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.

Our client is seeking a talented executive to be responsible with collaboration, design and implementation of the worldwide regulatory strategy for all products. The individual must have strong background in both the Medical Device Industry and Regulatory Strategy.

We are looking for an exceptional Senior Director, Clinical QA to join our team and manage clinical, laboratory and pharmacovigilance quality assurance. This role will manage all GCP, GLP and GVP quality oversight as it relates to the client's phase I, II and III clinical studies.

We are looking for an exceptional Director, Clinical Quality to join our team and manage clinical, laboratory and pharmacovigilance quality assurance. This role will manage all GCP, GLP and GVP quality oversight as it relates to the client's phase I, II and III clinical studies.

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.

This is a Sr. Director, Quality Control position in the Quality group. Primary responsibilities include leading all aspects of a Quality Control department including the following: hiring and developing management-level staff, providing strategic decision-making consistent with department and organizational goals, and ensuring phase-appropriate cGMP compliance throughout Quality Control laboratories and operations.

Reporting to senior leadership, this individual will play a critical role at the highest level in managing Big Pharma relationships pertaining to Discovery/R&D services. The team is seeking a seasoned Director coming from Big Pharma, experienced in managing External Discovery Collaborations hired to do the same job, except from a commercial CRO perspective (managing Big Pharma partnerships).

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.

This is a Sr. Director, Quality Control position in the Quality group. Primary responsibilities include leading all aspects of a Quality Control department including the following: hiring and developing management-level staff, providing strategic decision-making consistent with department and organizational goals, and ensuring phase-appropriate cGMP compliance throughout Quality Control laboratories and operations.

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.

Are you a Manufacturing Accounting Professional with 10+ years of experience? Do you have a mixture of Public and Private experience? Do you have your CPA? Do you have experience leading and managing teams? Do you have experience improving processes and procedures? If so, please read on and apply to the Director of Accounting - Manufacturing job posting located in Natick, MA. This will be a hybrid role - 3 days a week on site.

Reporting to senior leadership, this individual will play a key leadership role in identifying, developing and delivering new business opportunities across North America with an emphasis on Boston/Cambridge as it relates to the biotech/pharma landscape. This position will be remote with the expectation to meet clients across the territory, R&D facilities, and work closely with key internal stakeholders.

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 Renewable Energy - VP, Development - Remote will lead development activities across the company's pipeline in the USA. Working cross-departmentally with Procurement, Execution, and Finance teams.

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.

• Join a rapidly growing company in the aerospace & defense industry
• Role will directly sit on the leadership team

Michael Page is partnered with a reputable design firm in Boston that is seeking to hire a "Director of Project Management - Design Firm" to their team. If you are interested, please apply today for immediate consideration.

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

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.

• Do you want to join a market leader in steel manufacturing within Aerospace and Defense?
• Do you want the opportunity to be one of the first sales people, with potential to grow and scale a team, with a high growth industrial client?

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.

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.

Michael Page has partnered with a family-owned company that has been in business for over 20 years. They offer design-build, ground-up construction, and tenant improvement services for local companies and are looking to add a Director of Estimating to their team to oversee preconstruction and the bid coordinators. Please apply within.

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.

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 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.

This is a Sr. Director, Quality Control position in the Quality group. Primary responsibilities include leading all aspects of a Quality Control department including the following: hiring and developing management-level staff, providing strategic decision-making consistent with department and organizational goals, and ensuring phase-appropriate cGMP compliance throughout Quality Control laboratories and operations.