- 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 - 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 - 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 - 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 - 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 - BostonPermanent
The R&D Program Management & Operations, Director/Sr. Director will play an integral role in the project management of one or more of programs that are part of the client's wholly owned pipeline.
Join innovative biotech company
Manage lead drug/therapy from discovery to into Clinical Trials
Save Job View Job - BostonPermanentUSD180,000 - USD250,000
This role will be responsible for leading the day-to-day Quality operations at the cell/gene therapy manufacturing site. The role will also be a key contributor to the implementation and execution of quality systems including oversight of facility and equipment validation activities.
Globally recognized leader in the Pharmaceutical space
Massive growth potential
Save Job View Job - BostonPermanent
The Director will be responsible for leading the day-to-day Quality operations at the cell/gene therapy manufacturing site. The Director will also be responsible for the implementation of policies, practices, procedures, standards, and systems necessary to ensure the compliance of site operations to global GMP regulations.
Great opportunity to work with a top company in the field
Great growth potential!
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