Compliance Specialist (Global Regulatory Affairs and Drug Safety) jobs in United States
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Intelliswift - An LTTS Company · 7 hours ago

Compliance Specialist (Global Regulatory Affairs and Drug Safety)

Intelliswift, an LTTS Company, is seeking a Compliance Specialist focused on Global Regulatory Affairs and Drug Safety. This role involves executing regulatory and pharmacovigilance compliance activities, supporting quality management systems, and overseeing procedural deviations and inspections.

Big DataBusiness IntelligenceCloud ManagementEnterprise SoftwareInformation Technology
Hiring Manager
Basant Sharma
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Responsibilities

Support investigations, development of corrective and preventative action (CAPA) and effective measures for Regulatory and PV related change controls, deviations, audits and inspections
Support GRADS Regulatory and/or Labeling sub-functions to enhance compliance activities with a focus on inspection readiness
Perform quality review of assigned aggregate reports (PSUR, PADER, REMS Assessment Report, etc)
Support the management of Regulatory and Pharmacovigilance issues, deviations, CAPA development, and change control management
Collaborate with GRADS Compliance team members in executing global Regulatory and PV compliance activities
Identify and escalate critical quality issues to senior GRADS Compliance management
Support (as determined by line management) Regulatory and PV process improvements including authoring/updating controlled procedures as it relates to compliance activities
Assists with inspection related activities, (pre-, peri- and post-inspection)
Remain current with global regulatory affairs, labelling and PV regulations and requirements, evaluate legislative changes affecting Regulatory, Labeling and PV, and develop strategies to support patient safety
Monitor the PV Compliance mailbox to ensure timely actioning of communications

Qualification

PharmacovigilanceRegulatory AffairsCAPAQuality Management SystemChange ControlInspection ReadinessAggregate ReportsGeographical CollaborationWritten CommunicationVerbal CommunicationTime ManagementDetail OrientedFast-paced Environment

Required

Pharmacovigilance (PV) / Drug Safety
Regulatory Affairs (RA)
CAPA (Corrective and Preventive Actions)
Change Control & Deviations
Inspection Readiness / Audits
Aggregate Reports (PSUR, PADER, REMS)
Quality Management System (QMS)
Minimum 1 year business, pharmaceutical, or biotechnology industry experience
Can apply base level quality control technical concepts and skills
Developing written and verbal communications skills
Ability to work in a fast-paced environment
Individual contributor with oversight from line manager
Ability to work across geographical boundaries
Disciplined, detail oriented, and good time management skills
Bachelor's degree in business or life sciences required

Preferred

Lean Sigma certification, or equivalent certification, preferred but not required

Company

Intelliswift - An LTTS Company

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''Intelliswift, an LTTS Company, delivers world-class Digital Product Engineering, Data Management, Analytics & AI, and Digital Ent Solutions

Funding

Current Stage
Late Stage
Total Funding
unknown
2024-11-11Acquired

Leadership Team

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Pat Patel
Founder & Executive Chairman
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Company data provided by crunchbase