GCP Quality Associate Director
$160.6k - $240.8kVertex Pharmaceuticals
## GCP Quality Associate DirectorApplylocations: Boston, MAtime type: Full timeposted on: Posted Todaytime left to apply: End Date: June 18, 2026 (5 days left to apply)job requisition id: REQ-29374**Job Description****GENERAL POSITION SUMMARY:**The Associate Director, GCP Compliance is responsible for the quality assurance and compliance activities in support Quality Issues Management and other activities within RDQ. This role will support GCP related events and escalation of these events to Senior Management and other key stakeholders. This individual will work closely with Quality Leads, Study team members, and other pillars in the Quality organization and will demonstrate Vertex Core Values.**RESPONSIBILITIES:*** Assist in the continuous improvement of the Issue Management process- handling of QEs, trending, and updating processes.* Manage or assist in (internal and external) GCP Quality Events including, but not limited to investigations, CAPAs, Root Cause Analysis, Effectiveness Checks).* Perform initial triage of event criticality working with operational Quality, Global Clinical Quality and other Subject Matter Experts, as needed.* Escalate critical and major findings to Quality management and monitor key performance indicators.* Utilize quality tools and techniques to support or perform and document full root cause and investigations, to evaluate and resolve quality issues, and to enhance continuous improvement.* Assist in tracking of event completion in expected timeframes and monitor quality of investigation writing.* Create investigation and deviation records in the electronic Quality Management System..* Communicates proactively with internal and external partners and management.* Serve as a Subject Matter Expert in the risk-based approach to quality events, and using data to inform trends and next steps in continuous improvement process.* Generates Metrics / KPIs, Dashboards and Reports, as requested and present results, where needed.* Participate in inspection readiness and support activities* May assist with onboarding and ongoing training team members, and may manage direct reports, as needed.* Assist in additional Quality Assurance initiatives as applicable, including inspection, audit activities* Assist in Quality Risk Assessment and Management**REQUIRED KNOWLEDGE, SKILLS, AND COMPETENCIES*** Experience successfully leading event investigations, Root Cause Analysis and CAPA* Knowledge of current industry trends and ability to use the latest technologies* Highly organized with strong planning capabilities* Compliance and GCP quality management experience* Strong communication, problem solving and critical thinking skills* Knowledge of overall issue management processes, risk- based approaches, and best practices* Experience in quality analytics and using data to make decisions and identify trends* Experience in Health Authority inspections and audits**PREFERRED EDUCATION AND EXPERIENCE:*** Bachelor’s Degree and 10 years of relevant work experience or a combination of training and experience**Pay Range:**$160,600 - $240,800**Disclosure Statement:**The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.**Flex Designation:**Hybrid-Eligible Or On-Site Eligible**Flex Eligibility Status:**In this Hybrid-Eligible role, you can choose to be designated as: 1. **Hybrid**: work remotely up to two days per week; **or select** 2. **On-Site**: work five days per week on-site with ad hoc flexibility.Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.#LI-Hybrid #J-18808-Ljbffr
- ...Vertex Pharmaceuticals is hiring a GCP Quality Associate Director in Boston. The role involves overseeing quality assurance and compliance for GCP activities, including managing quality events and assisting in investigations. Candidates should possess a Bachelor's degree...Suggested
$148k - $222k
...Quality Product Complaints Associate Director The Quality Product Complaints Associate Director is responsible and accountable for providing quality oversight of the Product Complaint Quality System and the Global Recall and Defect Notification Systems. This role will...SuggestedContract workWork experience placementSummer workRemote workFlexible hours2 days per week$156.6k - $234.8k
**Job Description****General Summary:**The Manufacturing Process & Technical Quality Associate Director is accountable for end-to-end technical quality oversight of cell and genetic program throughout clinical development, commercialization, product launch and post approval...SuggestedWork experience placementSummer workRemote workFlexible hours2 days per week$164.5k - $222.5k
Associate Director, Clinical Quality and Continuous Improvement Overview Provides strategic QA oversight across clinical development procedures to ensure compliance with GCP requirements, regulatory expectations, and internal quality standards. Serves as the primary...SuggestedFull timeTemporary workLocal areaRemote workFlexible hours$160k - $180k
...latest corporate deck and other presentations here. About the Role Senior Manager, GCP Clinical Quality As the Senior Manager, GCP Clinical Quality reporting to the Senior Director GCP Quality Assurance, you will be partnering with Clinical Development/Operations, Pharmacovigilance...SuggestedWork at officeFlexible hours2 days per week$160k - $180k
...candidate, OP‑3136, is a potent KAT6 inhibitor with best‑in‑class potential. About the Role As the Senior Manager, GCP Clinical Quality reporting to the Senior Director GCP Quality Assurance, you will partner with Clinical Development/Operations, Pharmacovigilance and Safety...Work at office2 days per week$170k - $190k
...founded by Fairmount. For more information, visit JadeBiosciences.com and follow the Company on LinkedIn. Role Overview The Associate Director, Quality Control will lead critical Quality Control functions to support Jade’s product pipeline across various stages of...Remote work- Looking for a GCP Quality expert to work on implementing quality from work for our on going Phase I-III clinical trials. Responsible for support of phase-appropriate Monte Rosa Quality GCP and GCLP activities, including GCP quality oversight of ongoing quality activities...
- ...with strong discovery, clinical development, corporate, and commercial operations. About the Role: We are seeking a Director, Quality Assurance, GCP/GLP to join our team. We are building our Quality function to support Xenon’s clinical development programs, as well as...Contract workTemporary workWork at officeRemote work2 days per week
- ...pipeline into late-stage clinical development, we are building a fit-for-purpose Quality organization to support our growth. Position Overview The Senior Director, Quality Assurance GCP is a key role within Hemab's Quality function. Reporting to the Head of Quality, this...
$170k - $190k
...A clinical-stage biotechnology company is seeking an Associate Director, Quality Control to lead critical functions supporting their product pipeline. The successful candidate will develop QC strategies, oversee analytical methods, and ensure compliance with quality standards...Remote work- ...Vertex Pharmaceuticals in Boston is seeking an Associate Director for R&D Quality Regulatory & Risk Integration. This role involves establishing and maturing the Regulatory Intelligence & Surveillance process and serving as a key resource for quality consults and inspection...
$155k - $190k
...Associate Director, Clinical Quality Assurance Waltham, Massachusetts At Kailera, we are bold, authentic and committed to our mission of developing... ...: Oversee and ensure compliance with GCP/GVP regulations, guidelines, and internal policies throughout...Full timeLocal areaFlexible hours$137k - $235.75k
...championing patients every step of the way. Learn more at Johnson & Johnson Innovative Medicine (IM) is recruiting for an Associate Director of AI Quality and Governance - R&D Data Science & Digital Health. This position can be located in Titusville, NJ; New Brunswick, NJ;...Temporary workLocal areaImmediate start$160k - $175k
...unites us across functions and geographies. Location : Boston, MA preferred but can be remote Position : Sr. Manager/Associate Director GMP Quality Reporting to : Director, GMP Quality The position will be responsible for day-to-day operational support ensuring compliance...Contract workRemote workWorldwideFlexible hours- ...A leading biotechnology firm in Boston is seeking an Associate Director for Manufacturing Process & Technical Quality. This role is focused on ensuring technical quality oversight for cell and gene therapies throughout their lifecycle. The ideal candidate will have extensive...
- ...Associate Director of Compliance & Quality Improvement Casa Esperanza, Inc. is a bilingual/bicultural behavioral health treatment provider serving Boston and the Merrimack Valley. Our mission is to empower individuals and families to recover from addiction, trauma, mental...Full timeContract workFor contractorsWork at officeMonday to Friday
$160k - $240k
...curiosity and inclusivity, so that our people are valued, seen, and heard. How you'll make an impact: The Associate Director will act as a Quality subject matter expert for Good Manufacturing Practices (GMP) activities. The individual will be responsible for material...Contract work$148k - $236.5k
...Pioneering Medicines: Associate Director / Director, Clinical Operations Cambridge, MA USA What... ...data management, regulatory affairs, and quality. Lead or contribute to the design of clinical... .... Maintain current knowledge of ICH‑GCP, FDA, EMA, and other applicable...For contractors- ...Associate Director of Quality Assurance Summary: The Associate Director of Quality Assurance is responsible for designing, planning, implementing, directing and evaluating a quality assurance function and a quality management system which supports clinical development...Temporary workFor contractorsFor subcontractorFlexible hours
$154.4k - $242.55k
...Associate Director, Predictive Analytics We are seeking a hands-on innovative seasoned Data Science... ...project work and ensure high-quality, timely deliverables. Oversee project timelines... ...with cloud platforms (AWS, Azure, GCP). Experience with pharma data (e.g.,...Minimum wageTemporary workWork at officeLocal areaRemote work- ...Job Description Associate Medical Director in Neuroscience Therapeutic Area Unit, Cambridge, MA. Position Objectives The Associate Medical Director... ...preferred. Regional/global regulatory requirements. GCP/ICH. Travel Requirements Ability to drive or fly to meetings...Local areaNight shift
$198.5k - $311.85k
...that will inspire you and empower you to shine? Join us as an Associate Medical Director in our Neuroscience Therapeutic Area Unit in our Cambridge,... ...preferred. Regional/global Regulatory requirements. GCP/ICH. Travel Requirements Ability to drive to or fly to various...Minimum wageTemporary workWork at officeLocal areaRemote workNight shift$198.5k - $311.85k
...that will inspire you and empower you to shine? Join us as an Associate Medical Director in our Neuroscience Therapeutic Area Unit in our Cambridge,... ...is preferred Regional/global Regulatory requirements GCP/ICH TRAVEL REQUIREMENTS Ability to drive to or fly to various...Minimum wageFull timeTemporary workWork at officeLocal areaRemote workNight shift$155k - $214k
...About This Role:As the Associate Director, Global Quality Risk Management, you will be at the forefront of Biogen’s commitment to quality excellence. Leading the charge in designing, implementing, and sustaining the enterprise Quality Risk Management (QRM) capabilities...Temporary workLocal area$184k - $210k
...Summary: We’re looking for an experienced Associate Director, Trial Master File (TMF) Operations to... ...partner across Clinical Operations, Quality, Regulatory, IT, and external vendors to... ...reporting processes Deep understanding of ICH‑GCP requirements, TMF best practices, and...Work at office2 days per week3 days per week- ...Job Title: Associate Medical Director Location: Cambridge, MA (Remote) Duration: 12 months+ Pay Rate: $170/hr. on W2 Job Description... ...building skills Understanding guidelines (FDA, ICH, EMA and GCP) Working knowledge of biostatistics, data management,...Contract workRemote workShift work
$211.91k - $256.79k
...Associate Director, Global Clinical Science - Neuroscience Working with Us Challenging. Meaningful... ...comments and ensuring high clinical quality (collaboration with Medical Writing)... ...equivalent ~ Proficient knowledge of GCP/ICH, drug development process, study design...Hourly payFull timeTemporary workPart timeFor contractorsSummer workWork at officeRemote workFlexible hoursShift work$270k - $300k
...range of solid tumors. For more information, visit and follow the Company on LinkedIn and X. We are seeking a Senior Director, R&D Quality (GCP–GLP–GvP) is a key leader within Crescent’s Quality organization, responsible for providing strategic and hands-on Quality...Contract workTemporary workWork at officeLocal areaFlexible hours- ...represent a significant portion of Harvard's annual spend. The Associate Director partners closely with HUIT, school‑based IT leaders, General... ...such as Artificial Intelligence, machine learning, SaaS (GCP, AWS, etc.) and automation frameworks. Demonstrated expertise...Contract workWork experience placementWork at office2 days per week1 day per week
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