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VALIDATION - Validation Specialist

ECLARO

Lawrenceville, NJ

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JOB DETAILS
SALARY
$81.05–$85.96 Per Hour
SKILLS
Analysis Skills, Artificial Intelligence (AI), Atlassian JIRA, Best Practices, Biology, Biotech and Pharmaceutical, Change Control, Chemistry, Communication Skills, Computer Systems, Control Systems, Cross-Functional, Data Quality, Dental Insurance, Detail Oriented, Diversity, Document Management, Documentation, Documentation Review, English Language, FDA (Food and Drug Administration), FDA Requirements, Failure Mode and Effects Analysis (FMEA), GLP (Good Laboratory Practices), GMP (Good Manufacturing Practices), Genetics, GxP, Healthcare, ICH Regulations, IT Service Management (ITSM), Information Technology & Information Systems, Interpersonal Skills, Interviewing Skills, Manufacturing, Manufacturing Requirements, Medical Products, Microsoft Office, Microsoft SharePoint, Microsoft Visio, Multicultural, Organizational Skills, Presentation/Verbal Skills, Quality Assurance, Quality Control, Quality Management, Regulations, Regulatory Compliance, Risk Analysis, ServiceNow, Software Development Lifecycle (SDLC), Standard Operating Procedures (SOP), System Validation, Team Player, Technical Writing, Validation Plan, Vision Plan, Writing Skills
LOCATION
Lawrenceville, NJ
POSTED
3 days ago
Validation Specialist
Job Number: 26-00778
 
Be part of a company that delivers life-changing healthcare solutions. ECLARO is looking for a Validation Specialist for our client in Lawrenceville, NJ. 
 
ECLARO’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!
 
Position Overview:
  • This role will focus on the Computer System Validation (CSV) activities for enterprise GxP systems, specifically for a critical set of projects in the Cell Therapy functional area.
  • This role will be supporting validation leads to help ensure the required deliverables and testing are complete according to the Client CSV SOP.
  • Effective communication is key across a multi-functional team consisting of Business, IT, and Quality personnel.
  • Experience with current digital validation tools is required, use of AI as an accelerator is a plus.
  • Overall a solid CSV background and having a strong work ethic in an aggressive project setting will be key to being successful in this role.
 
Responsibilities:
  • 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.
 
Required Qualifications:
  • Bachelor's degree in Engineering, Pharmaceutical Sciences, Chemistry, Biology, or a related scientific or technical discipline
  • 8–10+ years of experience in pharmaceutical, biotechnology, or regulated manufacturing environments
  • 5+ years of experience in Data Integrity/ALCOA+ principles
  • 5+ years of experience with CSA principles
  • 5+ years of experience with technical writing
  • Working knowledge of GMP, GLP, and GAMP 5 principles
  • Strong understanding of FDA regulations, ICH guidelines, and EU Annex 11 (as applicable)
  • Experience developing, executing, and reviewing:
    • Validation protocols and reports
    • Risk assessments (FMEA, impact assessments)
    • SOPs, deviation investigations, and CAPAs
  • Ability to support regulatory inspections and audits (FDA, EMA, internal, or client audits)
  • Strong technical writing skills with attention to detail and data integrity
  • Proficiency with common pharmaceutical documentation systems and tools (e.g., EDMS, change control systems)
  • Excellent organizational, communication, and cross functional collaboration skills
  • 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.
 
Pay Rate: $81.05-$85.96/Hour
 
If hired, you will enjoy the following ECLARO Benefits:
  • 401k Retirement Savings Plan administered by Merrill Lynch
  • Commuter Check Pretax Commuter Benefits
  • Eligibility to purchase Medical, Dental & Vision Insurance through ECLARO
 
If interested, you may contact:
Paul Quibuyen
Christian.Quibuyen@eclaro.com
6466952942
Paul Quibuyen | LinkedIn
 
Equal Opportunity Employer: ECLARO values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status, in compliance with all applicable laws.
 

About the Company

E

ECLARO

Eclaro is a Business and Technology Consulting Firm that connects top talent with opportunities nationwide. We have direct access to Hiring Managers from leading Fortune 1000 organizations in almost every industry segment, with particular expertise in:

• Technology and Business Consulting
• Financial Services and Insurance
• Pharmaceuticals and Life Sciences
• Consumer Products, Public Sector, and Utilities

Eclaro provides fully customizable, comprehensive talent acquisition and management of seasoned professionals through a number of business models, including:

• Consulting
• Professional Hiring
• Global Integrated Delivery™
• Managed Services

Eclaro recruits and manages a staff of highly skilled individuals in an array of specialized disciplines enabling our clients to leverage new opportunities, respond to increased and changing demands, and increase their profitability.

Eclaro’s Management Team averages over 25 years of experience in partnering with clients in technical, corporate operations and human capital solutions. We hold ISO 9001:2008 certification and have achieved SOC 2 Type 2 certification in Security, Availability and Confidentiality. Eclaro’s decades of expertise and collaborative practice have proven that The Right People are The Answer.

COMPANY SIZE
500 to 999 employees
INDUSTRY
Staffing/Employment Agencies
FOUNDED
1999
WEBSITE
http://www.eclaroit.com