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Computerized System Validation Jobs In Danvers, Massachusetts - 16 Job Positions Available

1 – 15 of 16 jobs

Lead, QCTS Data Integrity & Computerized Systems Lexington, MA The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and

Genezen  2 days ago
Vertex jobs

Job Description JOB TITLE: Director, Information Systems Management LOCATION: 50 Northern Ave., Boston, Massachusetts, 02210 OPENINGS: 1 DUTIES: Provides strategic quality oversight across GxP computer systems and strategic direction to management of QA-owned systems in support of effective deployment

Vertex  11 days ago
Syner-G BioPharma Group jobs

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

Syner-G BioPharma Group  9 days ago
Alpha Business Solutions jobs

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

Alpha Business Solutions  22 days ago
Scholar Rock jobs

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

Scholar Rock  2 days ago
Dyne Therapeutics jobs

Company Overview: Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of

Dyne Therapeutics  11 days ago

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,

RIT Solutions  2 days ago

CMMS Specialist (Pharmaceutical Manufacturing) Job Category : Facilities Requisition Number : CMMSS003865 Posted : May 8, 2026 Full-Time On-site Bedford, MA Job Details Description Lantheus (NASDAQ: LNTH) is the leading radiopharmaceutical-focused company, delivering life-changing science to

Lantheus Brand  15 hours ago
Dyne Therapeutics jobs

Senior Director, Pharmacovigilance Quality Assurance Waltham, MA Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to

Dyne Therapeutics  2 days ago
US Tech Solutions jobs

Job Title Duration: 12 months (potential to extend) Onsite Expectations: For onboarding and training for the first few weeks should plan to be onsite 4-5 days a week. After onboarding and starting working on projects, it

US Tech Solutions  2 days ago
Beth Israel Lahey Health jobs

Join The BILH Team When you join the growing BILH team, youre not just taking a job, youre making a difference in peoples lives. Job Summary Responsible for reviewing electronic and scanned medical records of patients

Beth Israel Lahey Health  2 days ago
Medtronic Plc jobs

Quality Applications Manager - Quality Data Analytics Join us at Medtronic, where we are partnering across the industry to tackle systemic healthcare challenges with bold leadership. If you seek a challenging, energizing, and rewarding career that

Medtronic Plc  2 days ago
Corning jobs

Division Quality Engineer I Join us at Corning, one of the worlds leading innovators in glass, ceramic, and materials science. From the depths of the ocean to the farthest reaches of space, our technologies push the

Corning  2 days ago
USDM Life Sciences jobs

Risk Assessment/Technical Document Specialist The Risk Assessment/Technical Document Specialist serves as a subject matter expert across both IT systems and data integrity for a Takeda quality control lab systems engagement, ensuring solutions are compliant, inspection ready, and operationally

USDM Life Sciences  15 hours ago

Sr. Manager, Quality CSV Somerville, MA About Genetix Biotherapeutics At Genetix Biotherapeutics every role has meaning, every team member is respected, and every day is a chance to make a difference. When you join Genetix, youre

Genetix Biotherapeutics  2 days ago

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