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A leading Biopharma company are actively seeking a motivated candidate to fill their Vendor Outsourcing QC Associate I opportunity. B.Sc./ B.A. and 5+ years of relevant experience in the pharmaceutical or biopharma industry.
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The Technical Center Specialist will provide operational support to the North American Tech Center which includes customer cycle development, product testing, and assisting with sterilization training for customers within the biopharma and broader life sciences industry.
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Posted job title: Histologist. RTG Medical-Allied is seeking a travel Histology Technician for a travel job in Minneapolis, Minnesota. Specialty: Histology Technician. Posted job title: Histologist.
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GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organization where people can thrive.
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Responsible for change management strategies focused on delivering effective project and program management for high-level cross-functional initiatives associated with the effective combination of technology and biopharma.
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Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
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KBI Biopharma, Inc. (KBI) is committed to providing a safe and healthy workplace. KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application.
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The Quality Assurance Operations group has oversight of the manufacturing areas, including process technology transfer, master batch record review and approval, on-the-floor support, product disposition, and shipping.
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The site manufactures organic and vegan-based nutraceuticals via confection to enhance wellness for all consumers. Is able to communicate problems with the Production Supervisor, designated Production Worker Lead/Foreperson and/or mechanic on duty.
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Bridge to thousands of biopharma companies and their patients. Ensures validation representation on cross-functional and multi-site teams to support integrating risk management into various product quality systems such as Change Control and CAPA. Participates, present and provide rationale for the validation program during periodic audits and regulatory inspection and customer visits/conference calls as required.
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As an essential employee, facilities technician III, is responsible for the installation, 24/7, day-to-day operation, maintenance, and modification of all KBI Biopharma site systems. KBI Biopharma is committed to providing a safe and healthy workplace.
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Company: CBRE at GSK Biopharma. Leads a team responsible for complex preventive maintenance and corrective repair of commercial and industrial HVAC, refrigeration equipment, Pure water systems and other building systems/utilities.
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Knowledge of and adherence to all PCI, cGMP, and GCP policies, procedures, and rules. Ensure compliance of plant operations with company policy, and federal, state, and local regulations, including OSHA, FDA, and employment law.
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Experience with industrial facilities such as Dairy, Nutrition, Pharma, Biopharma & Medical Device manufacturing facilities. We are currently recruiting an experienced energy engineer based in Ireland to support our growing business.
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A minimum of 5 years related work experience in a pharma, biopharma, and/or biotech manufacturing environment. The Sr. Validation Engineer supports validation of cGMP equipment, facilities and processes.
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