OVERVIEW

Are you looking for a new career opportunity with an exciting biotech company?! Then we’ve got the right team for you! In this role, you’re responsible for the duties listed below.

Immediate opening for a QC Associate I/II with a biotech company in San Diego, CA who possesses:

• GMP experience
• Understanding of basic chemistry techniques (pH, osmolality, conductivity, agarose gel electrophoresis, restriction digest, ELISA, and qPCR)
• Strong documentation skills

Email resumes to tness@simplybiotech.com or call 858.258.6501

FULL DESCRIPTION:

The selected candidate will be responsible for:

• Perform routine analytical testing rigorously following established SOP’s. Analytical techniques include pH, osmolality, conductivity, agarose gel electrophoresis, restriction digest, ELISA, and qPCR.
• Strict adherence to cGMP’s, policies, procedures and SOP’s for testing, documentation, and processes.
• Perform routine laboratory maintenance including, monthly cleaning procedures to ensure instrument readiness, safety of laboratory personnel, continuous supply of disposable materials and reagents.
• Assist Quality Assurance in ensuring compliance with applicable quality standards and regulatory requirements.
• Collaborate with product development and manufacturing on tech transfer activities as well as provide support to any activities needed for manufacturing.

The selected candidate will also possess:

• Bachelor or Masters of Science Degree in the Biological Sciences, Bioengineering or Chemistry with a combination of education and experience performing biochemistry, molecular biology, microbiology, and chemistry.
• 2+ years relevant experience with BS
• 0+ years relevant experience with MS
• The QC Associate I/II must be accountable for the work performed, productive within the company, provide open communication, and exemplify effective teamwork skills.
• The QC Associate must be capable of reading, understanding, and adhering to relevant test methods, SOP’s, and industry guidance.
• The QC Associate must be knowledgeable in basic chemistry and analytical principles. They should understand basic statistical analysis.
• The position is responsible for performing and demonstrating the highest form of quality in the pharmaceutical industry, understanding the cGMP regulations, and implementing these practices on the work being performed.
• Knowledgeable using Microsoft Office as well as developing any documentation and creating tables for laboratory inventory and data entry.
• Highly organized, detail oriented, with excellent record keeping skills.
• Sound scientific judgement with good communication skills and the ability to work effectively with others.
• Experience working in a GMP facility is highly desirable.
• Experience analyzing plasmid DNA is highly desirable.

Salary Range: $36.10-$40.50/hr
For immediate and confidential consideration, please email your resume to tness@simplybiotech.com or call 858.258.6501. More information can be found at www.simplybiotech.com
Job Type: Full-time
Pay: $36.10 - $40.50 per hour

Schedule:

• Day shift

Work Location: In perso

• Perform routine analytical testing rigorously following established SOP’s. Analytical techniques include pH, osmolality, conductivity, agarose gel electrophoresis, restriction digest, ELISA, and qPCR.
• Strict adherence to cGMP’s, policies, procedures and SOP’s for testing, documentation, and processes.
• Perform routine laboratory maintenance including, monthly cleaning procedures to ensure instrument readiness, safety of laboratory personnel, continuous supply of disposable materials and reagents.
• Assist Quality Assurance in ensuring compliance with applicable quality standards and regulatory requirements.
• Collaborate with product development and manufacturing on tech transfer activities as well as provide support to any activities needed for manufacturing