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Looking for a motivated Assistant Construction Superintendent to join join one of Boston's most reputable General Contractors to support a $100M+ Life Science project in Downtown Boston!
Michael Page is partnered with one of Massachusetts' top General Contractors. They are actively looking for an experienced marketing professional to join their team as a Proposal Manager. Apply today for immediate consideration.
Michael Page is partnered with a leading General Contractor based West of Boston seeking to hire a highly experienced Project Executive to direct a mid sized team!
Looking for a motivated Assistant Construction Project Manager to support an exciting $100M+ life science build happening in Downtown Boson!
Currently seeking to hire a highly motivated Project Manager to join a leading General Contractor located in the Metro West area focusing heavily on life science and manufacturing projects!
APPLY TODAY FOR IMMEDIATE CONSIDERATION
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 role will have full control to strategies, plan and execute the companies' clinical assets in oncology and diseases with budget and direct line responsibility for patient advocacy, medical affairs, and clinical operations. This role will play a pivotal role in building the companies future vision with full access to the board.
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.
This Executive Director / Head of Clinical Operations will lead psychiatric programs. Highly visible role expected to interact with the executive team, design Clinical Studies, and build and manage CRO relationships.
Ideally, candidates are to have 15+ years of experience managing clinical trials execution in biotech / pharma and experience in CNS or psychiatric programs is preferred.
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.
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.
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).
Work in the preclinical team as the biomarkers lead to support in vitro and in vivo proof-of-concept and IND-enabling studies. You will be responsible for designing, developing, and executing molecular and other biologically relevant assays to support development efforts across their highly multidisciplinary organization.
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.
As Sr. Specialist, Quality Assurance, he/she will perform task that will uphold and improve the product quality of medical devices manufactured and meet regulatory requirement to stay in compliance.
The Senior Product Development Engineer in this role will be an integral member on a small development engineering team team, that will work in conjunction with internal Operations and Quality partners, to drive a life-changing technology to FDA approval.
The Principal Research and Development Engineer will be responsible for the adjustments of a micro catheter based product through design for manufacturing, lean processing and continuing to work with third party suppliers and contract manufacturers to make it the most efficient product possible.
The Sustaining Engineer II will be responsible for supporting product lines throughout the entire product lifecycle. You will work closely with R&D, Quality, Regulatory and Manufacturing teams to support regulatory submissions, maintain good market status, and engineer solutions that improve the safety, quality and efficacy of Class I, II and III medical devices.
The Electrical Engineer will work with a outside primary supplier int he beginning stages of a fifth generation medical device product. The first Electrical Engineer on the Research and Development Engineering team will be a leader of development of new electronic techniques and continue to grow out the team with the qualified individuals over the next three years.
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