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Senior CSV Engineer/Analyst - Senior Validation Engineer 5392

Verista’s 600 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 CSV Engineer Responsibilities:

We are seeking a skilled Computer System Validation (CSV) Specialist to support the commissioning and qualification (C&Q) efforts for a cell therapy manufacturing project. This role ensures that computer systems meet regulatory compliance standards and are validated to facilitate product manufacturing.

Responsibilities Include:

  • Develop and execute CSV protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), for manufacturing equipment
  • Collaborate closely with automation and validation teams to ensure systems meet project and regulatory compliance standards
  • Manage the document lifecycle, including creation, revision, and storage, in compliance with project documentation systems
  • Participate in weekly project meetings to coordinate with system owners and management for alignment on project needs and issue resolution
  • Conduct risk assessments and generate compliance reports, managing deviations and ensuring all required documentation meets quality and regulatory standards
  • Oversee vendor interactions, including reviewing and tracking vendor deliverables and system qualifications
  • Bachelor’s degree in a relevant field (e.g., Engineering, Computer Science, Life Sciences)
  • Minimum of 5 years of experience in Computer System Validation in a GMP-regulated environment, ideally within pharmaceuticals or biotechnology
  • Strong knowledge of regulatory compliance requirements (e.g., FDA regulations, cGMP standards) and quality systems
  • Experience with DeltaV control systems and document management systems
  • Excellent organizational, communication, and documentation skills
  • Ability to work effectively both independently and as part of an integrated project team
  • Must be available to work onsite at client site in Warren, NJ (On-site; some degree of remote work possible with approval)
  • Obvious business maturity and interpersonal skills to be able to effectively communicate and collaborate
  • Experience and capability of effectively communicating requirements (written and orally) with rationale to different levels of the client’s organization
  • Demonstrated ability to generate CSV deliverables independently
  • Ability to work independently and as part of a team, with the ability to transition between the two
  • Capacity to make independent sound decisions and independently manage priorities
  • Advanced Microsoft WORD, EXCEL, and PowerPoint capabilities
  • 5 years minimum of relevant experience

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

For more information about our company, please visit us at Verista.com

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.

$70,491-115,000

*Verista is an equal opportunity employer.

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Average salary estimate

$92745.5 / YEARLY (est.)
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$70491K
$115000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Senior CSV Engineer/Analyst - Senior Validation Engineer 5392, Verista

Are you ready to take your career to the next level with a company that truly values its people? Join Verista as a Senior CSV Engineer/Analyst and be part of a dedicated team that's on a mission to empower growth and innovation within the life sciences sector. At Verista, we pride ourselves on solving some of the world’s most pressing healthcare challenges through cutting-edge solutions and expert-driven strategies. As a Senior CSV Engineer, your role will be pivotal in supporting the commissioning and qualification efforts for an exciting cell therapy manufacturing project. You'll be responsible for developing and executing Computer System Validation (CSV) protocols, ensuring compliance with regulatory standards, and collaborating with a dynamic project team. We’re looking for individuals who not only have a deep understanding of regulatory compliance but also possess excellent communication and documentation skills. Your experience in Computer System Validation within the GMP-regulated environment will be crucial in managing vendor interactions and generating compliance reports. We're committed to your growth, offering a competitive salary and comprehensive benefits, including medical, dental, and vision insurance! At Verista, we value inclusivity, growth, and our mission to make a positive impact every day. If you're ready to thrive in a fast-paced environment where your expertise can genuinely make a difference, this role is for you!

Frequently Asked Questions (FAQs) for Senior CSV Engineer/Analyst - Senior Validation Engineer 5392 Role at Verista
What are the key responsibilities of the Senior CSV Engineer at Verista?

As a Senior CSV Engineer at Verista, your primary responsibilities will include developing and executing Computer System Validation (CSV) protocols, ensuring regulatory compliance for manufacturing equipment, and collaborating with automation and validation teams. You will also oversee document management in compliance with project standards, conduct risk assessments, and manage vendor interactions to track deliverables and system qualifications.

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What qualifications are required for the Senior CSV Engineer/Analyst position at Verista?

To qualify for the Senior CSV Engineer/Analyst position at Verista, candidates should have a Bachelor’s degree in a relevant field like Engineering or Computer Science, plus a minimum of 5 years of experience in Computer System Validation within a GMP-regulated environment. Strong knowledge of regulatory compliance requirements and excellent organizational skills are also essential.

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What opportunities for growth should candidates expect at Verista as a Senior CSV Engineer?

At Verista, the Senior CSV Engineer position presents significant growth potential within a fast-paced and people-focused culture. Employees are encouraged to acquire new skills and pursue professional development opportunities, including tuition reimbursement programs and performance-based incentives, ensuring that your career can continuously evolve.

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Can Senior CSV Engineers work remotely at Verista?

While the Senior CSV Engineer role at Verista primarily requires on-site work at the client site in Warren, NJ, some degree of remote work may be possible with approval. This flexibility can enhance work-life balance while still engaging fully with project teams.

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What kind of company culture can Senior CSV Engineers expect at Verista?

Verista fosters a culture that empowers and supports its colleagues, prioritizes client success, and actively encourages an inclusive environment. Employees are respected, challenged, and encouraged to grow and learn from their experiences, creating a rewarding workplace for Senior CSV Engineers and other team members.

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Common Interview Questions for Senior CSV Engineer/Analyst - Senior Validation Engineer 5392
Can you explain your experience with Computer System Validation in a GMP-regulated environment?

When answering this question, provide specific examples of past projects where you successfully developed and executed CSV protocols. Highlight your familiarity with regulatory requirements and how you ensured compliance throughout the project lifecycle.

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What strategies do you use to collaborate with automation and validation teams?

Discuss your approach to teamwork, including effective communication practices, regular meetings, and shared documentation tools that help align goals and ensure successful project outcomes in a collaborative environment.

Join Rise to see the full answer
How do you manage the document lifecycle for CSV projects?

Outline your proficiency in document management systems, discussing how you create, revise, and archive documents based on regulatory standards. Be sure to mention your attention to detail and organizational skills that prevent compliance issues.

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Describe a challenging situation you faced regarding regulatory compliance and how you resolved it.

Use the STAR method (Situation, Task, Action, Result) to narrate a specific challenge, focusing on your analytical skills and decision-making process. Highlight the positive impact your timely intervention had on project compliance.

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What is your experience with DeltaV control systems?

Be prepared to discuss any hands-on experience you've had with DeltaV systems, including specific projects and your role in ensuring system validation. Knowledge of this specific technology will be a plus in any interview for a Senior CSV Engineer position.

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Can you provide an example of a successful risk assessment you've conducted?

Describing a past risk assessment, detail the methodologies you used, the stakeholders involved, and how your assessment helped mitigate risks that could affect project success. Include any compliance reports generated from this process.

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How do you handle vendor interactions and deliverable tracking?

Discuss your communication skills and methodologies for maintaining clear expectations with vendors. Explain how you keep track of deliverables through regular updates and compliance documentation that keeps everyone informed and accountable.

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What steps do you take to ensure that documentation meets quality and regulatory standards?

Highlight your systematic approach to documentation, including thorough reviews, collaborative input from team members, and adherence to industry regulations, showcasing how you prioritize quality assurance in your work.

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How do you stay informed about changes in regulatory requirements in the life sciences field?

Showcase your commitment to continuous learning by discussing resources you follow, professional networks you are part of, and any certifications you pursue that help you keep up-to-date with regulatory changes and trends.

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What do you find most rewarding about working as a Senior CSV Engineer?

Reflect on your passion for ensuring compliance and improving processes in life sciences projects, emphasizing how making a positive impact on healthcare outcomes keeps you motivated and engaged in your work.

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We enable life sciences clients to improve lives.

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Full-time, hybrid
DATE POSTED
January 15, 2025

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