Award-winning printer of custom labels, shrink sleeves, flexible packaging, and packaging prototypes, seeking to bring a Director of Operations onboard to manage their state of the art 35,000 sq. ft. printing services facility as well as a second facility in Long Island. Our client has extensive background in all phases of co-packing and filling -- they produce over 600,000,000 printed units per year.

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.

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 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 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.

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.

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.

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.

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.

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 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 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.

• Are you in the Boston Area looking to grow your regional sales and management skills?
• Do you want to join a growing top consumer electronics company?

Michael Page is partnered with Boston's leading Real Estate Development firm on their search for an experienced Construction Manager. Apply today for immediate consideration.

A well known General Contractor is looking for a Construction Supervisor to come join their team!

The Development Manager will directly report into the Director and support all the major active projects.