Healthcare Pharmaceutical jobs

This is a leadership level position focused on IT Quality within a large portion of the company. It will have purview over IT Validation, compliance initiatives, and documentation.

This position will be reporting into the Manager of IT Audit and the VP of Audit at a well known Fortune 500 Company.

Work on the operations of Quality Engineering, Purchasing Controls and Supplier Quality processes related to the development, procurement and continuous improvement of products and materials used by our client. You will have responsibility for supplier management activity working with external suppliers and internal teams to assure that our products exceed the requirements and expectations of patients, physicians, regulatory agencies and the business

Our client is looking to hire a Senior Manufacturing Engineer for their New Product Development Team. The Engineer in this role will be responsible for Process Development support, implementation of cost effective manufacturing processes, and will also act as a project team lead with new up coming projects.

The Quality Assurance Lead will report directly to the QA Director.This position is responsible to actively participate in the ISO 9001 Quality Management System. This role will be responsible for the management of Quality Associates in support of product release. They are responsible for supervising the daily schedule and assigning tasks to their direct reports. Must work independently and manage short and long-term priorities.

This position will manage Incoming, In Process, and Outgoing Product evaluations, New Product Development design evaluations, Statistical Process Control, Supplier Part evaluation, Calibration systems, and Corrective Action Processes. Responsible to plan, develop, manage, and control programs and procedures used to define and monitor all levels of product quality.

This is a newly created role due to growth that will maintain and support the EHS Program. The ideal candidate will develop, implement and oversee procedures and programs to ensure Federal and State compliance with EPA and DEOP.

This role will be responsible for leading the day-to-day Quality operations at the cell/gene therapy manufacturing site. The role will also be a key contributor to the implementation and execution of quality systems including oversight of facility and equipment validation activities.

• The primary goal of this position is to devise and implement best in class marketing strategies in order to strengthen the position of the company in the marketplace and exceed business goals.
• You will utilize a myriad of skills including planning and executing complex projects on a global scale, build out a global web presence, and effectively multitask to tend to multiple company priorities.

The Associate Category Manager - Project Procurement will be responsible for the execution of strategies through strategic sourcing to significantly reduce costs. This role will partner with internal customers and build relationships with key stakeholders and be responsible for achieving savings and tracking impact. The goal is to achieve reductions in total costs of services while maintaining or improving supplier quality and service.

As a hands-on Director, this individual will lead as a "player/coach," leading a small team of 3 (with additional hires next year) to drive Quality Assurance across the company gene and cell therapy manufacturing unit. The GMP Quality Director will provide Quality Operations oversight and play a key role in implementing quality systems.

Reporting to the VP of Quality, the Supplier Quality Engineering Manager will be responsible for Supplier oversight to ensure, Quality, Compliance, and Regulatory requirements. This individual will work cross-functionally with the engineering team for both onboarding new suppliers, especially contract manufacturers,and monitor performance of existing suppliers in a sustaining role.

The Senior Regulatory Affairs Specialist is responsible for functioning as the regulatory lead on integrated project teams, and as a mentor within the Regulatory Affairs group. The Senior Regulatory Affairs Specialist contributes to corporate initiatives, interacting with clients, and ensuring accuracy, completeness and compliance of high-quality submissions to US and international regulatory authorities, from pre-submission phase through market launch.

The Lab Technician will assist in all laboratory procedures performed within Guilford, CT facilities. You will assist in processing RMA units which includes receiving, documentation, organization and low level assessment.

*4-6 month assignment in the Connecticut laboratory. Seeking local candidates only*