QC Analyst

Employment Type

: Full-Time

Industry

: Miscellaneous



For more than 75 years, Grifols has worked to improve the health and well-being of people around the world. We are a global healthcare company that produces essential plasma-derived medicines for patients and provides hospitals and healthcare professionals with the tools, information and services they need to deliver expert medical care. Headquartered in Barcelona, Spain, Grifols has over 20.000 employees in 30 countries. Grifols' three main divisions - Bioscience, Diagnostic and Hospital - develop, manufacture and market innovative products and services available in more than 100 countries. A leader in transfusion medicine, the Diagnostic Division is a global business focused on providing innovative solutions to help ensure the safety of the blood and plasma supply, detect human diseases and monitor therapies. The division advances patient care with diagnostic solutions to improve disease detection and management, and simplify laboratory operations. Job Summary: To provide expertise to their designated QC group, and to accurately assess the purity, potency, efficacy, and other performance characteristics for the purpose of supporting both manufacturing and quality assurance in the production, release, and monitoring of established product lines Essential Job Duties: * Perform assays for their designated laboratory: a. Routine in-process, final product (antigens) protein chemistry testing for release of product b. Routine in-process, final product (antigens) microbiological testing for release of product c. Routine testing for release of Raw Materials d. Routine testing for release of Seed Stock e. Antigen Stability, reference/reagent qualification testing f. Seedstock Stability testing g. Cleaning and or Process Validation testing h. Analytical Method Validation testing i. Product/Method development testing * Comply Site Environmental Health & Safety (EH&S) requirements Job Requirements: * Bachelor's degree in Biochemistry, Molecular Biology, Immunology with 1-2 years. * At least 1-2 years experience in a regulated GMP testing laboratory * Must have one or more assay testing experience in one of the main areas listed: * Protein chemistry methods such as Lowry, Bradford, BCA, SDS-PAGE, Western Blot, HPLC, Amino Acid Analysis, ELISA's and in vitro diagnostic test kits. * Microbiological methods such as Microbial Limits Test (bioburden), Sterility, Endotoxin, TOC, Microbial Identification, Contamination testing and Growth Promotion. * Bacterial and Yeast Seedstocks testing methods such as Microscopic examination, viability, contamination, purity and phenotype testing, DNA Plasmid isolation and restriction digest testing. * Environmental/Utility/facility Monitoring testing such as Sampling of and testing of manufacturing water by membrane filtration, viable and non-viable particulate testing of facilities and utilities, viable (surface) monitoring of manufacturing facilties, personnel and biological hoods, moisture and oil content testing of compressed gases * Analytical/Microbiological Method Validation testing such as Bacteriosis and Fungistasis, linearity, specificity and robustness tests in protein chemistry, microbiology or complendial test methods * Assay trouble shooting experience in their expert area * Pharmacoepeial (compendial) test methods for Raw Materials such as, but not limited to; melting point, loss on drying, color and appearance, identity by FTIR, heavy metals, arsenic, residual solvents, chloride, sulphate, insoluble matter * Proficient in MS Word, MS Powerpoint and MS Excel software * Must have good time management, effectively prioritizing tasks for completion * Individual must work in an ethical manner and ensure employees follow Grifols ethics and compliance guidelines. * Must meet the two (2) mission critical competencies:1)Customer Focus 2)Technical Skills * Timely execution and completion of release and stability testing for all antigen product lines * Timely execution and completion of stability testing for all seedstocks * Timely execution and completion of testing for RMs * Training in new assays within the required time * No safety incidents or HSE related observations. * This job description is accurate at the date of publication. It is intended to provide information essential to understanding the scope and general nature of the work performed by job holders within this position. This job description is not intended to be an exhaustive list of qualifications, skills, duties, responsibilities or working conditions associated with the position. Other duties may be assigned and qualifications required may change over time. EEO Minorities/Females/Disability/Veterans Grifols is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and local laws that prohibit employment discrimination on the basis of race, color, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability or veteran's status or any other classification protected by applicable State/Federal laws. We will consider for employment all qualified Applicants, including those with Criminal Histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. Job Summary: To provide expertise to their designated QC group, and to accurately assess the purity, potency, efficacy, and other performance characteristics for the purpose of supporting both manufacturing and quality assurance in the production, release, and monitoring of established product lines Essential Job Duties: * Perform assays for their designated laboratory: a. Routine in-process, final product (antigens) protein chemistry testing for release of product b. Routine in-process, final product (antigens) microbiological testing for release of product c. Routine testing for release of Raw Materials d. Routine testing for release of Seed Stock e. Antigen Stability, reference/reagent qualification testing f. Seedstock Stability testing g. Cleaning and or Process Validation testing h. Analytical Method Validation testing i. Product/Method development testing * Comply Site Environmental Health & Safety (EH&S) requirements Job Requirements: * Bachelor's degree in Biochemistry, Molecular Biology, Immunology with 1-2 years. * At least 1-2 years experience in a regulated GMP testing laboratory * Must have one or more assay testing experience in one of the main areas listed: * o Protein chemistry methods such as Lowry, Bradford, BCA, SDS-PAGE, Western Blot, HPLC, Amino Acid Analysis, ELISA's and in vitro diagnostic test kits. * o Microbiological methods such as Microbial Limits Test (bioburden), Sterility, Endotoxin, TOC, Microbial Identification, Contamination testing and Growth Promotion. * o Bacterial and Yeast Seedstocks testing methods such as Microscopic examination, viability, contamination, purity and phenotype testing, DNA Plasmid isolation and restriction digest testing. * o Environmental/Utility/facility Monitoring testing such as Sampling of and testing of manufacturing water by membrane filtration, viable and non-viable particulate testing of facilities and utilities, viable (surface) monitoring of manufacturing facilties, personnel and biological hoods, moisture and oil content testing of compressed gases * o Analytical/Microbiological Method Validation testing such as Bacteriosis and Fungistasis, linearity, specificity and robustness tests in protein chemistry, microbiology or complendial test methods * o Assay trouble shooting experience in their expert area * o Pharmacoepeial (compendial) test methods for Raw Materials such as, but not limited to; melting point, loss on drying, color and appearance, identity by FTIR, heavy metals, arsenic, residual solvents, chloride, sulphate, insoluble matter * • Proficient in MS Word, MS Powerpoint and MS Excel software * • Must have good time management, effectively prioritizing tasks for completion * • Individual must work in an ethical manner and ensure employees follow Grifols ethics and compliance guidelines. * • Must meet the two (2) mission critical competencies:1)Customer Focus 2)Technical Skills * • Timely execution and completion of release and stability testing for all antigen product lines * • Timely execution and completion of stability testing for all seedstocks * Timely execution and completion of testing for RMs * Training in new assays within the required time * No safety incidents or HSE related observations. * This job description is accurate at the date of publication. It is intended to provide information essential to understanding the scope and general nature of the work performed by job holders within this position. This job description is not intended to be an exhaustive list of qualifications, skills, duties, responsibilities or working conditions associated with the position. Other duties may be assigned and qualifications required may change over time. EEO Minorities/Females/Disability/Veterans Grifols is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and local laws that prohibit employment discrimination on the basis of race, color, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability or veteran's status or any other classification protected by applicable State/Federal laws. We will consider for employment all qualified Applicants, including those with Criminal Histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. Location: NORTH AMERICA : USA : CA-Emeryville:USSDW - San Diego CA - Willow Ct Mfg

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