The Superintendent will be managing large lab projects along the 495 belt. This leadership role will allow you to wear multiple hats and ensure the project is on track.

Responsible for selling company product to new and existing customers. This role requires the ability to effectively identify and translate the company's ability to provide solutions to customer needs.

Are you an experienced Project Manager in the Raleigh area? Would you like to work for one of the most reputable and established GCs in the market? Do you have experience working on life sciences renovation / upfit projects up to $20M? If yes, please apply now!

Top 100 ENR GC specializing in healthcare, life-science and higher education work. They are a leader in the US, establishing a track record of excellent clients and pipeline of projects. They pride themselves on their strong leadership & support, and have established a fantastic company culture.

Currently hiring a motivated Assistant Project Manager to work on high-profile lab projects throughout the Greater Boston area!

The Assistant Project Manager will be working with the Project Management team on projects in the life science space- both renovations & ground up.

Michael Page is partnered with one of Massachusetts' most reputable General Contractors with a strong hold on Boston's Lab/Life Science market. They are seeking an experienced Project Manager to join their team on Lab/Life Science projects worth up to $100M for a national real estate developer. Apply today for immediate consideration.

International pharmaceutical business seeks Associate Director of Talent Acquisition to support their American business operations.

Michael Page is partnered with one of Massachusetts' most reputable General Contractors with a strong hold on Boston's Lab/Life Science market. They are seeking an Assistant Project Manager to join their team. Apply today for immediate consideration.

Michael Page is partnered with one of Massachusetts' most reputable General Contractors with a strong hold on Boston's Lab/Life Science market. They are seeking an Assistant Project Manager to join their team. Apply today for immediate consideration.

Currently hiring a motivated Assistant Project Manager to work on high-profile lab projects throughout the area!

Michael Page is partnered with a General Contractor based South of Boston on their search for a Senior Project Manager. This Senior Project Manager will oversee complex Lab & Life Science projects. Apply today for immediate consideration.

The Senior Project Manager will take the lead on the firms ground-up, lab and life science projects. Projects are high-profile, up to $50M+ in value, and require strong technical skills.

The Senior Project Manager will take the lead on the firms ground-up, lab and life science projects. Projects are high-profile, up to $50M+ in value, and require strong technical skills.

International pharmaceutical business seeks Senior Manager of Employee Experience to support their American business operations.

The Senior QA Specialist - Plant Operations is responsible to provide QA support and expertise to manufacturing plant operations.

The Senior QA Operations Specialist is responsible to provide QA support and expertise to manufacturing operations. This includes review and approval of GMP documentation such as Batch Records, Deviations/Investigations, CAPA(s), Stability Protocols/Reports, Validation Protocols/Reports, and Calibration/Work Order Records.

Assist with the clinical development strategy, work with cross-functional multidisciplinary study teams on clinical trial strategy, design and execution. Serve as the Medical Lead and primary Medical Monitor for clinical trials that will be conducted with this compound.

Be a key member of senior leadership team with a high degree of visibility and impact across the organization. Bring a strong strategic mindset and have a proven track record of success in leading a company's technical operations, including process and analytical development, Clinical and Commercial Manufacturing.

This position will report to the VP of Clinical Operations and interact with the executive team. They will focus on building relationships with CROs and oversee the creation and implementation of standard operation procedures for clinical development.

The Director of Quality is responsible for oversight of the corporate quality program, including Quality Engineering, Quality Compliance, Quality Assurance, and Laboratory Quality Control.

Responsible for daily oversight of the Technical Operations team, facilitating the technical transfer of client processes and executing operational functions including design, document control & new product introduction to the manufacturing teams. The Manager will provide leadership and coaching to the Technical Operations team and will provide technical support to drive process improvements throughout operations.

The Manager, Operational Excellence will be responsible for developing and executing a focused effort to improve operational effectiveness and profitability for the site. This person will be measured annually on the ability to enhance a continuous improvement culture and the development and execution of cost reduction initiatives.

The Tech Ops Specialist is responsible for internally overseeing the manufacture and completion of client project activities to support release of products for clinical trials and ensure the delivery of batch manufacture and documentation to GMP standards, in line with client project timelines. The job holder will also be required to liaise, guide and develop the wider production team to ensure continuous development and successful delivery of projects.

• In-bounding client product/process in order to develop a GMP manufacturing processes and assist department and site management in developing client proposals.
• Facilitate the tech transfer of the developed processes into GMP Operations.
• Execute engineering functions including design and document controls.
• Co-lead and contribute to development team execution of product development within project timelines.

Write and/or review CMC part of the regulatory submission dossiers based on hands-on experiences and/or in-depth understanding of the relevant subjects. Partner and work collaboratively with cross-functional teams.

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.

The QC Supervisor will develop Quality Control systems to streamline process and drive efficiencies in support of Microbiological and Analytical methods at multiple sites. They will also be responsible for maintaining the day-to-day activities for product manufacture, test and release including deviation support, OOS support and root cause analysis.

The QC position is a key opportunity to support the delivery of treatment for patients, they prepare for the BLA filing. You will play a vital role in the bioanalytical lot release testings of commercial scale clinical supply and product stability testing.

The Quality Control Bioanalytics Analyst / Specialist will play a vital role in the bioanalytical lot release testing of commercial scale clinical supply and product stability testing, while also preparing the Quality Control processes for commercial launch.