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Senior CSV Engineer/Analyst - Senior Validation Engineer 5245

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 5245, Verista

Join Verista as a Senior CSV Engineer/Analyst and be part of a dedicated team where your contributions truly matter! At Verista, we believe in empowering growth and fostering innovation within the life sciences community. As a Senior CSV Engineer, you will play a crucial role in ensuring that computer systems are compliant and validated for a cutting-edge cell therapy manufacturing project. You'll be responsible for developing and executing comprehensive validation protocols, collaborating closely with automation teams, and overseeing necessary documentation to ensure it meets stringent regulatory standards. Working in a fast-paced environment, your analytical skills and attention to detail will help drive the success of critical projects. If you’re passionate about making an impact and want to work within a supportive team that values growth and collaboration, Verista is the perfect place for you! Not only do we provide a competitive salary and benefits, but we also encourage a fun and inclusive culture that respects and engages every team member. Your expertise in Computer System Validation and your experience within a GMP-regulated environment will shine here. If you're looking to advance your career in a place where you can learn and grow, we invite you to apply!

Frequently Asked Questions (FAQs) for Senior CSV Engineer/Analyst - Senior Validation Engineer 5245 Role at Verista
What responsibilities does a Senior CSV Engineer/Analyst have at Verista?

As a Senior CSV Engineer at Verista, you will be responsible for developing and executing Computer System Validation protocols, which include Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). You will collaborate closely with various teams to ensure regulatory compliance, manage document lifecycles, conduct risk assessments, and oversee vendor interactions to ensure all systems meet project needs.

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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 role at Verista, candidates must possess a Bachelor’s degree in a relevant field such as Engineering, Computer Science, or Life Sciences and have at least 5 years of experience in Computer System Validation within a GMP-regulated environment. Strong knowledge of regulatory requirements and experience with DeltaV control systems are also essential.

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How does Verista support employee growth as a Senior CSV Engineer?

Verista values continuous learning and supports employee growth through various initiatives, including a tuition reimbursement policy, access to training resources, and a collaborative work environment. As a Senior CSV Engineer, you will have the opportunity to enhance your skills while working alongside a talented team committed to making a difference in the life sciences sector.

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What can I expect regarding the work culture at Verista as a Senior CSV Engineer?

At Verista, the work culture is people-focused, emphasizing empowerment, support, and respect. As a Senior CSV Engineer, you will work in an inclusive environment where ideas are valued, and individuals are encouraged to learn from experiences. The company also promotes team-building activities and recognizes employee contributions regularly.

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What kind of challenges will I face as a Senior CSV Engineer/Analyst at Verista?

As a Senior CSV Engineer/Analyst at Verista, you will face challenges that include ensuring robust compliance with regulatory standards, managing complex documentation processes, and driving project tasks effectively. Your capacity to make independent decisions while collaborating with various teams will be critical in navigating these challenges successfully.

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Common Interview Questions for Senior CSV Engineer/Analyst - Senior Validation Engineer 5245
Can you explain your experience with Computer System Validation in a GMP environment?

Highlight specific projects or systems you have validated, focusing on your role and responsibilities. Discuss your understanding of regulatory requirements and any protocols you've developed, such as IQ, OQ, or PQ.

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How do you manage document lifecycle in compliance with industry standards?

Discuss your methods for creating, revising, and archiving documents, emphasizing your familiarity with validation documentation systems and compliance measures that ensure accuracy and accessibility.

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What steps do you take to conduct risk assessments for validation projects?

Outline your approach to identifying potential risks and the tools you use to analyze and mitigate these risks. Emphasize the importance of thorough checks and communication with relevant stakeholders.

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Describe a time when you had to resolve a significant compliance issue?

Provide a specific example where you successfully identified and corrected a compliance issue, detailing the process and the outcome, as well as any lessons learned from the experience.

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How do you ensure effective communication within an integrated project team?

Discuss your communication strategies, including regular updates, documentation practices, and how you facilitate meetings or discussions to keep everyone aligned on project goals.

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What experiences do you have with DeltaV control systems?

Elaborate on your hands-on experiences with DeltaV systems, including specific projects where you utilized them, your understanding of their functions, and any challenges you overcame regarding their validation.

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How do you prioritize tasks when managing multiple validation projects simultaneously?

Share your prioritization techniques, such as using project management tools or methodologies, and how you assess which tasks need immediate attention based on project deadlines and requirements.

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What are the most critical regulatory compliance standards you need to be aware of as a Senior CSV Engineer?

Mention key regulations such as FDA, cGMP, and any other relevant standards. Discuss your familiarity with these standards and how they impact your validation work.

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How do you handle vendor interactions during the validation process?

Detail your approach to managing vendor relationships, including how you perform reviews, track deliverables, and ensure that vendors meet project specifications effectively.

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What tools and software do you find essential in Computer System Validation?

Discuss specific tools and software you have experience with, such as document management systems or validation software, highlighting how they enhance your efficiency and compliance during validation processes.

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We enable life sciences clients to improve lives.

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Full-time, hybrid
DATE POSTED
December 13, 2024

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