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The Biologics Sales Specialist is responsible for achieving and exceeding sales goals to grow Implant Directs' biomaterials revenue through selling directly to clinicians and dental office staff.
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Partners with the Health Plan National Medical Officer for Pharmacy to develop and deploy clinical affordability solutions for drugs and biologics covered under the Medical Benefit. Collaborates with Cigna Ventures to identify and evaluate digital health, startup company and investment opportunities to advance Cigna Pharmacy services.
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Learn and maintain thorough familiarity and compliance with all state and federal regulations, U.S. Food and Drug Administration (FDA)-approved Standard Operating Procedure Manual, Occupational Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), Current Good Manufacturing Practice (cGMP) and internal company procedures.
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Mixes chemotherapy and biologics only within the biological safety cabinet (BSC) using proper aseptic technique. Mixes chemotherapy and biologics only within the biological safety cabinet (BSC) using proper aseptic technique.
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Must possess strong knowledge of SOPs, laboratory procedures, FDA and ICH guidance, USP regulations, analytical testing techniques, and cGMP. As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry.
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Must have past experience in wound care/biologics. We have an immediate opening for a Surgical Sales Specialist with a leading manufacturer of advanced wound care products. Must have past experience in wound care/biologics.
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We are looking for a talented individual to join our dynamic Drug Product Development team within the Company’s Biologics CMC organization, where we drive the maintenance and evolution of both clinical and commercial products and programs.
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You will be a product consultant in the Sports Medicine Biologics portfolio specializing in both Biologics and Sports Medicine soft tissue injury repair. You will work cross-divisionally to increase awareness and adoption of products including the Sports Medicine Biologics product portfolio.
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Must possess strong knowledge of SOPs, laboratory procedures, FDA and ICH guidance, USP regulations, microbiological testing techniques, and cGMP. Bachelor’s Degree in biology, or related science and 8-10 years of experience in a pharmaceutical laboratory management role.
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Supervise donor selection, plasma collection and all manufacturing records to maintain the highest production standards in accordance with Federal and State regulations, with FDA approved Standard Operating Procedure Manual, OSHA, CLIA and cGMP.
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The incumbent is responsible for tasks associated with the technology transfer for sterile drug products and Biologics. Knowledge and experience working in the sterile cGMP-based environment.
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Our integrated operating unit is comprised 3 global businesses, Spine and Biologics, Enabling Technologies and China Cranial, Spinal Orthopedic Technologies. At Medtronic, the Enabling Technologies (Advanced Energy) Sales Representative II has the responsibility and authority for creating an effective sales presence in his/her area, learning the product line and its applications under different environments, following-up on leads with a multi-prong contact approach, achieving sales targets, and utilizing the Medtronic Sales process for each class of customers.
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Strong understanding of drug acquisition and dispensing in the immunology specialty biologics space (Buy and Bill, Specialty Pharmacies, Specialty Distributors, etc.) We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio.
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The QA/QC Manager will have responsibility for the implementation and management of quality control/assurance programs, processes, and technicians for Vireo Systems operations to maintain compliance with all applicable regulatory and cGMP requirements.
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In addition, our team also works on projects with clients to manage these Quality business processes for supply chain, manufacturing, commercial operations and R&D. This includes analyzing various cGMP and 21 CFR Part 11 regulations in the Regulatory Compliance area to determine impact on risk exposure.
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biologics cgmp jobs in Antioch, TN
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