COMPANY DESCRIPTION: A career here is life-enhancing. At Syner-G, we enable our people to build careers that impact positively on their quality of life. Through our expertise, insight, consulting and management skills, we accelerate breakthrough science
Position: System Administrator Location: Lexington, MA (Hybrid remote) Duration: 6+ months (High possibility of extension) Application System Administrator (Contractor) 1. Services Overview / Objective The purpose of this Statement of Work (“SOW”) is to engage a contractor to
Scholar Rock Job Post Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As
Terrestrial (formerly known as Vaxess) is developing a pipeline of next-generation vaccines and therapeutics on our novel micro-array patch platform. With only five minutes of wear-time on the skin, the self-applied patch enables up to two
Validation Manager, Quality Assurance We are seeking an experienced Validation Manager, Quality Assurance to join Marianas Quality Assurance organization, advancing personalized medicine and radiopharmaceuticals. The Validation Manager, Quality Assurance is responsible for leading and overseeing the qualification and validation program
RSO Specialist Bachelors required (Masters OK), 26 years experience in Pharma / Biopharma Regulatory compliance and manufacturing Knowledge of GMP. Must have experience in Veeva Vault RIM - work within RSO, ensuring data alignment, submissions, approvals,
Head Of Quality (Vice President) Cambridge, MA (hybrid) Vedanta Biosciences is a late-stage biopharmaceutical company developing medicines for the treatment of gastrointestinal diseases. The companys lead asset is a potential first-in-class oral therapy, VE303, in a
CQV Specialist We are seeking a CQV Specialist to lead commissioning, qualification, and validation activities for facility, equipment, and computerized systems supporting GMP cell therapy manufacturing. This individual will own qualification strategy and execution, ensuring compliant, risk-based validation aligned with
CMMS Specialist (Pharmaceutical Manufacturing) Lantheus (NASDAQ: LNTH) is the leading radiopharmaceutical-focused company, delivering life-changing science to enable clinicians to Find, Fight and Follow disease to deliver better patient outcomes. Headquartered in Massachusetts with offices in New
Senior It Business Analyst, Glp And Gmp Systems Manager Wave Life Sciences is a biotechnology company focused on unlocking the broad potential of RNA medicines to transform human health. Our RNA medicines platform, PRISM, combines multiple modalities,
Location: Waltham (hybrid) Department: Quality Reports to: Sr. Director, Quality Assurance Role Summary The GCP Quality role provides quality oversight and compliance leadership for multiple multi-national clinical studies. This position partners with Clinical Operations, Data Management,
Senior Facility Manager - JLL Our people at JLL are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are committed to hiring
Job Description We are seeking an experienced IT Compliance leader to establish and oversee a robust, risk-based validation program supporting our regulated systems and data across the enterprise. This role ensures computerized systems remain compliant, inspection-ready, and aligned with global
Job Description We are seeking a Risk Assessment / Technical Documentation Specialist to support Quality Control Lab Systems in a GxP-regulated pharmaceutical or biotech environment. This role will serve as a subject matter expert across IT systems and