- Aequor (Thousand Oaks, CA)
- …evaluation of compliance issues, providing recommendations, and assuring progress of quality records to completion. The Sr. Associate will also represent ... SOPS, maintaining training, and good documentation practices. Also, ability to make Quality based decisions in order to ensure compliance . Experience managing… more
- Merck & Co. (Upper Gwynedd, PA)
- …Electronic Common Technical Document (eCTD), Immunochemistry, International Regulatory Compliance , Microbiology, Molecular Microbiology, Pharmaceutical Process ... Job DescriptionGRACS CMC - Associate Principal Scientist, CMC, R4 - Pharm Pre-approval...to the Sr Director/Director/Principal Scientist/Sr Principal Scientist in Pre-approval Pharmaceutical CMC is responsible for developing and implementing CMC… more
- Merck & Co. (Rahway, NJ)
- …Estimation and Planning, GMP Compliance , Management Process, Manufacturing Quality Control, Medical Supply Management, Medicinal Chemistry, Pharmaceutical ... in Rahway, New Jersey.The Sterile Process Engineer role at the Associate Director level will leverage the individual's leadership, technical, and communication… more
- Merck & Co. (San Francisco, CA)
- Job Description Position Description: Associate Director, DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) ... modalities. We are interdependent across our functional areas, Discovery, our Manufacturing Division Quality , and BARDS, to name a few, and with our partners in… more
- Eisai, Inc (Nutley, NJ)
- … compliance with regulatory and other ethical guidelines relevant to the pharmaceutical industry, and to ensure compliance with Eisai policies & ... Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and...is your profile, we want to hear from you. Associate Director, Medical Education - Oncology, is responsible for… more
- Merck & Co. (Durham, NC)
- …routine internal and external GMP and Financial audits, QSAT actions, to ensure compliance .- This is a fast-paced and multi-faceted role that provides leadership and ... external GMP and Financial audits, input to QSAT actions, to ensure compliance .Support the Master Data team with general Material Handling Steward tasksDrive safety,… more
- Merck & Co. (Durham, NC)
- …for establishing a strong business partnership and ensuring excellence in Compliance , Supply, Continuous Improvement, and Cost Management.--The Associate ... compliance goals through a risk-based approach (Safety Regulations, Quality Assurance, Risk Management, Deviation Management, Product Release, Change Control).-… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …design pull you in? Are you ready to experiment with us? The Position The Associate Director of Nephrology Key Opinion Leader Marketing will be a pivotal driver in ... responsible experience within sales, brand management/marketing experience within the pharmaceutical industry required Proven knowledge of the pharmaceutical … more
- Eisai, Inc (Exton, PA)
- …close-out of documentation, manufacture of DS/ADI materials, and suite change-over ensuring compliance to relevant regulations. The Associate Director is also ... Quality Control, Regulatory, and CMC Program Management departments.The Associate Director of Biologics Operations maintains knowledge of established and… more
- Merck & Co. (Rahway, NJ)
- …should have solid understanding of integration and partnering for Pharmaceutical development/ CMC with Quality , Regulatory, Operations, Non-clinical, ... This research opportunity is fast paced and contributes to the Pharmaceutical Sciences and Clinical Supplies (PSCS) deliverable which is the development… more
- Merck & Co. (Rahway, NJ)
- …Manufacturing Environments, Mechanical Apptitude, Pharmaceutical Development, Pharmaceutical Manufacturing, Pharmaceutical Quality Assurance, ... will provide hands on assistance for daily production activities while ensuring compliance with Safety & Environmental (S&E) and current Good Manufacturing Practices… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... to Biostatistics Data Management & Data Ops for EDC, edit checks, data quality listings, SAP, Data Management plan; Reviews patient population and protocol … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... preferred supplier list, maintains and tracks Procurement training for compliance , troubleshoots payment delays, and other duties as needed.ResponsibilitiesContract… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. This position carries ... option 14 weeks Paid Parental Leave Free access to Novo Nordisk-marketed pharmaceutical products At Novo Nordisk, you will find opportunities, resources and… more
- Merck & Co. (Durham, NC)
- …Maintenance Processes, Manufacturing Operations, Manufacturing Processes, Operations Support, Pharmaceutical Production, Pharmaceutical Quality Assurance, ... Production Operations, Production Scheduling, Safety, Health, Environment and Quality (SHEQ), Safety Procedures, Shift Work, Standards Compliance , Systems… more
- Novo Nordisk Inc. (Durham, NC)
- …improvement, & project management Serve as the Lead and SME to operate within compliance with a quality mindset that focuses on risk management & mitigation ... & projects Lead the team's Change Management standards and always manage assignments within compliance with a Quality Mindset that focuses on risk management and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ... execute daily production schedules.Will have 3-6 direct reports ranging from Associate Director, Senior Manager, and Manager.Oversee the hiring, development, and… more
- Merck & Co. (Durham, NC)
- Job DescriptionAre you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you!The ... Associate Specialist, Calibration is a member of the Engineering,...This includes Energy Center, Vaccine Bulk and Manufacturing Facilities, Quality Labs, Material Management Storage Facility (MMSF) and projects.… more
- Merck & Co. (Durham, NC)
- …pharmaceutical environment, operations, technical services, supply chain, and/or quality operationsExperience with aseptic processing operations such as bulk ... and drug product, including product inspection, warehouse, utilities, and quality control laboratories.The Specialist, Operations will be responsible for providing… more
- Merck & Co. (North Wales, PA)
- …(Ph.D.) or 20 years of work experience (MS) in the pharmaceutical industryStrong expertise in high- quality strategic statistical decision-making, development ... and vaccines for the benefit of patients and global human health.The Associate Vice President (AVP), Late Development Statistics, BARDS, is responsible and… more
