Search the 14 jobs at Mallinckrodt Pharmaceuticals

The Quality Coordinator oversees the nonconforming material report process, ensuring compliance with GMP standards. Responsibilities include analyzing nonconforming products, conducting failure mode and root cause analyses, preparing for material review board meetings, managing nonconforming parts in SAP, and performing internal and external audits.

The Product Manager/Associate Product Manager will lead marketing projects, manage project execution, support the marketing team, and liaise with external vendors. The role also involves developing marketing initiatives, managing marketing materials, and ensuring compliance throughout the promotional review process.

The Senior Product Manager will develop and execute a re-launch plan for a new medical device product in Japan, managing stakeholder relationships and collaborating with sales and marketing teams. Responsibilities include strategy development, issue resolution, and budget management, along with engagement in key marketing activities such as congresses and KOL relationships.

Manage the development and maintenance of quality programs in alignment with cGXP regulations. Oversee supplier quality and self-inspection programs, support regulatory compliance audits, and ensure quality assurance processes meet industry standards. Provide leadership in quality system initiatives and act as a subject matter expert in GxP compliance.

The Sr Quality Systems Admin supports the administration of laboratory systems such as LIMS and Chromeleon, providing user support, addressing technical issues, creating documentation, and ensuring compliance with regulations. This role also involves project participation and collaboration with various departments while adhering to safety protocols.

The EHS Specialist facilitates safety management activities, ensuring compliance with safety regulations, conducting hazard analyses, training employees, investigating incidents, and improving safety culture. They collaborate with departments to remediate hazards and assist in compliance reviews.

The EHS Manager at Mallinckrodt is responsible for leading and executing EHS strategies and compliance across the College Park campus in Dublin. This role involves managing environmental and safety programs, fostering a culture of safety, and ensuring effective risk management and regulatory compliance. The manager will also oversee sustainability initiatives and lead key EHS projects, while maintaining relationships with regulatory agencies.

The Payroll Specialist is responsible for preparing and processing payroll, auditing HR data, ensuring tax compliance, and managing payroll reports. They perform payroll adjustments and support system testing while aiding in mergers and acquisitions. The role includes adhering to payroll laws and supporting inquiry handling.

The In-Process Quality Engineer II oversees quality functions in manufacturing, managing customer complaints, and conducting investigations. Responsibilities include writing reports, regulatory support, and ensuring cGMP compliance, while leading process improvement initiatives and audits.

The Quality Tech II will perform analysis on various laboratory samples, document results, conduct testing, and participate in laboratory activities while maintaining safety and quality standards. Essential functions include using analytical instruments and ensuring compliance with good laboratory practices.

The Quality Tech III provides technical support in a laboratory environment, performing analysis on various samples, adhering to safety and quality standards, and participating in investigations of out-of-specification results. Responsibilities include wet chemistry testing, instrument maintenance, LIMS data entry, and training team members on laboratory protocols.

The Quality Assurance Technician III reviews product batch records for errors, ensures compliance with cGMP, resolves documentation discrepancies, performs batch record accountability, and manages product release processes. They also participate in efficiency improvement teams and ensure quality assurance compliance within the site.

The Operations Quality Engineer II is responsible for supporting various aspects of the Quality System in a cGMP manufacturing environment, including statistical analysis, root cause analysis, corrective actions, and continuous improvement initiatives. The role involves compliance efforts, risk analysis, and collaboration with production teams to enhance quality and efficiency.

The Buyer I is responsible for sourcing and contracting direct materials to ensure timely delivery while maintaining cost-effectiveness. The role involves negotiating with suppliers, monitoring supply agreements, and supporting inventory management processes to prevent interruptions in material supply.