Senior QC Chemist - Pharma

YO IT Group; Massachusetts; On-site; USD 60,000 - 90,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking a Quality Control Chemist. This role involves testing samples, ensuring product quality and compliance with safety standards, while utilizing specialized laboratory techniques. Qualified candidates with a Bachelor's degree in Chemistry and relevant experience in a cGMP environment are invited to apply.

Qualifications

• Minimum 2 years experience as a QC Chemist.
• Fluency in English.
• Authorized to work permanently in the U.S.

Responsibilities

• Conduct tests on various samples using laboratory equipment.
• Create and execute protocols for validating analytical methods.
• Maintain compliance with cGMP practices and documentation standards.

Skills

GMP

SOP

Lab Safety

Quality Control

HPLC

GC

Karl Fisher

ICP

Particle Size Analysis

Chemistry

Education

Bachelor's degree in Chemistry or related physical science

Job description

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