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Recruitment Consultant - Account Management US Contract
We are seeking a meticulous and experienced Quality Assurance Consultant to support our client in the scientific research industry on a 6 month contractual basis. Key Responsibilities: Develop, implement, and monitor quality assurance protocols aligned with industry standards (e.g., GLP, GMP). Conduct audits, inspections, and risk assessments to ensure regulatory compliance and identify areas for improvement. Collaborate with research teams to establish best practices and ensure adherence to quality management systems. Provide training and guidance to staff on quality standards, policies, and procedures. Review and approve documentation, including SOPs, reports, and validation protocols. Investigate quality issues, implement corrective actions (CAPAs), and oversee resolution processes. Stay updated on regulatory changes and advise on necessary adaptations to policies and practices. Requirements: Bachelor's or advanced degree in a relevant scientific discipline. Proven experience in quality assurance within the scientific research or pharmaceutical industry. Strong knowledge of regulatory standards (GMP). Excellent analytical, problem-solving, and communication skills. Attention to detail and ability to work collaboratively in a dynamic environment. Seniority level
Mid-Senior level Employment type
Contract Job function
Consulting, Science, and Quality Assurance Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Research Services
#J-18808-Ljbffr
We are seeking a meticulous and experienced Quality Assurance Consultant to support our client in the scientific research industry on a 6 month contractual basis. Key Responsibilities: Develop, implement, and monitor quality assurance protocols aligned with industry standards (e.g., GLP, GMP). Conduct audits, inspections, and risk assessments to ensure regulatory compliance and identify areas for improvement. Collaborate with research teams to establish best practices and ensure adherence to quality management systems. Provide training and guidance to staff on quality standards, policies, and procedures. Review and approve documentation, including SOPs, reports, and validation protocols. Investigate quality issues, implement corrective actions (CAPAs), and oversee resolution processes. Stay updated on regulatory changes and advise on necessary adaptations to policies and practices. Requirements: Bachelor's or advanced degree in a relevant scientific discipline. Proven experience in quality assurance within the scientific research or pharmaceutical industry. Strong knowledge of regulatory standards (GMP). Excellent analytical, problem-solving, and communication skills. Attention to detail and ability to work collaboratively in a dynamic environment. Seniority level
Mid-Senior level Employment type
Contract Job function
Consulting, Science, and Quality Assurance Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Research Services
#J-18808-Ljbffr
