Overview
On Site
USD 85.00 - 90.00 per hour
Contract - W2
Skills
ELC
Research and Development
Documentation
GDP
Writing
Risk Assessment
Regulatory Affairs
Test Plans
Reporting
Computer Science
Information Technology
Chemical Engineering
Biomedical Engineering
GAMP
GxP
Life Sciences
Computerized System Validation
Management
Reasoning
Analytical Skill
Conflict Resolution
Problem Solving
Data Integrity
Software Development
Project Scoping
Pharmaceutics
Regulatory Compliance
Communication
Leadership
Collaboration
Positive Attitude
Agile
MEAN Stack
Customer Service
Training And Development
SAP BASIS
Job Details
Software Guidance & Assistance, Inc., (SGA), is searching for an CSA Validation Subject Matter Expert (SME) for a RIGHT TO HIRE assignment with one of our premier Beauty clients in LIC , New York.
Responsibilities :
The CSA Validation SME is a key stakeholder in the ELC CSA Center of Excellence (COE). The primary function of this role is to ensure the integrity of CSA projects, with an eye to assessing risk and ensuring integrity. Their responsibilities serve as a key conduit between the COE leadership and the protocol author(s) and tester(s). The CSA Validation SME will ensure validation projects meet regulatory and data integrity requirements, and they will confirm validation projects meet R&D/GSC/IT policies.
Responsibilities:
Provide insight and expertise on validation project risk and complexity
Maintain validation best practices
Gather project information from system owner(s)
Collaborate with the Business Analyst on a frequent basis
Maintain compliance with Good Documentation Practices (GDP)
Aid in writing and reviewing of reports summarizing system CSA validation execution
Collect feedback from System Owner(s) on deliverables
Draft and execute of GxP Assessment, Risk Assessment (RA), Validation Plan (VP), Test Plan (TP), and Validation Summary Report (VSR) as necessary
Draft, review, and execute other validation documents when necessary
Qualifications:
Bachelor's Degree in Computer Science, Information Technology, Chemical Engineering, Biomedical Engineering, or related degree
7-10+ years of successful, progressive experience with Computer System Validation and Computer Software Assurance
Aptitude in GAMP 5 and 21 CFR Part 11 standards
Previous experience in a GxP industry or a life sciences industry is required
Technical competency in FDA regulations
Expertise in generating, reviewing, and addressing CAPAs
Strong written and verbal communication skills
Strong ability to collaborate with the team
Ability to work self-directed in the timely completion of project deliverables
Practical experience with Data Integrity and ALCOA+ is a plus
Demonstrated Competencies:
Technical Competency - Develop an understanding of business requirements and work to translate the business requirements to the necessary CSV documents and supporting materials
Time Management - Able to follow strict deadlines, prioritize tasks, and work well under pressure
Analytical Skills - Identifies, researches, and demonstrates logical reasoning to communicate critical information
Agility - Meets objectives by responding to competing and changing priorities and multiple tasks under inflexible timelines
Strong written and verbal communication skills
Strong ability to communicate with other COE team members
Strong analytical and problem-solving abilities
Understands the purpose of CSA, is passionate about customer safety, data integrity, and product quality
Adept at solution development and project scoping
Effectively collaborate with peers, cross-functional teams, and departments
Strong technical background is preferred
Must Have:
Extensive experience in the Medical, Pharma or Regulatory Compliance Industries
Strong CSA experience as they will be acting as the SME
Must have good communication and leadership skills, collaboration skills, must have a positive attitude and be easy to work with
Agile experience/knowledge highly preferred.
SGA is a technology and resource solutions provider driven to stand out. We are a women-owned business. Our mission: to solve big IT problems with a more personal, boutique approach. Each year, we match consultants like you to more than 1,000 engagements. When we say let's work better together, we mean it. You'll join a diverse team built on these core values: customer service, employee development, and quality and integrity in everything we do. Be yourself, love what you do and find your passion at work. Please find us at .
SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or Other Legally Protected Status. We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, and our services, programs, and activities. Please visit our company to request an accommodation or assistance regarding our policy.
#LI-JM1
Responsibilities :
The CSA Validation SME is a key stakeholder in the ELC CSA Center of Excellence (COE). The primary function of this role is to ensure the integrity of CSA projects, with an eye to assessing risk and ensuring integrity. Their responsibilities serve as a key conduit between the COE leadership and the protocol author(s) and tester(s). The CSA Validation SME will ensure validation projects meet regulatory and data integrity requirements, and they will confirm validation projects meet R&D/GSC/IT policies.
Responsibilities:
Provide insight and expertise on validation project risk and complexity
Maintain validation best practices
Gather project information from system owner(s)
Collaborate with the Business Analyst on a frequent basis
Maintain compliance with Good Documentation Practices (GDP)
Aid in writing and reviewing of reports summarizing system CSA validation execution
Collect feedback from System Owner(s) on deliverables
Draft and execute of GxP Assessment, Risk Assessment (RA), Validation Plan (VP), Test Plan (TP), and Validation Summary Report (VSR) as necessary
Draft, review, and execute other validation documents when necessary
Qualifications:
Bachelor's Degree in Computer Science, Information Technology, Chemical Engineering, Biomedical Engineering, or related degree
7-10+ years of successful, progressive experience with Computer System Validation and Computer Software Assurance
Aptitude in GAMP 5 and 21 CFR Part 11 standards
Previous experience in a GxP industry or a life sciences industry is required
Technical competency in FDA regulations
Expertise in generating, reviewing, and addressing CAPAs
Strong written and verbal communication skills
Strong ability to collaborate with the team
Ability to work self-directed in the timely completion of project deliverables
Practical experience with Data Integrity and ALCOA+ is a plus
Demonstrated Competencies:
Technical Competency - Develop an understanding of business requirements and work to translate the business requirements to the necessary CSV documents and supporting materials
Time Management - Able to follow strict deadlines, prioritize tasks, and work well under pressure
Analytical Skills - Identifies, researches, and demonstrates logical reasoning to communicate critical information
Agility - Meets objectives by responding to competing and changing priorities and multiple tasks under inflexible timelines
Strong written and verbal communication skills
Strong ability to communicate with other COE team members
Strong analytical and problem-solving abilities
Understands the purpose of CSA, is passionate about customer safety, data integrity, and product quality
Adept at solution development and project scoping
Effectively collaborate with peers, cross-functional teams, and departments
Strong technical background is preferred
Must Have:
Extensive experience in the Medical, Pharma or Regulatory Compliance Industries
Strong CSA experience as they will be acting as the SME
Must have good communication and leadership skills, collaboration skills, must have a positive attitude and be easy to work with
Agile experience/knowledge highly preferred.
SGA is a technology and resource solutions provider driven to stand out. We are a women-owned business. Our mission: to solve big IT problems with a more personal, boutique approach. Each year, we match consultants like you to more than 1,000 engagements. When we say let's work better together, we mean it. You'll join a diverse team built on these core values: customer service, employee development, and quality and integrity in everything we do. Be yourself, love what you do and find your passion at work. Please find us at .
SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or Other Legally Protected Status. We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, and our services, programs, and activities. Please visit our company to request an accommodation or assistance regarding our policy.
#LI-JM1
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.