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One or more years of experience working in a Laboratory Animal Facility or performing work in cGMP environment. As is typical of a pharmaceutical manufacturing-based role, employees must be able, with or without an accommodation to: frequently lift/carry 15/30 pounds unassisted/assisted; stand for prolonged periods of time; walk and move for prolonged periods of time; climb stairs or ladders; gown/degown PPE and uniforms; use a computer with a keyboard and mouse; collaborate with others; maintain general availability during standard business hours.
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B.A./B.S degree in Chemical Engineering, Biology, or similar relevant field with at least 6 years of direct GMP manufacturing experience in a biotechnology manufacturing facility or Pilot Plant OR a High School Diploma with 10 years of experience in protein purification in Biotech/Pharmaceutical industry.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Company Overview: Synergy Bioscience, a pharmaceutical contract research organization (CRO), provides Product development, analytical chemistry, microbiology testing, as well as quality compliance consulting services to the FDregulated companies.
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Experience: 2-4 years in the Pharmaceutical or Biotechnology with emphasis in aseptic processing, QC microbiology, environmental monitoring, water system, quality control, validation and manufacturing processes.
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Minimum of 0-3+ years post-Bachelors degree experience in a cGMP environment (e.g. Production, Development, Process Engineering, Technical Services or related field) in pharmaceutical/ biotech industry.
ExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Demonstrated work experience in compliance with cGMP and FDA requirements, including Good Documentation Practices (GDP). Innova Solutions offers benefits( based on eligibility) that include the following: Medical & pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Ensure timely manufacturing of all liquid parenteral cGMP products using aseptic processing technology to deliver high-quality sterile products to the pharmaceutical industry. High School Diploma or GED and a minimum of five (5) years of relevant related work in the pharmaceutical industry experience, plus one (1) year in a team leadership role.
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The QC Analyst II will be responsible for analytical testing and data verification supporting both late-stage clinical and commercial small molecule and biosimilar products in cGMP-compliant laboratories.
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We are looking for a Quality Control Tech. I who thrives in a fast-paced environment, that will support a wide variety of Quality responsibilities including raw material sampling, setting up testing profile and perform physical testing adhere to follow all cGMP and HACCP guidelines.
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Scientist I: Bachelor of Science (MS preferred) in a Life Sciences discipline with 1-3 years of relevant experience working in a Quality Control work environment, preferably in the pharmaceutical industry with knowledge of cGMP is a plus.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Relevant experience and knowledge of manufacturing, batch record review, incoming material release, logbook review and/or analytical analyses for the biotech/pharmaceutical industry. Experience in a cGMP manufacturing environment, with strong working knowledge of FDA requirements and guidance documents.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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The Quality Lab Associate I will be located at the Drug Delivery Chemistry Laboratories, Round Lake, IL. The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs.
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6+ years cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, and bulk formulation. Coordinate daily operations and lead on the floor manufacturing employees to complete production activities safely and compliantly in accordance with OSHA and cGMP guidelines.
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Minimum of 1 - 5 years of experience in quality and/or manufacturing in a pharmaceutical, biotech, or biologics cGMP regulated manufacturing environment preferred. Ensure that products are manufactured in compliance with site procedures, regulatory and cGMP guidelines.
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EDUCATION and/or EXPERIENCE: Preferred 4 year BS, BA or BT degree in a technical discipline or 2 year associates degree with 1 to 2 years pharmaceutical packaging experience or an equivalent training and/or experience.
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