Quality Control Chemist-Pharma

YO IT Group; Massachusetts; On-site; USD 65,000 - 90,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking a Quality Control Chemist to ensure safety and quality of products. This role involves conducting analytical tests, maintaining compliance with industry standards, and collaborating with colleagues in a cGMP laboratory environment. Ideal candidates will possess a Bachelor's in Chemistry, relevant experience, and strong analytical skills. Join our team and contribute to advancements in high-quality pharmaceutical products.

Qualifications

• Minimum of 2 years as a QC Chemist in a pharmaceutical environment.
• Fluency in English, strong analytical skills, and teamwork.
• Hands-on experience with laboratory instruments and cGMP environment.

Responsibilities

• Conduct tests on samples using advanced lab techniques.
• Create and execute protocols for method validation.
• Maintain compliance with data integrity standards.

Skills

GMP

SOP

Lab Safety

ICP

HPLC

GC

Quality Control

Analytical Method Validation

Data Integrity

Particle Size Analysis

Education

Bachelor's degree in Chemistry or related field

Tools

Microsoft Office

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,data integrity,gc,quality control,sop,usp,chemist,lab safety,hplc,high-performance liquid chromatography (hplc),pharmaceutical companies,analytical method validation,particle size analysis,pharma,microsoft office,qc chemist