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Marking Jobs in Massachusetts (NOW HIRING)

G3 Staffing LLC

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CNC Laser Operator

Devens, MA · On-site

$30 - $32/hr

Devens, MA Primary responsibilities will include, but not limited to, the set up and running of different (CNC) computer numeric controlled equipment within the Marking Department. Minimum ...

Private Company

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Mechanical Assembly (4 day work week)

Tyngsboro, MA · On-site

$25/hr

... marking equipment. · Support general production needs, including material handling and preparation. · Inspect assemblies and finished components for accuracy · Record accurate time and count data ...

Spartan Race, Inc

Manager, Course

Boston, MA · On-site

$20 - $23/hr

With minimal direction, sufficiently marks a course using marking tape and directional arrows based on Race Director guidelines and an existing course design * Ensures the core product of Spartan ...

IPG Photonics

Integration Engineer

Marlborough, MA · On-site

$107K - $145K/yr

Job Summary We are looking for a laser system integration engineer to help us support our subsystems on different laser applications (in welding, marking and cutting). This includes the development ...

McBride

Security Assistant

Hanscom Air Force Base, MA · On-site

$100K - $110K/yr

Review documentation for public release and verify proper Controlled Unclassified Information (CUI), classification markings, and distribution statements. * Assist with the development and ...

IPG Photonics

Integration Engineer

Marlborough, MA · On-site

$107K - $145K/yr

Job Summary We are looking for a laser system integration engineer to help us support our subsystems on different laser applications (in welding, marking and cutting). This includes the development ...

Kept Companies, Inc

General Labor

Lowell, MA · On-site

$16 - $20/hr

Duties include cleaning kitchen exhaust hood systems, assisting with pavement marking and line striping projects, operating and maintaining specialized trucks and field service equipment, and loading ...

DCS Corporation

$66K - $90K/yr

Review documentation for public release and verify proper Controlled Unclassified Information (CUI), classification markings, and distribution statements. * Assist with the development and ...

Kept Companies Inc

General Labor

Lowell, MA · On-site

$16 - $20/hr

Duties include cleaning kitchen exhaust hood systems, assisting with pavement marking and line striping projects, operating and maintaining specialized trucks and field service equipment, and loading ...

Connexion Systems & Engineering, Inc.

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Electromechanical Assembler

Andover, MA · On-site

$20 - $24/hr

Following established methods and procedures builds flexible cable assemblies; makes bulk cables, cuts and strips wires, crimps, cleaning operations, marking operations * Work from production ...

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Showing results 21-40

All JobsMarking JobsMarking Jobs in Massachusetts

Marking information

See Massachusetts salary details

$14

$35

$61

How much do marking jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for marking in Massachusetts is $35.70, according to ZipRecruiter salary data. Most workers in this role earn between $23.61 and $47.26 per hour, depending on experience, location, and employer.

What is a marking?

A marking job typically involves assessing and grading students' work, such as exams, essays, or assignments, based on specific criteria. Markers ensure that grading is fair, consistent, and aligned with institutional or organizational guidelines. This role is common in educational institutions, testing agencies, and professional certification bodies. Strong attention to detail and subject expertise are essential for accuracy in evaluation. Some marking jobs may also involve providing feedback to help students improve their performance.

What are the typical daily responsibilities of a marking?

In a Marking role, your daily responsibilities usually include labeling products or components, verifying part numbers and specifications, and ensuring all marked items meet quality and compliance standards. You may operate specialized marking machines, apply barcodes or serial numbers, and track marked items using inventory software. Collaboration with quality control and warehouse teams is common, as accuracy and coordination are essential for smooth production and shipping processes. The work is generally active and may involve periods of standing or repetitive tasks, with opportunities to cross-train in related production areas.

What are the key skills and qualifications needed to thrive in marking, and why are they important?

To thrive in a Marking role, you need strong attention to detail, manual dexterity, and familiarity with production or warehouse settings, typically supported by a high school diploma or equivalent. Experience with labeling machines, barcode systems, and inventory tracking software is often required. Dependability, efficiency, and the ability to communicate well with team members are valuable soft skills. These abilities ensure that products are correctly identified, tracked, and prepared for shipping, minimizing errors and maintaining supply chain accuracy.

What are the most commonly searched types of Marking jobs in Massachusetts?

The most popular types of Marking jobs in Massachusetts are:

What are popular job titles related to Marking jobs in Massachusetts?

For Marking jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Marking jobs in Massachusetts look for?

The top searched job categories for Marking jobs in Massachusetts are:

What cities in Massachusetts are hiring for Marking jobs?

Cities in Massachusetts with the most Marking job openings:

Marking jobs near you
Infographic showing various Marking job openings in Massachusetts as of August 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 100% In-person job distribution, with an average salary of $74,254 per year, or $35.7 per hour.

Senior Regulatory Affairs Specialist

BRIOHEALTH SOLUTIONS INC

Burlington, MA • On-site

$115K - $130K/yr

Full-time

Re-posted yesterday

Key responsibilities

  • Prepare, review, and maintain FDA submissions supporting the BrioVAD System and the INNOVATE™ Trial, including IDE submissions, supplements, amendments, and annual reports.

  • Partner with Clinical, R&D, Quality, Medical Affairs, and other cross-functional teams to incorporate regulatory requirements into clinical and product development activities.

  • Support EU MDR regulatory strategy and CE marking activities, including planning for conformity assessment, Notified Body interactions, and maintenance of EU regulatory deliverables.

Job description

About Us

We are a global team of like-minded Med-Tech professionals focused on patient centric solutions in a collaborative environment leading to excellent outcomes. We have developed an advanced and unique heart failure therapy technology in the BrioVAD® Left Ventricular Assist System (LVAS). We are introducing the BrioVAD LVAS to Heart Failure clinicians for use with the large number of indicated and untreated patients who could benefit from chronic mechanical circulatory support. The initiation of our INNOVATE™ Trial in the US is only the beginning. We are building a team to develop advanced technology intended to further improve patient outcomes, increase therapy acceptance, and enabling chronic MCS therapy to be accessible to more patients across the globe.


The Role

BrioHealth Solutions is seeking a skilled and self-motivated Senior Regulatory Affairs Specialist to support the BrioVAD® Left Ventricular Assist System. This individual will partner with cross-functional teams to support product development activities, US and EU clinical studies and regulatory planning and submission activities.


What You’ll Do

  • Prepare, review, and maintain FDA submissions supporting the BrioVAD System and the INNOVATE™ Trial, including IDE submissions, supplements, amendments, and annual reports.
  • Partner with Clinical, R&D, Quality, Medical Affairs, and other cross-functional teams to incorporate regulatory requirements into clinical and product development activities.
  • Provide regulatory guidance on clinical protocols, informed consent materials, investigator communications, labeling, device changes, and other study-related documentation.
  • Assess product, manufacturing, software, labeling, and clinical study changes to determine their regulatory impact and applicable FDA reporting or submission requirements.
  • Support FDA communications and meetings by preparing materials, coordinating cross-functional input, and tracking regulatory questions and commitments.
  • Review technical, clinical, and quality documentation for accuracy, consistency, and submission readiness.
  • Monitor changes to U.S. regulations, FDA guidance, and relevant industry standards; evaluate their impact and communicate applicable requirements to internal stakeholders.
  • Maintain accurate regulatory records, submission files, agency correspondence, approvals, and commitments in accordance with internal procedures.
  • Manage multiple regulatory deliverables and timelines while proactively identifying and escalating risks or potential delays.
  • Support EU MDR regulatory strategy and CE marking activities for the BrioVAD® LVAS, including planning for conformity assessment, Notified Body interactions, and maintenance of EU regulatory deliverables.
  • Contribute to preparation, review, and lifecycle maintenance of EU technical documentation, including General Safety and Performance Requirements (GSPR) evidence, clinical evaluation documentation, post-market surveillance inputs, and related submission-ready records.
  • Support EU clinical and post-market obligations, including clinical investigation documentation, PMCF planning, vigilance inputs, field safety communications, periodic reporting, and responses to regulatory or Notified Body questions, as applicable.
  • Evaluate design, manufacturing, software, labeling, supplier, and clinical study changes for EU regulatory impact, including potential effects on CE marking, technical documentation, GSPR compliance, UDI/EUDAMED data, and Notified Body notification requirements.
  • Coordinate with Authorized Representative, importer/distributor, Notified Body, and internal stakeholders to ensure EU regulatory commitments, timelines, and evidence needs are identified, tracked, and fulfilled.


What You Bring

  • Bachelor’s degree in life sciences, engineering, or a related technical discipline required; advanced degree preferred. 
  • At least five years of medical device regulatory affairs experience with a bachelor’s degree, or at least three years with an advanced degree. 
  • Working knowledge of applicable U.S. medical device regulations, including 21 CFR Parts 11, 50, 54, 56, 812, and 820. 
  • Experience preparing or supporting FDA medical device submissions, such as IDE or PMA submissions, supplements, amendments, annual reports, and regulatory responses. 
  • Working knowledge of EU MDR 2017/745 requirements, including CE marking, technical documentation, GSPR, clinical evaluation/PMCF, PMS, vigilance, UDI, and EUDAMED expectations.
  • Experience supporting Notified Body submissions or interactions, EU technical documentation, and/or CE mark maintenance for Class III, implantable, active, cardiovascular, or life-sustaining medical devices preferred.
  • Familiarity with ISO 13485, ISO 14971, applicable harmonized standards, MDCG guidance, and EU medical device regulatory intelligence processes preferred.
  • Experience supporting medical device clinical studies and collaborating with clinical, technical, and quality teams. 
  • Class III medical device experience strongly preferred; experience with active implantable, cardiovascular, or life-sustaining devices is highly desirable. 
  • Ability to assess regulatory requirements and implications across product, software, manufacturing, labeling, and clinical study changes. 
  • Strong technical writing, communication, analytical, and organizational skills. 
  • Ability to manage competing priorities, exercise sound judgment, and work independently in a fast-paced environment.