Senior EHS Specialist Stanley Black & Decker, Inc.Senior EHS SpecialistAllentown, PA$77,600–$124,900 / yearLearning & Development: Our lifelong learning philosophy means you'll have access to a wealth of state-of-the-art learning resources, including our Lean Academy and online university (where you can get certificates and specializations from renowned colleges and universities). Join our top-notch team of approximately 43,000 diverse and high-performing professionals globally who are making their mark on some of the world's most beloved brands, including DEWALT, BLACK+DECKER, CRAFTSMAN, STANLEY, CUB CADET, and HUSTLER.
Senior Scientist, Regulatory Affairs- CMC - Synthetic Moieties of ADC''''s and Bioconjugates Merck & Co IncSenior Scientist, Regulatory Affairs- CMC - Synthetic Moieties of ADC''''s and BioconjugatesNorth Wales, PA$117,000–$184,200 / yearManage preparation and execution of Chemistry, Manufacturing and Control documentation including Investigational New Drug Applications, Investigational Medicinal Product Dossiers, original Biologics License Applications, Marketing Authorization Applications, post-approval submissions/variations, agency meeting background packages, and responses to health authority questions. Required Experience and Skills: At least 5 years of Regulatory CMC or directly relevant pharmaceutical development experience in small molecules or other chemically synthesized modalities, including experience in process chemistry, analytical development, manufacturing, testing, quality, technical operations, or CMC product development.
Sr. Principal Scientist, Nonclinical Drug Safety Merck & Co IncSr. Principal Scientist, Nonclinical Drug SafetyWest Point, PA$190,800–$300,300 / yearStrategically influence nonclinical drug safety considerations for Immunology programs by providing drug development mentorship and partnering with Compound Leaders on time-critical matters, including nonclinical program design and toxicology study design, weight-of-evidence risk assessments, science-based waiver strategies, and integrated safety development plans that support clinical trials, global registration, and timely resolution of nonclinical development issues. Provide scientific and strategic oversight for Immunology candidates through close collaboration with Program Coordinators, Discovery Preclinical Leaders, Compound Leaders, and scientists across NDS and/or Preclinical Development, while ensuring strong partnership with key Research and Development Division functions, including Discovery, chemistry, regulatory affairs, translational medicine, clinical development, and CMC.
NewSenior Scientist, Biologics Drug Substance Commercialization Process Analytics Merck & Co IncSenior Scientist, Biologics Drug Substance Commercialization Process AnalyticsWest Point, PA$117,000–$184,200 / yearSupport and oversee the establishment of new methods within BDSC Process Analytics team, including handoff from research analytic teams to BDSC Process Analytics, ensuring technical readiness for implementation. As a Senior Scientist in Process Analytics, you'll be at the forefront of scientific problem-solving and technical leadership, partnering cross-functionally to support process development, method establishment, and lifecycle activities for a diverse biologics pipeline.
Senior Staff Industrial Hygienist Terracon Consultants IncSenior Staff Industrial HygienistBlue Bell, PAPerform field studies including airborne chemical monitoring, noise monitoring, indoor air quality, asbestos surveys and Phase I preliminary site assessments. Implements technical requirements to complete client projects by directing and supervising field staff to sample, test and collect data and/or document site activities.
Director Product Portfolio - Life Sciences RELX GroupDirector Product Portfolio - Life SciencesHorsham, PA$136,100–$252,800 / yearWork directly with customers and prospects to understand regulatory operations pain points, validate product-market fit, and ensure the roadmap is grounded in real-world workflows across labeling, submissions, compliance, and lifecycle change management. Shape the Life Sciences AI strategy in partnership with technical leaders, with a focus on intelligent workflows, explainable decision support, governed automation, and future agentic capabilities that operate safely inside regulated processes.
Senior Validation Specialist Karwell TechnologiesSenior Validation SpecialistFort Washington, PAThe ideal candidate will be responsible for planning, executing, reviewing, and approving validation documentation for equipment, facilities, utilities, processes, and computerized systems while ensuring compliance with FDA, EMA, and cGMP regulations. Responsibilities: Lead validation lifecycle activities including Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
Senior Automation Engineer Georgia IT Inc.Senior Automation EngineerWest Point, PASeeking a Senior Automation Engineer with strong DeltaV and Allen-Bradley/Rockwell PLC configuration and troubleshooting experience in a regulated Life Sciences/GMP environment. Preferred: Sterile manufacturing, biologics/cell therapy/fill-finish, ISA-88/ISA-95, ERP/LIMS/Data Historian.
Sr. Project Engineer - Data Centers Thermal Engineering InternationalSr. Project Engineer - Data CentersTrevose, PA$130,000–$160,000 / yearTo provide greater transparency to candidates, we include base pay ranges for all US-based job postings that encompass all potential locations and levels for the open positions. In this critical role, you will be responsible for maintaining the overall design responsibility for specific projects to which he/she has been assigned, and is the primary contact for the project manager, workshops, vendors, and the client.
Senior Veeva Technical Architect Tata Consultancy Services LtdSenior Veeva Technical ArchitectTitusville, NJ$140,000–$180,000 / yearStrong architecture expertise across Veeva QualityDocs, Veeva eTMF, Veeva PromoMats, and Veeva MedComms, with the ability to provide cross-platform architectural leadership across ECM and Commercial content domains. Demonstrated ability to lead distributed cross-functional teams, including architects, product owners, business analysts, configuration teams, integration teams, QA/validation teams, vendors, and implementation partners.
Senior Controls Engineer Barry-WehmillerSenior Controls EngineerEaston, PADesign Group is widely known as an industry leader, recognized as a top system integrator, ranking #7 in the 2023 System Integrator Giants; as a Rockwell Platinum Integrator, the highest designation given to Rockwell partners; and as an Ignition Enterprise Premier Integrator. By blending people-centric leadership with disciplined operational strategies and purpose-driven growth, Barry-Wehmiller has become a $3 billion organization with nearly 12,000 team members united by a common belief: to use the power of business to build a better world.
Sr. Manager Quality Systems & Compliance Piramal Enterprises LtdSr. Manager Quality Systems & ComplianceSellersville, PAThis enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. The incumbent will be primarily responsible to ensure the Quality Assurance team delivers the following through effective leadership, mentoring and management: Audits: Support internal and external audits and regulatory inspections.
Senior Medical Writer Nucleus Global LtdSenior Medical WriterYardley, PADrawn together from several backgrounds including the pharmaceutical industry, research, marketing, medical and regulatory writing, sales, publishing, digital media and design, we have the experience and all-round ability to conceive and deliver the best quality medical communications programs. We consider compensation more than just a base salary - that's why we also offer an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work.
Senior Clinical Trial Manager ICON PlcSenior Clinical Trial ManagerBlue Bell, PAClose collaboration with the assigned Local Trial Manager(s) (LTMs), Lead Site Manager (LSM), Site Managers (SMs), Clinical Trial Associates (CTAs), and Site Contract Managers (SCMs) to outline accountabilities/responsibilities and provide support and training, where necessary. The Sr LTM will manage and oversee the following throughout the study: Central IRB and other local vendors (Greenphire, Drug Destruction services, etc.…) including set up of vendor purchase orders, invoice review and approval, and change-orders, as applicable.
NewSr. Manager, Pooled Screening Core - CAR Screening & Lead Selection, Cell & Genetic Medicines 6084-Janssen Research & Development Legal EntitySr. Manager, Pooled Screening Core - CAR Screening & Lead Selection, Cell & Genetic MedicinesSpring House, PennsylvaniaAnalytical Reasoning, Biochemistry, Chemistry, Manufacturing, and Control (CMC), Clinical Research and Regulations, Clinical Trial Designs, Developing Others, Drug Discovery Development, Inclusive Leadership, Leadership, Molecular Diagnostics, Pharmacovigilance, Process Improvements, Productivity Planning, Program Management, Quality Assurance (QA), Scientific Research, Tactical Planning, Team Management, Troubleshooting The successful candidate will bring technical depth, operational discipline, and a collaborative leadership style to build a trusted Core that accelerates discovery, strengthens partnerships, and advances our cell therapy portfolio.
Sr. Manufacturing Automation Engineer DeltaV / Allen-Bradley ICONMA, LLCSr. Manufacturing Automation Engineer DeltaV / Allen-BradleyWest Point, PA$48.57–$53.57 / hourResponsibilities: Senior Automation Engineer is responsible for supporting manufacturing business, project team and Quality in designing / configuring / updating / troubleshooting / documenting Automation systems. Life Sciences industry understanding of GMP concepts: data integrity (ALCOA+), electronic signatures, validation requirements, audit trails, controlled documents, deviations/CAPA, and change control.
Senior Medical Writer Health InteractionsSenior Medical WriterYardley, PADrawn together from several backgrounds including the pharmaceutical industry, research, marketing, medical and regulatory writing, sales, publishing, digital media and design, we have the experience and all-round ability to conceive and deliver the best quality medical communications programs. We consider compensation more than just a base salary - that's why we also offer an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work.
Sr. Manager Quality Systems & Compliance Piramal PharmaSr. Manager Quality Systems & ComplianceSellersville, PennsylvaniaThis enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. The incumbent will be primarily responsible to ensure the Quality Assurance team delivers the following through effective leadership, mentoring and management: Audits: Support internal and external audits and regulatory inspections.
Sr. CSV/CSA/Validation Engineer Katalyst HealthCares & Life Sciences IncSr. CSV/CSA/Validation EngineerRaritan Township, NJCSV/CSA/Validation Engineer leads and independently executes computerized system validation, computer software assurance, infrastructure qualification, and business system validation activities within GxP-regulated pharmaceutical, biotechnology, or medical device environments. Ability to manage end-end from Inventory, assessments, remediations to final dispositions; Infrastructure Qualifications & Business Systems Validations 7-10 years of relevant experience; has experience of leading/advising Junior and Senior resources.
NewSr. Manager, Pooled Screening Core - CAR Screening & Lead Selection, Cell & Genetic Medicines Johnson and JohnsonSr. Manager, Pooled Screening Core - CAR Screening & Lead Selection, Cell & Genetic MedicinesSpring House, PAFull timeAnalytical Reasoning, Biochemistry, Chemistry, Manufacturing, and Control (CMC), Clinical Research and Regulations, Clinical Trial Designs, Developing Others, Drug Discovery Development, Inclusive Leadership, Leadership, Molecular Diagnostics, Pharmacovigilance, Process Improvements, Productivity Planning, Program Management, Quality Assurance (QA), Scientific Research, Tactical Planning, Team Management, Troubleshooting . The successful candidate will bring technical depth, operational discipline, and a collaborative leadership style to build a trusted Core that accelerates discovery, strengthens partnerships, and advances our cell therapy portfolio.