PCI Pharma Services

HQ
Philadelphia, Pennsylvania, USA
2,259 Total Employees

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Jobs at PCI Pharma Services

Search the 64 jobs at PCI Pharma Services

Pharmaceutical
The Testing Coordinator will oversee the software testing process for PCI's pci | bridge™ platform, including developing and executing UAT plans, coordinating with teams, improving testing procedures, and ensuring compliance with standards. They will also maintain documentation, utilize testing tools like Cypress, and interact with JIRA for project management.
Pharmaceutical
The Commercial Project Manager manages customer projects, serving as the main contact for timelines, budgets, and client satisfaction. Responsibilities include project planning, compliance with regulations, expense management, team leadership, and continuous improvement initiatives to achieve project deliverables.
2 Days Ago
Red Lion, PA, USA
Pharmaceutical
The Project Engineer is responsible for providing technical and operational support, focusing on process improvement and equipment optimization. Key tasks include analyzing sales requests, designing production lines, managing project budgets, and overseeing equipment acquisition, installation, and validation protocols. The role entails collaboration with various departments and managing project timelines effectively.
Pharmaceutical
The Quality Engineer Associate I supports the Consumer Complaints and Quality Engineering Team by managing customer complaints, maintaining tracking systems, and ensuring compliance with GMP regulations. Responsibilities include logging complaints, communicating with customers, generating metrics, and assisting with various documentation tasks.
3 Days Ago
Northern Ireland, GBR
Pharmaceutical
The Projects Engineering Manager oversees the Engineering Projects Team, ensuring adherence to EHS, cGMP, and engineering standards. This role involves managing project timelines, costs, and quality while fostering a culture of continuous improvement and efficiency. Responsibilities include technical support for new product introductions, maintenance of project documentation, and mentoring team members.
Pharmaceutical
The Quality Engineer - NPI role involves onboarding new customer programs, transitioning products from engineering to manufacturing, and collaborating with teams to ensure compliance with quality standards. Responsibilities include developing workflows, driving root cause analysis, maintaining project timelines, and supporting documentation processes.
Pharmaceutical
The Associate Quality Account Manager I coordinates quality activities for a customer-focused team, ensuring objectives are met on time and within budget. Responsibilities include document creation, batch record reviews, quality metrics population, and acting as the liaison with customers, while adhering to cGMP guidelines.
3 Days Ago
Red Lion, PA, USA
Pharmaceutical
The Quality Analyst will conduct customer complaint investigations, log complaints in the QMS system, perform root cause analysis, draft investigation reports, and maintain Quality Management Systems through internal audits, CAPAs, and change controls.
Pharmaceutical
The Associate Quality Account Manager I facilitates quality activities for customer-focused teams to meet goals and deadlines. Responsibilities include reviewing and updating packaging instructions, performing batch record reviews, liaising with customers on quality documentation, tracking quality metrics, and assisting in training new Quality Coordinators.
Pharmaceutical
The Associate Quality Account Manager I assists with coordinating quality activities to achieve team goals and ensure project success, focusing on compliance with guidelines and customer requirements. Responsibilities include reviewing documentation, conducting batch record reviews, communicating with customers, resolving quality issues, and mentoring new staff.
3 Days Ago
Red Lion, PA, USA
Pharmaceutical
The Quality Auditor is responsible for ensuring compliance with GMP standards, auditing production processes, documenting findings, and leading continuous improvements in quality metrics. The role involves reviewing batch records, equipment calibration, safety protocols, and overall quality documentation to enhance operational efficiency and product integrity.
3 Days Ago
Red Lion, PA, USA
Pharmaceutical
The Quality Auditor is responsible for ensuring compliance with cGMP standards by auditing production documentation, performing inspections, and reviewing processes. They drive improvements in operational practices while mentoring staff, ensuring quality control, and documenting audits effectively.
Pharmaceutical
The Associate Quality Account Manager I assists with quality activities for a dedicated customer team, ensuring goals are met within timelines and budgets. They create and review documentation, perform compliance checks, facilitate communication with clients, and drive project success in quality management.
Pharmaceutical
The EHS Specialist will promote environmental health and safety, ensuring compliance with regulations, guiding teams, managing incidents, conducting safety training, and supporting audits. They will actively contribute to a safety culture and assist in risk management and EHS system development.
3 Days Ago
Red Lion, PA, USA
Pharmaceutical
The Quality Auditor ensures cGMP compliance and directs the organization of production processes. Responsibilities include reviewing production documentation, performing real-time batch record audits, leading continuous quality improvements, and training operational staff while ensuring timely processing of customer orders.
Pharmaceutical
The Commercial Project Manager oversees customer project execution and order fulfillment, ensuring objectives are met on time and within budget while adhering to regulations. Responsibilities include managing production schedules, procurement processes, order statuses, and documentation, while maintaining high client satisfaction and tracking performance metrics.
3 Days Ago
Großbeeren, Brandenburg, DEU
Pharmaceutical
The Qualified Person will implement and execute QP duties related to compliance with GMP, manage audits, certify medicinal products, support training, and enhance internal processes across PCI Pharma Services.
3 Days Ago
Großbeeren, Brandenburg, DEU
Pharmaceutical
The Quality Assurance Specialist will be responsible for the qualification and validation of various processes and equipment, conducting risk analyses, creating related documentation, and ensuring compliance with quality systems within the pharmaceutical sector. This role requires collaboration with other departments, handling audits, and supporting regulatory inspections.
6 Days Ago
Northern Ireland, GBR
Pharmaceutical
The Reliability Engineer analyzes processes to improve equipment reliability and maintenance. Responsibilities include root cause analysis, project management, and leading system improvements while ensuring compliance with safety regulations. The role emphasizes collaboration with the Continuous Improvement team to enhance operational excellence.
7 Days Ago
San Diego, CA, USA
Pharmaceutical
The Project Manager oversees clinical customer projects to achieve goals within time frames and budgets, fostering strategic relationships and ensuring high-quality deliverables. Responsibilities include project planning, leading teams, managing customer interactions, and ensuring adherence to regulatory standards. They also support business development efforts and manage project finances effectively.