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Additional responsibilities will include executing CIP, SIP, aseptic sampling, parts washing, inventory management, documentation, work order generation, and data entry/evaluation. The Andover Pilot Facility process technician will be part of a diverse team of scientists, engineers and technicians focused on media and buffer solution preparation as well as scale up and optimization of mammalian processes to enable the production of toxicology drug substance and process development material in support of Pfizer’s Biotherapeutics portfolio.
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Must possess a working knowledge of epidemiology, microbiology, infectious diseases, and aseptic techniques to include Standard Precautions. We are hiring a Director of Staff Development/Infection Control Nurse to join our dynamic care team at Northwood Rehab in Lowell.
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Responsible for Patient Safety, including pre-screening for contra-indications, aseptic injection technique and may require remote MR Technologists Assistant oversite. As an MRI Technologist, you are responsible for patient safety and the performance of high-quality MR studies, including radiologists as necessary.
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Demonstrated experience in aseptic manufacturing and other pharmaceutical manufacturing activities (API, DP, Biotech, Oral Solid Dosage) applicable to the role. Advanced computer skills for MSOffice and enterprise systems such SAP, QTS, Vault, Documentum platforms, Minitab.
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Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.
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Understanding of aseptic/sterile technique. Title: Equipment QC Analyst II. BS degree in Biochemistry or related Life Science and/or 3-5 yrs. Understanding of aseptic/sterile technique. Record, document, and summarize calibration and testing data.
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The QC Analyst I is an entry-level, non-exempt position that reports to the QC Management Team. The QC Analyst I is responsible for performing quality control testing on various state-of-the-art diagnostic tests, components and standards for the food and beverage industries.
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Expected to meet the allotted time goals assigned per calibration. Calibrate equipment manufactured by client and ensure that it meets the quality standards. Document, troubleshoot, and report problems/discrepancies to the Manager.
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The QA Compliance Specialist performs quarterly audits, supports customer and regulatory audits as part of the Audit Team. Some microbiological knowledge/experience with aseptic technique is preferred as candidate may provide some additional support to quality control testing laboratory.
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0 to 2 years GMP/GLP experience. Able to safely handle antibiotics and mycotoxins in dry powder and concentrated liquid form in a laboratory setting. Be part of a QC team dedicated to assuring the quality of these diagnostic tests for food safety.
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GMP – Aseptic and non-Aseptic Areas and Non GMP Area – Offices spaces. Test continuity of circuit to insure electrical compatibility and safety of components, using testing instruments, such as ohmmeter, battery and buzzer, and oscilloscope.
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