Planet Pharma
Job Description
QC Analyst In this role, you will support QC GMP operation and key assays for release, in-process, and stability testing; Other activities include but not limited to data trending, archiving, lab/equipment maintenance, reagent preparation/supplies ordering, supporting EM and microbiology testing. Final job title will be determined based on candidate experience level. Key Responsibilities include but not limited to:
Support routine laboratory management and instrument maintenance Support sample and data management duties Support contract testing lab management, e.g., coordinate sample shipments, obtain results, and follow up on open action items Perform testing in support of GMP Manufacturing and stability program Perform environmental monitoring (EM) and microbiology testing Document, evaluate, and review data and trend results Requirements:
Bachelor's or master's degree in biology, Biochemistry, or a related field and a minimum of 1 year of hands-on laboratory experience in an assay development and/or QC laboratory environment Experience working in a cGMP environment is a plus Expertise in one or more of the following is a plus: cell culture, qPCR/ddPCR, viral genome titer, capsid titer, ELISA, cell-based transgene potency, electrophoretic assays, EM Self-motivated, able to multitask and deliver results with a high degree of attention to detail to drive projects forward in a timely manner Capable of lifting up to 40 pounds
Equal Opportunity Employer: We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
Fraud Alert: Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it's from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.
QC Analyst In this role, you will support QC GMP operation and key assays for release, in-process, and stability testing; Other activities include but not limited to data trending, archiving, lab/equipment maintenance, reagent preparation/supplies ordering, supporting EM and microbiology testing. Final job title will be determined based on candidate experience level. Key Responsibilities include but not limited to:
Support routine laboratory management and instrument maintenance Support sample and data management duties Support contract testing lab management, e.g., coordinate sample shipments, obtain results, and follow up on open action items Perform testing in support of GMP Manufacturing and stability program Perform environmental monitoring (EM) and microbiology testing Document, evaluate, and review data and trend results Requirements:
Bachelor's or master's degree in biology, Biochemistry, or a related field and a minimum of 1 year of hands-on laboratory experience in an assay development and/or QC laboratory environment Experience working in a cGMP environment is a plus Expertise in one or more of the following is a plus: cell culture, qPCR/ddPCR, viral genome titer, capsid titer, ELISA, cell-based transgene potency, electrophoretic assays, EM Self-motivated, able to multitask and deliver results with a high degree of attention to detail to drive projects forward in a timely manner Capable of lifting up to 40 pounds
Equal Opportunity Employer: We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
Fraud Alert: Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it's from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.