Hiring.Camp

Analytical Chemist

Itw

·

Today

Salary
$94k – $115k
Location
Burlington - 01803, United States of America
Type
Full-time
Education
Master
Source
Workday

Description

Job Description:

Analytical Chemist – 2nd Shift
Burlington, MA

ABOUT THE COMPANY:

QSA Global, a division of Illinois Tool Works (ITW), specializes in supplying state-of-the-art gamma radiography and portable X-ray systems used in non-destructive testing (NDT), as well as high-performance radiation sources for oil well logging (OWL), industrial processes, and nuclear medicine. With more than 100 years of organizational experience, we have established ourselves as leading experts in radiation source design and radioisotope solutions. We are now focused on expanding our work in medical applications of radioisotopes—an area where chemistry plays a direct role in improving patient care. This includes growing our presence in radiopharmaceuticals and brachytherapy, building on decades of experience in radioisotope technology, design, and manufacturing.

JOB SUMMARY:

An analytical chemist responsible for supporting and expanding QSA's analytical chemistry capabilities in support of radiochemistry, manufacturing, quality assurance, product development, and regulatory compliance. This role develops and validates analytical methods, performs analytical testing, establishes laboratory procedures, and collaborates with cross-functional teams to generate accurate, defensible analytical data that supports manufacturing, customer requirements, and future business growth. The ideal candidate combines strong analytical chemistry fundamentals with excellent laboratory practices, technical problem-solving skills, and a continuous improvement mindset.

Note: The hours on this position are Monday – Thursday, 1pm – 11:30 pm.  Enjoy a four-day work week while receiving a 15% pay differential for working second shift.  

KEY RESPONSIBILITIES:

  • Develop and maintain analytical methods that support manufacturing, product development, and quality objectives.
  • Perform analytical testing using ICP-OES, ICP-MS, and other analytical instrumentation to generate accurate, reliable, and defensible analytical data.
  • Collaborate with Chemistry, Engineering, Manufacturing, Quality, and Regulatory personnel to support investigations, process improvements, and new product development.
  • Establish and maintain analytical laboratory procedures, specifications, QA/QC practices, and supporting documentation.
  • Support laboratory qualification activities, instrument calibration, preventive maintenance, and troubleshooting.
  • Interpret analytical data and communicate results through technical reports and scientific documentation.
  • Support investigations involving deviations, CAPAs, non-conformances, and out-of-specification analytical results.
  • Assist in evaluating and implementing new analytical techniques and laboratory capabilities to support future business needs.
  • Ensure analytical activities comply with applicable quality systems, laboratory safety requirements, and radiation safety standards.

EDUCATION & EXPERIENCE REQUIREMENTS

(or equivalent combination of education and experience)

  • Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, Radiochemistry, or a related scientific discipline required.
  • Advanced degree (M.S.) preferred.
  • Minimum of five years of experience operating ICP-OES and ICP-MS, including method development, validation, troubleshooting, and data interpretation.
  • Demonstrated experience developing, validating, and improving analytical methods.
  • Strong technical report writing and scientific documentation skills.
  • Experience establishing and maintaining QA/QC laboratory processes and procedures.
  • Experience working in regulated analytical laboratory environments.

PREFERRED QUALIFICATIONS:

  • Experience with radioisotope analysis.
  • Experience supporting radiopharmaceutical manufacturing.
  • Experience with Agilent instrumentation
  • Experience with GMP, GLP, ISO 17025, or comparable quality systems.
  • Experience supporting laboratory audits and regulatory inspections.

SUCCESS PROFILE

The strongest candidates will demonstrate:

  • Scientific Curiosity – enjoys understanding analytical results and continuously improving laboratory methods.
  • Attention to Detail – consistently produces accurate, reliable, and well-documented analytical data.
  • Problem Solving – approaches technical challenges with sound scientific reasoning and practical solutions.
  • Collaboration – works effectively across Chemistry, Engineering, Manufacturing, Quality, and Regulatory teams.
  • Accountability – takes ownership of assigned work and follows projects through completion.
  • Continuous Improvement – seeks opportunities to improve laboratory processes, analytical methods, and overall efficiency.

COMPENSATION INFORMATION:

The annual base salary starting range for this position is $94,000 – 115,000 annually plus a 15% differential for 2nd shift. Please note that this salary information serves as a general guideline. The company considers various factors when extending an offer, including but not limited to the scope and responsibilities of the position, the candidate's work experience, education and training, key skills, as well as geographic location, market, and business considerations.

We believe our people are our greatest asset. That’s why we invest in creating an environment where you can thrive—both personally and professionally.  For more details, visit our Benefits page

ADDITIONAL INFORMATION:

QSA Global is an equal opportunity employer. We value our colleagues’ unique perspectives, experiences and ideas and create workplaces where everyone can develop their careers and perform to their full potential.

All qualified applicants will receive consideration for employment based on qualifications, merit, and business needs, without regard to any characteristic protected by applicable federal, state, or local laws. Qualified applicants with disabilities and protected veterans are encouraged to apply.  Reasonable accommodation is available during the application and hiring process upon request.

Compensation Information:

94,000 - 115,000 plus 15% 2nd shift differential

ITW is an equal opportunity employer. We value our colleagues’ unique perspectives, experiences and ideas and create workplaces where everyone can develop their careers and perform to their full potential. 


As an equal employment opportunity employer, ITW is committed to equal employment opportunity and fair treatment for employees, beginning with the hiring process and continuing through all aspects of the employment relationship. 


All qualified applicants will receive consideration for employment without regard to race, color, sex, gender identity, sexual orientation, religion, national origin, age, disability, protected Veteran status or any other characteristic protected by applicable federal, state, or local laws.

Skills

GMPPatient CareCompliance

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