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This role requires a candidate who has an understanding of and several years of experience with the legal and business risks specific to pharmaceutical product pricing and reporting, public and private third-party payer and PBM, GPO and specialty pharmacy contracts, product labeling, negotiating and drafting complex contracts for other functional areas and the advertising and promotion of approved products.
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Resource Label Group, LLC is a leading full-service provider of label and packaging solutions with a diverse product offering which includes pressure sensitive labels, shrink sleeves, RFID/NFC technology, sustainable product solutions, scent activation technology, pharmaceutical packaging and fulfillment services.
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With approximately 750 employees and laboratories in four countries, CIL specializes in the process of labeling biochemical and organic compounds with highly enriched, stable (nonradioactive) isotopes of carbon, hydrogen, nitrogen and oxygen.
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Princeton Legal Search Group is retained on an exclusive basis with Otsuka America Pharmaceutical US to lead the search for an experienced attorney familiar with pharmaceutical pricing, reimbursement, market access contracting strategies, and commercializing approved products.
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Manual to Semi-automatic manufacturing and packaging, wet and dry weigh & fill-line equipment, agitators, dispensers, liquid and solid encapsulation, compression, rolling, packaging and labeling to produce MedMen products including tinctures, lotions, capsules, vape pens and pre-rolls.
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CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. Minimum of 5 years of experience working in a chemical manufacturing, biotech or pharmaceutical GMP regulated environment.
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Tasks to be completed may include fermentation, protein purification, solvent extractions, tissue culture, preparation of bulk solutions, aseptic fills of buffers, filling and labeling of vials under sterile and non-sterile conditions, routine buffer and media preparation, filtration, vial preparation and sterilization.
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CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists.
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From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labeling is accurate.
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Minimum of 3 years of experience in a Pharmacovigilance/Drug Safety environment with experience in managing adverse event and SAE processing, medical surveillance and risk management, signal detection, on a global basis within the pharmaceutical industry.
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Technical Expertise 4.1 Demonstrate proficiency and mastery of various technology utilized in the provision of pharmaceutical care, including, but not limited to: EMR, ADS, Inventory Management software, carousel, Packaging software, Sterile Product Pharmacy Workflow Manager, Barcode Labeling Programs, RFID Technology (usage varies depending upon hospital.
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Community/retail pharmacy technician experience or academic training /experience in health related fields (Laboratory Sciences or Pharmaceutical Sciences) also considered. 1.5 Demonstrate reliability in providing assistance to the pharmacist in regards to the provision of pharmaceutical care.
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Health Care Professional degree required (e.g., RN/BSN/MSN, NP, PharmD) and 10-12+ years of pharmaceutical industry experience in drug safety & pharmacovigilance as a Safety Scientist for products in the clinical trial and post-marketing environments.
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Excellent understanding of US regulations for drug promotion/advertising and US labeling, and experience interacting with FDA OPDP• Experience with Veeva Vault PromoMats and MedComms, Trackwise, or similar document management systems a plus• Demonstrated expertise in regulatory requirements for labeling and advertising materials.
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Our Specialty Additives product line provides mineral-based technologies serving Paper, Packaging, Sealants & Adhesives, Paint & Coatings, Ceramics, Plastics, Food & Pharmaceutical markets. The Quality Assurance (QA) Manager is responsible for the planning, execution, and overall management of an FDA and GMP regulated Quality Unit which governs the site's manufacturing, packaging, labeling, testing, and holding activities of goods produced.
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labeling pharmaceutical jobs
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