Process Validation Engineer
Aequor JD ·www.aequor.com
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Direct Contingent Worker
Posting Title Direct Contingent Worker
Division ***
Country USA
Work Location Houston, TX
Functional Area Technical Operations
Job Type Full Time
Employment Type Contract
Job Description
Development of New Injection Molding Processes using scientific molding principles.
Lead complete IQ/OQ/PQ validation activities of both thermoplastic and silicone injection molds working
with all stakeholders including Engineering, Production and Quality
Troubleshoot molding processes to mitigate production defects and or improve efficiency
Participate in design reviews of new tooling and equipment working with both external and internal
injection mold makers
Lead technology improvements that advance our molding processes for new and existing products.
Prepare complete and accurate records/documentation of assigned project activities per the established
Quality System and Validation Guidelines
Participate in regular project meetings, publishes timely project updates, and follows-up continuously
on all open critical path items
Generate and maintain documentation for applicable internal processes and procedures, inspection
criteria, Bill of Materials, Validation Protocols/Reports and other manufacturing and quality records
Identify, initiate and implement technology improvements, which increase productivity and reduce
scrap/reject rates through effective training of production personnel and process enhancements
Maintain and improve product quality by performing and documenting robust root cause investigations
and implementing effective corrective and preventive actions
Develop and leverage product knowledge to ensure Critical Quality Attributes (CQAs) are consistently
met
Minimum Education Requirements
Bachelor degree in Engineering or equivalent years of directly related experience (or high school 8yrs;
Assoc. 4 yrs; Scientific Molding Certifications (master molder) 2yrs)
Direct Contingent Worker
Preferred: Bachelor degree in Plastics Engineering or Scientific Molding Certification completion.
Minimum Experience Requirements
Minimum: 2 years experience in high volume molding and manufacturing environment
Preferred: 2 years experience in medical device manufacturing or other highly regulated industry
Working knowledge of Validation processes (IQ/OQ/PQ)
Technical expertise in injection molding of thermoplastics related to Design for Manufacturability of
molds, processing of thermoplastics, robotics, automation and hot runner system
Comprehensive knowledge and thorough understanding of troubleshooting techniques for the
injection molding process, machine, robot and auxiliaries.
Experience with advanced processing techniques (eDart), robot programming, hot runner molds,
tooling issue diagnostics, molding machine diagnostics, central material handling systems and color
blending.
Processing knowledge of Polycarbonate, Acrylic, ABS, Polysulfone, and various commodity resins
Familiar with SPC methodologies and the scientific molding process.
Data driven, disciplined, objective and detail oriented.
Ability to read and interpret part and mold drawings
Ability to work with minimal supervision and/or guidance
Familiarity with statistical problem solving techniques
Excellent organization and communication skills.
Knowledge of FDA regulations and other international compliance standards
Competency in the following software: MS Project, Excel, Word, PowerPoint
EEO Statement
Company is committed to diversity and inclusion. We are an equal opportunity
employer including veterans and people with disabilities.
Posting Title Direct Contingent Worker
Division ***
Country USA
Work Location Houston, TX
Functional Area Technical Operations
Job Type Full Time
Employment Type Contract
Job Description
Development of New Injection Molding Processes using scientific molding principles.
Lead complete IQ/OQ/PQ validation activities of both thermoplastic and silicone injection molds working
with all stakeholders including Engineering, Production and Quality
Troubleshoot molding processes to mitigate production defects and or improve efficiency
Participate in design reviews of new tooling and equipment working with both external and internal
injection mold makers
Lead technology improvements that advance our molding processes for new and existing products.
Prepare complete and accurate records/documentation of assigned project activities per the established
Quality System and Validation Guidelines
Participate in regular project meetings, publishes timely project updates, and follows-up continuously
on all open critical path items
Generate and maintain documentation for applicable internal processes and procedures, inspection
criteria, Bill of Materials, Validation Protocols/Reports and other manufacturing and quality records
Identify, initiate and implement technology improvements, which increase productivity and reduce
scrap/reject rates through effective training of production personnel and process enhancements
Maintain and improve product quality by performing and documenting robust root cause investigations
and implementing effective corrective and preventive actions
Develop and leverage product knowledge to ensure Critical Quality Attributes (CQAs) are consistently
met
Minimum Education Requirements
Bachelor degree in Engineering or equivalent years of directly related experience (or high school 8yrs;
Assoc. 4 yrs; Scientific Molding Certifications (master molder) 2yrs)
Direct Contingent Worker
Preferred: Bachelor degree in Plastics Engineering or Scientific Molding Certification completion.
Minimum Experience Requirements
Minimum: 2 years experience in high volume molding and manufacturing environment
Preferred: 2 years experience in medical device manufacturing or other highly regulated industry
Working knowledge of Validation processes (IQ/OQ/PQ)
Technical expertise in injection molding of thermoplastics related to Design for Manufacturability of
molds, processing of thermoplastics, robotics, automation and hot runner system
Comprehensive knowledge and thorough understanding of troubleshooting techniques for the
injection molding process, machine, robot and auxiliaries.
Experience with advanced processing techniques (eDart), robot programming, hot runner molds,
tooling issue diagnostics, molding machine diagnostics, central material handling systems and color
blending.
Processing knowledge of Polycarbonate, Acrylic, ABS, Polysulfone, and various commodity resins
Familiar with SPC methodologies and the scientific molding process.
Data driven, disciplined, objective and detail oriented.
Ability to read and interpret part and mold drawings
Ability to work with minimal supervision and/or guidance
Familiarity with statistical problem solving techniques
Excellent organization and communication skills.
Knowledge of FDA regulations and other international compliance standards
Competency in the following software: MS Project, Excel, Word, PowerPoint
EEO Statement
Company is committed to diversity and inclusion. We are an equal opportunity
employer including veterans and people with disabilities.
Frequently asked questions
Who is hiring for the Process Validation Engineer role?
Aequor JD is hiring for the Process Validation Engineer position, a Shazamme client. Apply directly on the employer's career site.
Where is the Process Validation Engineer job located?
The Process Validation Engineer role with Aequor JD is based in Houston, TX, US.
Is the Process Validation Engineer role full-time or contract?
This is a full time position at Aequor JD.
What experience level is the Process Validation Engineer role?
The Process Validation Engineer position is aimed at mid-level candidates.
How do I apply for the Process Validation Engineer role at Aequor JD?
Apply directly on Aequor JD's career page via the Apply button on this listing. ZammeJobs links straight through to the employer's ATS — no third-party form, no resume database.