Summary

PCI Pharma Services is a global contract development and manufacturing organization (CDMO) that provides comprehensive pharmaceutical supply chain solutions to pharmaceutical and biopharmaceutical companies worldwide. Founded in 1991 and headquartered in Philadelphia, Pennsylvania, the company has established itself as a trusted partner in the healthcare industry, offering integrated services that span the entire drug development lifecycle. PCI specializes in drug development support, clinical trial supply management, contract drug manufacturing, sterile and non-sterile drug product packaging, and global pharmaceutical logistics. With a global footprint encompassing 30 GMP-compliant facilities across multiple continents, the company serves as a strategic partner that follows the molecule from early development through commercial launch. PCI's expertise enables clients to accelerate time-to-market while ensuring regulatory compliance and quality standards. The company's comprehensive service portfolio includes analytical services, formulation development, commercial manufacturing, packaging, supply chain management, and distribution, making it a one-stop solution for pharmaceutical companies seeking to outsource their development and manufacturing needs.

Job description

Essential Job Functions

Supervise and mentor process equipment maintenance staff and direct day-to-day work assignments.
Oversee timely troubleshooting of complex problems, complete emergency repairs, and guide staff in implementing repairs.
Maintain equipment in use-ready, compliant state. Major equipment includes lyophilizer, PLC, SCADA, HMI, clean steam, WFI, and others.
Monitor, respond to, and correct issues generating equipment alarms.
Provide recommendation for, and implement upgrades and improvements.
Author, review, and update maintenance procedures and forms.
Complete CMMS entries and required training activities.
Travel between facilities to support all functional areas.
Regular and reliable attendance on a full time basis.
Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
Foster a safe and environmentally sustainable workplace by ensuring compliance with all PCI EHS policies and procedures.
Embodies PCI Pharma Service’s cultural values and aligns daily actions with department goals and company culture.

Education and Experience

Associate’s degree or equivalent experience required.
High school diploma or equivalent experience required.
Certification preferred.
Minimum twelve (10) plus years of relevant experience required.
Minimum eight (8) years of cGMP experience required.
Mastery of troubleshooting.
Mastery of process and support equipment for pharmaceutical manufacturing including lyophilization system, clean steam, WFI, PLC, SCADA, HMI, and others.
Advanced understanding of cGMP.
Ability to work in a group, and independently.

Requirements

Associate’s degree or equivalent experience required
High school diploma or equivalent experience required
Certification preferred
Minimum 10+ years of relevant experience required
Minimum 8 years of cGMP experience required
Mastery of troubleshooting
Mastery of process and support equipment for pharmaceutical manufacturing including lyophilization system, clean steam, WFI, PLC, SCADA, HMI, and others
Advanced understanding of cGMP
Ability to work in a group, and independently

Benefits

Paid time off
Health insurance
Dental insurance
Vision insurance
Flexible spending account
401(k)

Company overview

PCI Pharma Services is a global contract development and manufacturing organization (CDMO) that provides comprehensive pharmaceutical supply chain solutions to pharmaceutical and biopharmaceutical companies worldwide. Founded in 1991 and headquartered in Philadelphia, Pennsylvania, the company has established itself as a trusted partner in the healthcare industry, offering integrated services that span the entire drug development lifecycle. PCI specializes in drug development support, clinical trial supply management, contract drug manufacturing, sterile and non-sterile drug product packaging, and global pharmaceutical logistics. With a global footprint encompassing 30 GMP-compliant facilities across multiple continents, the company serves as a strategic partner that follows the molecule from early development through commercial launch. PCI's expertise enables clients to accelerate time-to-market while ensuring regulatory compliance and quality standards. The company's comprehensive service portfolio includes analytical services, formulation development, commercial manufacturing, packaging, supply chain management, and distribution, making it a one-stop solution for pharmaceutical companies seeking to outsource their development and manufacturing needs.