Validation Lead CaaS Engagement
Job
Sikich LLC
Princeton, NJ (In Person)
Full-Time
Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
76
out of 100
Average of individual scores
Skill Insights
Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.
Job Description
Validation Lead CaaS Engagement Sikich LLC paid time off, paid holidays, sick time, tuition reimbursement, flex time, 401(k) United States, Jersey, Princeton May 05, 2026 Description Valuation Lead CaaS Engagement
What to expect when you join Sikich
Team members at Sikich have a lot in common while also being part of a rich and varied group of contributors, creating a distinct and thriving culture. Chief among our commonalities is a desire for growth and a shared unity of purpose in our professional lives. We believe that through diverse perspectives, challenging the status quo and rewarding action, we accelerate innovation and drive growth
- for our clients, for ourselves and for our communities.
About This Role:
The Validation is responsible for leading and managing software implementation and development projects, executing and guiding IT Quality, validation, and compliance service engagements in the Life Sciences industry. This role involves working with clients to implement new computerized systems, upgrades, and enhancements, while providing subject matter expertise in computer system validation (CSV) and Computer Software Assurance (CSA) and ensuring compliance with regulatory standards. Experience with current digital validation tools is required, use of AI as an accelerator is a plus. Overall, a solid CSV background and a strong work ethic in an aggressive project setting will be key to being successful in this role.Essential Job Duties:
Support creation, review, and approval of all CSV deliverables for custom in-house solutions. Maintain close communication with stakeholders and team members to keep apprised of CSV needs, interpretation of requirements, impacts on compliance of an application, project status, and other relevant issues Ability to create documents to an existing document standard Obtain and respond to review by Business, IT, and Quality stakeholders Follow SOPs and industry best practices Advanced knowledge of complete MS Office suite and Visio. Firm understanding of technology platforms as needed for project. Experience with electronic document management systems (e.g. Qumas, SharePoint etc.); application development and lifecycle management (e.g. ALM, JIRA, etc.); and IT service management systems (e.g. ServiceNow) Excellent oral and written communication skills in English. Strong expertise and ability to interview and accurately interpret communication requirements of team members. Familiarity with using AI as an accelerator for creation and review of documents and testing.Key Competency Requirements:
Cross-functional experience in one or more regulated areas (i.e. Research, Analytical/QC, QA, Engineering, Manufacturing, Regulatory, IT etc.) is desired. Ability to provide innovative ideas to improve quality and compliance that create value including seeking new information and external insights. Excellent interpersonal skills, including written and verbal communication. Strong sense of ethics, diplomacy and discretion. Commitment to Quality. Strong critical thinking to analyze complex situations and discern critical issues. Able to work effectively with highly-matrixed and multi-cultural workforce and build strong relationships by being transparent, reliable and delivering on commitments. Excellent team player attitude. Ability to manage competing priorities.Knowledge, Skills, and Abilities:
Bachelor's degree in a related field or equivalent experience. 12+ years of experience in software validation/testing in regulated environments. 10+ years of experience in CSV/CSA and GAMP 5 risk-based validation in FDA or EMA regulated environments. Excellent understanding of GAMP 5 Risk-Based Validation Approach. Strong understanding of Risk Assessment and Data Integrity Principles. Knowledge of 21 CFR Part 11 and EU Annex 11 compliance. Detail-oriented with best practices in testing and documentation in Life Sciences. Excellent documentation and communication skills. Must have hands-on validation experience on the following systems: TrackWise, TrackWise Digital, Salesforce, NetSuite, Emerson Syncade/DeltaV and Instruments/Equipment in Pharma/BioPharma. Must have hands-on experience on the followingVLMS:
Kneat, Veeva and ValGenesis Must have hands-on using Testing Management Testing tools such as: JIRA, HPALM, qTest and Azzure DevOps and Tricentis Tosca and Testim automated testing tool, is a plus. Must have experience managing validation activities to implement enterprise applications by engaging global cross-functional teams Experience with systems integrations and data migration/extraction to/from EQMS. Ability to quickly learn new technologies and product functionality. Experience withISO 9001, FDA 21CFR
Part 11, and EU Annex 11 compliance. Strong leadership, consulting, and interpersonal skills. Entrepreneurial nature with a strong sense of ownership. Strong problem-solving and analytical skills. Ability to manage competing priorities in a fast-paced team environment. Team player with strong collaboration skills. In addition, specific skills/experience required are as follows: Values driven- You embody and model absolute integrity and servant leadership and you have a bias for action and continuous innovation. Uncompromising problem solver
- You see opportunities in every business challenge and can develop, articulate and implement solutions. Collaboration
- You are a relationship builder across all levels of the organization and across all business units. Instills trust
- You do what you say, without ego, and you follow through on commitments consistently and credibly. Impact & influence
- Youare relentlessly focused on making a difference and can gainsupport for ideas, proposals and solutions.
- Sikich community volunteer program enabling each team member to use up to four hours of paid time annually to volunteer and make a difference in their localcommunities.
Similar remote jobs
Wells Fargo
Chandler, AZ
Posted2 days ago
Updated4 hours ago
Similar jobs in Princeton, NJ
Similar jobs in New Jersey
Hackensack Meridian Health
Brick Township, NJ
Posted2 days ago
Updated4 hours ago
Compass Group, North America
Jersey City, NJ
Posted2 days ago
Updated4 hours ago
Red Bank Regional High School
Little Silver, NJ
Posted2 days ago
Updated4 hours ago
AbbVie
Florham Park, NJ
Posted2 days ago
Updated4 hours ago
Intermountain Health
Trenton, NJ
Posted2 days ago
Updated4 hours ago