Engineering Pharma Technical Recruiter This role is 100% remote. Recruiting primarily for US & Canada roles. Excellent English communication skills are required. MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical/biotechnology and highly regulated industries. Its
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
Reporting to the Director, Data Analytics and Technical Solutions, this position is responsible for designing, maintaining and governing the Technical Solutions’ clinical data ecosystem. This position will bridge the gap between complex clinical data sources and
Our story began with a passionate idea that we could change the world. And to be honest, we’ve never stopped believing that. In 1986 it was a simple concept that microbiology teamed with innovation and clinical
PsiQuantum’s mission is to build the first useful quantum computers—machines capable of delivering the breakthroughs the field has long promised. Since our founding in 2016, our singular focus has been to build and deploy million-qubit, fault-tolerant
Lead Auditor - GMP Quality Audits will perform high level assessments of quality systems in a variety of manufacturing sites, farms, processing plants and/or other work related sites throughout a region or country. Assess and report
Work Location: Kankakee, Illinois Shift: No Department: LS-PS-ATA PDS Region 1 Recruiter: Jennifer Lovell This information is for internals only. Please do not share outside of the organization. Your role: MilliporeSigma is looking for a Process
Job SummaryResponsible for managing the quality and compliance for applicable products and processes for assigned department(s). Adapt departmental plans and priorities to address resource and operational challenges. Job Description Responsibilities: Ensure quality and regulatory compliance with
Job SummaryResponsible for the validation of facility utilities, equipment processes and cleaning for cGMP products such as pharmaceuticals, medical devices, and cosmetic products to adhere to 21 CFR 211/210, 21 CFR 820, and other applicable regulatory requirements.
Job Summary Job Description JOB SUMMARY: Audit a broad, global supplier base against FDA regulations, ISO standards, and other applicable global regulatory requirements across the full spectrum of Medline products including sterile products, APIs, raw materials,
About the role Binocs is our cutting-edge SaaS solution designed to help laboratories and cell & gene therapy teams optimize their scheduling, planning, and resource management. Trusted by leading pharmaceutical and life sciences companies, Binocs empowers teams
About Us:BW Packaging is driving performance at the intersection of people, technology, and customer care. As part of the privately held Barry-Wehmiller family, we unite a global team of packaging experts with a clear purpose: People
You’ve Never Been Satisfied with Good Enough. You want to make an impact, not just manage projects, but change how the world gets built. At Accenture Infrastructure & Capital Projects, you’ll do exactly that. You’ll help
Our story began with a passionate idea that we could change the world. And to be honest, we’ve never stopped believing that. In 1986 it was a simple concept that microbiology teamed with innovation and clinical