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Our client, a world-leading Pharmaceutical Company in Sanford, NC is currently looking for a Microbiologist to join their expanding team. As a Microbiology Scientist, you will be a member of Pharmaceutical's dedicated and highly effective quality assurance and control team.
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We design, supply, and service a range of water systems and monitoring equipment in industries ranging from pharmaceutical to food and beverage applications, and from microelectronics ultrapure water to municipal water and industrial wastewater treatment.
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Experience of working under own initiative and in planning and prioritizing workloads University or technical college degree or equivalent qualification in relevant sciences such as: Medicine, Pharmacy, Chemistry, Biochemistry, Biology, Microbiology, Biotechnology, Health Technology, Toxicology, Physics, Biophysics, Material Science Biomedical Engineering, Mechanical, Electrical or Electronic Engineering, Computer & Software Technology, Human Physiology, Nursing, Quality Management.
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The BioMonitoring business field of MilliporeSigma Corporation is seeking a Digital Contract & Service Sales Specialist to support the growth strategy in the microbiology quality control field, with a strong focus on pharmaceutical, food, beverage, and other microbiological testing markets.
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Education and Experience:A MS/BS degree in life sciences, microbiology or chemistry, medical technology, biology or related field and a minimum of 15 + years’ experience in the pharmaceutical or biotechnology industry is required.
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We look for Science – Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We are searching for a talented Bioinformatics Analyst to join our team. Requirements: Bachelor's or Master’s degree in bioinformatics, Computational Biology, Biological Sciences, or a related field.
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Opportunity to explore the application of cutting-edge technologies in the field of mycology and to learn key concepts, and develop skills pertaining to infectious diseases pharmacotherapy, microbiology, and molecular genetics.
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QualificationsTo be considered for this role, you’ll require a minimum of 5 years of professional experience in relevant field of healthcare products or related activities e.g.:Work in medical devices industry and/or in vitro diagnostic devices(preferred) or closely related industries (e.g., pharmaceutical industry) such as research and development, manufacturing, quality management, regulatory affairs.
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Complete audits to assess accuracy and quality of scientific data submitted to the regulatory agencies in support of in vivo medical devices and in vitro diagnostic devices' application. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self.
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These groups include Maintenance, Quality, Automation, Operations, Microbiology, Labs, Packaging, and Environmental Health & Safety. Manage 7+ active capital design/construction projects ($75,000-$1,000,000) with varying complexity, in both GMP and non-GMP areas, including but not limited to clean rooms, pharmaceutical injectable filling lines, dirty utilities, and general facility improvements.
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Complete deviations and Environmental monitoring trend reports Compendial Endotoxin Testing Requirements: Bachelor's degree in microbiology (or closely related subjects), Higher level degree in Microbiology preferred Experience in a sterile manufacturing pharmaceutical laboratory.
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B.S. in Science (Chemistry, Pharmacy, Biology, Microbiology or related sciences) or Business/Finance is required. Minimum of 5 years of pharmaceutical experience in business development, alliance management, and/or portfolio management is required.
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The position will report directly to the analytical development manager or a quality control manager and work in close collaboration with the microbiology QC team and project team, as well as periodically interfacing directly with external customers as a technical subject matter expert.
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Kelly Science & Clinical is seeking a Validation Engineer near Morton Grove, IL. Direct Hire Shift: Monday - Friday 8am-5pm Compensation: Based on experience Position Summary: Are you ready to join a dynamic team to ensure the utmost cleanliness and safety standards in a cutting-edge pharmaceutical environment.
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Manage audit observations and audit reports through the internal audit database and CAPA process. Plan, conduct, and lead complex clinical study audits (Sponsor, Investigator Sites and Clinical Suppliers) (either remote or on site) in accordance with all applicable regulations, standards, mentorship, and the established procedures, maintaining a high standard of service delivery that ensures effective customer relationships.
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