As a member of project teams, this consultant identifies client's strategic issues, evaluates their company, industry, and rivals, structures issues, conducts executive interviews, conducts quantitative analysis, uses spreadsheet modeling, develops and improves complex business models, and prepares and delivers client presentations.

An engagement manager or principal will manage all facets of customer interactions and engagements. On matters of the utmost strategic importance to the client organization, they communicate with C-level executives, leadership groups, and boards of directors. Through the process of developing a plan, they assist and direct client teams.

Michael Page is working with one of Boston's fastest growing general contractors as they seek to hire a "Construction Superintendent - Biotech Projects" to their team. If interested, please apply today for immediate consideration within 12 business hours.

The Project Scheduler will be responsible for managing time and resources to ensure work/project is completed on time. Experience with technical/complex construction projects or projects in the lab/life science space preferred.

Are you a Superintendent ready to take your career to the next level? This opportunity allows you to gain autonomy while working alongside some of the best in the business. Put your excellent verbal and written communication and management skills on display while building state of the art Life Science facilities in greater Boston.

Looking for a motivated Construction Project Manager to join a well established and reputable General Contractor building high-profile Life Science projects throughout the local area.

Currently hiring a motivated Senior Project Manager to manage high-profile Life Science projects throughout the local area!

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. Apply today for immediate consideration.

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

The Senior Project Manager will be incharge of leading projects in their life science sector. They have a large back-log of life science/pharma projects, primarily North of Boston, up to $50M+ in value.

• Join one of the top Commercial General Contractors in Boston!
• Manage high-profile Lab, Life Science & Biotech projects throughout Boston

Looking for a motivated Construction Project Manager to join a well established and reputable General Contractor building high-profile Life Science projects throughout the local area.

Michael Page is partnered with a well-known and respected General Contractor based North of Boston. They are seeking a Project Executive to join their team, overseeing and supporting multiple Project Management teams from a high level. Please apply today for immediate consideration.

Looking for a motivated Construction Project Manager to join a well established and reputable General Contractor building high-profile Life Science projects throughout the local area.

• Join one of Boston's leading General Contractor with a strong pipeline of work!
• Competitive pay, 100% paid health insurance, Car allowance & Bonus structure!

The Senior Project Manager will be incharge of leading projects in their life science sector. They have a large back-log of life science/pharma projects, primarily North of Boston, up to $200M+ in value.

Monitor the project from beginning to end while updating all parties involved on project status and budget.

• Responsible for locating, creating, and implementing business prospects in the biotech and pharmaceutical sectors on a global scale in order to strategically expand the company.
• Develop strategies to turn opportunities into new business and revenue by identifying feasible short- and long-term commercial opportunities in the CDMO sector, including CMC and GMP production.

The VP of Quality will build and lead the Quality Assurance team and processes in support of the company's portfolio of products in clinical development and through commercialization

• Responsible for locating, creating, and implementing business prospects in the biotech and pharmaceutical sectors on a global scale in order to strategically expand the company.
• Develop strategies to turn opportunities into new business and revenue by identifying feasible short- and long-term commercial opportunities in the CDMO sector, including CMC and GMP production.

Establishing, developing, and finalizing business deals will fall under the purview of the vice president of business development. This person will negotiate contract terms, evaluate opportunities, and lead outreach efforts to prospective partners. Long-term goals include cultivating and maintaining solid connections with partners, potential partners, and influential figures in business and academia.

The Senior Program Manager provides strategic and operational leadership across the portfolio pipeline, integrating drug development across all functions, and tracking progress to plan. This includes driving execution of pre-clinical development plans and regulatory efforts for multiple programs to meet corporate time-lines and budgets.

Scientist Assay Validation efforts in preparation for regulatory filing and product commercialization.

Prepare for regulatory filings and product commercialization. Support of documentation for compliance with FDA.

Join the CMC group and help int he development, qualification, and execution of analytical methods and bioassays in support of clinical development of protein therapeutics. Work in cross functional environment and provide support for Process Development and Research and Discovery groups.

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.

• Responsible for locating, creating, and implementing business prospects in the biotech and pharmaceutical sectors on a global scale in order to strategically expand the company.
• Develop strategies to turn opportunities into new business and revenue by identifying feasible short- and long-term commercial opportunities in the CDMO sector, including CMC and GMP production.

Work cross functionally with project teams to define and execute bioanalytical and bio-marker strategies using LC/MS and other technical platforms. Expand the bioanalytical assay portfolio to align with preclinical and clinical program requirements while mentoring and teaching junior scientist along the way.

The Director of Global Regulatory Affairs will define company regulatory strategy for biologic and small molecule programs, overseing regulatory matters and lead all regulatory initiatives.

The Director will provide expert modeling input into exploring the PK/PD/Efficacy in pre-clinical models as well as build an understanding of the requirements for therapeutic intervention across patient populations.