Email Alert for
ⓘ There was an unexpected error processing your request.
Please refresh the page and try again.
If the problem persists, please contact us with your issue.
You can always manage your preferences and update your interests to ensure you receive the most relevant opportunities.
Get ready to discover your next great opportunity.
Randstad
Norwood, MA, United States
Randstad is partnering with a global pharmaceutical and biotechnology company. This role will be responsible for enabling GMP production of sterile drug product manufactured at the Norwood site. Specifically, the role will be tasked with performing deviation investigations, root cause analysis and CAPA management. Additionally, the role will be acc
Job Source: RandstadGardner Resources Consulting
Boston, MA, United States
Our Pharma client is currently searching for a Quality Operations Specialist with expertise in both development and commercialization of products. The primary responsibility of this position will be to ensure quality oversight of assigned projects/CMO's for the clinical/commercial product manufactured and to work cross-functionally providing updat
Job Source: Gardner Resources ConsultingCeres Group
Boston, MA, United States
Responsible for providing the independent monitoring of investment compliance requirements so as to ensure the firms ongoing compliance; advise key business units in related regulatory and client compliance requirements; train investment compliance professionals and key business stakeholders on regulatory and client requirements; and support the ma
Job Source: Ceres GroupPSG Global Solutions
Boston, MA, United States
Description We're looking for a Compliance Specialist I , working in Pharmaceuticals and Medical Products industry in 500 Soldiers Field Road, Boston, Massachusetts, 02134, United States . Performs audits necessary to ensure the compliance of manufacturing procedures to in-house specifications and government regulation. Conducts internal
Job Source: PSG Global SolutionsLincoln Institute of Land Policy
Cambridge, MA, United States
Job Details Level Experienced Job Location Cambridge, MA - Cambridge, MA Remote Type Hybrid Position Type Regular Full Time Education Level 4 Year Degree Salary Range $64,000.00 - $75,000.00 Salary Travel Percentage None Job Shift Any Job Category Other Description Position Overview The Lincoln Institute of Land Policy is lookin
Job Source: Lincoln Institute of Land PolicyLexisNexis
Cambridge, MA, United States
About the Business LexisNexis Risk Solutions is the essential partner in the assessment of risk. Within our Business Services vertical, we offer a multitude of solutions focused on helping businesses of all sizes drive higher revenue growth, maximize operational efficiencies, and improve customer experience. Our solutions help our customers solve
Job Source: LexisNexisNortheastern University
Boston, MA, United States
About the Opportunity This job description is intended to describe the general nature and level of work being performed by people assigned to this classification. It is not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. JOB SUMMARY The Compliance Specialist supports
Job Source: Northeastern UniversityAzzur Group
Waltham, MA, United States
Description Azzur COD is looking for a GMP Facility Manager. This employee will be a Cleanrooms On-Demand Burlington business unit (Facility Solutions) leader, who will be responsible for employees supporting the facility, client start-up, and continuous business improvement at COD. The Facility Manager will perform repairs, Maintenance, and impro
Job Source: Azzur GroupNorwood, MA, United States
Randstad is partnering with a global pharmaceutical and biotechnology company. This role will be responsible for enabling GMP production of sterile drug product manufactured at the Norwood site. Specifically, the role will be tasked with performing deviation investigations, root cause analysis and CAPA management. Additionally, the role will be accountable to coordinating and monitoring performance metrics around deviation performance. This role will work cross functionally with Engineering, MS&T and Quality Assurance partners to ensure a culture of continuous improvement and right first time are imbedded in day-to-day operations.
Key Responsibilities and if appropriate Authorities of the Position:
GMP Documentation: Write, review, and approve deviation investigation and CAPA plans.
Monitor CAPA completion progress and provide support to stakeholder departments to ensure on-time completion.
Identify and coordinate continuous improvement opportunities across the department.
Metrics and Reporting: Generate targeted metrics for Quality Management Review and support data collection for regulatory filings.
Regulatory Compliance: Ensure operational compliance with relevant FDA, EU, ICH guidelines, and regulations.
(Must Have) Required Background:
Experience (Sr. Specialist): Science or Engineering background (B.S.) with 5+ years of experience or MS with 3+ years of experience in a pharmaceutical or biotechnology company.
Experience (Specialist): Science or Engineering background (B.S.) with 3+ years of experience or MS with 2+ years of experience in a pharmaceutical or biotechnology company.
Other Quantifiable Preference: Experience in biopharmaceutical & GMP.
Email Alert for GMP Compliance Specialist jobs in Norwood, MA, United States
ⓘ There was an unexpected error processing your request.
Please refresh the page and try again.
If the problem persists, please contact us with your issue.
You can always manage your preferences and update your interests to ensure you receive the most relevant opportunities.
Get ready to discover your next great opportunity.