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BS degree in Mechanical, Chemical Engineering, or related discipline with at least 5 years of engineering or manufacturing experience in a cGMP context. DPS Group Global is seeking a Facilities Engineer with experience within the Biopharmaceutical industry.
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Ensure performance of all qualification activities is in accordance with internal procedures, cGMP industry and regulatory guidance. Must have demonstrated understanding of cGMP. Seeking a capable Validation Engineer to work in the RI area.
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The Document Control Specialist is responsible for managing and maintaining all pharmaceutical CGMP related documents within the organization. Document Management: Create, Review, and Revise CGMP related documents and records.
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Downstream biologics process development technology transfer, scale-up and ongoing manufacturing of biologics (cGMP) including technical support for nonconformance investigations and other commercial support activities.
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Critical to the success of this position is adherence to cGMP and OSHA Process Safety Management regulations, development of robust, reliable production processes, and cost-effective installation of durable, multi-purpose (flexible) chemical and solids processing equipment.
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Quality Control Chemist will also be responsible for method validation and release & stability testing for clinical trial and commercial drug products; therefore, verifying all products and/or substances meet acceptable quality standards and that they are in accordance with the company’s policies & procedures, FDA policies & procedures, and any applicable cGMP requirements.
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This position will develop and review protocols for new and existing cGMP systems, including manufacturing equipment, laboratory instrumentation, and processes, across our network of manufacturing facilities.
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Seeking a talented and collaborative Construction Project Manager with experience managing projects in the healthcare and/or life sciences sector, which may include hospitals, medical facilities, biology, cell/gene therapy, chemistry, pharmaceutical, cGMP process manufacturing, bio-containment, public health and/or clinical labs.
$120,000 - $160,000 a yearExpandUpdated 4 days ago - UpvoteDownvoteShare Job
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CGMP/cGDP Experience (preferred) or other regulated environment experience (Required)ISO / ISO Information Analysis (Mini-Tab experience preferred)Quality Engineering DOE, Inference Tests, Normality/Capability Analyses, Correlation Studies, Gage RR, etc.
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Responsible for complying with applicable regulations as required in a cGMP environment. Monday-Friday NO weekends, NO holidays. Remnant donor sample tube management: sort, prepare aliquot specimens, label, document data, freeze samples, and pack.
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Comply with cGMP, safety, and audit standards. Fully cGMP compliant. Blue Cross Blue Shield Medical, Vision, & Dental. Our client is a pharmaceutical manufacturer of formulation and packaging solutions located in Lincoln, RI. Privately owned with two sophisticated laboratories on-site.
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Experience in a regulated environment such as cGMP, ISO, or FDA preferred. The Sourcing Manager will support single use fluid handling commodities to include bags, filters, fluid transfer, sensors, pumps, clamps, fittings, gaskets, etc.
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Completes documents/records following cGMP documentation practices. Bradford offers a full benefits package that includes full medical, vision and dental coverage, employee wellness programs, 401(k), paid vacations and more.
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What We Offer:Bradford offers a full benefits package that includes full medical, vision and dental coverage, employee wellness programs, 401(k), paid vacations and more. We are the world's leading manufacturer of specialty bar soap and solid cleansing products, which include cleansing sticks; solid shampoos and conditioners; bath bombs; and moisturizing sticks.
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Experienced in critical regulations (occupational health & safety, radiation safety, devices, and quality standards (cGMP, Eudralex, ICH). In addition to a robust proprietary pipeline, Fusion has a collaboration with AstraZeneca to jointly develop novel targeted alpha therapies (TATs) and combination programs between Fusion's TATs and AstraZeneca's DNA Damage Response Inhibitors (DDRis) and immune-oncology agents.
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cgmp job in Providence, RI
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