Scientist (2nd Shift) - Pharmaceutical Analytical Sciences (Onsite) Merck & Co IncScientist (2nd Shift) - Pharmaceutical Analytical Sciences (Onsite)Rahway, NJ$87,300–$137,400 / yearEducation Minimum Requirements: Minimum 3 years relevant industry experience for applicants with a Bachelor of Science degree, or 1 year of relevant industry experience for applicants with a Master of Science degree in Chemistry, Pharmaceutical Sciences, or other Life Sciences. Primary Responsibilities: Support execution of Good Manufacturing Practices (GMP) activities such as release and stability testing to support development of active pharmaceutical ingredients (APIs), pharmaceutical formulations, and manufacturing processes using both traditional and advanced analytical tools.
Director of GMP Analytical, Pharmaceutical Analytical Sciences Merck & Co IncDirector of GMP Analytical, Pharmaceutical Analytical SciencesRahway, NJ$173,200–$272,600 / yearRequired Skills: Analytical Method Development, Analytical Reports, Analytical Testing, Biologics License Application (BLA), Chromatographic Techniques, Compliance Oversight, Dosage Forms, GMP Compliance, Inspection Readiness, People Leadership, Pharmaceutical Management, Process Analytical Technology (PAT), Project Management, Regulatory Compliance, Regulatory Submissions, Risk Analysis, Risk Assessments, Risk Evaluation And Mitigation Strategy (REMS), Spectroscopy, Talent Development, Team Leadership, Technical Writing. In this role, the Director will lead a team of scientists in Rahway supporting various GMP analytical activities including method validation, clinical release, and stability testing for drug substance and drug product across the entirety of our small molecule clinical portfolio (oral solid dosage forms and sterile liquids).
Principal Scientist, Pharmaceutical Analytical Sciences Merck & Co IncPrincipal Scientist, Pharmaceutical Analytical SciencesRahway, NJ$156,900–$247,000 / yearRequired Skills: Analytical Characterization, Analytical Chemistry, Analytical Method Development, Assay Development, Bioanalysis, Chromatographic Techniques, Chromatography, Clinical Judgment, Clinical Trials, Conducting Experiments, Data Science, Liquid Chromatography (LC), Matrix Management, Mentoring Staff, Method Validation, Product Development, Scientific Study Design, Stability Testing. Your main responsibilities, in not particular order and by no means complete, include: Driving our company's Pipeline: Leading analytical teams driving the development of drugs in our company's pipeline, with a deep understanding of product development from early stage through commercialization.
Associate Director, Compliance Business Partner (Pharmaceuticals) Asahi Kasei Plastics North America, Inc.Associate Director, Compliance Business Partner (Pharmaceuticals)New York, New York$160,000–$175,000Our purpose is to transform transplant medicine as the primary partner to the community of transplant healthcare providers and their patients; our focus is in developing new therapies and programs to help transplant healthcare providers and the patients they treat. This role serves as a trusted advisor to assigned business functions, providing strategic and operational leadership across core compliance activities, including guidance and advisory support, training, monitoring, policy governance, investigations support, and issue resolution.
Pharmaceutical Technician I, 2nd Shift ArdenaPharmaceutical Technician I, 2nd ShiftSomerset, New JerseyPerforms all the duties necessary to compress and encapsulate drug products, which includes the disassembly, cleaning, set-up and operation of manufacturing equipment such as but not limited to Tablet Presses, Capsule Fillers, Dedusters, Metal Detectors, Disintegration Testers, Friabilators, Tablet and Capsule In Process Weight Check Systems, Hardness Testers and Micrometers. As a leading Contract Development and Manufacturing Organization (CDMO), Ardena partners with pharmaceutical companies of all sizes—from emerging biotech to global industry leaders—united by the mission to help biopharma innovators navigate drug development with precision, quality, and speed, bringing their molecules from discovery to the clinic and market.
NewProcess Engineer – Pharmaceutical Synerfac Technical StaffingProcess Engineer – PharmaceuticalWhippany, NJBy applying for this job, you agree to receive calls, Al-generated calls, text messages, or emails from Synerfac Technical Staffing and our contracted partners. A contract development and manufacturing organization that specializes in producing topical, semi-solid, and liquid pharmaceutical products for both prescription and over-the-counter markets.
NewPharmaceutical Operators 2nd, & 3rd shift Synerfac Technical StaffingPharmaceutical Operators 2nd, & 3rd shiftWest Caldwell, NJ$20–$24 / hourAble to wear safety glasses, hearing protection, full face/half mask respirator, latex gloves, Tyvek suit and other safety equipment as needed. Communicate with IPC Operator and Supervisor on all issues concerning quality, components, and machine performance.
Senior Lab Systems Support Engineer (GxP/CSV – Pharmaceutical Lab IT) IconmaSenior Lab Systems Support Engineer (GxP/CSV – Pharmaceutical Lab IT)Rahway, NJ$42.85–$46.42 / hourLab System Lifecycle Management: Manage end to end lab system lifecycle including implementation validation maintenance and decommissioning. Our Client, an IT Services and Consultant company, is looking for a Senior Lab Systems Support Engineer (GxP/CSV – Pharmaceutical Lab IT) for their Rahway, NJ location.
Associate Director, Compliance Business Partner (Pharmaceuticals) Asahi Kasei Battery Separator Canada CorporationAssociate Director, Compliance Business Partner (Pharmaceuticals)New York, New York$160,000–$175,000Our purpose is to transform transplant medicine as the primary partner to the community of transplant healthcare providers and their patients; our focus is in developing new therapies and programs to help transplant healthcare providers and the patients they treat. This role serves as a trusted advisor to assigned business functions, providing strategic and operational leadership across core compliance activities, including guidance and advisory support, training, monitoring, policy governance, investigations support, and issue resolution.
Project Manager, Healthcare and Pharmaceutical Advertising Precision Medicine Group LLCProject Manager, Healthcare and Pharmaceutical AdvertisingNY$60,000–$90,000 / yearThis compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com.
2026 Sun Pharmaceutical Intern - New Brunswick, NJ & Cranbury, NJ Sun Pharmaceutical Industries Ltd2026 Sun Pharmaceutical Intern - New Brunswick, NJ & Cranbury, NJNew Brunswick, NJResponsibilities: The Sun Internship Program will allow students the opportunity to gain valuable experience that will integrate the knowledge and theory learned in the classroom with practical application and skill development in a professional setting. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors.
2026 Sun Pharmaceutical Intern - Hawthorne, NY Sun Pharmaceutical Industries Ltd2026 Sun Pharmaceutical Intern - Hawthorne, NYNYResponsibilities: The Sun Internship Program will allow students the opportunity to gain valuable experience that will integrate the knowledge and theory learned in the classroom with practical application and skill development in a professional setting. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors.
Project Coordinator, Healthcare and Pharmaceutical Agency Precision Medicine Group LLCProject Coordinator, Healthcare and Pharmaceutical AgencyNY$40,000–$60,000 / yearThis compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com.
Associate Director, Compliance Business Partner (Pharmaceuticals) Asahi Kasei Semiconductor, Inc.Associate Director, Compliance Business Partner (Pharmaceuticals)New York, New York$160,000–$175,000Our purpose is to transform transplant medicine as the primary partner to the community of transplant healthcare providers and their patients; our focus is in developing new therapies and programs to help transplant healthcare providers and the patients they treat. This role serves as a trusted advisor to assigned business functions, providing strategic and operational leadership across core compliance activities, including guidance and advisory support, training, monitoring, policy governance, investigations support, and issue resolution.
Radio Pharmaceuticals QA Auditor BioHire HealthRadio Pharmaceuticals QA AuditorParamus, NJThis role supports the Pharmaceutical Quality System (PQS) by identifying gaps, recommending corrective actions, and driving continuous improvement across manufacturing, testing, and distribution processes. Conduct routine, for-cause, and risk-based audits of internal processes, RPT CMOs, and suppliers.
Associate Director, Compliance Business Partner (Pharmaceuticals) Asahi Kasei America, Inc.Associate Director, Compliance Business Partner (Pharmaceuticals)New York, New York$160,000–$175,000Our purpose is to transform transplant medicine as the primary partner to the community of transplant healthcare providers and their patients; our focus is in developing new therapies and programs to help transplant healthcare providers and the patients they treat. This role serves as a trusted advisor to assigned business functions, providing strategic and operational leadership across core compliance activities, including guidance and advisory support, training, monitoring, policy governance, investigations support, and issue resolution.
Associate Director, Compliance Business Partner (Pharmaceuticals) Crystal IS, Inc.Associate Director, Compliance Business Partner (Pharmaceuticals)New York, New York$160,000–$175,000Our purpose is to transform transplant medicine as the primary partner to the community of transplant healthcare providers and their patients; our focus is in developing new therapies and programs to help transplant healthcare providers and the patients they treat. This role serves as a trusted advisor to assigned business functions, providing strategic and operational leadership across core compliance activities, including guidance and advisory support, training, monitoring, policy governance, investigations support, and issue resolution.
Associate Director, Compliance Business Partner (Pharmaceuticals) Asahi Kasei Bioprocess America, IncAssociate Director, Compliance Business Partner (Pharmaceuticals)New York, New York$160,000–$175,000Our purpose is to transform transplant medicine as the primary partner to the community of transplant healthcare providers and their patients; our focus is in developing new therapies and programs to help transplant healthcare providers and the patients they treat. This role serves as a trusted advisor to assigned business functions, providing strategic and operational leadership across core compliance activities, including guidance and advisory support, training, monitoring, policy governance, investigations support, and issue resolution.
NewSenior Lab Systems Support Engineer (GxP/CSV - Pharmaceutical Lab IT) Iconma LLCSenior Lab Systems Support Engineer (GxP/CSV - Pharmaceutical Lab IT)Rahway, NJResponsibilities: Lab System Lifecycle Management: Manage end to end lab system lifecycle including implementation validation maintenance and decommissioning. Our Client, an IT Services and Consultant company, is looking for a Senior Lab Systems Support Engineer (GxP/CSV - Pharmaceutical Lab IT) for their Rahway, NJ location.
NewAssociate Director/Director Pharmaceutical Development BridgeBio Pharma IncAssociate Director/Director Pharmaceutical DevelopmentNYRemote$223,000–$239,000 / yearThe final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process. Skill Development & Career Paths: People are part of our growth and success story - from discovery to active drug trials and FDA pipelines, there are endless opportunities for skill development and internal mobility.