Sokol Materials & Services
CQV Validation Engineer Senior-Level
Sokol Materials & Services, Skillman, New Jersey, us, 08558
CQV Validation Engineer Senior-Level
Apply Now (https://forms.monday.com/forms/3cdf5bfb73703e4a3aa29c55653510f4?r=use1)
Job Type
Validation Engineer
Workspace
On-site position (no remote or hybrid options)
Target Hiring Date
January 2025
Salary
$50-60 Per Hour
Work Authorization
Applicants must have the legal right to work in the United States without requiring sponsorship. Corp-to-Corp (C2C) arrangements are not accepted.
Requirements
Education and Experience :
Bachelor's degree in Engineering , Science, or a related field is preferable; an advanced degree is preferred.
Minimum of 7 years of CQV experience in pharmaceutical, biotechnology, cell therapy, or medical device industries, with at least 5 years focused on utilities and facility qualification.
Strong understanding of validation principles, methodologies, and regulatory requirements, including FDA, EMA, and ICH guidelines.
Knowledge, Skills & Abilities:
Proficient in risk-based validation approaches.
Strong analytical, problem-solving, and communication skills.
Ability to work effectively in team settings and collaborate with cross-functional teams.
Physical Requirements :
Prolonged periods of sitting and computer use.
Must be able to lift up to 15 pounds occasionally.
About the Role
As a Senior-Level Validation Engineer at Sokol GxP Services, you will be instrumental in commissioning, qualifying, and validating laboratory equipment, facility systems, and utilities at multi-use sites. Collaborating with internal teams and external service providers, you will ensure that critical CQV activities align with regulatory standards and best practices. This role requires a professional with analytical acumen, problem-solving expertise, and the ability to work seamlessly with cross-functional teams.
Supervisory Responsibilities: None.
DUTIES / RESPONSIBILITIES
Develop and execute CQV protocols for equipment, facility systems, and utilities, covering Commissioning, Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
Conduct comprehensive risk assessments and impact analyses to ensure validation accuracy and compliance.
Collaborate with cross-functional teams to coordinate and manage CQV activities.
Develop and maintain CQV documentation, including plans, test protocols, summary reports, and traceability matrices, ensuring technical accuracy and compliance with regulatory requirements.
Investigate and resolve deviations encountered during qualification/validation, working with stakeholders to identify root causes and implement corrective actions.
Provide guidance on qualification/validation principles, requirements, and best practices to internal stakeholders.
Stay up-to-date with regulatory guidelines, industry trends, and best practices related to validation and quality assurance.
About the Company
Join Sokol GxP Services – Where Innovation Meets Integrity!
Join Sokol GxP Services, where we partner with leading pharmaceutical and biotech companies to provide exceptional Commissioning, Qualification, and Validation (CQV) services. We are committed to fostering diversity, empowering local talent, and building strong community connections to bring the best-qualified candidates to our clients in the Summit, NJ area. Our inclusive and collaborative culture promotes growth and innovation, offering competitive health benefits, PTO, holiday pay, volunteer hours, a relocation budget*, a 401K** program, and professional development opportunities. Plus, take advantage of our Employee Referral program! Be part of a dynamic team with fantastic opportunities for growth and professional development!
Let’s shape the future of life sciences together!
All applicants will receive an acknowledgement that their application has been received within 2-3 weeks from the from the date of receipt.
Equal Opportunity Employer Statement:
Sokol GxP Services is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
*Relocation support will be determined on a case-by-case basis.
**Our 401K program is set to launch in the 2025 fiscal year.
By submitting your application and resume, you consent to have your information retained in our repository for six months. This allows us to consider you for future opportunities that may align more closely with your skills and qualifications. If a suitable position becomes available, we will contact you directly.
Apply Now (https://forms.monday.com/forms/3cdf5bfb73703e4a3aa29c55653510f4?r=use1)
Job Type
Validation Engineer
Workspace
On-site position (no remote or hybrid options)
Target Hiring Date
January 2025
Salary
$50-60 Per Hour
Work Authorization
Applicants must have the legal right to work in the United States without requiring sponsorship. Corp-to-Corp (C2C) arrangements are not accepted.
Requirements
Education and Experience :
Bachelor's degree in Engineering , Science, or a related field is preferable; an advanced degree is preferred.
Minimum of 7 years of CQV experience in pharmaceutical, biotechnology, cell therapy, or medical device industries, with at least 5 years focused on utilities and facility qualification.
Strong understanding of validation principles, methodologies, and regulatory requirements, including FDA, EMA, and ICH guidelines.
Knowledge, Skills & Abilities:
Proficient in risk-based validation approaches.
Strong analytical, problem-solving, and communication skills.
Ability to work effectively in team settings and collaborate with cross-functional teams.
Physical Requirements :
Prolonged periods of sitting and computer use.
Must be able to lift up to 15 pounds occasionally.
About the Role
As a Senior-Level Validation Engineer at Sokol GxP Services, you will be instrumental in commissioning, qualifying, and validating laboratory equipment, facility systems, and utilities at multi-use sites. Collaborating with internal teams and external service providers, you will ensure that critical CQV activities align with regulatory standards and best practices. This role requires a professional with analytical acumen, problem-solving expertise, and the ability to work seamlessly with cross-functional teams.
Supervisory Responsibilities: None.
DUTIES / RESPONSIBILITIES
Develop and execute CQV protocols for equipment, facility systems, and utilities, covering Commissioning, Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
Conduct comprehensive risk assessments and impact analyses to ensure validation accuracy and compliance.
Collaborate with cross-functional teams to coordinate and manage CQV activities.
Develop and maintain CQV documentation, including plans, test protocols, summary reports, and traceability matrices, ensuring technical accuracy and compliance with regulatory requirements.
Investigate and resolve deviations encountered during qualification/validation, working with stakeholders to identify root causes and implement corrective actions.
Provide guidance on qualification/validation principles, requirements, and best practices to internal stakeholders.
Stay up-to-date with regulatory guidelines, industry trends, and best practices related to validation and quality assurance.
About the Company
Join Sokol GxP Services – Where Innovation Meets Integrity!
Join Sokol GxP Services, where we partner with leading pharmaceutical and biotech companies to provide exceptional Commissioning, Qualification, and Validation (CQV) services. We are committed to fostering diversity, empowering local talent, and building strong community connections to bring the best-qualified candidates to our clients in the Summit, NJ area. Our inclusive and collaborative culture promotes growth and innovation, offering competitive health benefits, PTO, holiday pay, volunteer hours, a relocation budget*, a 401K** program, and professional development opportunities. Plus, take advantage of our Employee Referral program! Be part of a dynamic team with fantastic opportunities for growth and professional development!
Let’s shape the future of life sciences together!
All applicants will receive an acknowledgement that their application has been received within 2-3 weeks from the from the date of receipt.
Equal Opportunity Employer Statement:
Sokol GxP Services is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
*Relocation support will be determined on a case-by-case basis.
**Our 401K program is set to launch in the 2025 fiscal year.
By submitting your application and resume, you consent to have your information retained in our repository for six months. This allows us to consider you for future opportunities that may align more closely with your skills and qualifications. If a suitable position becomes available, we will contact you directly.