This is a contract job opportunity. potential for permPosition : Senior Quality Assurance Compliance Auditor Drug Development 9354Location : Indianapolis INSchedule : M-F 8AM - 5PMProjected duration : 6 months + potential for permJob code : CVDJP00029354 W2 pay rate - $38.
40 per hour Benefits are available
Essential duties :
- Conduct workasidentifiedontheauditactivitylist
- ContributestoglobalQApoliciesoninterpretation / applicationofregulations
- ProvidesubjectmatterexpertisetoprojectsSupportteaminCAPAplancreation
- Hostsexternalaudits / inspectionse.g.regulatoryinspections,strategicclients.Assistswiththe facilitation of audit responses
- SupportstheQA to-QArelationshipwithkeyclient(s)
- Deliveryoftraininginperformanceofaudits(basic,intermediate,complex)
- Participate(formulti-regulatorytopicsinareaofexpertise)globalQualityinitiative(s)aimedat improving compliance and / or efficiency of the QA organization
- Supportsthereportingofqualitymetricsandimplementationofnecessarycorrectiveactions and / or process improvements via appropriate forum (e.
g. Monthly Reports, Site Quality Review, Liaison meetings)
- EnsureRegulatoryComplianceandQualityAssurance(RC&QA)responsibilities,asindicated in applicable controlled documents, are followed
- Otherdutiesasassignedbymanagement.
Summary : The main function of a compliance analyst is to ensure the organizations operations and procedures meet government and industry compliance standards.
A compliance analyst may research regulations and policies, communicate requirements, and apply for compliance certifications on behalf of the organization.
Job Responsibilities : Researching industry compliance regulations and policies.Evaluating internal operational and procedural compliance.
Analyzing and updating existing compliance policies and related documentation. Communicating compliance policies and guidelines to Management and designated departments.
Developing and executing new compliance policies and procedures as required.Applying for compliance certification and regulatory approval.
Developing and maintaining a compliance record keeping system.Training employees on industry compliance requirements.Maintaining communication with compliance regulators and following up on applications.
Keeping up with compliance requirements and amendments to regulations. Requirements : Industry related bachelors degree or related experience.
Compliance management certification preferred.Knowledge of compliance management software.Advanced analytical abilities. Good communication and interpersonal skills.5-7 years of experience.
Senior Quality Assurance Compliance Auditor Drug Development 8926
This is a contract job opportunity.Position: Phlebotomist 8580Location: Holyoke MASchedule: see belowProjected duration: 3 months + potential for permJob code:CVDJP00028580 Benefits are available will be floating, various hours between Monday-Friday 6am-6pm.Greenfield area, Northampton area, Westfie...
Senior Quality Assurance Compliance Auditor Drug Development 8926
Position: Senior Quality Assurance Compliance Auditor Drug Development 8926Location: Indianapolis INSchedule: M-F 8AM - 5PMProjected duration: 6 months + potential for permJob code: CVDJP00028926 Benefits are available This is a hybrid position, where the candidate can work from home but will need t...
Senior Quality Assurance Compliance Auditor Drug Development 8926
Position: Senior Quality Assurance Compliance Auditor Drug Development 8926Location: Indianapolis INSchedule: M-F 8AM - 5PMProjected duration: 6 months + potential for permJob code: CVDJP00028926 Benefits are available This is a hybrid position, where the candidate can work from home but will need t...
Senior Quality Assurance Compliance Auditor Drug Development 8926
Position: Senior Quality Assurance Compliance Auditor Drug Development 8926Location: Indianapolis INSchedule: M-F 8AM - 5PMProjected duration: 6 months + potential for permJob code: CVDJP00028926 W2 pay rate - $38. Summary:The main function of a compliance analyst is to ensure the organizations oper...
Senior Quality Assurance Compliance Auditor Drug Development 8926
Position: Senior Quality Assurance Compliance Auditor Drug Development 8926Location: Indianapolis INSchedule: M-F 8AM - 5PMProjected duration: 6 months + potential for permJob code: CVDJP00028926 Benefits are available This is a hybrid position, where the candidate can work from home but will need t...
Senior Quality Assurance Compliance Auditor Drug Development 8926
Position: Senior Quality Assurance Compliance Auditor Drug Development 8926Location: Indianapolis INSchedule: M-F 8AM - 5PMProjected duration: 6 months + potential for permJob code: CVDJP00028926 W2 pay rate - $33. Summary:The main function of a compliance analyst is to ensure the organizations oper...
Senior Quality Assurance Compliance 13485 ISO Certified Auditor 9354
Position: Senior Quality Assurance Compliance 13485 ISO Certified Auditor 9354Location: Indianapolis INSchedule: M-F 8AM - 5PMProjected duration: 6 months + potential for permJob code: CVDJP00029354 Ideal Candidate is a 13485 ISO Certified Auditor. Summary:The main function of a compliance analyst i...
Senior Quality Assurance Compliance 13485 ISO Certified Auditor 9354
Position: Senior Quality Assurance Compliance 13485 ISO Certified Auditor 9354Location: Indianapolis INSchedule: M-F 8AM - 5PMProjected duration: 6 months + potential for permJob code: CVDJP00029354 Ideal Candidate is a 13485 ISO Certified Auditor. Summary:The main function of a compliance analyst i...
Senior Quality Assurance Compliance 13485 ISO Certified Auditor 9354
Position: Senior Quality Assurance Compliance 13485 ISO Certified Auditor 9354Location: Indianapolis INSchedule: M-F 8AM - 5PMProjected duration: 6 months + potential for permJob code: CVDJP00029354 Ideal Candidate is a 13485 ISO Certified Auditor. Summary:The main function of a compliance analyst i...
Quality Assurance Compliance Specialist
Title : Quality Assurance Compliance Specialist (13485 ISO Certified). Ensure Regulatory Compliance and Quality Assurance (RC&QA) responsibilities, as indicated in applicable controlled documents, are followed. Participate (for multi-regulatory topics in area of expertise) global Quality initiative(...