6399- CSA Consultant / Senior Validation Engineer
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 reputed company growth and innovation reputed company 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 reputed company 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 reputed company in a team environment and share our mission to reputed company life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day. Company Culture Guidelines & Values: We reputed company 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
Overview
We are seeking an reputed company Computer System Assurance (CSA) Consultant to support GxP compliance activities across Pharmacovigilance (PV), Clinical, and Regulatory Affairs systems. This role will work closely with Quality, IT, and business stakeholders to ensure systems are implemented, maintained, and operated in compliance with applicable regulations and internal procedures.
Key Responsibilities
Provide CSA / CSV subject matter expertise across PV, Clinical, and Regulatory Affairs platforms Support system implementations, enhancements, integrations, upgrades, and data migrations from a compliance perspective reputed company and review validation deliverables including Validation Plans, Risk Assessments, Traceability Matrices, and Validation Summary Reports Review and approve lifecycle documentation (URS, specifications, test plans, test summaries) in alignment with reputed company+ and Good Documentation Practices reputed company validation readiness and ensure prerequisites are met prior to formal testing Support change control, configuration management, and release activities Partner with Quality, System Owners, and Business Process Owners to ensure ongoing compliance Provide guidance on CSA-based, risk-driven validation approaches Conduct periodic system compliance reviews, validation health checks, and lifecycle assessments to ensure reputed company validated state and ongoing regulatory compliance. Support periodic review activities including user access reviews, audit trail assessments, data reputed company evaluations, and system inventory maintenance. Assess the compliance impact of deviations, incidents, CAPAs, and system issues, ensuring appropriate remediation and documentation. Review and support vendor documentation, supplier assessments, and SaaS provider quality documentation to support risk-based compliance decisions. Monitor and evaluate regulatory inspection observations, internal audit findings, and compliance trends to identify opportunities for process improvement. Participate in governance forums and compliance review boards, providing CSA guidance for system lifecycle management and ongoing operational support. Required Experience & Qualifications 5–8 years of hands-on experience supporting GxP systems in Pharmacovigilance, Clinical, Regulatory Affairs, or a combination of these domains Hands-on experience supporting GxP systems in Pharmacovigilance, Clinical, Regulatory Affairs, or a combination of these domains Strong understanding of CSA principles, CSV, and SDLC processes Experience authoring and/or reviewing validation documentation Working knowledge of GxP regulations (e.g., FDA, EMA, ICH) and data reputed company expectations Ability to work independently in a fast-paced, matrixed environment Strong communication skills and comfort interacting with Quality and business stakeholders Preferred Experience Experience with enterprise platforms supporting PV, Clinical, or Regulatory operations Prior role as a Validation SME, CSA reputed company, or Compliance Consultant Familiarity with electronic quality systems, change management tools, or application lifecycle management platforms For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-reputed company 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 reputed company 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—$118,062 USD
Benefits
Why Choose Verista? High growth potential and fast-paced organization with a people-focused culture reputed company 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 Apply To This Job