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GMP or GLP and/or FDA manufactured component experience/knowledge preferred. Mitsubishi Chemical Performance Polymers, Inc. (MCPP) a subsidiary of Mitsubishi Chemical is wholly owned, MCC and its twenty group companies provide products and services to customers in North and South America providing a broad range of businesses including chemical, petrochemical, composite materials, pharmaceuticals, electronics, and other businesses.
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Support site LIMS team during internal and regulatory GMP system audits. Experience using databases and/or data trending/analysis tools (Microsoft Access, statistical programs) and basic coding capability (such as SQL, R, Python) is preferred.
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We are seeking a highly skilled and detail-oriented GMP Test Technician to join our team. The GMP Test Technician will play a crucial role in maintaining the highest standards of quality assurance in a regulated manufacturing environment.
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Must demonstrate a working knowledge of standard manufacturing operations, FDA and ISO regulations, Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) requirements, and standard problem solving techniques.
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Perform general plant cleaning, housekeeping, and sanitation to support the sanitation, GMP, and safety programs. Work on GMP action items generated from internal / external audits and the quality department.
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Job Title: GMP Business Analyst. SAP Fiori App integration. Plant Maintenance Master Data: Equipment/Functional Location/Maintenance. Able to create SAP reports from Plant Maintenance Master Data.
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1 - 3 years GMP/GLP experience. Electro-Mechanical assembly skills. The Electronics Assembly Technician I is a non-exempt position that reports to the Electronics Management Team. The Electronics Assembly Technician I is responsible for assembling and testing full assembly and individual sub assembly parts for Charm Sciences equipment.
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Adhere to Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP). Strong understanding of GDP and GMP. Excellent English communication skills. The primary responsibility of the Quality Inspector will be to ensure compliance with quality standards and regulations in a manufacturing environment, specifically focusing on paperwork, line clearance, 5S (Sort, Set in order, Shine, Standardize, Sustain), MPIs (Manufacturing Process Instructions), and QIs (Quality Inspections.
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The micro-cleaner is a critical role in the company which ensures the proper cleaning of the cleanroom, controlled environment and GMP laboratory environments. Responsible for participating in continuous training: cGMP training, technical skills, safety, performance improvement.
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Position : Packaging Operator (Must Have Clean room, GMP & SOP Exp) Some Clean Room experience, Knowledge of Computer basics and GMP knowledge. Position : Packaging Operator (Must Have Clean room, GMP & SOP Exp.
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Additional duties as may be assigned from time to time Education & Qualifications 4 years of experience in the pharmaceutical/biotech industry Demonstrated aptitude or ability to learn to gain a strong understanding of GxP regulations (specify GMP, GLP, GCP, GVP or other applicable standards.
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Working knowledge of GMP and FDA regulatory requirements for Class III medical devices or equivalent. Working knowledge of GMP and FDA regulatory requirements for Class III medical devices or equivalent.
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Utilizing state of the art strategies, processes and human capital, CCS ensures the highest degree of service and integrity for the sensitive environment we support; impacting those industries that impact the world.
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Work under the Production Department director to support production by performing GMP radiochemistry processes in a safe, efficient and timely manner. GMP CHEMIST (This is a hands on position with production responsibilities, not a QC position.
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Provide technical leadership and subject matter expertise to the Nucleic Acids testing team to ensure the successful execution of all GMP release and stability PCR testing executed in support of Sarepta' s Gene Therapy programs (currently 1 commercial program and 5+ active clinical programs.
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gmp job in North Reading, MA
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