... with FDA, GMP, and site regulatory standards Required Experience: • Strong hands-on Commissioning & Qualification (C&Q) background in pharma manufacturing • Experience supporting packaging ...
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... with FDA, GMP, and site regulatory standards Required Experience: • Strong hands-on Commissioning & Qualification (C&Q) background in pharma manufacturing • Experience supporting packaging ...
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... with FDA, GMP, and site regulatory standards Required Experience: • Strong hands-on Commissioning & Qualification (C&Q) background in pharma manufacturing • Experience supporting packaging ...
Ensure compliance with GMP, FDA, and SOP standards * Document maintenance activities and support cross-functional teams * Provide real-time support to maintain production uptime Preferred ...
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Ensure compliance with GMP, FDA, and SOP standards * Document maintenance activities and support cross-functional teams * Provide real-time support to maintain production uptime Preferred ...
Expert-level working knowledge of FDA 21 CFR Part 820 / Quality Management System Regulation (QMSR), including its incorporation of ISO 13485:2016 effective February 2026. * Strong applied ...
Expert-level working knowledge of FDA 21 CFR Part 820 / Quality Management System Regulation (QMSR), including its incorporation of ISO 13485:2016 effective February 2026. * Strong applied ...
Expert-level working knowledge of FDA 21 CFR Part 820 / Quality Management System Regulation (QMSR), including its incorporation of ISO 13485:2016 effective February 2026. * Strong applied ...
Expert-level working knowledge of FDA 21 CFR Part 820 / Quality Management System Regulation (QMSR), including its incorporation of ISO 13485:2016 effective February 2026. * Strong applied ...
$17 - $20.50/hr
This role requires a strong understanding of CGMP (Current Good Manufacturing Practices) and FDA regulations, as well as mechanical knowledge to operate and maintain packaging equipment.
$17 - $20.50/hr
This role requires a strong understanding of CGMP (Current Good Manufacturing Practices) and FDA regulations, as well as mechanical knowledge to operate and maintain packaging equipment.
Columbus, OH · On-site
$68K - $92K/yr
Completes intake, document, and submit all Adverse Events and Product Complaints within 24-hour FDA and manufacturer SLA requirements * Investigates patient-reported events by gathering complete and ...
Columbus, OH · On-site
$68K - $92K/yr
Completes intake, document, and submit all Adverse Events and Product Complaints within 24-hour FDA and manufacturer SLA requirements * Investigates patient-reported events by gathering complete and ...
Columbus, OH · On-site
$16 - $22/hr
This role requires a strong understanding of CGMP (Current Good Manufacturing Practices) and FDA regulations, as well as mechanical knowledge to operate and maintain packaging equipment.
Columbus, OH · On-site
$16 - $22/hr
This role requires a strong understanding of CGMP (Current Good Manufacturing Practices) and FDA regulations, as well as mechanical knowledge to operate and maintain packaging equipment.
$17 - $20.50/hr
This role requires a strong understanding of CGMP (Current Good Manufacturing Practices) and FDA regulations, as well as mechanical knowledge to operate and maintain packaging equipment.
$17 - $20.50/hr
This role requires a strong understanding of CGMP (Current Good Manufacturing Practices) and FDA regulations, as well as mechanical knowledge to operate and maintain packaging equipment.
FDA 21 CFR Part 11 (Electronic Records and Electronic Signatures). * Data Integrity principles ( ALCOA/ALCOA+ ). * GMP regulations and Quality Management Systems (QMS). * CAPA, deviations, change ...
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FDA 21 CFR Part 11 (Electronic Records and Electronic Signatures). * Data Integrity principles ( ALCOA/ALCOA+ ). * GMP regulations and Quality Management Systems (QMS). * CAPA, deviations, change ...
... GMP, FDA, and site SOP standards • Document maintenance activities and collaborate with Production, Quality, and Engineering teams Preferred Qualifications: • Experience in pharmaceutical ...
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... GMP, FDA, and site SOP standards • Document maintenance activities and collaborate with Production, Quality, and Engineering teams Preferred Qualifications: • Experience in pharmaceutical ...
Maintain a safe, compliant, and audit-ready facility through adherence to FDA, GMP, OSHA, and company requirements. * Ensure maintenance activities are executed in accordance with approved procedures ...
Maintain a safe, compliant, and audit-ready facility through adherence to FDA, GMP, OSHA, and company requirements. * Ensure maintenance activities are executed in accordance with approved procedures ...
Maintain a safe, compliant, and audit-ready facility through adherence to FDA, GMP, OSHA, and company requirements. * Ensure maintenance activities are executed in accordance with approved procedures ...
Maintain a safe, compliant, and audit-ready facility through adherence to FDA, GMP, OSHA, and company requirements. * Ensure maintenance activities are executed in accordance with approved procedures ...
Be Seen First
New Albany, OH · On-site
$32 - $35/hr
This position supports non-standard shifts and plays a key role in maintaining compliance with FDA regulations, industry standards, and company quality requirements while driving continuous ...
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Be Seen First
New Albany, OH · On-site
$32 - $35/hr
This position supports non-standard shifts and plays a key role in maintaining compliance with FDA regulations, industry standards, and company quality requirements while driving continuous ...
Ensure compliance with GMP, FDA, and site procedures * Document maintenance activities and repairs accurately * Work closely with Production, Quality, and Engineering teams Preferred Qualifications:
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Ensure compliance with GMP, FDA, and site procedures * Document maintenance activities and repairs accurately * Work closely with Production, Quality, and Engineering teams Preferred Qualifications:
The role ensures that packaging lines are installed, tested, and documented in compliance with GMP, FDA, and internal quality requirements while supporting project schedules and startup activities.
The role ensures that packaging lines are installed, tested, and documented in compliance with GMP, FDA, and internal quality requirements while supporting project schedules and startup activities.
The role ensures that packaging lines are installed, tested, and documented in compliance with GMP, FDA, and internal quality requirements while supporting project schedules and startup activities.
The role ensures that packaging lines are installed, tested, and documented in compliance with GMP, FDA, and internal quality requirements while supporting project schedules and startup activities.
Ensure all commissioning activities comply with FDA, GMP, and company standards * Apply manufacturing process knowledge to verify systems meet operational and production requirements * Support clean ...
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Ensure all commissioning activities comply with FDA, GMP, and company standards * Apply manufacturing process knowledge to verify systems meet operational and production requirements * Support clean ...
Ensure all maintenance activities follow GMP, FDA, safety, and company SOP requirements * Complete maintenance documentation, repair logs, and corrective action records accurately * Work closely with ...
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Ensure all maintenance activities follow GMP, FDA, safety, and company SOP requirements * Complete maintenance documentation, repair logs, and corrective action records accurately * Work closely with ...
Ensure all maintenance activities comply with GMP, FDA, and site SOPs * Document maintenance work, repairs, and corrective actions accurately * Collaborate with Production, Quality, and Engineering ...
Quick apply
Ensure all maintenance activities comply with GMP, FDA, and site SOPs * Document maintenance work, repairs, and corrective actions accurately * Collaborate with Production, Quality, and Engineering ...
Ensure all maintenance activities comply with GMP, FDA, and site SOPs * Document maintenance work, repairs, and corrective actions accurately * Collaborate with Production, Quality, and Engineering ...
Quick apply
Ensure all maintenance activities comply with GMP, FDA, and site SOPs * Document maintenance work, repairs, and corrective actions accurately * Collaborate with Production, Quality, and Engineering ...
$13.46 - $19.23
11% of jobs
$23.90 is the 25th percentile. Wages below this are outliers.
$19.23 - $25
18% of jobs
$25 - $30.77
16% of jobs
The median wage is $33.65 / hr.
$30.77 - $36.54
12% of jobs
$36.54 - $42.31
11% of jobs
$46.63 is the 75th percentile. Wages above this are outliers.
$42.31 - $48.08
12% of jobs
$48.08 - $53.85
9% of jobs
$53.85 - $59.62
5% of jobs
$59.62 - $65.38
3% of jobs
$65.38 - $71.15
2% of jobs
$71.15 - $76.92
2% of jobs
$13
$39
$76

Contractor
Posted yesterday
Key Responsibilities:
• Lead commissioning and qualification activities for new packaging equipment installations
• Execute equipment walkdowns, system verifications, and commissioning checks on the manufacturing floor
• Author and execute commissioning plans, protocols, punch lists, and turnover packages
• Support SAT (Site Acceptance Testing) activities with equipment vendors
• Coordinate with Engineering, Construction, Manufacturing, and Quality teams
• Drive punch list resolution through system acceptance and GMP turnover
• Ensure compliance with FDA, GMP, and site regulatory standards
Required Experience:
• Strong hands-on Commissioning & Qualification (C&Q) background in pharma manufacturing
• Experience supporting packaging equipment installations and startup activities
• Knowledge of secondary and tertiary pharmaceutical packaging operations
• Experience with GMP/FDA-regulated environments
• Strong understanding of system turnover, commissioning execution, and manufacturing processes
Sourced by ZipRecruiter
51 - 200 Employees
Iselin, NJ, US
2018