DevOps Engineer
epias GmbH
Join epias GmbH to support medical process management software through CI/CD, Kubernetes, infrastructure automation, and dependable platform operations.
Open
Clarkston Consulting is a strategic business consultancy supporting organizations in life sciences, consumer products, and retail. Its work spans business strategy, operations, implementation, managed services, change management, and data-driven transformation. The firm also provides expertise in business process consulting, clinical research, digital and technology consulting, and supply chain management, helping clients address complex operational and organizational challenges.
Senior Veeva Quality Systems Consultant
Lead Veeva Quality and Vault RIM implementations for life sciences clients, from requirements workshops through configuration and validation. The role also covers project planning, client training, and team guidance, with 30–50% travel and home-office work between trips.
Description
- Design and deploy Veeva solutions for life sciences and consumer products clients.
- Configure and implement Veeva Quality and Veeva Vault RIM capabilities.
- Lead requirements workshops and design, prototype, configure, and document content management and QMS data solutions.
- Build lasting client relationships that continue beyond individual projects.
- Develop and oversee project and workstream plans and timelines.
- Set deliverables, allocate team roles and resources, track issues and resolutions, and help manage scope and requirements.
- Support computer system validation in GMP environments.
- Draft and update standard operating procedures.
- Deliver knowledge transfer and end-user training, sharing best practices.
- Guide junior systems analysts and client staff.
- Serve clients across life sciences, consumer products, and retail.
- Travel an estimated 30–50% according to client and project needs, working from a home office between trips.
Requirements
- At least five years of experience working with or for life sciences companies.
- Experience implementing document or quality management systems in life sciences, as a consultant or business or IT representative.
- Experience with regulatory information management systems, including registrations and submissions, is preferred.
- Understanding of global quality requirements, compliance considerations, and processes.
- Hands-on experience with systems such as Veeva Vault, EtQ, TrackWise, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, or other quality information or content management platforms.
- Team lead experience.
- Adaptability to work from design through hands-on configuration and take on new responsibilities.
- Strong client service orientation and active involvement in delivering engagements and project plans or tasks.
- Strong analytical skills.
- Excellent presentation and publication-quality writing skills for communicating findings and recommendations.
- Four-year degree from an accredited college or university.
- Use AI responsibly and authentically; real-time AI-generated or scripted interview responses are prohibited.
Benefits
- Comprehensive medical, dental, vision, and other health and wellness benefits.
- 401(k) plan with company contributions.
- Paid vacation, personal days, holidays, and sick leave.
- Paid parental leave and family-building support for adoption, surrogacy, and infertility.
- Life and disability insurance.
- Investment in training and professional development.
- Tuition assistance.
- Support for accommodations during the interview process.
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