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Quality systems manager Jobs in Boston, MA

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Quality systems manager • boston ma

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Director, Quality Systems & Compliance

Director, Quality Systems & Compliance

ElevateBioWaltham, MA, United States
Full-time
ElevateBio is a technology-driven cell and gene therapy company, accelerating access to the cutting‑edge technologies and expertise to change the future of medicine. Our integrated technologies mode...Show moreLast updated: 1 hour ago
Quality Manager

Quality Manager

Admiral MetalsWoburn, MA, US
Full-time
Admiral Metals is a leading Metal Service Center based in Woburn, MA servicing the Northeast, Mid-Atlantic, Mid-West and we are hiring. QMS and AS9100 & ISO Certification.Manage the QMS to ensur...Show moreLast updated: 30+ days ago
  • Promoted
Quality Systems Specialist

Quality Systems Specialist

Advantage TechnicalWaltham, MA, United States
Full-time
Hybrid (Onsite Tuesday, Wednesday, Thursday).The Quality Systems Specialist, under the direction of the QS&C management team, supports global Quality Systems to ensure compliance, operational effec...Show moreLast updated: 22 days ago
Manager, Quality Systems Cell and Gene

Manager, Quality Systems Cell and Gene

VertexBoston, MA
Full-time
This position focuses not just on the “what” but the “how.Key Duties and Responsibilities : .Supports local Quality system oversight, metrics, and improvement including change control, events, CAPA, ...Show moreLast updated: 30+ days ago
Manager Quality Assurance

Manager Quality Assurance

Boston StaffingBoston, MA, US
Full-time
This position will be remote, but with a preference for candidates in Ohio, Missouri, Texas, or Louisiana.This is your chance to be part of an in-house Brands team of industry experts in the domain...Show moreLast updated: 12 days ago
Manager, Quality Assurance

Manager, Quality Assurance

Alnylam PharmaceuticalsCambridge, MA, United States
Full-time
This role is primarily responsible for day-to-day operations within the Document Control team, as well as support QMS procedural improvements and document workflow optimization.Summary of Key Respo...Show moreLast updated: 8 days ago
  • Promoted
USA_Quality Manager

USA_Quality Manager

VariteQuincy, MA, US
Full-time
Work closely with Business SMEs and Application Vendor teams to understand Business requirements for ongoing projects, upgrades, and enhancements. Develop Test Strategy to provide adequate test cove...Show moreLast updated: 7 days ago
  • Promoted
Quality Systems Lead

Quality Systems Lead

AlkermesWaltham, MA, United States
Full-time
Govern owned QMS applications, including harmonization of processes across sites.Responsible for requirements authoring and ongoing maintenance by leading and facilitating meetings / workshops with S...Show moreLast updated: 30+ days ago
  • Promoted
Lead Quality Systems Auditor

Lead Quality Systems Auditor

Fresenius Medical CareWaltham, MA, US
Full-time
Fresenius Medical Care (FMC) is a people business.Our success depends on having the best and brightest employees and helping them attain their personal and professional goals while delivering excel...Show moreLast updated: 30+ days ago
  • Promoted
Senior Manager, Quality Systems Readiness (Commercial Launch)

Senior Manager, Quality Systems Readiness (Commercial Launch)

JMD Technologies Inc.Boston, MA, United States
Full-time
Senior Manager, Quality Systems Readiness (Commercial Launch).Greater Boston Area, MA (Hybrid 3 days onsite).This role supports commercial launch readiness by ensuring GMP Quality Systems and docum...Show moreLast updated: 15 days ago
Quality Manager

Quality Manager

Consigli ConstructionBoston, MA, US
Full-time
The Quality Manager (QM) will collaborate with several project teams throughout the lifecycle of their assigned projects. Their main responsibility is to support and be a technical and field resourc...Show moreLast updated: 30+ days ago
  • Promoted
Clinical Systems / EHR Quality Data Specialist

Clinical Systems / EHR Quality Data Specialist

US Tech SolutionsBoston, MA, United States
Full-time
This position is responsible for working with the care team to support the development of quality measures, code the technical specifications to operationalize the measures, and create the reportin...Show moreLast updated: 10 days ago
Lead, Quality Systems

Lead, Quality Systems

GenezenLexington, MA, US
Full-time
The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients.We provide process development, produce GMP viral vectors, and provide cell transduction f...Show moreLast updated: 30+ days ago
Quality Systems Specialist I

Quality Systems Specialist I

New England Donor ServicesWaltham, Massachusetts, USA
Full-time
This is a hybrid role that requires 1-2 days in office per week after a successful orientation period.During orientation expect to be in Waltham more. There is also a weekend coverage rotation among...Show moreLast updated: 12 days ago
Quality Manager

Quality Manager

PSIBoston, MA, US
Full-time
The Quality Assurance (QA) Manager in Boston, MA is responsible for leading the quality function at a cooked and raw, multi-protein retail production facility. This role ensures all products meet re...Show moreLast updated: 30+ days ago
Quality Manager

Quality Manager

FloodGate Medical IncBoston, MA, United States
Full-time
Cytrellis is seeking a hands?on Quality Manager to support a fast?growing medical device organization that develops FDA?cleared capital equipment and consumables. Youll own day?to?day quality execut...Show moreLast updated: 16 days ago
Associate Director, Quality Systems

Associate Director, Quality Systems

Mariana OncologyWatertown, MA, US
Full-time
Vice President, Quality Assurance.We are seeking an experienced Associate Director, Quality Systems to join Marianas Quality Assurance organization, advancing personalized medicine and.Illustrative...Show moreLast updated: 30+ days ago
Quality Engineer-Systems

Quality Engineer-Systems

BoydWoburn, MA
Full-time
The Boyd Quality Engineer is responsible for ensuring that Boyd products exceed the requirements and expectations of our customers. This individual will assume full responsibility for all aspects of...Show moreLast updated: 30+ days ago
Experienced Quality Systems Specialist (Regulatory Regulations)

Experienced Quality Systems Specialist (Regulatory Regulations)

BoeingEverett, Massachusetts, USA
Full-time +1
Experienced Quality Systems Specialist (Regulatory Regulations).Experienced Quality Systems Specialist.As a member of the Designated Regulatory Office (DRO) you will support FAA Certification activ...Show moreLast updated: 5 days ago
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Director, Quality Systems & Compliance

Director, Quality Systems & Compliance

ElevateBioWaltham, MA, United States
1 hour ago
Job type
  • Full-time
Job description

ElevateBio is a technology-driven cell and gene therapy company, accelerating access to the cutting‑edge technologies and expertise to change the future of medicine. Our integrated technologies model offers turnkey scale and biotechnological capabilities to power genetic medicines processes, programs, and companies to their full potential.

The Role :

The Director, Quality Systems and Compliance provides strategic direction and oversight of the Quality Systems and Quality Compliance functions at ElevateBio to ensure execution and performance meets regulatory requirements and current industry best practices. You will be responsible for ensuring that ElevateBio’s Quality Management System (QMS) enables and facilitates compliance in a phase‑appropriate manner from early clinical phase projects through commercial operations. In this role you will manage the teams responsible for providing day‑to‑day support of the Quality Systems, Compliance and Supplier Quality functions.

The successful candidate will also actively communicate goals and timelines to align team members and cross‑functional stakeholders on Quality milestones and deliverables. You will further develop, maintain, and continually improve the QMS. Additionally, this role is responsible for the audit programs, including self‑inspections, client audits, supplier audits, and regulatory inspections at our BaseCamp facility.

Here’s What You’ll Do :

Responsible for the Quality Systems of :

  • Documents and Records Management
  • GxP Training and Learning Management
  • CAPA, Deviation and Change Control Management
  • Quality Risk Management
  • Supplier Quality Management
  • Audits and Inspection Management
  • Digital Quality Management
  • Manage and develop the teams responsible for the Quality Systems and Compliance.
  • Serve as the business system owner for the electronic DMS, LMS and QMS.
  • Drive strategic planning for the QMS, including establishing short and long‑range quality planning objectives in collaboration with cross‑functional stakeholders for continuous improvements.
  • Manage key quality performance metrics and data, collaborating with stakeholders to continually review and refine the quality metrics.
  • Ensure the site remains inspection‑ready through self‑inspection, internal quality audit and inspection‑readiness programs.
  • Host and coordinate client quality audits.
  • Lead and facilitate Quality meetings, Supplier Review Board and Quality Management Review.
  • Responsible for efficient and phase‑appropriate Supplier Quality Management program elements, with close interdependence to the Material Quality program.
  • Promote a culture of Quality and GxP continuous improvement across the organization including training initiatives.
  • Support new GxP business opportunities, address GxP risks or enhancements to cross‑functional quality systems.

Requirements :

  • Minimum of 12+ years biopharmaceutical experience; 7+ years management experience in Quality Operations and Quality Management Systems.
  • Expert knowledge in global GxP regulations and the ability to interpret and implement these requirements.
  • Experience in regulatory inspections.
  • Ability to think strategically and to influence others.
  • Ability to identify, prioritize, and implement actions to continuously improve operations and systems and manage risks.
  • Experience in electronic Enterprise Management systems, Quality Management Systems, Document Management Systems.
  • Appreciation and desire to operate within a completely digital environment.
  • The budgeted range for this position is$220,000 - $250,000. This range is a good faith estimate of the expected salary range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.

    Why Join ElevateBio?

    ElevateBio is a technology‑driven company built to power transformative genetic medicines today and for many decades to come. The Company commercializes its enabling technologies, manufacturing capabilities, and industry‑leading expertise through partnerships to accelerate development across a breadth of therapeutic approaches and modalities. The ElevateBio ecosystem combines multiple R&D technology platforms – including Life Edit, a next‑generation, full‑spectrum gene editing platform; comprehensive cell engineering technologies; and an expanded viral and non‑viral therapeutic delivery platform – with BaseCamp®, its end‑to‑end genetic medicine cGMP manufacturing and process development business, to accelerate the discovery and development of advanced therapeutics.

    We aim to be the dominant engine inside the world’s greatest scientific advancements harnessing human cells and genes to alter disease.

    Our Mission :

    To power the creation of life‑transforming cell and gene therapies, at a speed the world deserves.

    Our Vision :

    We seek to be the world’s most indispensable cell and gene therapy technology company, redefining how companies operate, how products are created and how disease is treated.

    ElevateBio is committed to equal employment opportunity and non‑discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

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