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120 jobs near Columbus, OH

Diamond Mowers, LLC

$100 - $140/hr

Senior Validation Engineer Full Time Regular Non COGS Sioux Falls, SD, US 8 days ago Requisition ID: 1510 Senior Validation Engineer Position Summary This is not a remote position, you will be ...

INCOG

Senior Validation Engineer

Fishers, IN

The Senior Validation Engineer is a key individual contributor role within the INCOG BioPharma Validation Department. The Senior Validation Engineer is responsible for understanding and implementing ...

Fujifilm

Sr. Validation Engineer

College Station, TX · On-site

Position Overview Sr. Validation Engineer for FUJIFILM Diosynth Biotechnologies Texas, LLC, located in College Station, TX. Company Overview The work we do at FUJIFILM Biotechnologies Texas has never ...

Fujifilm

Sr. Validation Engineer

College Station, TX

Position Overview Sr. Validation Engineer for FUJIFILM Diosynth Biotechnologies Texas, LLC, located in College Station, TX. Company Overview The work we do at FUJIFILM Biotechnologies Texas has never ...

Fujifilm

Sr. Validation Engineer

College Station, TX · On-site

Sr. Validation Engineer for FUJIFILM Diosynth Biotechnologies Texas, LLC, located in College Station, TX. The work we do at FUJIFILM Biotechnologies Texas has never been more important--and we are ...

FUJIFILM Biotechnologies

College Station, TX. Sr. Validation Engineer for FUJIFILM Diosynth Biotechnologies Texas, LLC, located in College Station, TX. Responsible for providing scientific and technical support of product ...

Alcami Corporation

Sr. Validation Engineer

Pepperell, MA · On-site

$43.27 - $53.49/hr

The Sr. Validation Engineer will execute protocols for Installation, Operational and Performance Qualification testing on chambers and rooms including: autoclaves, cryo-freezers, cold rooms ...

Compli

Senior Validation Engineer

Milwaukee, WI · On-site

Senior Validation Engineer Location : Milwaukee, WI. Lead Projects. Inspire Teams. Build What Matters. We serve pharmaceutical companies across the United States, offering a vast array of services ...

New

Syner-G

Sr. Validation Engineer

Raleigh, NC

The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...

Netpace, Inc.

Sr Validation Engineer

Foster City, CA · On-site

Sr Validation Engineer who has a solid experience on laboratory instrumentation as well as CSV. * Responsible for planning, scheduling, and executing validation efforts for LabX system. * Ensures ...

GBA Companies

Senior Validation Engineer

Milwaukee, WI · On-site

Senior Validation Engineer Location : Milwaukee, WI. Lead Projects. Inspire Teams. Build What Matters. We serve pharmaceutical companies across the United States, offering a vast array of services ...

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Senior Validation Engineer

Sterling Engineering Inc.

Greenville, NC • On-site

$75/hr

Contractor

Medical, Dental, Vision, Retirement, PTO

This job post has expired 6 days ago. Applications are no longer accepted.

Job description

Job Title: Senior Validation Engineer (Revalidation/Requalification)
Location: Greenville, NC (Onsite)
Hire Type: 6-Month Contract-to-Hire
Target Pay Rate: $75.00/hour (W2)
Benefits: PTO, paid holidays, BCBS medical plans, dental/vision plans, 401(k), & ESOP
Additional Benefits:
  1. Opportunity for long-term employment through contract-to-hire conversion
  2. Opportunity to support a leading pharmaceutical manufacturing organization
  3. Work within a highly regulated aseptic manufacturing environment
Job Summary:
Seeking a Senior Validation Engineer with Revalidation/Requalification experience to support aseptic manufacturing validation activities within a highly regulated pharmaceutical environment. This role will serve as a subject matter expert (SME) supporting revalidation and requalification activities for critical manufacturing systems and equipment. The ideal candidate will have extensive experience in aseptic manufacturing validation, including hands-on expertise with autoclaves, isolators, sterilization-in-place (SIP) systems, and validation lifecycle activities. The Senior Validation Engineer will work closely with Quality, Manufacturing, Engineering, and Validation teams to ensure equipment and processes remain compliant with cGMP, FDA, and global regulatory requirements.
Must Have Skills:
  • Bachelor's degree in Engineering, Life Sciences, or related technical discipline
  • 10+ years of aseptic manufacturing validation experience
  • Extensive experience with revalidation and requalification activities
  • Strong expertise with:
    • Autoclave validation
    • Isolator validation
    • Sterilization-in-place (SIP) systems
    • Equipment qualification and lifecycle management
    • Validation protocols and reports
    • cGMP and FDA regulatory requirements
    • Strong technical writing and documentation skills
    • Ability to work independently as a validation subject matter expert
Job Duties:
  • Lead and support revalidation and requalification activities for aseptic manufacturing equipment and systems.
  • Develop, execute, and review validation protocols, qualification documents, and final reports.
  • Provide SME support for autoclave, isolator, and SIP validation activities.
  • Evaluate validation requirements related to equipment changes, process updates, and lifecycle management.
  • Partner with Engineering, Manufacturing, Quality Assurance, and Validation teams to ensure successful execution of validation activities.
  • Support deviation investigations, risk assessments, and corrective/preventive actions (CAPAs).
  • Ensure validation activities comply with cGMP, FDA, and applicable regulatory standards.
  • Maintain accurate validation documentation and support audit and inspection readiness.
Qualifications:
  • Bachelor's degree in Engineering, Life Sciences, or related technical field
  • 10+ years of validation experience within pharmaceutical or biotechnology manufacturing
  • Proven experience supporting aseptic processing and sterile manufacturing environments
  • Deep knowledge of equipment qualification and requalification processes
  • Experience with autoclaves, isolators, and SIP systems required
  • Strong understanding of validation lifecycle principles and regulatory expectations
  • Excellent communication, organization, and problem-solving skills


Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.