QC Chemist II & III

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 to ensure product quality and safety. You will conduct rigorous testing protocols using advanced laboratory techniques, operating in a compliant cGMP environment. This role requires a Bachelor's degree in Chemistry, a solid understanding of quality control processes, and proficiency in laboratory instruments.

Benefits

Opportunity for career advancement

Access to cutting-edge laboratory technologies

Qualifications

• Minimum 2 years as a QC Chemist with strong GMP knowledge.
• Fluency in English with communication skills in science.
• Ability to interpret complex data sets.

Responsibilities

• Conduct tests and ensure quality and safety of products.
• Create and validate analytical methods.
• Lead investigation activities for quality assurance.

Skills

GMP

Lab Safety

HPLC

ICP

Quality Control

SOP

USP

Analytical Chemistry

Education

Bachelor's degree in Chemistry or a related field

Tools

HPLC

Karl Fischer

GC

Microsoft Office

Relevant Scientific Software

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: 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