{"id":4586,"date":"2026-04-19T19:07:57","date_gmt":"2026-04-19T23:07:57","guid":{"rendered":"https:\/\/mivado.com\/mgp\/?post_type=jobpost&p=4586"},"modified":"2026-04-19T19:37:36","modified_gmt":"2026-04-19T23:37:36","slug":"gxp_compliance_advisor","status":"publish","type":"jobpost","link":"https:\/\/mivado.com\/mgp\/jobs\/gxp_compliance_advisor\/","title":{"rendered":"GxP Compliance Advisor"},"content":{"rendered":"

[vc_row][vc_column][vc_column_text css=””]Mivado GlobalPerformance is seeking a GxP Compliance Advisor who will act as the organization\u2019s authority on GMP, GAMP, QA\/QC workflows, and regulatory compliance.<\/p>\n

This role ensures that every solution designed and implemented using a low-code platform aligns with real-world pharma operations and global regulatory expectations.<\/p>\n

The incumbent will act as the credibility anchor during sales cycles, the process architect during implementation, and the compliance guardian throughout the customer lifecycle.[\/vc_column_text][\/vc_column][\/vc_row][vc_row][vc_column][vc_column_text css=””]<\/p>\n

Key Responsibilities<\/strong><\/h1>\n

1. Regulatory & Compliance Leadership<\/strong><\/h2>\n
    \n
  • – Interpret and apply global regulatory frameworks: GMP, GAMP 5, 21 CFR Part 11, Annex 11, WHO, MHRA, PIC\/S.<\/li>\n
  • – Ensure that all solution designs adhere to data integrity principles (ALCOA+).<\/li>\n
  • – Advise clients on audit readiness and best practices for compliance.<\/li>\n
  • – Review validation deliverables (URS, FRS, Risk Assessments, IQ\/OQ\/PQ).<\/li>\n<\/ul>\n

    2. Process Mapping & Digital Transformation<\/strong><\/h2>\n
      \n
    • – Analyze existing pharma workflows (QA, QC, Manufacturing, R&D, Engineering).<\/li>\n
    • – Translate manual or legacy processes into optimized digital workflows.<\/li>\n
    • – Define functional requirements for modules such as:\n
        \n
      • \n
          \n
        • — eQMS (CAPA, Deviations, Change Control, Complaints)<\/li>\n
        • –LIMS (sample management, stability, COA)<\/li>\n
        • –MES\/eBR (batch records, equipment logs)<\/li>\n
        • –DMS (SOPs, controlled documents)<\/li>\n
        • –EMS\/eLogbook (equipment management)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<\/li>\n
        • – Identify process gaps and recommend improvements aligned with industry standards.<\/li>\n<\/ul>\n

          3. Client Engagement & Advisory<\/strong><\/h2>\n
            \n
          • – Lead discovery workshops with QA Heads, QC Managers, Plant Managers, and IT teams.<\/li>\n
          • – Provide domain expertise during pre?sales demos and solution presentations.<\/li>\n
          • – Act as a trusted advisor throughout the customer journey.<\/li>\n
          • – Support Business Development with domain?specific insights and proposal content.<\/li>\n<\/ul>\n

            4. Implementation Support<\/strong><\/h2>\n
              \n
            • – Collaborate with implementation teams to ensure functional accuracy.<\/li>\n
            • – Validate workflow configurations, forms, dashboards, and reports.<\/li>\n
            • – Ensure system configurations align with regulatory expectations.<\/li>\n
            • – Participate in UAT planning, execution, and documentation.<\/li>\n<\/ul>\n

              5. Documentation & Validation<\/strong><\/h2>\n
                \n
              • – Review and approve:\n
                  \n
                • \n
                    \n
                  • –URS\/FRS<\/li>\n
                  • –Process maps<\/li>\n
                  • –Validation protocols (IQ\/OQ\/PQ)<\/li>\n
                  • –SOPs and training materials<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<\/li>\n
                  • – Ensure documentation meets GxP and audit standards.<\/li>\n<\/ul>\n

                    [\/vc_column_text][\/vc_column][\/vc_row][vc_row][vc_column][vc_column_text css=””]<\/p>\n

                    Required Skills & Qualifications<\/strong><\/h1>\n

                    Education<\/strong><\/h2>\n
                      \n
                    • Bachelor\u2019s or Master\u2019s degree in Pharmacy, Biotechnology, Chemistry, Life Sciences, or related field.<\/li>\n<\/ul>\n

                      Industry Experience<\/strong><\/h2>\n
                        \n
                      • _\u00a0 3+ years in pharma\/biotech operations, QA, QC, manufacturing, or regulatory affairs.<\/li>\n
                      • _ Experience with QMS, LIMS, MES, DMS, or other GxP systems is a strong asset.<\/li>\n
                      • _ Hands?on involvement in audits, CAPA, deviations, change control, batch release, or lab operations.<\/li>\n
                      • _ Deep understanding of GxP processes and digitalization trends.<\/li>\n
                      • _ Ability to map business processes to software capabilities.<\/li>\n
                      • _ Familiarity with CSV (Computer System Validation) principles.<\/li>\n
                      • _ Strong analytical and documentation skills.<\/li>\n<\/ul>\n

                        Soft Skills<\/strong><\/h2>\n
                          \n
                        • _ Excellent communication and presentation abilities.<\/li>\n
                        • _ Strong stakeholder management and influence.<\/li>\n
                        • _ Ability to simplify complex regulatory concepts.<\/li>\n
                        • _ Close attention to detail and structured thinking.<\/li>\n<\/ul>\n

                          [\/vc_column_text][\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"

                          A GxP Compliance Advisor is essentially the strategic brain behind compliant digital transformation in pharma and life sciences. This person will ensure every digital solution you deliver is audit-ready, GxP-aligned, and operationally correct for real pharma environments.<\/p>\n","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","jobpost_category":[43,46],"jobpost_job_type":[50,118,49],"jobpost_location":[189,53,54,138,56],"jobpost_tag":[],"class_list":["post-4586","jobpost","type-jobpost","status-publish","hentry","jobpost_category-contract","jobpost_category-permanent","jobpost_job_type-full-time","jobpost_job_type-hybrid","jobpost_job_type-part-time","jobpost_location-canada","jobpost_location-montreal-quebec","jobpost_location-quebec-qc","jobpost_location-togo-west-africa","jobpost_location-toronto-on"],"_links":{"self":[{"href":"https:\/\/mivado.com\/mgp\/wp-json\/wp\/v2\/jobpost\/4586","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/mivado.com\/mgp\/wp-json\/wp\/v2\/jobpost"}],"about":[{"href":"https:\/\/mivado.com\/mgp\/wp-json\/wp\/v2\/types\/jobpost"}],"author":[{"embeddable":true,"href":"https:\/\/mivado.com\/mgp\/wp-json\/wp\/v2\/users\/1"}],"wp:attachment":[{"href":"https:\/\/mivado.com\/mgp\/wp-json\/wp\/v2\/media?parent=4586"}],"wp:term":[{"taxonomy":"jobpost_category","embeddable":true,"href":"https:\/\/mivado.com\/mgp\/wp-json\/wp\/v2\/jobpost_category?post=4586"},{"taxonomy":"jobpost_job_type","embeddable":true,"href":"https:\/\/mivado.com\/mgp\/wp-json\/wp\/v2\/jobpost_job_type?post=4586"},{"taxonomy":"jobpost_location","embeddable":true,"href":"https:\/\/mivado.com\/mgp\/wp-json\/wp\/v2\/jobpost_location?post=4586"},{"taxonomy":"jobpost_tag","embeddable":true,"href":"https:\/\/mivado.com\/mgp\/wp-json\/wp\/v2\/jobpost_tag?post=4586"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}