Final Release Specialist II - Devens, MA

The Quality Assurance (QA) Final Release Specialist position supports the batch final release processes. Performs functions necessary to ensure that all relevant manufacturing records and documentation are assembled, reviewed, and completed in a compliant efficient manner. · Main ...

The Quality Assurance (QA) Final Release Specialist position supports the batch final release processes.This role requires attention to detail and must be performed in accordance with standard operating procedures as well as all applicable requirements. · ...

The Quality Assurance (QA) Final Release Specialist position supports the batch final release processes. · Performs functions necessary to ensure that all relevant manufacturing records and documentation are assembled, reviewed, and completed in a compliant efficient manner. · ...

About Us · Founded in 2015 to develop the world's first industrially scalable laser metal additive manufacturing solution, VulcanForms is reshaping how the world manufactures critical products. We build and operate advanced digital infrastructure that enables innovation, accelera ...

Overview · Responsible for processing requests for health information (medical records) in a timely manner, ensuring accuracy in the release of records, and providing customers with the highest quality product and service. Specialist must at all times safeguard the patient's righ ...

Responsible for processing requests for health information (medical records) in a timely manner, ensuring accuracy in the release of records, and providing customers with the highest quality product and service. Specialist must at all times safeguard the patient's right to privac ...

The HIM Release of Information (ROI) Specialist coordinates the release of Protected Health Information (PHI) for the Hospital for Behavioral Medicine and from multiple storage media while utilizing ROI software to process medical record requests. · ...

Responsible for processing requests for health information (medical records) in a timely manner, ensuring accuracy in the release of records, and providing customers with the highest quality product and service. Specialist must at all times safeguard the patient's right to privac ...

This is a part time position at the Hospital for Behavioral Medicine in Worcester, MA. · ...

The CDS Release Management Specialist will plan, coordinate, and execute the deployment of technology changes into production across the CDS enterprise environment.This role is Hybrid at either our Tewksbury MA, Richardson TX, or Tucson AZ facility. · Active and transferable U.S. ...

The AQ&C Specialist will focus on Quality Assurance (QA) review and approval of technical documents pertaining to GMP analytical methods for biologics (large molecules) drug substances and drug products. · Perform the QA review/approval of technical documentation, including but n ...

The AQ&C Specialist will focus on Quality Assurace (QA) review and approval of technical documents pertaining to GMP analytical methods for biologics (large molecules) drug substances and drug products.Specific technical document types include analytical method prodedures, method ...

The Quality Assurance Product Disposition Specialist is responsible for supporting quality and disposition activities at the Devens MA Cell Therapy manufacturing facility in accordance with Client policies standards procedures and Global cGMP The role will aid in the routine and ...

The Analytical Quality & Compliance Specialist will focus on QA review and approval of technical documents pertaining to GMP analytical methods for biologics drug substances and drug products. · Analytical method validation protocols and reports for in process, release, and stabi ...

Performs and troubleshoots routine and advanced processing and data review of raw materials, in-process, batch release, and/or stability samples of Bulk Drug Substance in a cGMP compliant environment. · Author revisions to SOPs for managerial review and approvalMay author protoco ...

The Supplier Quality Specialist will focus on Quality review and approval of supplier documents to support qualification of GMP starting materials for biologics (large molecules) drug substances. · Assist with the lifecycle management of material qualifications, including reduced ...

Discover Veranova · At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do ...

+ Working at Bristol Myers Squibb is anything but usual + Here uniquely interesting work happens every day in every department - From optimizing a production line to the latest breakthroughs in cell therapy this is work that transforms lives of patients and careers of those who d ...

We are hiring SR Quality Specialist for one of our clients. · We offer a wide gamut of consulting solutions customized to our 450+ clients ranging from Fortune 500/1000 to Start-ups across various verticals like Technology, Financial Services, Healthcare, Life Sciences, Oil & Gas ...

Provide human resources support for DC management and team members including recruiting and hiring applicants according to staffing needs. · Maintain close contact with corporate human resources to ensure compliance with O'Reilly policies and procedures, · and state/federal emplo ...