- 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 will be part of a team responsible for supporting GMP medicines.
Join a rapidly growing biotech company
Be part of a team developing innovative medicines
Save Job View Job - MarlboroughPermanent
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.
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 - 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 - FayettevillePermanentUSD100,000 - USD135,000
The Quality Assurance AD sits on the Quality team and is responsible for championing a world-class quality system, developing a quality culture within the organization, implementing and monitoring quality metrics throughout the organization to ensure it is achieving its goal of 100% out-of-box quality, ensuring company-wide compliance with ISO 9001 and that all process controls are in place to achieve the highest level of product quality in design, manufacturing and service.
Join a growing team with internal growth opportunity and career longevity.
Outstanding salary and benefits package
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 - 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 - WalthamPermanent
This role will be responsible for the management of Quality Associates in support of product release. The QA Lead will manage, mentor and motivate their direct reports. 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.
Competitive Compensation and Bonus
Step up into a management position
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