QC Inspector

Bruker Corporation

Bothell (WA)

On-site

USD 41,500 - 66,000

Full time

14 days+

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Benefits offered by this job

401(k) with company match
Employee stock purchase plan
Medical and dental plans
Paid time off

Job summary

Bruker Corporation in Bothell, Washington, is seeking a Quality Control Inspector (QCII) responsible for ensuring that all incoming materials and finished instruments meet quality specifications. Key responsibilities include conducting inspections, recording non-conformances, and collaborating with various departments to manage quality processes.

The ideal candidate has a Bachelor’s degree, 3-5 years of quality experience in regulated environments, and knowledge of ISO standards. The position offers a competitive salary and benefits, and supports growth within the role.

Qualifications

  • 3-5 years of quality-related experience in biotech or pharmaceutical industry.
  • Experience in leading process improvement projects.
  • Understanding of FDA/ISO regulations.

Responsibilities

  • Perform incoming and final quality control inspections.
  • Update inspection specifications and procedures.
  • Record non-conformances and manage material disposition.
  • Conduct lot validation testing.
  • Support review of SOPs related to Quality Control.

Skills

Analytical decision-making skills
Knowledge of ISO 9001 and ISO 13485
Problem-solving skills
Communication skills
Ability to work independently
Multi-tasking abilities

Education

Bachelor’s degree in a related field

Job description

Overview

As one of the world’s leading analytical instrumentation companies, Bruker covers a broad spectrum of advanced solutions in all fields of research and development. All our systems and instruments are designed to improve safety of products, to accelerate time-to-market, and to support industries in successfully enhancing quality of life. We have been driving innovation in analytical instrumentation for over 60 years now. Today, more than 8,500 employees distributed across 90 locations around the world continue to delight our customers with innovative solutions.

Bruker Nano, one of Bruker’s four operating segments, provides customers in academic and governmental institutions, life science, materials, and applied industries with the tools to determine the characteristics of matter and visualize the structure of molecules. Divisions within BNANO include Bruker AXS, Bruker Nano Analytics, Bruker Nano Surfaces and Metrology, Fluorescence Microscopy, and Canopy.

The Quality Control Inspector (QCII) is primarily responsible for Quality Control inspections of all Bruker Spatial Biology incoming raw materials, components and sub-assemblies received at our facilities per inspection plan meeting applicable material specifications. QCII is also responsible for all finished instrumentation testing of all final assembled instruments per inspection plan.

Responsibilities

The scope of this position includes performing all necessary quality control checks, including FAI's and associated reports (First Article Inspection & Reports), using appropriate testing procedures and test instrumentation supported with appropriate documentation for all Bruker Spatial Biology products to manage quality risk and provide oversight over manufacturing processes. This position reports into the Sr. Quality Manager which is part of Quality organization and support associated tasks and activities coordinated and integrated with production and inventory control. The individual ensures consistent implementation, improvement, and compliance to the Bruker Spatial Biology, ISO 13485 and ISO 9001 Quality Management Systems.

  • Perform timely incoming and final quality control inspections to support Manufacturing and Operations quality for all Bruker Spatial Biology instruments following approved and active Incoming Specifications
  • Update incoming inspection specifications and procedures as required, in collaboration with other cross-functional departments.
  • Record non conformances and support in conducting root cause investigations.
  • Manage nonconforming (or potentially nonconforming) material through disposition.
  • Perform lot validation testing while monitoring and adjusting testing frequencies.
  • Support review and updating of SOPs relating to Quality Control Procedures.
  • Collaborate with Manufacturing, Manufacturing Engineering, New Product Introduction, Procurement, Quality, and Supply Chain partners as well as vendors on the above activities.
  • Basic application of statistical tools and methods
  • Participates in FDA/ISO inspections and customer audits and maintain ongoing audit readiness
  • Perform other relevant duties as may be assigned by management
  • Act as Quality ambassador providing decisive approach for implementation to manage Quality Management System with various tasks, projects, as required
Skills and Abilities
  • Analytical decision-making skills to apply logical or Quality control thinking principles to operations using pragmatic approaches.
  • Demonstrates working knowledge of ISO 9001, ISO 13485 quality system and/or FDA 21 CFR 820 quality regulations as applicable to products.
  • Analytical and creative problem-solving skills that include experience in leading and or participating on process improvement/lean projects.
  • Excellent written and oral communication skills
  • Ability to work independently and collaboratively in cross-functional teams
  • Ability to multi‑task with demonstrated problem solving skills in a fast paced complex environment
Specialized Knowledge
  • GD&T and CMM skills is preferred
  • At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry.
Qualifications
Minimum Education

Bachelor’s degree in a related field strongly preferred OR High school STEM or technical diploma or equivalent BS in technical discipline, real world hands‑on regulated industry experience may also be considered.

Minimum Experience

3-5 years quality-related experience in biotech, the pharmaceutical or consumer regulated device industry.

At Bruker, base salary is part of our total compensation. The estimated base salary range for this full‑time position is between $41,500 and $66,000 provides an opportunity to progress as you grow and develop within a role. The base salary for the role will depend on a several job‑related factors, including, but not limited to education, training, experience, the geographic location of the successful candidate, skills, competencies, job‑related knowledge and travel requirements for this position. Full‑time employees may also be eligible for a performance‑related incentive in addition to a full range of benefits including 401(k) with company match, an employee stock purchase plan, medical and dental plans, life insurance, short‑term and long‑term disability insurance, employee assistance program and paid time off including vacation, sick time and holidays, and more.

Bruker is an equal‑opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.

Certain positions at Bruker require compliance withexport control laws and as a result, all interviewed candidates for all positions will be screened pre‑interview to determine theireligibility in light of export control restrictions

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