Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific
Career CategoryOperations Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that
Career CategoryOperations Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that
Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality. Every member of
Deviation Investigator I Location: This position is based in our Portsmouth, NH office. The typical work schedule is Monday through Friday, 8:00 AM–4:30 PM EST. What you will get: Below you will find a comprehensive summary of
Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific
Career CategoryManufacturing Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that
At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of
Job Title: Deviation Writer Location: Bloomington, IN Position Overview :We are seeking motivated and detail-oriented Deviation Writers with 2–4 years of experience in GMP-regulated environments to support investigation and documentation activities within pharmaceutical, biotechnology, or life sciences manufacturing
WHO? INCOG BioPharma Services is seeking an experienced and detail-oriented Deviation Writer to join our Manufacturing Engineering team. This role is crucial for translating a variety of complex technical events into clear, accurate, and robust investigations. The
Title: Deviation Investigation Writer / Associate Location: Concord, NC Duration: 6 month contract (potential of extension or conversion) Summary We are seeking a detail-oriented and technically skilled Deviation Investigator to support PAR Operations. This role is responsible for
QA Compliance Specialist Responsible for review and approval of Deviations and CAPAs in support of GMP manufacturing operations. Support timely review of events for classification, initiation in EtQ and closure. Support external client review and resolution of
Job Title Responsible for review and approval of Deviations and CAPAs in support of GMP manufacturing operations and other functional groups as required (e.g. Facilities Engineering, IT, Supply Chain, etc.). Support timely review of events for classification,
Sr. Specialist Ready to transform complex manufacturing anomalies into flawless, inspection-ready narratives? As a Sr. Specialist, youll dive into the heart of GMP operations-spearheading high-impact deviation investigations, mastering root cause analysis, and orchestrating cross-functional compliance excellence. Location:
Deviation Supervisor Work Schedule: Standard (Mon-Fri) Environmental Conditions: Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description:
Computer Systems Validation Specialist III Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed. The Computer Systems Validation (CSV) Specialist III leads teams in assessing new and changing computer systems
Today, Lonza is a global leader in life sciences, operating across three continents. While our work is grounded in science, our success is driven by talented people collaborating to develop innovative solutions that help businesses bring
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The Advanced Processing Team Member must be able to demonstrate they can perform tasks listed within a 90-day period in that position. Each Processing Team Member is expected to have three certifications within 1 year of
Position Title:Director of Spiritual Diversity Position Type:Regular Hiring Range: $102,800 - $115,560 per year; Compensation will be based on education, experience, skills relevant to the role, and internal equity. Pay Frequency:Annual A. POSITION PURPOSE The Director