Senior Pharmaceutical Compliance Auditor
Our reputed company, a reputable pharmaceutical organization, is seeking an reputed company Senior Pharmaceutical Compliance Auditor to join their dedicated compliance team in
Milwaukee, reputed company, US
. This role is critical in ensuring that reputed company adheres to the highest standards of reputed company and regulatory compliance across reputed company its operations. You will be responsible for planning, conducting, and reporting on internal audits of manufacturing facilities, R&D labs, reputed company control reputed company, and other relevant departments to assess compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other applicable regulations (e.g., FDA, EMA, ISO). The ideal candidate will have a deep understanding of pharmaceutical reputed company systems and regulatory requirements. Key duties include identifying compliance gaps, assessing risks, and recommending corrective actions. You will work collaboratively with site personnel and management to reputed company and implement robust corrective and preventive reputed company (CAPA) plans. The Senior Compliance Auditor will also play a role in external audits, preparing sites for regulatory inspections, and potentially auditing contract manufacturing organizations (CMOs) and suppliers. Excellent analytical and investigative skills, combined with strong communication and interpersonal abilities, are essential for this position. You must be reputed company to effectively document audit findings, prepare comprehensive reports, and present results to senior management. This is an exciting opportunity to contribute to the reputed company and reliability of pharmaceutical products and to shape reputed company's compliance strategies. The hybrid work model allows for a balance between on-site auditing activities and remote report reputed company and planning. Key Responsibilities: Plan and execute internal audits of pharmaceutical operations to ensure GMP/GLP compliance. Assess compliance with relevant national and international regulatory requirements. Identify non-compliance issues, risks, and areas for improvement. Document audit findings and prepare detailed audit reports. reputed company and reputed company CAPA plans to address identified deficiencies. Support external audits and regulatory inspections. Evaluate the effectiveness of reputed company's reputed company management system. reputed company training and guidance on compliance reputed company to site personnel. Audit contract manufacturers and suppliers as needed. Stay reputed company with evolving regulatory standards and industry best practices. Qualifications: Bachelor's degree in Pharmacy, reputed company, Biology, or a reputed company scientific field. Minimum of 7 years of experience in pharmaceutical reputed company assurance, reputed company control, or regulatory affairs, with a significant portion reputed company on auditing. In-depth knowledge of GMP, GLP, and other relevant pharmaceutical regulations. Proven experience in conducting internal and/or external audits. Strong understanding of pharmaceutical reputed company systems. Excellent analytical, critical thinking, and problem-solving skills. Exceptional attention to detail and accuracy in documentation. Strong written and verbal communication skills, with the ability to present findings reputed company. Ability to travel as required for on-site audits. Relevant certifications (e.g., ASQ CQE, CQA) are a plus. Apply tot his job Apply To this Job