Process Validation Specialist
1 week ago
Technical Source is seeking Validation Engineers to engage in process validation tasks within cGMP pharmaceutical production environments. In these positions, you will collaborate with colleagues to establish process control parameters and develop validation protocols aimed at assessing and confirming process reliability.
This role requires full on-site presence, with a need for flexibility in working rotating shifts. These are long-term contract opportunities that span multiple years. Please note that sponsorship or C2C employment options are not available at this time.
Key Responsibilities
- Develop and author Process Validation plans, which may encompass the creation of product-specific process requirements and specification drafts necessary for executing process performance qualifications and media fill protocols.
- Conduct technical reviews of deviations and planned deviations, manage change controls, oversee process monitoring, and facilitate activities related to lot releases.
- Assist in evaluating the implications of change control on the qualified processes and aseptic operations.
- Collaborate effectively with other validation professionals and ensure seamless cross-functional teamwork with various departments.
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Process Validation Specialist
2 weeks ago
Columbia, South Carolina, United States Technical Source Full timeTechnical Source is seeking experienced Validation Engineers to engage in critical process validation initiatives within the pharmaceutical manufacturing sector. In these positions, you will be responsible for executing validation tasks that ensure compliance with current Good Manufacturing Practices (cGMP).This role requires full-time on-site presence, with...
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Process Validation Specialist
1 week ago
Columbia, South Carolina, United States Technical Source Full timeOverviewTechnical Source is seeking Validation Engineers to engage in critical process validation tasks within the realm of cGMP pharmaceutical production. In these positions, you will collaborate with colleagues to establish process control parameters and develop validation protocols aimed at assessing and confirming process reliability.This role requires...
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Process Validation Specialist
2 weeks ago
Columbia, South Carolina, United States Technical Source Full timeTechnical Source is seeking experienced Validation Engineers to engage in critical process validation initiatives within the realm of cGMP pharmaceutical production. In these positions, you will collaborate with team members to establish process control parameters and develop validation protocols aimed at assessing and confirming process reliability.This...
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Process Validation Specialist
2 weeks ago
Columbia, South Carolina, United States Technical Source Full timeTechnical Source is seeking experienced Validation Engineers to engage in critical process validation initiatives within cGMP pharmaceutical production environments. In these positions, you will collaborate with team members to establish process control parameters and develop validation protocols aimed at assessing and confirming process reliability.This...
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Process Validation Specialist
1 week ago
Columbia, South Carolina, United States Technical Source Full timeTechnical Source is seeking skilled Validation Engineers to engage in process validation initiatives that support cGMP pharmaceutical production environments. In these positions, you will collaborate with team members to establish process control parameters and develop validation protocols aimed at assessing and confirming process integrity.This role...
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