Quality Control Technician (Sr. Inspector)

PSG Global Solutions

Littleton (MA)

On-site

USD 65,000 - 85,000

Full time

14 days+

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Benefits offered by this job

Training and career development opportunities

Job summary

A reputable staffing agency in healthcare is seeking a Quality Control Technician (Sr. Inspector) in Littleton, Massachusetts. This role demands a comprehensive understanding of quality assurance practices within FDA regulated environments. Candidates should have over 5 years of technical experience and proficiency in various measuring tools. The position offers opportunities for training and professional growth while ensuring compliance with quality standards and regulations.

Qualifications

  • 5+ years of experience in a technical field working with mechanical and electromechanical parts.
  • Experience working in regulatory/FDA or ISO manufacturing setting.
  • Previous experience with inspection of Machine parts, plastic covers, injection molding parts, and O-Arm scanner is beneficial.

Responsibilities

  • Follow all Quality System Practices and SOP’s to ensure compliance with regulations.
  • Provide leadership direction and coaching to production employees.
  • Perform data collection, interpret and analyze information for continuous improvement.
  • Ensure documentation results and Quality Record accuracy.

Skills

Proficiency in measuring and testing devices including calipers, microscopes, pin gages
Good writing and verbal skills
Ability to utilize complicated drawings and follow technical instructions
Demonstrated good judgment and discretion
Strong team skills

Education

High School or equivalent
2 year Associates Degree in a Technical Field or equivalent

Tools

Calipers
Microscopes
Pin gages

Job description

Quality Control Technician (Sr. Inspector)

Contract

At Real we're always looking for new and ambitious people to help deliver exceptional service levels, change the lives of the candidates we represent and partner with some of the world's best pharmaceutical, biotechnology and medical companies.

As specialists in recognizing talent we pride ourselves on not just finding the best people for our client partners but on our ability to spot the best and brightest talent to work for us. We are also renowned for providing training and long‑term career opportunities to help our employees be the best they can be, so they can continue to deliver the expertise Real has become famous for.

Relationships are at the heart of everything we do and ensure that our clients and candidates continue to work with us again and again. This ethos is also what shapes how we work as a business. We encourage and reward knowledge sharing and have various support networks and international forums to enable our employees to keep up‑to‑date with changes happening across their industries and share local insight to deliver true global perspectives.

POSITION DESCRIPTION:

Uses a variety of technical precision measuring instruments to ensure acceptance and/or performance of components or finished devices according to established engineering instructions or quality practice standards. May provide training or job coaching to inspectors or production employees and works with independence of action and minimal supervision.

Please Note: Contractors are required to bring their own safety shoes.

POSITION RESPONSIBILITIES:

  • Follow all Quality System Practices and SOP’s as defined by Medtronic policies, practices and procedures to ensure that FDA and ISO/MDD regulations are met
  • Participate within both departmental and cross-functional teams to assure compliance to regulatory and quality systems including both internal and external audits
  • Recommend and develop process, inspection testing and procedural initiatives to support production and Quality Systems
  • Provide leadership direction and coaching to inspectors or production employees for inspecting and/or testing parts, finished goods or re‑worked items according to established specification and testing methods; provide training as necessary
  • Ensure documentation results, approve/reject items according to established standards
  • Ensure Quality Record accuracy for traceability according to established practices
  • Perform data collection, interpret and analyze information, provide recommendations for solution and continuous improvement
  • Demonstrate leadership and a service attitude throughout the organization
  • Identify and recommend training needs within manufacturing as it relates to quality
  • Work within multi‑functional teams, QA or production
  • All activities must be performed in compliance with the Quality System
  • Performs duties in compliance with environmental, health and safety related site rules, policies or governmental regulations
  • All other duties as assigned
  • Travel requirement: Less than 10%

EDUCATION REQUIRED:

  • High School or equivalent

YEARS OF EXPERIENCE

  • 5+ years of experience in a technical field working with mechanical and electromechanical parts
  • 5+ years of experience in manufacturing or technical setting in inspection and measurement systems

SPECIALIZED KNOWLEDGE REQUIRED

  • Experience working in regulatory/FDA or ISO manufacturing setting
  • Proficiency in measuring and testing devices including calipers, microscopes, pin gages
  • Ability to utilize complicated drawings, follow technical instructions and mathematical/handbook formulas
  • Good writing and verbal skills
  • Performs with minimal supervision and has demonstrated good judgment and discretion
  • Previous experience with the inspection of Machine parts, plastic covers, injection molding parts and O-Arm scanner is VERY beneficial.

PREFERRED QUALIFICATIONS

  • 2 year Associates Degree in a Technical Field or equivalent
  • PCBA Inspection (current or expired)
  • Strong working knowledge of mechanical assemblies and electromechanical assemblies
  • Experience in the medical device industry with emphasis on capital equipment a plus
  • Knowledge of engineering methods and practices.
  • Motivated Self‑starter
  • Strong team skills

All your information will be kept confidential according to EEO guidelines.

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