- J&J Family of Companies (Raritan, NJ)
- …essential for enabling the CARVYKTI network's technical, supply chain, and compliance -related objectives. Collaborating across a complex network of internal and ... with 10-12 years of overall experience is required; 7+ years of biotech/ pharmaceutical experience or equivalent industry experience is highly preferred. + Hands-on… more
- Eliassen Group (Montpelier, VT)
- **Senior Tableau Developer** **Anywhere** **Type:** Contract **Category:** Data **Industry:** Life Sciences **Workplace Type:** Remote **Reference ID:** JN ... in a fast-paced environment. **Preferred Qualifications:** + Experience in the pharmaceutical or healthcare industry. + Familiarity with other data visualization… more
- Astrix Technology (Concord Township, OH)
- …80000 + Added - 06/05/2025 Apply for Job Our client is a contract research and development manufacturing service provider to chemical-based industries, and they're ... cGMP Laboratory. This role involves supporting analytical stability studies in compliance with regulatory guidelines. The ideal candidate will have hands-on… more
- Curia (Albany, NY)
- …of the general facility, including custodial functions. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience ... partnering with pharmaceutical and biotech companies to provide life-saving treatments to...light construction. Assures that these functions are performed in compliance with workplace safety procedures, OSHA requirements, and all… more
- System One (Horsham, PA)
- Job Title: Logistics Coordinator Location: Horsham, PA Type: Contract (through December 31) Schedule: Monday-Wednesday, 8:00 AM-4:30 PM (on-site, 24 hours/week) Pay ... shipping requirements + Maintain accurate shipping/receiving records and SOP compliance + Support additional operations and warehouse-related tasks as needed… more
- US Tech Solutions (RI)
- …Prior Authorization Specialist** **Location: Fully remote** **Duration: 12 months contract ** **Job Description:** + Prior Authorization Specialist takes in-bound ... Advocates and management team as needed. + Must maintain compliance at all times with CMS and department standards....center environment managing 75 calls/day. + Six months of PBM/ pharmaceutical related work strongly desired + At least two… more
- Catalent Pharma Solutions (Madison, WI)
- …Quality Control** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... a Patient First culture through excellence in quality and compliance , and to the safety of every patient, consumer...the requirements of clinical and commercial programs for active pharmaceutical ingredients and bulk drug substances. + Ability to… more
- Charles River Laboratories (Reno, NV)
- …projects such as redesign of SOPs and basic research procedures. * Maintain compliance with all applicable laws and regulations including the Animal Welfare Act. * ... Safety Assessment facilities. **About Charles River** Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of… more
- Charles River Laboratories (Boston, MA)
- …+ Work with researchers in pre-study designs of projects and ensuring appropriate compliance for new projects including ordering supplies for cases. + Order and ... leveraging available space. **About Charles River** Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of… more
- AbbVie (North Chicago, IL)
- …and mentor staff on statistical methodology and operations. May supervise contract statisticians or junior statisticians. Gain expertise in innovative statistical ... regulatory agencies as needed. Validate external statistical software to ensure compliance with SOPs and regulatory requirements. + (SSG) Lead statistical support… more