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Pharmatech Associates, Inc. seeks an experienced GLP Auditor, Contract/Project Consultant to support audits for clients conducting regulated nonclinical research and animal studies. The role requires evaluating GLP compliance and data integrity across laboratory environments and study documentation. Responsibilities
Pharmatech Associates is seeking a Regulatory Affairs Consultant to support multiple projects on a remote basis, approximately 10-20 hours per week. The role centers on developing regulatory strategies to enable successful registrations and post-approval commercialization for pharmaceutical/biotech products
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