QC Chemist II - III

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

Job summary

A leading company in the IT consulting sector is seeking a Quality Control Chemist in Fall River, MA. This position involves ensuring product safety and quality through rigorous testing and validation in a GMP laboratory environment. Ideal candidates will possess a Bachelor's degree in Chemistry and experience within a pharmaceutical context, with proficiency in laboratory techniques and compliance protocols.

Qualifications

• Bachelor's degree required.
• 2 years as QC Chemist in pharma is preferred.
• Fluency in English essential.

Responsibilities

• Conduct tests on various samples using lab equipment.
• Perform cleaning validation and residue analysis.
• Maintain compliance with cGMP practices.

Skills

Quality Control

GMP

Lab Safety

HPLC

GC

ICP

Microsoft Office

Pharmaceutical Industry

Education

Bachelor's degree in Chemistry or related field

Tools

HPLC

GC

Karl Fisher

ICP

Job description

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

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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