6437 - Senior Quality Engineer / Senior Quality GxP Auditor

Posted 7/7/2026 · last confirmed live 8/26/2026

Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities. Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day. Company Culture Guidelines & Values: We empower and support our colleagues We commit to client success at every turn We have the courage to do the right thing We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged. We constantly acquire new skills and learn from our experiences to enhance our collective expertise Senior Quality Engineer Responsibilities: Quality Oversight & GMP Operations Provide Quality Assurance oversight for GMP manufacturing operations supporting both clinical and commercial Cell & Gene Therapy products. Partner with Manufacturing, Validation, Engineering, Facilities, Laboratory Operations, Materials Management, and Capital Project teams to ensure GMP compliance throughout the product lifecycle. Represent Quality on cross-functional project teams while serving as the primary QA resource for assigned initiatives. Identify compliance risks and proactively communicate quality gaps, recommending practical, risk-based solutions. Validation & Engineering Support Provide QA review and approval of: Validation protocols and reports Equipment, utility, facility, and computer system qualification documentation Risk assessments Engineering change documentation Support commissioning, qualification, and validation activities associated with manufacturing equipment, facilities, utilities, and capital projects. Review qualification activities for laboratory instruments and manufacturing systems. Quality Systems & Compliance Provide Quality support for: Change Controls Deviations and GMP Investigations Root Cause Analysis Corrective and Preventive Actions (CAPA) Ensure investigations are scientifically sound, timely, and compliant with regulatory expectations. Evaluate quality issues using a risk-based decision-making approach. Facilities & Utility Oversight Provide Quality oversight for: Preventive Maintenance (PM) Calibration programs Electronic Change Requests (eCRs) Work Orders Review and approve equipment, utility, and facility trending programs. Support Environmental Monitoring (EM), routine facility monitoring, and utility control programs. Provide oversight of facility monitoring systems including Building Management Systems (BMS), Environmental Monitoring Systems (EMS), ViewLinc, pest control, and related GMP-controlled programs. Cross-Functional Collaboration Foster strong collaboration across Quality, Manufacturing, Engineering, Validation, Facilities, and Laboratory organizations. Participate in project meetings and provide quality guidance throughout project execution. Communicate effectively with stakeholders at all organizational levels while balancing quality, compliance, and business objectives. Requirements: Master's degree with 3–5 years of relevant Quality or Validation experience OR Bachelor's degree in Engineering, Life Sciences, Scientific, or related discipline with 8+ years of relevant industry experience, or equivalent combination of education and experience. Experience providing QA oversight of GMP manufacturing operations. Experience supporting validation programs and capital projects within regulated pharmaceutical, biotechnology, or Cell & Gene Therapy environments. Strong knowledge of cGMP regulations, quality systems, and validation principles. Experience supporting aseptic manufacturing operations. Demonstrated experience leading: GMP investigations Root Cause Analysis CAPA development and effectiveness Experience reviewing validation documentation, engineering documentation, and quality system records. Experience working with electronic quality systems such as: Veeva Nuvolo ViewLinc Other enterprise GMP quality applications Onsite job requirement in Boston, MA For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future. *Verista is an equal opportunity employer. National (US) Range $70,491 — $113,521 USD Benefits Why Choose Verista? High growth potential and fast-paced organization with a people-focused culture Competitive pay plus performance-based incentive programs Company-paid Life, Short-Term, and Long-Term Disability Insurance. Medical, Dental & Vision insurances FSA, DCARE, Commuter Benefits Supplemental Life, Hospital, Critical Illness and Legal Insurance Health Savings Account 401(k) Retirement Plan (Employer Matching benefit) Paid Time Off (Rollover Option) and Holidays As Needed Sick Time Tuition Reimbursement Team Social Activities (We have fun!) Employee Recognition Employee Referral Program Paid Parental Leave and Bereavement Verista collects and processes personal data in accordance with applicable data protection laws.  If you are a California Job Applicant, see the privacy notice for further details.  For more information about our company, please visit us at Verista.com

This role is published by Verista, Inc. on greenhouse. SwiftFit is not the employer and does not accept applications.