Director, Process Optimization Lead BeOne Medicines AGDirector, Process Optimization LeadNY$171,900–$231,900 / yearCollaborates with the P&SM team, other GCO functional teams, and cross-functional teams on process optimization and strategy alignment at both regional and global levels, ensuring that operational processes effectively meet business needs. Inspires and leads initiatives to enhance the necessary technical skills and competencies within the Global Clinical Study Management team, facilitating more efficient clinical study execution while ensuring patient safety, compliance, and data integrity through optimized operational processes.
Administrative Assistant II - Center for Discovery and Innovation- CDI Hackensack Meridian HealthAdministrative Assistant II - Center for Discovery and Innovation- CDINutley, New JerseyFull timeThe Center for Discovery and Innovation- CDI was established by Hackensack Meridian Health (HMH) as an academic basic and translational research enterprise to rapidly translate science innovation to the clinic and to improve outcomes for patients with cancer, infectious diseases, autoimmune disease and other acute and chronic diseases. The posted rate of pay in this job posting is a reasonable good faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package.
Associate Director, Drug/Device Combination Products - Method Development & Testing Merck & Co IncAssociate Director, Drug/Device Combination Products - Method Development & TestingRahway, NJ$142,400–$224,100 / yearRequired Skills: Analytical Chemistry, Biocompatibility, Biomedical Engineering, Chemical Biology, Computer-Aided Design (CAD), GMP Compliance, Process Engineering, Product Development, Product Risk Management, Project Management, Project Management Support, Quality Control Management, Quality Management, Risk Management, Statistical Analysis, Technical Writing, Verification and Validation (V&V). The Associate Director of Method Development & Testing is responsible for leading a Center of Excellence (CoE) focused on developing and validating platform and innovative device/CP functional test methods with high technical rigor to support development, IND-enabling stability, commercial stability, and Design Verification.
Assistant Research Associate - Center for Discovery and Innovation- CDI Hackensack Meridian HealthAssistant Research Associate - Center for Discovery and Innovation- CDINutley, New JerseyFull timeThe Center for Discovery and Innovation- CDI was established by Hackensack Meridian Health (HMH) as an academic basic and translational research enterprise to rapidly translate science innovation to the clinic and to improve outcomes for patients with cancer, infectious diseases, autoimmune disease and other acute and chronic diseases. Qualifications: Education, Knowledge, Skills and Abilities Required : Bachelor's Degree with a minimum of 1-2 years of related research and/or science experience, or Bachelor's Degree and a post graduate certification in a science or research discipline with 0-1 year relative experience, or a Masters/Post graduate degree.
Associate Principal Scientist, Biostatistics Merck & Co IncAssociate Principal Scientist, BiostatisticsRahway, NJ$142,400–$224,100 / yearIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Required Skills: Biostatistics, Clinical Development, Clinical Trials, Clinical Trials Analysis, Data Analysis, Data Management, Data Science, Numerical Analysis, Project Management, Regulatory Compliance, Scientific Modeling, Statistical Analysis, Statistical Methods, Statistics.
Medical Laboratory Technician I Quest Diagnostics IncMedical Laboratory Technician IClifton, NJ$23.10–$38.12 / hourPhysical and Mental Requirements: The normal performance of duties may require lifting and carrying objects: Objects 1 to 10 pounds are lifted and carried frequently; objects 11 to 25 pounds are lifted and carried occasionally; objects 36 to 50 pounds are seldom lifted or carried and objects over 50 pounds are not to be lifted or carried without assistance. Depending on whether it is a part-time or full-time position, some of the benefits offered may include: Part-time employees (29 hours or less per week) are eligible for: Vacation and Health/Flex Time (part-time employees scheduled to work at least 20 hours per week).
Senior Engineer, Facility Operations (On-site) Merck & Co IncSenior Engineer, Facility Operations (On-site)Rahway, NJ$117,000–$184,200 / yearEducation: Bachelor's degree in chemical/biochemical engineering, pharmaceutical sciences, chemistry, biochemistry, biology, microbiology, or related discipline with minimum of 5 years relevant experience, or a Master's degree with minimum 3 years of relevant experience. It can meet all historic, currently existing, and cutting-edge biologics program demands from supporting development to pilot scale, small and large scale potent material handling, and the ability to integrate new technologies and cell-line platforms.
Cardiovascular Account Specialist - U.S. Sales, Hackensack, NJ Cytokinetics IncCardiovascular Account Specialist - U.S. Sales, Hackensack, NJHackensack, NJRemote$162,180–$189,210 / yearDevelop territory-specific account plans that identify, assess, and prioritize opportunities to meet customer needs by coordinating the efforts of a local integrated field team consisting of medical, payer, and patient navigation/support colleagues. Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction.
Technical Product Specialist - PAT Bio Nova Biomedical CorpTechnical Product Specialist - PAT BioNew York, NY$90,000–$140,000 / yearNova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences. This position works in close partnership with North American Key Account Managers (KAMs) to develop new opportunities, manage complex sales processes, and ensure a high-quality customer journey from initial engagement through evaluation and close.
Training Specialist Sofie Biosciences IncTraining SpecialistTotowa, NJ2) assessing the needs of the SOFIE network, implementing training, assisting in developing plans, and facilitating a variety of training initiatives and programs that enhance the effectiveness of the SOFIE workforce. The Training Specialist supports quality, manufacturing, and operational initiatives for the SOFIE network by (1) assisting in developing, facilitating, and supervising training programs for employees.
Quality Team Leader QA Compliance Novartis AGQuality Team Leader QA ComplianceEast Hanover, NJ$114,100–$211,900 / yearThis is an exciting opportunity to influence site quality performance, develop high-performing teams, and help ensure life-changing medicines are delivered to patients with the highest level of quality and integrity. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1(877)395-2339 and let us know the nature of your request and your contact information.
Quality Assurance Officer Operations Novartis AGQuality Assurance Officer OperationsEast Hanover, NJ$30,200–$56,000 / yearContribute in maintaining the local quality system as per GMPs and corporate guidelines and in assuring the respect of the GMPs and Health Authorities requirements at local levelSupport the QP in the preparation of batches release documentsCollaborate in redaction of site GMP documentation and preparation and printing of batch documentationCollaboration in data compilation of Product Reviews, oversight on investigations and monitoring of resulting actions are checked and approved. Major accountabilities: Supervise the general conditions of hygiene of the premises subject to its managementContribute in assuring the validation/qualification status of the production site, equipment, training of personnel and management of quality documentationResponsible for the provisional release for the shipment of batchesWork in shift with other QA officers to oversight the production and quality control activities.
Medical Assistant - Morristown ENT and Allergy AssociatesMedical Assistant - MorristownMorristown, New JerseyEach ENTA clinical office is comprised of world-class physicians who are specialists and sub-specialists in their respective fields, delivering the highest level of expertise and care to patients of all ages. ENT and Allergy Associates (ENTA) is the largest ENT, Allergy, and Audiology practice in the country, with over 475 clinicians practicing across 70+ clinical locations in New York, New Jersey, Pennsylvania, and Texas .
NewValidation Specialist – Aseptic Process Simulation Synerfac Technical StaffingValidation Specialist – Aseptic Process SimulationWhippany, NJInterface with IQ/OQ/PQ activities for the sterile filling line, SKAN isolator, environmental monitoring systems, and associated critical utilities (compressed air, nitrogen, WFI, clean steam) as they relate to APS readiness. * Establish and maintain APS bracketing and worst-case rationale documentation (e.g., shift duration, personnel interventions, line speed, container-closure configurations).
AS&T Expert Novartis AGAS&T ExpertEast Hanover, NJLife-cycle management of analytical methods, including control of method performance, analytical method validation, pharmacopoeia and health authority compliance and definition of method improvementsHandling of deviations, investigation, OOS/OOE/OOT cases as well as changes and complaintsPerson of contact for analytical questions from health authorities and analytical subject matter expert during audits and inspectionsCross-functional interface with Manufacturing Science & Technology team, analytical development, production, quality assurance and regulatory departmentImplementation of GMP requirements. Compilation and Review of documents (analytical protocols and reports, annual performance quality reports, ongoing process verification reports, registration documents)Budgeting and cost control of external analytical activitiesManagement of reference substances and control samplesMinimum Requirements:University degree or FH with natural science/technical background (e.g.
Principal Scientist I/II, Study Quality and Compliance - Nonclinical Safety/Toxicology Novartis AGPrincipal Scientist I/II, Study Quality and Compliance - Nonclinical Safety/ToxicologyEast Hanover, NJ$119,700–$222,300 / yearEssential Requirements: Degree in biological related sciences8+ years of relevant experience working in a pharmaceutical settingExperience working in GLP setting, and general regulatory compliance and animal welfare knowledge related to conduct of toxicology studiesGood communication skills, and excellent logistical/planning skillsFluent in English (spoken and written)Desirable Requirements: Previous experience with SEND packages is desirablePrevious experience with software for online information and program management is a plusThis is a dual level posting. Support SEND package creation and quality review for FDA submissionsSupport the Study Quality and Compliance team's effort for tracking and managing study-related information through input of information types from the areas of responsibility above and generally support the effort in various workstreams or initiatives.
Executive Director, IP 4D Molecular Therapeutics IncExecutive Director, IPNY$309,000–$350,000 / yearStrongly preferred: Experience in counseling life sciences R&D and CMC teams with respect to day-to-day transactions, including experience reviewing and negotiating confidentiality agreements, manufacturing agreements, material transfer agreements, sponsored research agreements, master services agreements, consulting agreements, and licenses. Directs outside counsel in the preparation and prosecution of applications and responding to office actions; directs outside counsel in evaluating the patentability of invention submissions and registrability of trademarks globally; manages related outside counsel budgets.
Precision Medicine Experts Diaceutics PlcPrecision Medicine ExpertsParsippany-Troy Hills, NJSupport the exchange of ideas, identification of barriers to adoption and represent laboratory staff on behalf of our Pharma partners, to appropriately support both our customer and partner needs, Be responsible for effectively communicating with targeted stakeholders using effective listening, proper terminology, and approved messaging, drawing on your experienced scientific knowledge, understanding of the diagnostic testing landscape and approved educational materials to support program objectives. Testing and Diagnostics: A robust understanding of the testing practices and diagnostic pathways for pathology and oncology, as well as knowledge of the laboratory network within the US is desirable, however the aptitude to understand and digest key scientific communication messaging and be able to engage in conversation with lab stakeholders to convey this messaging and answer set questions is necessary.
Technical Sales Consultant *PC 1414 Miltenyi BiotecTechnical Sales Consultant *PC 1414Newark, New JerseyYour Role: Responsible for sales of instruments, services, reagents and other consumables, from new and existing accounts in a defined territory through in-depth knowledge of market segments, technical knowledge and selling skills. Travel throughout assigned territory to call on regular and prospective customers to develop and maintain knowledge of accounts, solicit orders, perform product demonstrations, attend trade shows and perform troubleshooting.
Senior Manager, Clinical Diagnostics Cdx (Precision Medicine) Regeneron PharmaceuticalsSenior Manager, Clinical Diagnostics Cdx (Precision Medicine)Tarrytown, NY$150,500–$245,500 / yearIn this role, you will translate scientific needs into fit-for-purpose assays for global decisions, owning programs from feasibility through validation, registration, launch, and post-market sustainment, while partnering with biomarker, clinical, regulatory, commercial, and IVD collaborators. We are seeking a Senior Manager, Clinical Diagnostics to support end-to-end companion diagnostics (CDx) strategy and execution across our therapeutic indications.