Top 1074 Medical devices Jobs in Boston, Ma

Consultant - Product Quality & Safety - Life Sciences & Healthcare
Deloitte —Boston, MA
- $88,700 - $170,900 a year
- Full-time
- Up to 50% travel
- Bachelor's degree
- Product management
Advanced Surgical Consultant (Boston Central) - Johnson & Johnson MedTech - Heart Recovery
Johnson & Johnson Services, Inc. —Boston, MA
- $96,000 - $155,250 a year
- Full-time
- Nursing
- Surgery
- Bachelor of Science
Medical Device Assembler
StemWave —Woburn, MA
- $24 - $28 an hour
- Full-time
- Computer literacy
- High school diploma or GED
- Computer skills
- Health savings account
- Paid holidays
Engineer I (Lab Testing & Operations)
Amgen —Cambridge, MA
- $88,281 - $119,439 a year
- Master's degree
- High school diploma or GED
- Organizational skills
- Disability insurance
- Health insurance
Research Associate
Eight Sleep —Boston, MA
- $70,000 - $100,000 a year
- Weekends as needed
- Computer Science
- HIPAA
- Mid-level
Clinical Specialist, ENT - Boston, MA
Medtronic —Boston, MA
- $60,800 - $91,200 a year
- Weekends as needed
- Nursing
- RN License
- Mid-level
- Health savings account
- Employee stock purchase plan
11d
Biomedical Equipment Technician 2
Sodexo —Melrose, MA
- $37.37 - $48.28 an hour
- Full-time
- Hospital
- Customer service
- Mid-level
- Paid holidays
- Health insurance
Senior Mechanical Engineer, Team Lead
Medica Corporation —Bedford, MA
- $102,000 - $125,000 a year
- Full-time
- Analysis skills
- Supervising experience
- Mentoring
- Health insurance
- Dental insurance
Quick Apply
10d
Quality Inspector
Primo Medical Group —Stoughton, MA
- $21 - $25 an hour
- Full-time
- Background check
- Basic math
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Senior Mechanical Engineer
Manta Product Development —Cambridge, MA
- $100,000 - $200,000 a year
- Full-time
- Customer service
- Bachelor of Science
- Office
- Health insurance
- Dental insurance
Quick Apply
Quality Inspector 2nd Shift
Primo Medical Group —West Bridgewater, MA
- $21 - $25 an hour
- Full-time
- Background check
- Basic math
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
In-Vivo Veterinary Surgical Research Technician
CBSET, Inc. —Lexington, MA
- From $24.99 an hour
- Full-time
- OSHA
- Bachelor of Science
- Laboratory experience
- Health savings account
- Disability insurance
Quick Apply
CNC Machinist - 1st Shift
Primo Medical Group —Stoughton, MA
- $24 - $40 an hour
- Full-time
- Background check
- 5 years
- Basic math
- Health savings account
- Health insurance
Quick Apply
14d
QA Senior Calibration Technician
Primo Medical Group —Stoughton, MA
- $28 - $32 an hour
- Full-time
- Background check
- Computer literacy
- Basic math
- Health insurance
- Dental insurance
Quick Apply
14d
Senior Manager, Regulatory Affairs NAM
Straumann —Andover, MA
- Up to $145,000 a year
- Full-time
- 5 years
- Office
- Analysis skills
- Health insurance
- Dental insurance
Production Supervisor - (Lead Manufacturing Technician)
AVAVA, Inc. —Waltham, MA
- From $80,000 a year
- Full-time
- Background check
- Mid-level
- 3 years
- Health savings account
- Health insurance
Quick Apply
1d
Internal Service Engineer
Hologic —Marlborough, MA
- $78,000 - $122,100 a year
- Full-time
- Computer literacy
- Bachelor of Science
- Mid-level
Regulatory Affairs Spec
Draeger Medical Systems, Inc. —Andover, MA
- $84,100 - $100,900 a year
- Hybrid work
- Bachelor of Science
- Research
- Mid-level
- Free parking
- Paid holidays
10h
Business Capability Specialist
BioNTech AG —Cambridge, MA
- $113,600 - $181,600 a year
- Full-time
- Background check
- Computer Science
- 5 years
- Health savings account
- AD&D insurance
Military Service - U.S. Air National Guard, Biomedical Equipment
Military Service - U.S. Air National Guard Recruiting —Massachusetts
- From $49,838.78 a year
- Full-time
- 18 years or older
- Military
- High school diploma or GED
- Health insurance

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Consultant - Product Quality & Safety - Life Sciences & Healthcare

Deloitte -
Boston, MA

Apply Now

Job Details

Full-time
$88,700 - $170,900 a year

Qualifications

AI tools proficiency
Employee relationship building
Reporting and dashboarding tools
Bachelor's degree
Management consulting experience
Managing projects
Cross-functional collaboration
Data-driven decision making
Data analytics technologies
Cross-functional communication

Full Job Description

Consultant - Product Quality & Safety - Life Sciences & Healthcare

Enterprise Operations & Risk

Our Deloitte Regulatory, Risk & Forensic team helps client leaders translate multifaceted risk and an evolving regulatory environment into defensible actions that strengthen, protect, and transform their organizations. Join our team and use advanced data, AI, and emerging technologies-combined with industry insight-to help clients bring clarity from complexity and accelerate their path to value creation.

Work You'll Do

As a Consultant, you will support the delivery of client projects while continuing to grow your subject matter expertise and consulting skills. You will work with teams helping life sciences clients address quality, regulatory, operational, and technology-related challenges across pharmaceutical, biotech, and medical device environments. This could include:

Support clients in pharmaceutical and medical device Regulatory Affairs and Quality Assurance strategy, process, operating model, and governance improvements
Assist with quality and regulatory due diligence for mergers and acquisitions, including document review, evidence gathering, interview support, risk tracking, and diligence summaries
Support separation and integration activities for QA/RA functions, including Day 1 planning, governance coordination, TSA support, and cutover readiness activities
Help assess quality management system and regulatory compliance gaps across areas such as SOPs, training, deviation management, CAPA, change control, complaints, and audit readiness
Support inspection readiness efforts, including mock inspection preparation, issue tracking, and remediation planning support
Assist with QA/RA technology enablement efforts, including business requirements gathering, process documentation, test script development, validation support, training coordination, and deployment activities
Support implementation and optimization of systems such as eQMS, document management systems, learning management systems, complaint handling, CAPA, change control, audit management, supplier quality, and regulatory information management platforms
Develop portions of client-ready deliverables, including assessments, process flows, requirements, status reports, business cases, and implementation plans
Track project activities, risks, dependencies, and action items, and support stakeholder coordination across workstreams
Continue building subject matter knowledge in Regulatory Affairs, Quality Assurance, and Commercial/Medical Content Management

The successful candidate would possess these skills

Ability to work independently and collaborate as part of a team
Effective written and verbal communication skills
Meticulous attention to detail and quality of work product
Ability to build and sustain professional relationships
Ability to lead projects or workstreams
Ability to manage and prioritize multiple tasks in a fast-paced and dynamic environment
Strong interpersonal skills and professional demeanor
Ability to meet deadlines
Ability to provide clear guidance to others

The Team
Our Enterprise Operations & Risk offering enables clients to achieve profitable growth and competitive advantage by optimizing the heart of the business. We leverage deep domain expertise to extend enterprise resilience, agility, and remediation. Our professionals address client needs that span the organization and impact strategy, operations, performance, and reputation.

Qualifications

Required:

Bachelor's degree required
2+ years of experience focused on Life Sciences in a consulting and/or industry role
Experience or exposure to the use of data, analytics, and/or AI-enabled tools to support business processes or decision-making
Foundational experience in pharmaceutical QA/RA (e.g., GMP, quality systems, compliance support) and/or medical device QA/RA (e.g., design controls, risk management, post-market processes)
Working knowledge of common regulatory and quality requirements applicable to pharmaceutical and/or medical device organizations
Experience supporting the translation of regulatory and quality requirements into business processes, documentation, or controls
Experience supporting project delivery in areas such as compliance remediation, process improvement, system implementation, diligence, or integration planning
Familiarity with quality and regulatory systems and capabilities such as document control, training, deviations, CAPA, change control, audits, complaints, supplier quality, and/or submission or product registration data management
Experience supporting data analysis, reporting, dashboards, KPI tracking, or process monitoring
Experience in project management, PMO support, or workstream coordination
Ability to manage multiple assignments and work effectively in a deadline-driven environment
Strong attention to detail and ability to produce polished, client-ready deliverables
Strong written and verbal communication skills and ability to work effectively in cross-functional teams
Must be legally authorized to work in the United States without the need for employer sponsorship, now or at any time in the future
Ability to travel up to 50%, based on the work you do and the clients and industries/sectors you serve

Preferred

Experience in the pharmaceutical, biotech, and/or medical device industries
Experience supporting eQMS, RIM, DMS, LMS, or related quality/regulatory technology initiatives
Experience with compliance assessments, inspection readiness, remediation, or QA/RA process improvement

Information for applicants with a need for accommodation: https://www2.deloitte.com/us/en/pages/careers/articles/join-deloitte-assistance-for-disabled-applicants.html

The wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Deloitte, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current range is $88700 - $170900.

You may also be eligible to participate in a discretionary annual incentive program, subject to the rules governing the program, whereby an award, if any, depends on various fac tors, including, without limitation, individual and organizational performance.

Apply Now

Refine Your Search

medical devices jobs in boston, ma

Consultant - Product Quality & Safety - Life Sciences & Healthcare

Advanced Surgical Consultant (Boston Central) - Johnson & Johnson MedTech - Heart Recovery

Medical Device Assembler

Engineer I (Lab Testing & Operations)

Research Associate

Clinical Specialist, ENT - Boston, MA

Biomedical Equipment Technician 2

Senior Mechanical Engineer, Team Lead

Quality Inspector

Senior Mechanical Engineer

Quality Inspector 2nd Shift

In-Vivo Veterinary Surgical Research Technician

CNC Machinist - 1st Shift

QA Senior Calibration Technician

Senior Manager, Regulatory Affairs NAM

Production Supervisor - (Lead Manufacturing Technician)

Internal Service Engineer

Regulatory Affairs Spec

Business Capability Specialist

Military Service - U.S. Air National Guard, Biomedical Equipment

I want to receive the latest job alert for medical devices in boston, ma

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