... validation protocols for facilities, utilities, and process equipment. * Oversee and review design ... Degree in Chemical, Mechanical, or Biochemical Engineering. * Minimum of 3 years of experience ...
61 Propharma Group Process Validation Engineer Jobs Hiring Near You
... validation protocols for facilities, utilities, and process equipment. * Oversee and review design ... Degree in Chemical, Mechanical, or Biochemical Engineering. * Minimum of 3 years of experience ...
The Impact You Will Make The Process Validation Engineer is a member of the Manufacturing Science & Technology (MS&T) organization responsible for supporting the development, execution, and lifecycle ...
The Impact You Will Make The Process Validation Engineer is a member of the Manufacturing Science & Technology (MS&T) organization responsible for supporting the development, execution, and lifecycle ...
The Impact You Will Make The Process Validation Engineer is a member of the Manufacturing Science & Technology (MS&T) organization responsible for supporting the development, execution, and lifecycle ...
The Impact You Will Make The Process Validation Engineer is a member of the Manufacturing Science & Technology (MS&T) organization responsible for supporting the development, execution, and lifecycle ...
The Impact You Will Make The Process Validation Engineer is a member of the Manufacturing Science & Technology (MS&T) organization responsible for supporting the development, execution, and lifecycle ...
The Impact You Will Make The Process Validation Engineer is a member of the Manufacturing Science & Technology (MS&T) organization responsible for supporting the development, execution, and lifecycle ...
The Impact You Will Make The Process Validation Engineer is a member of the Manufacturing Science & Technology (MS&T) organization responsible for supporting the development, execution, and lifecycle ...
The Impact You Will Make The Process Validation Engineer is a member of the Manufacturing Science & Technology (MS&T) organization responsible for supporting the development, execution, and lifecycle ...
The Impact You Will Make The Process Validation Engineer is a member of the Manufacturing Science & Technology (MS&T) organization responsible for supporting the development, execution, and lifecycle ...
The Impact You Will Make The Process Validation Engineer is a member of the Manufacturing Science & Technology (MS&T) organization responsible for supporting the development, execution, and lifecycle ...
Senior Process Validation Engineer Location: Raynham, MA (Onsite - Local candidates preferred) Type: Contract (1 year + long-term extensions) Industry: Medical Device Manufacturing | Supply Chain ...
Quick apply
Senior Process Validation Engineer Location: Raynham, MA (Onsite - Local candidates preferred) Type: Contract (1 year + long-term extensions) Industry: Medical Device Manufacturing | Supply Chain ...
Validation Engineer
Barceloneta, PR ยท On-site
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Perform process validation activities related to sterile manufacturing, including media fills (APS)
Validation Engineer
Barceloneta, PR ยท On-site
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Perform process validation activities related to sterile manufacturing, including media fills (APS)
Support process validation (IQ/OQ/PQ) and device master record (DMR) creation. 4. Stakeholder ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
Support process validation (IQ/OQ/PQ) and device master record (DMR) creation. 4. Stakeholder ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
Support on Executing other duties assigned by his Process Validation Lead & other supervisors Qualifications Knowledge and Skills: * Bachelor's degree in engineering * Experience in the Medical ...
Support on Executing other duties assigned by his Process Validation Lead & other supervisors Qualifications Knowledge and Skills: * Bachelor's degree in engineering * Experience in the Medical ...
Validation Engineer - Newaygo Area
$80K - $120K/yr
The Pivot Group Network, a West Michigan manufacturing-focused recruiting group, is committed to ... Develop and execute validation protocols (IQ, OQ, PQ) for equipment, processes, and software.
Validation Engineer - Newaygo Area
$80K - $120K/yr
The Pivot Group Network, a West Michigan manufacturing-focused recruiting group, is committed to ... Develop and execute validation protocols (IQ, OQ, PQ) for equipment, processes, and software.
Validation Engineer - DeWitt Area
$74K - $113K/yr
The Pivot Group Network, a West Michigan manufacturing-focused recruiting group, is committed to ... Support continuous improvement initiatives for validation processes and procedures. Recommended ...
Validation Engineer - DeWitt Area
$74K - $113K/yr
The Pivot Group Network, a West Michigan manufacturing-focused recruiting group, is committed to ... Support continuous improvement initiatives for validation processes and procedures. Recommended ...
Validation Engineer - Holt Area
$75K - $114K/yr
The Pivot Group Network, a West Michigan manufacturing-focused recruiting group, is dedicated to ... Develop and execute validation protocols for equipment, processes, and software. * Perform IQ, OQ ...
Validation Engineer - Holt Area
$75K - $114K/yr
The Pivot Group Network, a West Michigan manufacturing-focused recruiting group, is dedicated to ... Develop and execute validation protocols for equipment, processes, and software. * Perform IQ, OQ ...
Support process validation (IQ/OQ/PQ) and device master record (DMR) creation. 4. Stakeholder ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
Support process validation (IQ/OQ/PQ) and device master record (DMR) creation. 4. Stakeholder ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
Validation Engineer - Whitehall Area
Whitehall, MI ยท On-site
$77K - $117K/yr
The Pivot Group Network, a West Michigan manufacturing-focused recruiting group, is committed to ... Develop and execute validation protocols (IQ, OQ, PQ) for equipment, processes, and software.
Validation Engineer - Whitehall Area
Whitehall, MI ยท On-site
$77K - $117K/yr
The Pivot Group Network, a West Michigan manufacturing-focused recruiting group, is committed to ... Develop and execute validation protocols (IQ, OQ, PQ) for equipment, processes, and software.
Validation Engineer - Mattawan Area
$78K - $118K/yr
The Pivot Group Network, a West Michigan manufacturing-focused recruiting group, is dedicated to ... Process Validation Engineer, Equipment Validation Engineer, Software Validation Engineer, QC ...
Validation Engineer - Mattawan Area
$78K - $118K/yr
The Pivot Group Network, a West Michigan manufacturing-focused recruiting group, is dedicated to ... Process Validation Engineer, Equipment Validation Engineer, Software Validation Engineer, QC ...
Validation Engineer
Concord, NC ยท On-site
The Validation Engineer will be responsible for equipment qualification, process validation, utility validation, and cleaning validation activities to ensure compliance with FDA, cGMP, and industry ...
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Validation Engineer
Concord, NC ยท On-site
The Validation Engineer will be responsible for equipment qualification, process validation, utility validation, and cleaning validation activities to ensure compliance with FDA, cGMP, and industry ...
Validation Engineer - Jenison Area
$80K - $120K/yr
The Pivot Group Network, a West Michigan manufacturing-focused recruiting group, is dedicated to ... Develop and execute validation protocols (IQ, OQ, PQ) for equipment, processes, and software.
Validation Engineer - Jenison Area
$80K - $120K/yr
The Pivot Group Network, a West Michigan manufacturing-focused recruiting group, is dedicated to ... Develop and execute validation protocols (IQ, OQ, PQ) for equipment, processes, and software.
Engineer-Process Validation
Boulder, CO ยท On-site
The Process Validation Engineer will ensure consistent implementation of corporate and regulatory compliance of validation activities within a pharmaceutical manufacturing facility. Primary functions ...
Engineer-Process Validation
Boulder, CO ยท On-site
The Process Validation Engineer will ensure consistent implementation of corporate and regulatory compliance of validation activities within a pharmaceutical manufacturing facility. Primary functions ...
Regeneron is seeking a Process Controls & Validation Engineer to join our Process Sciences Drug Product Engineering department. Process Sciences is a technical services department that deals with a ...
Regeneron is seeking a Process Controls & Validation Engineer to join our Process Sciences Drug Product Engineering department. Process Sciences is a technical services department that deals with a ...
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Full-time
Re-posted 26 days ago
Job description
Responsibilities:
- Write and execute commissioning, qualification, & validation protocols for facilities, utilities, and process equipment.
- Oversee and review design and construction work related to cGMP manufacturing facility.
- Review submittals, IOM, control sequences, and start up procedures.
- Perform Walk Downs of As-Built P&IDs and Redlining P&IDs as required.
- Document and manage all punch lists and deviations.
- Write and review deviations, CAPAs, Change Controls, etc.
- Perform basic revisions as needed to accurately reflect current procedures.
- Must be able to wear appropriate cleanroom attire and all Personal Protective Equipment (PPE) i.e., scrubs, gowning coverall, masks, gloves, etc.
- Work in both an office and a manufacturing lab setting.
- Work in a lab setting with various chemical/biochemical exposures, including latex and bleach.
- Work in a cleanroom with biohazards, human blood components, and chemicals.
- Support project management initiatives to ensure efficient and timely progress.
- Additional relevant duties as needed.
- Degree in Chemical, Mechanical, or Biochemical Engineering.
- Minimum of 3 years of experience writing and executing CQV in the Pharmaceutical Industry.
- Able to read and understand system drawings, diagrams, and specifications.
- Experience collaborating with other design disciplines such as automation, facility design, and mechanical design groups.
- Experience working closely with CQV and operations teams is essential.
- Meticulous attention to detail and commitment to follow-through.
- Experience in working in cleanrooms and familiar with gowning requirements.
- Capable of standing and/or walking for 90% (and sitting for 10%) of a 10-hour day, which may involve climbing ladders or steps.
- Must have near vision acuity for viewing samples at close range.
- Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, and analytical skills.
- Must be able to manage multiple priorities simultaneously and have the ability to meet deadlines.
About Katalyst Healthcares & Life Sciences
Sourced by ZipRecruiter
Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.
Industry
Scientific research and development services
Company size
51 - 200 Employees
Headquarters location
South Plainfield, NJ, US