ApTask
Quality Control Chemist - I*
ApTask, Maryland Line, Maryland, us, 21105
About Client:The client is a leading American biopharmaceutical company. It specializes in the discovery, development, and commercialization of innovative therapeutics, particularly in antiviral drugs for HIV, hepatitis B, hepatitis C, and influenza. Known for key products like Truvada, Biktarvy, and Sovaldi, it invests heavily in research and development to address unmet medical needs. The company also focuses on expanding its portfolio through strategic acquisitions and collaborations, while maintaining a commitment to improving global health and access to medications.
Rate Range: $30-$35.54/Hr
Job Description:Roles and Responsibilities:
Perform testing of raw materials, intermediates and final products by following analytical methods: Cell based bioassays, Flow Cytometry, ELISA and qPCR assays.Work with internal and external resources to maintain lab in an optimal state.Assist with monitoring and trending data, complete routine record review of test data and related documents for in-process testing, drug substance and drug product release. Supply information to support generation of CoAs for product release.Maintains laboratory instruments for calibration and routine maintenanceAuthor or revise SOPs, qualification/validation protocols and reports.Asist with lab investigations regarding out of specifications (OOS) results. Participate in determination of root cause for deviations related to analytical procedures.Provide updates at daily and weekly meetings.Monitor the GMP systems currently in place to ensure compliance with documented policies.Review proposed changes to systems, procedures, methods, and submissions to regulatory agencies, as appropriate.Gather metric information for use in continuous improvement of areas of responsibility.Perform other duties as required.Basic Qualifications:
Bachelor's Degree ORAA Degree and 2+ years' experience in biotechnology or related field and Quality Control experience ORHigh School Degree and 3+ years' experience in biotechnology or related field and Quality Control experiencePreferred Qualifications:
Strong knowledge of GMP, SOPs and quality control processes.Identifying, writing, evaluating, and closing OOS's and investigations.Proficient in MS Word, Excel, Power Point and other applications.Strong written and verbal communication skills.Ability to communicate and work independently with scientific/technical personnel.Well versed in various analytical techniques such as Flow Cytometry, ELISAs, PCR, and cell bioassays and other applicable methods to the testing of biopharmaceuticals.Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211).Preferred: Experience in the biotech and/or pharmaceutical industry.
Non-benefitted (other than those mandated under state or federal law).Please note that this position does not include paid time off benefits. ApTask offers subsidized insurance coverage to our employees.
About ApTask:ApTask is a leading global provider of workforce solutions and talent acquisition services, dedicated to shaping the future of work. As an African American-owned and Veteran-certified company, ApTask offers a comprehensive suite of services, including staffing and recruitment solutions, managed services, IT consulting, and project management. With a focus on excellence, collaboration, and innovation, ApTask provides unparalleled opportunities for professional growth and development. As a member of the ApTask team, you will have the chance to connect businesses with top-tier professionals, optimize workforce performance, and drive success across diverse industries. Join us at ApTask and be part of our mission to empower organizations to thrive while fostering a diverse and inclusive work environment.
Applicants may be required to attend interviews in person or by video conference. In addition, candidates may be required to present their current state or government issued ID during each interview.
Candidate Data Collection Disclaimer:At ApTask, we prioritize safeguarding your privacy. As part of our recruitment process, certain Personally Identifiable Information (PII) may be requested by our clients for verification and application purposes. Rest assured, we strictly adhere to confidentiality standards and comply with all relevant data protection laws. Please note that we only collect the necessary information as specified by each client and do not request sensitive details during the initial stages of recruitment.
If you have any concerns or queries about your personal information, please feel free to contact our compliance team at businessexcellence@aptask.com
Rate Range: $30-$35.54/Hr
Job Description:Roles and Responsibilities:
Perform testing of raw materials, intermediates and final products by following analytical methods: Cell based bioassays, Flow Cytometry, ELISA and qPCR assays.Work with internal and external resources to maintain lab in an optimal state.Assist with monitoring and trending data, complete routine record review of test data and related documents for in-process testing, drug substance and drug product release. Supply information to support generation of CoAs for product release.Maintains laboratory instruments for calibration and routine maintenanceAuthor or revise SOPs, qualification/validation protocols and reports.Asist with lab investigations regarding out of specifications (OOS) results. Participate in determination of root cause for deviations related to analytical procedures.Provide updates at daily and weekly meetings.Monitor the GMP systems currently in place to ensure compliance with documented policies.Review proposed changes to systems, procedures, methods, and submissions to regulatory agencies, as appropriate.Gather metric information for use in continuous improvement of areas of responsibility.Perform other duties as required.Basic Qualifications:
Bachelor's Degree ORAA Degree and 2+ years' experience in biotechnology or related field and Quality Control experience ORHigh School Degree and 3+ years' experience in biotechnology or related field and Quality Control experiencePreferred Qualifications:
Strong knowledge of GMP, SOPs and quality control processes.Identifying, writing, evaluating, and closing OOS's and investigations.Proficient in MS Word, Excel, Power Point and other applications.Strong written and verbal communication skills.Ability to communicate and work independently with scientific/technical personnel.Well versed in various analytical techniques such as Flow Cytometry, ELISAs, PCR, and cell bioassays and other applicable methods to the testing of biopharmaceuticals.Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211).Preferred: Experience in the biotech and/or pharmaceutical industry.
Non-benefitted (other than those mandated under state or federal law).Please note that this position does not include paid time off benefits. ApTask offers subsidized insurance coverage to our employees.
About ApTask:ApTask is a leading global provider of workforce solutions and talent acquisition services, dedicated to shaping the future of work. As an African American-owned and Veteran-certified company, ApTask offers a comprehensive suite of services, including staffing and recruitment solutions, managed services, IT consulting, and project management. With a focus on excellence, collaboration, and innovation, ApTask provides unparalleled opportunities for professional growth and development. As a member of the ApTask team, you will have the chance to connect businesses with top-tier professionals, optimize workforce performance, and drive success across diverse industries. Join us at ApTask and be part of our mission to empower organizations to thrive while fostering a diverse and inclusive work environment.
Applicants may be required to attend interviews in person or by video conference. In addition, candidates may be required to present their current state or government issued ID during each interview.
Candidate Data Collection Disclaimer:At ApTask, we prioritize safeguarding your privacy. As part of our recruitment process, certain Personally Identifiable Information (PII) may be requested by our clients for verification and application purposes. Rest assured, we strictly adhere to confidentiality standards and comply with all relevant data protection laws. Please note that we only collect the necessary information as specified by each client and do not request sensitive details during the initial stages of recruitment.
If you have any concerns or queries about your personal information, please feel free to contact our compliance team at businessexcellence@aptask.com