Are you an experienced architect looking to put your knowledge and skills into state of the art lab/life science facilities? Work for one of the nation's most established architecture/design firms on large projects. Apply today for immediate consideration.

Michael Page is partnered with one of Massachusetts' most reputable General Contractors in the Lab, Life Science, and Healthcare spaces. They are actively looking to hire an Assistant Superintendent. Apply today for immediate consideration.

Michael Page is partnered with a leading General Contractor in Boston's Lab, Life Science, and Healthcare spaces. They are actively seeking an experienced Superintendent to join their team. Apply today for immediate consideration.

We are partnered with one of the top General Contractor's in Boston seeking to hire a highly motivated Project Manager to join their team!

Currently hiring for a Construction Project Manager to join one of Boston's most established General Contractors in Boston!

Currently hiring for a Construction Assistant Project Manager to join one of Boston's most established GCs to work on complex healthcare & life science projects in Boston!

Michael Page is currently hiring for a Construction Project Manager to join one of Boston's most established General Contractors in Boston!

Michael Page is partnered with one of Massachusetts' most reputable General Contractors in the Lab, Life Science, and Healthcare spaces. They are actively looking to hire an Assistant Superintendent. Apply today for immediate consideration.

Lead and manage pharmaceutical analytical development and cGMP quality actions. Identify and assess regulatory and quality risks from clinical development, commercial development, and product launch.

This client is seeking a technically accomplished scientist with a thorough understanding of Biologics/Cell Gene therapy related assays and technology. Reporting to the CEO, this role will have responsibility for the oversight of Analytical QC operations. The role will be of high visibility and expected to partner with Analytical Development, Quality Assurance and Manufacturing in supporting operational needs for the site.

This position will be primarily responsible for generating revenues and sales for drug discovery R&D business in the target markets / segments in the USA. The position will be our front face to customer and will be expected to build a strong network of global clients in the above domain through close interaction with senior level contacts in the relevant industries and delivery of differentiated customer services.

The position will be our front face to customer and will be expected to build a strong network of global clients in the above domain through close interaction with senior level contacts in the relevant industries and delivery of differentiated customer services.

In this highly visible role, this individual's primary responsibilities are focused on several areas including, but not limited to, design and implementation of clinical studies; building and managing relationships with CROs and academic collaborators; implementation of standard operating procedures for clinical development; contributing to the creation and implementation of the overall clinical strategy of of the business.

Design and implementation of clinical studies; building and managing relationships with Contract Research Organizations (CROs) and academic collaborators. This includes implementation of standard operating procedures for clinical development; contributing to the creation and implementation of the overall clinical strategy.

This position will be primarily responsible for generating revenues and sales for drug discovery R&D business in the target markets / segments in the USA. The position will be our front face to customer and will be expected to build a strong network of global clients in the above domain through close interaction with senior level contacts in the relevant industries and delivery of differentiated customer services.

Management of Big Pharma partnerships in the areas of Chemistry, Screening and other discovery-related activities. Build and manage a robust pipeline of partnerships aligned with the company's value creation strategy for customers, based on their current and future product positions.

Build an implement Clinical Development strategy globally. Serve as member of the executive leadership team among other key responsibilities.

• Executive leadership role to advance company's Clinical assets into late stages.
• Biotech start-up with therapies in metabolic and immune-related disease areas.

This candidate will be coming from big pharma and will be managing/overseeing the external collaboration.

Reporting to the CEO, the CMO is expected to build and implement the Clinical development strategy globally, drive the Company's Clinical assets, provide oversight for the Clinical Organization, and serve as a member of the executive leadership team among other key responsibilities.

This is a key role within the Commercial/Business Team with primary function being business development and supporting discussions between Clients and the Scientific/Technical team. The individual will use his/her strong technical/lab work knowledge in the field of large molecules/biologics to understand the Client's challenges and design solutions. The requests can range from R&D through clinical stage and product commercialization.

This is not a sales role, the client wants experienced scientist with minimal BD experience previously. You are responsible for supporting business development activities within an specific area of focus.

The individual will use his/her strong technical/lab work knowledge in the field of large molecules/biologics to understand the Client's challenges and design solutions. The requests can range from R&D through clinical stage and product commercialization. The individuals must have strong verbal and written communication skills and the ability to use their scientific prowess and business skills to win business from the assigned Clients.

As a Director or Senior Director of Business Development, Cell & Gene Therapy, you will be responsible for supporting business development activities for our CDMO's US-based cell and gene therapy business line and the UK based GMP gene therapy manufacturing CDMO.

Currently hiring for a Construction Project Manager to join one of Boston's most established General Contractors in Boston!

The Program Manager will oversees full product life cycle through budgeting, time-line materials and more. They will be the lead with new clients on the potential to manufacture medical device products across the world.

The Director of Regulatory CMC is responsible for leading the development and implementation of regulatory strategies for the chemical, manufacturing, and control (CMC) aspects of drug and biologics development programs. The Director will be responsible for interacting with regulatory agencies and internal teams to ensure timely and successful regulatory approvals for new and existing products.

The Director of Regulatory CMC is responsible for leading the development and implementation of regulatory strategies for the chemical, manufacturing, and control (CMC) aspects of drug and biologics development programs. The Director will be responsible for interacting with regulatory agencies and internal teams to ensure timely and successful regulatory approvals for new and existing products.

The Process Engineer will be on the front end of design manufacturing processes for printed circuit boards within medical device systems. The Process Engineer will be hands on in the development, sustaining and adjustments of health-care products.

The Principal Product Development Engineer will be responsible for the early stage development of plastic and disposable medical device products for one of the industry leading blood therapy devices in the world. This individual will continue to sustain as well a contribute to the development of new products in the catalog.