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Design and execute experiments to fully characterize the oligonucleotide drug substance and drug product materials. Additionally, you’ll design and execute experiments to fully characterize oligonucleotide drug substances and drug product materials.
$120,000 - $140,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Well versed in FDA, EMA and ICH guidelines relating to registration, quality, and compliance concerning drug substance and authored CMC sections in commercial filings (BLA, MAA) and post approval changes.
$237,660 - $307,560ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Review documents associated with drug substance and product development and manufacturing, including but not limited to change controls, methods, monographs, protocols, and reports, and organize and archive documents in Veeva Quality Docs System.
$123,000 - $144,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Qualifications: Bachelor of Science degree or work experience equivalent to a minimum of 5-7 years of experience in a GMP quality (Mfg/QA/QC) environment, experience in drug substance. Responsibilities:Note: The following is meant to be representative but not necessarily all inclusive of the duties and responsibilities for this position title: Good knowledge base and direct experience Drug Substance/API production and QA oversight.
$110,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Treatment Setting Responsibilities: Facilitates educational groups related to substance use disorders, community meetings and supports with independent living skills in the Laurel house residential setting.
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We are seeking a candidate with clinical-stage QA background in drug substance biologics manufacturing (e.g. antibodies, proteins, reagents), at the supervisor/manager level, and a strong desire to learn.
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The QC Analyst is responsible for performing drug substance and drug product in-process, release, and stability testing activities in support of CGMP manufacturing of clinical trial materials.
$60,000 - $85,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Williams Lea is a drug-free workplace and performs pre-employment substance abuse testing. Williams Lea is hiring for Office Services Associate for our Menlo Park office to work Monday to Friday, 9:30 am to 6:30 pm.
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We are accountable for direct technical support of drug substance and drug product operations, with responsibility for all aspects of process engineering: tech transfer, process validation, GMP manufacturing support, process monitoring and data analytics.
$237,660 - $307,560 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Scientist - PhD in analytical, organic chemistry or a related discipline with minimum of 1 year of direct experience in oligonucleotide analysis and formulation. Scientist - PhD in analytical, organic chemistry or a related discipline with minimum of 4 years of direct experience in oligonucleotide analysis and formulation.
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The Development Sciences Biologics CMC Drug Substance Cell Line Development Group in South San Francisco, CA is seeking a Scientist to join a talented and collaborative team developing CHO cell lines for GMP applications.
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We maintain a drug-free workplace and perform pre-employment substance abuse testing. Focal Point for one or two major areas such as: Labor Relations, Compliance, Start Ups, Learning, Leave/FMLA. Knowledge, Experience and Skill Requirements Bilingual in English and Spanish requiredPeople management skillsAnalytical and goal orientedWorking knowledge of current labor legislationKnowledge of HR functions and practicesExperience with labor unions and employee relations Work Experience years of related Business Partner experience.
Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Determine the reason for the patient's visit, identify lifestyle needs, and deliver recommendations to patients for eyewear needs following the prescription given by their optometrist. Recommend specific lenses, lens coatings, and frames to suit customer needs, occupations, habits, and facial features.
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Forms cross-functional alliances with Small Molecule Drug Substance Development, Small Molecule Drug Product Development, CMC Regulatory Affairs, Quality Control and Manufacturing Operations by providing SMEs to these functions and project teams.
$221,170 - $286,220 a yearExpandUpdated 2 days ago - UpvoteDownvoteShare Job
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Manage manufacturing activities for viral vector and cell therapy, including cGMP aseptic qualification, in support of manufacturing and formulation of viral vectors as drug substance and of cell therapeutics as drug products.
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drug substance jobs in San Mateo, CA
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