- WakefieldPermanentUSD120,000 - USD140,000
Michael Page is partnered with a reputable General Contractor based just north of Boston. They are seeking a skilled Superintendent with Life Science project experience to join their team. Apply today for immediate consideration.
Join a Reputable General Contractor in a promising market!
Base salary up to $140k, health benefits, 2+ weeks & more!
Save Job View Job - BurlingtonPermanentUSD120,000 - USD140,000
Michael Page is partnered with a reputable General Contractor based just north of Boston. They are seeking an experienced Superintendent with Life Science project experience to join their team. Apply today for immediate consideration.
Join a General Contractor that specializes in high-profile Life Science projects
Base salary up to $140K, 2+ weeks PTO, health & dental, and more!
Save Job View Job - LexingtonPermanentUSD100,000 - USD120,000
Are you a technical accountant, looking for a more your next great career opportunity? My client is seeking strong Technical Accountants to join their business in a newly created role. This is an excellent opportunity for any accounting professional looking to expand their technical skills while working in a high growth environment. If you are interested, please read on and apply for immediate consideration.
Join one of the fastest growing Biotech companies in New England
Excellent Opportunity for any Accountant looking to advance their career
Save Job View Job - MedwayPermanent
The Quality Engineer will be responsible for working in a GMP environment.
Excellent benefit package
Join a rapidly growing global leader in medical device/life sciences
Save Job View Job - BostonPermanentUSD48,000 - USD65,000
Sitting among our Team at Michael Page Boston, this position will drive business development through developing relationships, negotiating contracts, visiting clients, and closing lucrative deals.
This offers a definitive career growth plan with a strong development plan.
Dynamic Sales position with our team located right in Boston!
Save Job View Job - BrocktonPermanentUSD130,000 - USD160,000
Michael Page is working with one of Massachusetts' fastest growing General Contractors. They are seeking a Project Manager with Life Science experience to work on high-profile projects throughout the Greater Boston Area. Apply today for immediate consideration.
Work for one of New England's fastest growing General Contractors!
Base salary up to $160K, health benefits, 401k, 3 weeks PTO, & more!
Save Job View Job - WalthamPermanent
The Quality Assurance Lead will report directly to the QA Director.This position is responsible to actively participate in the ISO 9001 Quality Management System. This role will be responsible for the management of Quality Associates in support of product release. They are responsible for supervising the daily schedule and assigning tasks to their direct reports. Must work independently and manage short and long-term priorities.They will work closely with the manufacturing team assisting with Qu
Opportunity to lead and develop a team of innovate QA Associates
Join a growing med device/biotech company seeing a lot of success in 2020
Save Job View Job - FraminghamPermanent
The Safety Manager will monitor and enforce the individual Health & Safety plans of each project in conjunction with the safety managers to ensure that the following requirements are fulfilled for each project.
ENR TOP 400 General Contractor firm | 100% Employee-Owned Organization
Highly-Competitive Benefits Package + Employee Stock Ownership Program
Save Job View Job - CambridgePermanentUSD70,000 - USD85,000
The Property Manager will directly report into the General Manager and oversee multiple properties within an office complex that entails and life science component.
Join an entrepreneurial company in growth mode
Work on both office properties and with life science components
Save Job View Job - BostonPermanentUSD140,000 - USD170,000
Michael Page is partnered with a leading Developer and Owner's Project Management firm based in Boston. They have an increased pipeline of work and are seeking a Senior Project Manager with Life Science experience to join their team. Apply today for immediate consideration.
Work for an industry-leading development firm with high-profile clients/projects
Base salary up to $170K, health benefits, 3 weeks PTO, annual bonus & more!
Save Job View Job - BrooklinePermanentUSD130,000 - USD140,000
Michael Page is working with a reputable Top 400 ENR firm as they seek to hire a "Lead Construction Superintendent - Life Science Projects" to their team. If you are interested, please apply today for immediate consideration within 8 business hours.
Build complex projects for the Boston area's most high profile clients!
Total salary over $150,000!
Save Job View Job - BurlingtonPermanentUSD80,000 - USD150,000
Work on large scale, complex projects in the lab/life science space. Have the ability to develop in your career with a company that is almost doubling in size.
Develop in your career with a company that is growing substantially into 2021.
Opportunity to wear multiple hats and work on complex lab/life science projects.
Save Job View Job - BridgewaterPermanentUSD90,000 - USD135,000
Core responsibilities of this position will be maintaining client relationships by keeping open communication through all parties, and managing all phases of construction.
Five plus years of Life Science Experience Preferred
Must Have Ground up Construction Experience
Save Job View Job - WoburnPermanentUSD90,000 - USD120,000
The selected Project Manager for this firm will be working with a reputable OPM Firm in an office based role, working on high profile Life Science projects that are based around New England. As the Project Manager, you will be overseeing all phases of the building process, and collaborate with your team and clients to achieve and go above and beyond with consistently achieving goals and taking initiative.
Career Development- This firm highly believes in Promote/Develop from within.
Team Culture- This firm emphasizes quality of life & rewarding work environment.
Save Job View Job - CambridgePermanentUSD150,000 - USD220,000
Reporting to the SVP & Head Business Development, CMC, the BD Director, CMC will play a key leadership role in identifying, developing and delivering new business opportunities in the North East territory including: Boston/New England, NY, NJ, CT, and PA. This position will be remote with the expectation to meet customers across the territory (virtually for now) and work closely with key internal stakeholders.
Expected to establish and lead business development across US North East
Global Life Sciences CDMO looking to aggressively expand its US market presence
View Job - BostonPermanentUSD70,000 - USD80,000
The Document Control Specialist will be responsible for the management of the document control system and assist with internal/external audits. This job is a great opportunity to work with a hands-on quality team and develop a broad level of experience within Quality & Document Control.
Our client is an essential business and has seen exponential growth.
This is an opportunity to work with an innovate product and culture.
Save Job View Job - WalthamPermanent
The Director of Regulatory Affairs will be accountable for delivery of regulatory affairs for the product portfolio, both strategy and operations. This role will need to provide key input into non-clinical and clinical aspects of regulatory preparation, delivering a regulatory strategy for novel therapeutics in oncology and autoimmune disease areas.
Opportunity to build out and own Regulatory Function
Join a rapidly scaling biotech with aggressive growth plans for 2021
Save Job View Job - BostonPermanentUSD90,000 - USD120,000
The Design Quality Engineering will be responsible for the design quality, risk management and design control with an emphasis on sustaining. Works cross-functionally in the development and implementation of prevention-based methodologies used in design, manufacturer, test, sustainability and correction of products and services.
A fast paced and competitive work environment in a constantly evolving market.
This is an opportunity for clearly defined internal growth.
Save Job View Job - CantonPermanentUSD50 - USD90,000
The individual in this role will be part of a cohesive team responsible for production of medicines in clinical trials. He/she will apply existing and new knowledge of bioprocess unit operations and cGMPs to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations.
Global biopharmaceutical company in Canton MA expanding aggressively
Hands-on Manufacturing Associate with growth trajectory/upward mobility
Save Job View Job - WalthamPermanent
The Director of Regulatory Affairs will serve as the head of the function; providing oversight, planning, and delivery of Regulatory strategy & operations for the company's portfolio of lead therapies. As the first Regulatory hire, this individual will be tasked with building and implementing a culture of Regulatory & Quality.
Head position; Regulatory Affairs oversight of company's portfolio
Biotech start-up in Boston, supporting oncology and autoimmune disease therapies
Save Job View Job - CambridgePermanent
The Director of Regulatory Affairs will be accountable for delivery of regulatory affairs for the product portfolio, both strategy and operations. This role will need to provide key input into non-clinical and clinical aspects of regulatory preparation, delivering a regulatory strategy for novel therapeutics in oncology and autoimmune disease areas.
Great opportunity to work with a top company in the field
Key hire- first Regulatory Hire
Save Job View Job - CambridgePermanent
The individual in this role will be responsible for antibody/protein engineering and characterization in a dynamic and highly interdisciplinary environment. He/she will also be involved in antibody/protein engineering/optimization using phage display or other molecular evolution techniques.
Great step into leadership
Rapidly growing company
Save Job View Job - WalthamPermanentUSD120,000 - USD150,000
The RA Manager will be responsible for oversight of 510k submissions, registrations and other US and European submissions. This opportunity allows for responsibility and an opportunity to grow within the Regulatory field.
Join a rapidly growing Class II Medical Device start-up.
This role will allow for autonomy and growth opportunities.
Save Job View Job - WalthamPermanent
The candidate will contribute to advancement of the research and early development pipeline of novel biotherapeutics targeting Oncology. This individual is expected to have a strong foundation in molecular biology techniques and a high attention to detail. Primary responsibilities include generating antibody leads using phage display, and protein engineering.
Join innovative biotech company with exciting growth plans for 2021
Opportunity to mentor and develop leadership skills
Save Job View Job - WalthamPermanent
The Director of Regulatory Affairs will be accountable for delivery of regulatory affairs for the product portfolio, both strategy and operations. This role will need to provide key input into non-clinical and clinical aspects of regulatory preparation, delivering a regulatory strategy for novel therapeutics in oncology and autoimmune disease areas.
Growth opportunity to build out and own Regulatory Function
Join a rapidly growing biotech with aggressive growth plans for 2021
Save Job View Job - CambridgePermanent
This individual will be responsible for antibody/protein engineering and characterization in a dynamic and highly interdisciplinary environment. He/she will also be involved in antibody optimization using phage display or other molecular evolution techniques. This position will CONTRIBUTE to therapeutic mAb discovery and Ab fusion protein engineering/optimization by using microbial display and mammalian transient expression/protein production technology.
Great opportunity to work with a top company in the field
Growth Potential
Save Job View Job - BostonPermanentUSD160,000 - USD220,000
As a hands-on Director, this individual will lead as a "player/coach," leading a small team of 3 (with additional hires next year) to drive Quality Assurance across the company gene and cell therapy manufacturing unit. The GMP Quality Director will provide Quality Operations oversight and play a key role in implementing quality systems.
Global biopharmaceutical company in Boston which has doubled size and revenue
Hands-on Director to lead oversight for Quality Operations in gene therapy
Save Job View Job - NorwoodPermanent
The individual in this role will perform cGMP QC tasks and also support environmental monitoring and sample management activities as needed.
Bonus and equity stake
Growth Opportunity
Save Job View Job - NorwoodPermanent
The individual will be part of a team responsible for supporting GMP medicines.
Industry Leader
Rapid growth opportunity
Save Job View Job - NorwoodPermanent
The individual in this role will perform cGMP QC tasks and also support environmental monitoring and sample management activities as needed.
Join an innovative and quickly growing biotech company
Opportunity to grow and develop under a highly motivated and talented team
Save Job View Job
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