
This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (“Vertex”). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements
By applying for this position, you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials, which may include your CV/Resume, email address or phone number, with Vertex. For more information on how Vertex handles your personal data related to your job application, please see Vertex’s Careers Privacy Notice. Agreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners
(collectively, “Atrium Alerts”). Atrium Alerts may be sent by email, phone, or text message. Your personal information will be safely stored within the Atrium & Vertex databases. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time, please contact Atrium at [email protected].
If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at [email protected]. Please include the job title in the subject of your email.
Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious diseases and has made significant advancements in cystic fibrosis, sickle cell disease, transfusion-dependent beta thalassemia, and acute pain — and continues to progress clinical and research programs in these diseases. We also have a robust clinical pipeline of investigational therapies across a range of modalities in other serious diseases where we have deep insight into causal human biology, including acute and neuropathic pain, APOL1-mediated kidney disease, IgA nephropathy, autosomal dominant polycystic kidney disease, type 1 diabetes and myotonic dystrophy type 1.
Our global headquarters is in Boston, and we have research and development (R&D) sites and commercial offices worldwide.
Vertex is consistently recognized as one of the industry’s top places to work by Science Magazine, The Boston Globe, Boston Business Journal and the San Diego Business Journal. We have also earned a spot on TIME Most Influential Companies, TIME Best Inventions, and Fast Company Most Innovative Companies lists. Our research and medicines have received esteemed recognitions, including the Robert J. Beall Therapeutics Development Award, the Prix Galien, the Scrip Award and the Breakthrough Prize awards.
Read our community guidelines: https://www.vrtx.com/vertexs-community-guidelines/
Offices: Vertex Pharmaceuticals Inc., 50 Northern Avenue, Boston, MA 02210, US · 2 Kingdom Street, Paddington, London W2 6BD, GB · 3215 Merryfield Row, San Diego, California 92121, US · Calle Marqués de Villamagna, Madrid, Spain 28001, ES · 601 Pacific Hwy, Sydney, NSW 2065, AU
How much do Science & Research jobs in Massachusetts pay?
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