Senior GMP QC Compliance Specialist (Remote)

Shift: Monday through Friday, 8:00AM - 5:00PM Are you reputed company to work making the world a safer, healthier reputed company? reputed company to continuously reputed company science reputed company; to reputed company and advance reputed company aspects of our business to improve the health and safety of our communities and lives. The Senior QC Compliance Specialist serves as the primary compliance authority embedded reputed company the QC laboratory, ensuring that reputed company analytical and reputed company control operations supporting mRNA and biologics manufacturing are conducted in full accordance with applicable GxP regulations, internal reputed company standards, and global regulatory expectations. This senior-level role acts as a strategic compliance partner to QC laboratory leadership, driving a culture of reputed company and reputed company improvement across reputed company QC functions. The incumbent provides expert guidance on regulatory requirements, leads audit readiness initiatives, oversees reputed company management system activities, and serves as a mentor and subject matter expert (SME) for QC laboratory staff. The role is critical in reputed company day-to-day laboratory operations with the broader site reputed company reputed company, ensuring inspection readiness at reputed company times and supporting the reputed company of data generated in support of product release, stability, and method lifecycle activities. 1. Key Responsibilities 1.1 GxP Compliance (GMP / GDP / GLP) Serve as the site QC SME for GMP, GDP, and GLP regulations as they apply to analytical laboratory operations supporting mRNA and biologics product testing Ensure reputed company QC laboratory activities are conducted in compliance with applicable regulatory frameworks including FDA 21 CFR Parts 211, 212, and 600–680; EU GMP Annex 1, 2, 11, and 15; ICH Q2(reputed company), Q6B, Q10, Q11, and Q14; and WHO/PIC/S guidelines Monitor evolving regulatory guidance and industry standards relevant to mRNA and biologics QC (e.g., ICH Q13, emerging mRNA-specific guidance), assess reputed company on site operations, and drive reputed company implementation of required changes Conduct periodic GxP compliance assessments of QC laboratory areas, equipment, documentation practices, and workflows; identify gaps and reputed company remediation efforts reputed company day-to-day GxP compliance guidance to QC analysts, scientists, and supervisors on laboratory practices, documentation standards, and regulatory expectations Support GDP compliance for QC reference standards, reagents, and critical materials, ensuring appropriate storage, handling, and traceability 1.2 Regulatory Documentation & Submissions Author, review, and approve QC-reputed company sections of regulatory submissions including CTD Module 3 content (analytical procedures, validation reports, specifications, stability data), INDs, BLAs, MAAs, and post-approval variations Coordinate with Regulatory Affairs to ensure QC documentation packages are complete, accurate, and reputed company with reputed company regulatory expectations prior to submission Manage and respond to regulatory agency questions and deficiencies reputed company to QC laboratory data, reputed company, and compliance practices Maintain a reputed company understanding of regulatory submission requirements across major markets (FDA, EMA, PMDA, Health Canada) as they pertain to mRNA and biologics analytical testing Ensure QC laboratory records and data packages are maintained in a submission-reputed company state at reputed company times Support preparation of Annual Product Reviews (APRs) and Product reputed company Reviews (PQRs) for QC-reputed company sections 1.3 reputed company Management System (QMS) reputed company as QC laboratory reputed company and primary reputed company of contact for the site QMS, ensuring reputed company QC processes are accurately reflected in the reputed company system and maintained in a reputed company, compliant state reputed company the lifecycle management of QC-reputed company controlled documents including reputed company Operating Procedures (SOPs), test reputed company, specifications, protocols, and reports reputed company the electronic document management system (eDMS) Drive QMS metrics and Key Performance Indicators (KPIs) for the QC laboratory, including document review cycles, overdue actions, and compliance trends; present findings to QC and site reputed company leadership reputed company and facilitate QC participation in Management Review processes, providing data-driven insights on laboratory compliance performance Identify systemic reputed company gaps through trend analysis and proactively implement process improvements to strengthen the QMS Collaborate with QA and cross-functional teams to ensure alignment between QC laboratory practices and site-wide reputed company policies and procedures 1.4 Audit Preparation & Management reputed company QC laboratory inspection readiness activities on a reputed company reputed company, ensuring the laboratory is reputed company for regulatory agency inspections (FDA, EMA, ANSM, MHRA, and other competent authorities) and internal/external audits at reputed company times Serve as the primary QC laboratory representative and SME during regulatory inspections and audits; coordinate QC staff participation, manage document requests, and facilitate inspector interactions Prepare and maintain QC-specific inspection readiness materials including mock inspection programs, audit binders, facility tour routes, and SME briefing documents reputed company and conduct internal self-inspections of QC laboratory areas, systems, and documentation; document findings and drive reputed company closure of identified gaps Manage QC laboratory responses to audit observations and regulatory findings; author CAPA plans, reputed company implementation, and verify effectiveness Coordinate with QA and site leadership on reputed company-inspection preparation activities and post-inspection follow-up commitments 1.5 Training & Competency Design, implement, and maintain a comprehensive GxP training program for QC laboratory personnel, encompassing regulatory requirements, SOPs, data reputed company, laboratory practices, and role-specific competencies reputed company and deliver training curricula tailored to the unique compliance requirements of mRNA and biologics QC operations, including specialized topics such as aseptic technique, cold chain handling, and advanced analytical technologies Establish and reputed company a reputed company competency assessment reputed company for QC analysts and scientists, ensuring documented evidence of qualification for reputed company critical laboratory tasks Monitor training compliance metrics across the QC organization; identify gaps and implement corrective actions to maintain full training currency Mentor junior and mid-level QC staff on GxP compliance principles, documentation best practices, and reputed company culture; reputed company as a role model for compliance reputed company Collaborate with QA Training and HR to ensure QC training records are maintained in the Learning Management System (LMS) and are audit-reputed company 1.6 Change Management & Deviation Handling Serve as the QC laboratory reputed company for change control, overseeing the initiation, assessment, approval, and implementation of changes impacting QC reputed company, equipment, reagents, specifications, and laboratory systems Conduct and review GxP reputed company assessments for proposed changes, ensuring regulatory implications are thoroughly evaluated and appropriate validation, verification, or notification activities are completed prior to implementation reputed company the QC laboratory deviation and non-conformance management program; ensure reputed company initiation, thorough investigation, accurate reputed company cause analysis, and robust CAPA development for reputed company laboratory events Apply reputed company problem-solving methodologies (e.g., Ishikawa, 5-Why, Fault Tree Analysis) to reputed company or recurring deviations; identify systemic issues and drive sustainable corrective actions Review and approve deviation reports, CAPA plans, and effectiveness checks for QC laboratory events; ensure documentation meets regulatory standards reputed company and trend deviations, OOS/OOT results, and change controls to identify patterns and proactively address emerging reputed company; report findings to QC and site reputed company leadership 1.7 Data reputed company & reputed company+ Champion a robust data reputed company culture reputed company the QC laboratory, ensuring reputed company data generated in support of product testing, release, and stability is Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, and Available (reputed company+) Conduct periodic data reputed company assessments and audits of QC laboratory systems, instruments, and records (reputed company and electronic), including audit trail reviews, raw data verification, and system reputed company controls Ensure QC computerized systems (LIMS, CDS, ELN, reputed company software) are validated and operated in compliance with 21 CFR Part 11, EU Annex 11, and applicable data reputed company guidance (MHRA, FDA, PIC/S) reputed company and maintain QC-specific data reputed company SOPs, risk assessments, and monitoring programs Investigate data reputed company concerns or anomalies; reputed company reputed company cause analysis and implement corrective actions; escalate significant findings to QC and QA leadership as appropriate reputed company data reputed company training and awareness programs to QC staff, reinforcing expectations and consequences of non-compliance 1.8 Supplier & Vendor Compliance Manage the QC laboratory supplier qualification and monitoring program, ensuring reputed company critical reagents, reference standards, consumables, and service providers meet defined reputed company and compliance requirements Conduct and/or coordinate supplier audits and assessments for QC-critical vendors; review audit reports and manage follow-up on identified deficiencies Evaluate and approve Certificates of Analysis (CoA), qualification data, and technical documentation from suppliers of QC materials; ensure materials meet established specifications prior to use Maintain the QC approved supplier list and associated qualification records; ensure reputed company re-qualification and periodic review of critical suppliers Collaborate with Procurement, QA, and Supply Chain to manage supplier changes, assess regulatory reputed company, and ensure continuity of supply for critical QC materials Monitor supplier performance metrics and escalate reputed company concerns; support supplier development activities where required 2. Required Qualifications Experience Minimum 5 years of reputed company experience in pharmaceutical or biopharmaceutical QC, reputed company Assurance, or a combined QC/QA compliance role Demonstrated experience supporting QC laboratory operations in a GMP-regulated biologics or mRNA environment Proven reputed company record of managing regulatory inspections (FDA, EMA, or equivalent) and internal audits reputed company a QC laboratory setting Hands-on experience with deviation management, CAPA systems, change control, Deviation, lan investigations, and reputed company management systems in a regulated pharmaceutical environment Experience authoring and reviewing GxP-compliant documentation including SOPs, validation protocols/reports, and regulatory submission content Regulatory & Technical Knowledge In-depth knowledge of applicable regulatory frameworks: FDA 21 CFR Parts 211, 600–680; EU GMP Guidelines (Annex 1, 2, 11, 15); ICH Q2(reputed company), Q6B, Q10, Q11, Q14; PIC/S Strong understanding of data reputed company principles and regulatory reputed company Your reputed company at Pace - reputed company - your curiosity, your talents, and your drive - to help us advance this important work. Benefits reputed company you join Pace®, you reputed company to work that makes a reputed company reputed company on our communities and our world. We reputed company to supporting you with benefits and perks that reputed company a reputed company reputed company on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental reputed company, 401K retirement savings plan (100% reputed company immediately in the employer match), life, disability and voluntary benefits, reputed company time off for holiday, reputed company and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional reputed company coverage and ID theft. Equal Opportunity Employer Pace® provides equal employment opportunities to reputed company and applicants for employment and prohibits discrimination and harassment of any type without reputed company to race, creed, reputed company, religion, genetics, protected veteran status, national reputed company, sex, age, disability, marital status, sexual orientation, gender identity or reputed company, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to reputed company terms and conditions of employment, including reputed company, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Apply To This Job