As a Quality Coordinator, you will coordinate quality activities to meet team objectives and ensure compliance with customer standards and cGMP regulations. Responsibilities include preparing and distributing documentation, reviewing customer specifications, organizing batch records, and assisting in resolving document-related issues. You will communicate with customers and maintain adherence to quality policies.

The Quality Supervisor - Complaints will oversee a team conducting customer complaint investigations, ensuring investigations are conducted thoroughly and efficiently. Responsibilities include communicating with customers, logging complaints in the Quality Management System, conducting root cause analysis, drafting investigations, compiling metrics, and maintaining overall Quality Management principles within the organization.

The Accountant will join a finance team to handle month/year-end closes, revenue/cost forecasting, intercompany reporting, external audits, and budget preparation. Responsibilities include ensuring compliance with accounting standards, preparing management accounts, and managing company expenses.

The Compliance and Administration Engineer at PCI Pharma Services will oversee engineering compliance and administrative tasks, including resolving discrepancies and conducting audits. The role requires training on analysis tools, managing compliance documentation, and supporting engineering workflows and contractor interactions while ensuring adherence to standards and best practices.

The Label Designer is responsible for printing labels in compliance with cGMPs, managing the daily schedule for label production, overseeing quality inspections, and ensuring accurate timelines and customer requirements. The role involves working closely with cross-functional teams and mentoring label technicians while maintaining all standard operating procedures and quality compliance.

The Facilities Operative will maintain and present facility equipment and buildings, performing tasks like plumbing, carpentry, and painting. Responsibilities include conducting general maintenance, coordinating with contractors, and adhering to GMP standards while ensuring workspace cleanliness and safety compliance.

The Automation Engineer leads efforts in developing and implementing manufacturing processes and automation solutions for new products, ensuring specifications are met and projects are completed efficiently. Responsibilities include equipment validation, process optimization, statistical analysis, and team collaboration to improve productivity and quality.

The Process Engineer I will provide technical leadership in product launches and process improvements, focusing on production efficiency, packaging issues, and quality enhancement. Responsibilities include engineering reviews, process design, documentation preparation, cross-functional collaboration, and adherence to compliance standards, while utilizing lean and six sigma techniques.

The Process Engineering Analyst will lead technical initiatives to enhance production efficiency and quality in biopharma operations. Responsibilities include process adherence, mechanical troubleshooting, documentation preparation, project management, and leveraging Lean Six Sigma methods for continuous improvement.

The Process Engineering Analyst will lead technical support in production environments, optimizing processes, mitigating issues, and ensuring compliance with safety and quality standards. Responsibilities include project management, process improvement, and cross-functional collaboration.

The Business Unit Intern will support documentation preparation for the production environment, manage the creation of forms and documentation related to lot/expiration, and ensure compliance with regulatory policies. The role involves identifying process improvements for enhancing efficiency in operations.

The Mechanical Supervisor oversees mechanical personnel, manages manpower, coordinates equipment setups and repairs, ensures compliance with regulations, interacts with customers and management, trains employees, manages inventories, and supports mechanical activities, while maintaining safety standards.

The Mechanical Supervisor will oversee mechanical personnel, manage manpower, ensure schedule adherence, coordinate equipment repairs, maintain safety compliance, update job assignments based on production needs, and handle payroll activities for mechanical staff. Overtime and weekend work may be required, and the role involves training and coaching employees while addressing production complaints.

As an Automation Engineer Intern, you will contribute to the development and implementation of automated solutions that improve processes and enhance the delivery of therapies to patients. This role focuses on supporting engineering teams and gaining practical experience in automation within the biopharma sector.

The Associate Quality Account Manager I coordinates quality activities for a customer-focused team, ensuring project goals are met on time and within budget. Duties include creating and reviewing packaging instructions, conducting batch record reviews, liaising with customers, and initiating quality investigations. The role involves training new coordinators and requires adherence to PCI, cGMP, and GCP policies.

The Commercial Associate Project Manager assists with managing customer projects and order fulfillment, ensuring they are completed on time and within budget while complying with pharmaceutical regulations. Responsibilities include scheduling production, placing purchase orders, tracking deliveries, and maintaining documentation accuracy.

As an Operator II, you will operate production equipment, assist line personnel, maintain a safe and organized production area, and ensure the stocking of components needed for operations. You will also monitor fill operations and handle the movement of materials within the production area.

The Automation Engineer Intern will support software systems by maintaining production data collection systems and assisting in creating electrical schematics and control systems. The role includes troubleshooting and implementing various monitoring and printing systems, working closely with colleagues to ensure connectivity and cyber security compliance.

The Commercial Associate Project Manager I is responsible for managing customer projects and order fulfillment within the pharmaceutical sector, ensuring timely delivery, maintaining schedules, and tracking metrics. This role involves document creation, purchasing, and working closely with clients to ensure project requirements are met while adhering to pharmaceutical regulations.

The Process Engineer I will provide technical leadership for new product launches and improve production processes, focusing on mitigating packaging issues and optimizing operational efficiency. Responsibilities include designing production lines, collaborating with teams, leading project management, and utilizing lean six sigma techniques to enhance performance and quality compliance.