Senior QC Chemist

YO IT Group; Fall River (MA); On-site; USD 65,000 - 90,000; Full time

Job summary

A leading company in IT Services and IT Consulting is seeking a Quality Control Chemist in Fall River. The role involves testing products to ensure quality and safety while performing various analytical techniques in a regulated environment. Candidates should possess strong analytical abilities and relevant experience in the pharmaceutical industry.

Qualifications

• Experience as a QC Chemist required with minimum 2 years in a pharmaceutical environment.
• Knowledge of GMP, SOP, and Lab Safety is crucial.
• Fluency in English with strong analytical skills preferred.

Responsibilities

• Conduct tests on samples and ensure product quality per cGMP standards.
• Create and execute validation protocols for analytical methods.
• Perform routine and advanced testing and lead investigation activities.

Skills

GMP

SOP

Lab Safety

USP

Quality Control

Analytical Techniques

Education

Bachelor's degree in Chemistry or a related physical science field

Tools

Karl Fisher

HPLC

GC

ICP

Microsoft Office

Job description

2 days ago Be among the first 25 applicants

This range is provided by YO IT Group. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$65,000.00/yr - $90,000.00/yr

Experience: 2 - 15 Years

Must Have

• Possess recent experience within a Pharmaceutical Company
• At least 2 years of experience as a QC Chemist
• Hands-on experience and strong familiarity with GMP, SOP, Lab Safety, and USP
• Practical knowledge of instruments such as Karl Fisher, HPLC, GC, Particle Size Analysis, and ICP
• Proficiency in reading, writing, and speaking English
• Experience with Inhalation products (MDI) is preferred, though candidates with experience in liquids, solids, tablets, and capsules are also welcome
  
  

Job Description

• The Quality Control Chemist plays a vital role in ensuring the safety and quality of our products. You will be conducting tests on various samples using innovative laboratory equipment and techniques.
  
  

Duties And Responsibilities

• Create and execute protocols for validating and transferring analytical methods.
• Perform cleaning validation and residue analysis.
• Conduct routine and advanced testing within our department.
• Operate specialized laboratory instruments.
• Test raw materials and facilitate their release.
• Lead investigation activities to ensure the highest standards of quality.
• Maintain strict compliance with data integrity, cGMP practices, and documentation standards.
• Additional responsibilities as assigned by your supervisor.
  
  

Education And Experience

• Bachelor's degree in Chemistry or a related physical science field.
• Fluent in English, with the ability to communicate scientific concepts clearly.
• Authorized to work permanently in the United States without sponsorship.
• Excellent organizational and teamwork skills.
• Strong analytical abilities to interpret complex data sets.
• Proficiency in Microsoft Office and relevant scientific software.
• Experience with Inhalation products (MDI) is a plus.
  
  

Working Conditions

• This role involves working in a cGMP laboratory or manufacturing environment which requires appropriate personal protective equipment.
• Interaction with solvents, powders, and other laboratory materials is a core aspect of this position.
• Shifts may vary, including day, evening, and night schedules.
• Weekend or Holiday work may be requested or required.
  
  

Skills: karl fisher,sop,quality control,mdi,scientific software,gmp,quality control chemist,usp,lab safety,qc chemist,pharma,chemist,icp,microsoft office,chemistry,pharmaceutical companies,hplc,high-performance liquid chromatography (hplc),particle size analysis,gc

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  IT Services and IT Consulting

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