About the Role

• We are seeking a skilled and detail-oriented individual to join our Quality Control laboratory team.
• The successful candidate will perform a variety of chemical analyses on drug substances, ensuring accuracy and compliance with cGMP standards.
• This role requires working a 12-hour rotating shift schedule.

Pay Range: $30- $39

Responsibilities 

• Conduct analytical testing on various samples/products using methods such as HPLC, ICP, plate reader-based assays, gel electrophoresis, dynamic light scattering, and qPCR.
• Ensure all test data is accurate and adhere to the Right-First Time principle.
• Collaborate with team members to maintain high levels of cGMP compliance and inspection readiness.
• Assist with laboratory activities including second-person review, instrument calibration, troubleshooting, and deviation investigations.
• Utilize and understand various data acquisition and management software.

Education Qualification

• Bachelor's degree preferred; a Master's degree will be considered if applicable to the role.

Required Skills 

• Proficiency in performing chemical analyses using HPLC and ICP. 
• Familiarity with plate reader-based assays, qPCR, dynamic light scattering, and gel electrophoresis.
• Minimum of 1+ years of experience in a GMP laboratory setting utilizing the listed methods.
• Ability to work a 12-hour rotating shift schedule, with start times between 7 am and 8 am.
• Strong attention to detail and commitment to maintaining high-quality standards.