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GMP Data Reviewers and Chemists

2 months ago

Wilmington, North Carolina, United States Quality Chemical Laboratories Full time

**Quality Chemical Laboratories (QCL)** is a leading pharmaceutical testing and development laboratory seeking highly motivated professionals to join our team as analytical data reviewers, LabWare LIMS development/configuration/validation specialists, document control associates, computer system validation and data integrity specialists, and scientists with expertise in various fields.

**Key Responsibilities:**

  • Review and validate analytical data to ensure accuracy and compliance with regulatory requirements
  • Develop and configure LabWare LIMS systems to meet laboratory needs
  • Implement document control processes to maintain accurate and up-to-date documentation
  • Validate computer systems to ensure data integrity and security
  • Conduct method development and validation in various analytical techniques, including Mass Spec, LC, GC, QC compendial testing, Wet Chemistry, Microbiology, Sterility, Synthetic Chemistry, and Pharmaceutical Formulation

**Requirements:**

  • Advanced degree in Chemistry or a related science
  • Experience in method development and validation, particularly in Mass Spec, LC, GC, and Wet Chemistry
  • Strong understanding of regulatory requirements, including GMP and GLP
  • Excellent communication and teamwork skills

**What We Offer:**

  • Competitive salaries commensurate with experience
  • Excellent benefits package
  • Opportunities for career advancement and leadership development

**Equal Employment Opportunity:**

Quality Chemical Laboratories (QCL) is an Equal Opportunity Employer and does not discriminate on the basis of race, color, national origin, religion, gender, age, veteran status, political affiliation, sexual orientation, marital status, or disability.