Flexible Hybrid Contract Jobs
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QMS Consultant
OverviewWe are seeking an experienced Quality Systems Manager to lead and continuously improve the Quality Management System (QMS) within a GMP-regulated pharmaceutical environment. This role will be responsible for ensuring compliance with global regulatory requirements while driving quality excellence across manufacturing, laboratory, supply chai...
QA Specialist Serialization and Automation (12 months)
OverviewWe are seeking an experienced Quality Assurance professional to represent Global Quality on two strategic cross-functional programmes within a pharmaceutical manufacturing environment.The primary focus of the role is a global serialization transformation initiative, where the successful candidate will lead the development and deployment of ...
Interim QA Director
OverviewAn established pharmaceutical organisation is seeking an experienced Interim QA Director to support a critical sterile manufacturing operation in Tampa, Florida. This is a high-priority 12-month contract requiring an accomplished quality leader with a substantial track record leading Quality Assurance functions within regulated sterile fill...
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Clinical Trial Liaison
🚨 Respiratory Clinical Trial Liaison - Contract OpportunityI'm looking to connect with professionals from a respiratory, pulmonary or nursing background for an exciting contract opportunity I'm recruiting for within EPM Scientific's Clinical Contractor Division.My client is confidential, but they are looking for someone with strong knowledge of th...
Senior Accountant Revenue, Contractor
OverviewWe are supporting a growing pharmaceutical organization seeking a Senior Accountant - Revenue Contractor to assist with upcoming month-end close activities and provide ongoing support through the audit cycle. This is an immediate need, and the ideal candidate will have strong Gross-to-Net (GTN) accounting experience within the life science...
Unblinded CRA Italy
Role OverviewWe are seeking an experienced Unblinded CRA to support an ongoing clinical study in Italy. The successful candidate will be responsible for monitoring unblinded aspects of the study, with particular focus on investigational product (IP/IMP) activities, while ensuring the integrity of the study blind is maintained.Unblinded CRAs monitor...