Email Alert for
ⓘ There was an unexpected error processing your request.
Please refresh the page and try again.
If the problem persists, please contact us with your issue.
You can always manage your preferences and update your interests to ensure you receive the most relevant opportunities.
Get ready to discover your next great opportunity.
EPM Scientific
Billerica, MA, United States
Title: Sr. Quality Assurance Specialist Location: Billerica, MA A pharmaceutical company is seeking a Sr. Quality Specialist to spearhead Quality activities related to their combination products. The Sr. QA Specialist will be responsible for all aspects of QA for medical devices manufactured on site or through third party contractors. Responsibil
Job Source: EPM ScientificCATALDO AMBULANCE
Danvers, MA, United States
Job Description Job Description ALS Quality Assurance (QA) Specialist Job Summary Works with each division Clinical Manager as well as the Senior Clinical Director to monitor and maintain clinical standards. Duties and Responsibilities Work collaboratively with the Clinical Director and Mangers to ensure that proper clinical standards are being
Job Source: CATALDO AMBULANCEArcaea
Boston, MA, United States
Arcaea is building a new ingredient toolset for the beauty and personal care industry - one rooted in biotechnology with the aim of delivering radical performance and unparalleled sustainability that will also present new opportunities for storytelling. Arcaea is seeking an experienced Quality Assurance Specialist to join our team and play a criti
Job Source: ArcaeaCambridge Isotope Laboratories, Inc.
Tewksbury, MA, United States
Cambridge Isotope Laboratories (CIL) has an outstanding opportunity for a Quality Assurance Specialist I to join the team responsible for the quality of several new and existing active pharmaceutical ingredients (APIs) and medical device components based onsite in our Tewksbury, MA location. CIL is the global leading company in a highly technical,
Job Source: Cambridge Isotope Laboratories, Inc.Arcaea
Boston, MA, United States
Arcaea is a biology-first beauty company building a new ingredient toolset for the beauty and personal care industry. We are creating pioneering ingredients, products, and stories accessible uniquely through biology. Arcaea is building a new ingredient toolset for the beauty and personal care industry - one rooted in biotechnology with the aim of
Job Source: ArcaeaAzzur Group
Waltham, MA, United States
Description About Azzur Cleanrooms on Demand As you look to start your journey on the next cure that can heal patients and save lives, lack of space to manufacture and properly follow cGMP processes can be a major hurdle. To address the unique needs of start-ups in your position, Azzur Cleanrooms on Demand is here to support production for early-
Job Source: Azzur GroupGardner Resources Consulting
Boston, MA, United States
Our Pharma client, located in Boston, MA, is currently searching for a Senior Quality Assurance Contractor to help maintain quality systems with a focus on GMP Compliance. The Senior QA Contractor will assist with batch record review and will provide a thorough review and analysis of mission critical data focused on QMS trending and reporting and
Job Source: Gardner Resources ConsultingFractyl Health, Inc
Burlington, MA, United States
Reports to: Sr. Manager of Regulatory Affairs Position Summary As our Clinical Quality Assurance Specialist, you will be a champion for Good Clinical Practices (GCP) compliance across our medical device development programs. You will ensure adherence to ICH requirements, manage clinical vendor selection and oversight, oversee clinical Standard
Job Source: Fractyl Health, IncBoston, MA, United States
Description:
seeking a Quality Assurance Sr. Specialist for real time on the floor quality oversight and lot disposition of Small Molecule GMP manufacturing facility at Moderna Inc. This position will be based in our cGMP Small Molecule Manufacturing site in Cambridge, MA.
The individual in this role will be part of a cohesive team responsible for supporting cGMP small molecules produced internally at Moderna. He/she will provide quality oversight and expertise to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will have experience in quality oversight or manufacturing experience in early-stage clinical products. They will be able to interact fluidly with peers and supervisors in Manufacturing, and cross-functionally with Quality Control, Manufacturing, Logistical and Process Development Technology Transfer counterparts.
Here's What You'll Do: Provide on-the-floor Quality support to manufacturing, review documentation, and make quality decisions and/or escalate issues to management that may impact operations.
Participate in quality oversight of manufacturing through real-time observations of activities.
Participate in quality focused teams across Moderna's broad ecosystem of functions.
Authors and reviews SOPs, policies, and batch production/testing records to ensure compliance and adherence to regulations/cGMP operations.
Oversee and review batch record documentation.
Review/Approve manufacturing deviations, change controls and CAPAs.
Closely partner with peers for disposition of Small Molecules.
Demonstrate general knowledge of standard manufacturing compliance, quality disposition, quality system review.
Enforce adherence to current good manufacturing practices, standard operating procedures, and manufacturing documentation. Establish and follow written procedures for the clear and accurate documentation of equipment operation and process instructions, and of process data.
Monitor process operations to ensure compliance with specifications.
Utilize knowledge to improve operational efficiency.
Here's What You'll Bring to the Table:
A minimum of 5 years' experience in a GMP manufacturing environment with a bachelor's degree in biology, Chemistry, Chemical engineering, Biomechanical engineering, Bioengineering, Biomedical engineering, Biochemistry or related field or seven years of experience in a clinical quality assurance environment
#J-18808-Ljbffr
Email Alert for Quality Assurance Sr. Specialist jobs in Boston, MA, United States
ⓘ There was an unexpected error processing your request.
Please refresh the page and try again.
If the problem persists, please contact us with your issue.
You can always manage your preferences and update your interests to ensure you receive the most relevant opportunities.
Get ready to discover your next great opportunity.