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5697 - Sr. Systems Validation Specialist / Lead Validation Engineer

Verista

West Point (AL)

On-site

USD 87,000 - 137,000

Full time

21 days ago

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Job summary

A leading company in the pharmaceutical industry is seeking a Senior Systems Validation Specialist to promote quality and operational excellence. This full-time role at the West Point site involves managing validation tasks, mentoring junior scientists, and ensuring compliance in a GMP environment. The position requires strong metrology expertise and project leadership skills, with a focus on creating life-changing medicines. Competitive salary and comprehensive benefits are offered.

Benefits

Competitive pay
Performance incentives
Comprehensive insurance
401(k)
Paid time off
Tuition reimbursement

Qualifications

  • 5-7 years with M.S. or 7-10 years with B.S. in relevant field.
  • Experience with Computer System Validation and GMP audits.

Responsibilities

  • Manage project plans for validation tasks.
  • Oversee laboratory equipment maintenance and qualification.
  • Support internal and external audits.

Skills

Metrology
Project Leadership
Communication
Problem Solving

Education

M.S.
B.S.

Job description

5697 - Sr. Systems Validation Specialist / Lead Validation Engineer

Join to apply for the 5697 - Sr. Systems Validation Specialist / Lead Validation Engineer role at Verista.

Job Overview

The Senior Systems Validation Specialist will work within the Global Quality Large Molecule Analytical Science (GQLMAS) group, promoting quality and operational excellence across labs in West Point and North Wales. The role involves supporting the maintenance and qualification of analytical equipment in GMP and non-GMP environments, working independently and with teams, and collaborating with scientific and technical staff to create life-changing medicines.

Responsibilities
  • Manage project plans for metrology and validation tasks, ensuring alignment with goals and timelines.
  • Provide strategic direction in metrology, mentor junior scientists, and oversee daily assignments.
  • Collaborate with internal teams and external partners to ensure compliance and operational excellence.
  • Oversee laboratory equipment maintenance and qualification.
  • Support internal and external audits, maintaining inspection readiness.
Qualifications
  • M.S. with 5-7 years or B.S. with 7-10 years of relevant experience.
  • Extensive metrology expertise and understanding of measurement principles.
  • Experience with instrument Computer System Validation and supporting GMP audits.
  • Knowledge of GMP policies, pharmaceutical compliance, change, and deviation management.
  • Proven project leadership, teamwork, and problem-solving skills.
  • Excellent communication skills; PMP certification preferred.
Additional Details

This is a full-time, on-site role at the West Point (North Wales), PA site.

Salary range (US): $87,780—$136,225 USD, dependent on experience and other factors.

Benefits
  • Competitive pay, performance incentives, comprehensive insurance, 401(k), paid time off, tuition reimbursement, and more.
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