- Insmed Incorporated (Bridgewater, NJ)
- …MPH, PharmD, PhD, MD) advantageCombination of pharmaceutical industry experience in Medical Affairs, Development, or Commercial and/or prior consulting ... in New York™, and Best Workplaces for Millennials™ lists.OverviewThe Director of Medical Process Excellence will be responsible to develop and evolve strategic… more
- Sofo Foods (Columbus, OH)
- …plans based on a customer's needs and sales objectives. Requirements: Prior outside consultative sales experience with continuous repeat customers.Working knowledge ... industry. Preferably experience in the ethic/Italian food market.Proven track record of prospecting and opening new customer accounts.Analytical ability to… more
- Option Care Health (Columbus, OH)
- …Responsible for developing marketing campaigns and materials that reflect the analysis of prior marketing data to build on the success or failure of prior ... market conditions and information gathered in the sales process.Maintain adequate records of sales calls and interactions with clients through appropriate expense… more
- Merck & Co. (North Wales, PA)
- …A minimum of 5 years regional medical affairs experience (eg, Regional Director Medical Affairs) with proven track record of contribution to medical ... Job DescriptionRole Summary:The Global Senior Director Medical Affairs (GDMA) Immunology/Pipeline & Biomarkers will be responsible for driving execution of… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product… more
- Merck & Co. (North Wales, PA)
- …the Director may be responsible for: Providing scientific and medical leadership for strategic alliances and Co-partnership opportunities.-Supporting the team ... Required: MD or MD/PhD combinationBoard Certified or Eligible in Medical Oncology (and/or Hematology), Radiation Oncology, Surgical Oncology or a… more
- Catalent (Philadelphia, PA)
- …every patient, consumer, and Catalent employee. The Role Review and approve all batch records prior to production to ensure that they conform to requirements of ... responsible in preparing customer files, review and approve batch records , and release batch records and finished...liaison to our customer's quality assurance groups for batch record review and release. The Quality Assurance Document Control… more
- Novo Nordisk Inc. (Oklahoma City, OK)
- …live with the disease of obesity, yet only 2% of them receive dedicated medical treatment. By joining the Obesity Commercial team, you will have the opportunity to ... a rare opportunity backed by Novo Nordisk's long term commitment and track record in helping people living with chronic disease achieve greater health outcomes. If… more
- Greater Baltimore Medical Center (GBMC) (Baltimore, MD)
- …Performs initial history and physical and documents same appropriately in Electronic Medical Record .* Writes standard orders in accordance with hospital policy.* ... fully vaccinated against Covid-19 or obtain a GBMC approved medical or religious exemption prior to starting employment at GBMC Healthcare, to include Gilchrist… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product… more
- Catalent (Philadelphia, PA)
- …errors made during the packaging operation and again when the job is completed prior to submitting the batch record for final review and release. Prints ... and understands both the Production Protocol and QA Protocol prior to starting the packaging process. Performs and documents...that the drug product quantities documented in the batch record match those that are entered in the Inventory… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product… more
- Novo Nordisk Inc. (Suffern, NY)
- …I maintains relationships with physicians, physician assistants, nurse practitioners, medical assistants, pharmacists, nurses and other paramedical customers and ... Demonstrates understanding of territory customer groups and affiliations such as IPAs, Medical Groups, Health Systems, and Local Clinics and uses this to identify… more
- Merck & Co. (Rahway, NJ)
- …regulated environmentsDevelopment project leadership with a proven track record collaborating with and managing external vendors/manufacturers.Preferred Experience ... methods as needed in tech transfer or lifecycle.Experience with medical device development with understanding of Design Controls (21...of twelve (12) months of service in current position prior to applying for open positions.If you have been… more
- Merck & Co. (South San Francisco, CA)
- …driving scientific or platform innovationsDemonstrated passion for, and a track record of talent development. Prior direct people management.Established external ... experience, OR BS with 14+ years of substantial industry experience.Track record in leadership and managerial roles in Biologics Discovery.Experience in advancing… more
- Lundbeck (Las Vegas, NV)
- …procedures and FDA regulations regarding the promotion of pharmaceutical and medical products.REQUIRED EDUCATION, EXPERIENCE and SKILLS: Bachelor of Arts or Bachelor ... accredited college or university 2+ years pharmaceutical, biopharmaceutical, biologics, medical device sales or related healthcare sales experience Must demonstrate… more
- Merck & Co. (Rahway, NJ)
- …with Regional Commercial Leaders, international markets and cross-functional partners ( medical , policy, outcomes research, access, advocacy, etc.) to optimize the ... key market dynamics and seize business opportunities. Proven track record of high-performance launches and driving business results.Strategic Planning: Proven… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …cell, and CAR-T process) according to standard operating procedures and batch records and ensure safe and compliant manufacturing operations according to cGMP ... create/revise operational procedures, including manufacturing work instructions, master batch records , forms, and support and manage change controls. Work closely… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …Electronic Notebooks, laboratory formbooks, training formbooks, instrument logbooks, and records . Utilization of electronic systems (LIMS) for execution and ... able to accommodate unplanned overtime (including nights and weekends) on little to no prior notice. The candidate must be highly organized and capable of working in… more
- Lundbeck (Rockford, IL)
- …procedures and FDA regulations regarding the promotion of pharmaceutical and medical products.REQUIRED EDUCATION, EXPERIENCE and SKILLS: Bachelor of Arts or Bachelor ... accredited college or university 4+ years pharmaceutical, biopharmaceutical, biologics, medical device sales or related healthcare sales experience Must demonstrate… more
