- Boehringer Ingelheim (Columbus, OH)
- …completed according to specifications. + products are manufactured in accordance with Quality Assurance Agreements (QAAs)as required. + discrepancies have been ... of 2-3 days per week on-site.** **Duties & Responsibilities** + Independently performs batch record review and/or final disposition of drug products manufactured… more
- Catalent Pharma Solutions (Harmans, MD)
- …therapies and vaccines. **Position Overview:** The Lead Specialist , QA Batch Disposition is responsible for providing Quality Assurance support for ... **Job Title:** Lead Specialist , QA Batch Disposition...documentation practices (GDP), including but not limited to: executed batch records , master batch … more
- Catalent Pharma Solutions (Harmans, MD)
- **Job Title:** Senior Specialist , QA Batch Disposition **Location:** Harmans, Maryland **Company:** Catalent Inc. **About Us:** Catalent, Inc. is a leading ... viral vector-based therapies and vaccines. **Position Overview:** The Senior Specialist , QA Batch Disposition supports...documentation practices (GDP), including but not limited to executed batch records , master batch … more
- Regeneron Pharmaceuticals (Rensselaer, NY)
- We are currently looking to fill a Quality Assurance Specialist position. This position performs activities supporting dispositioning product and/or raw ... materials while ensuring compliance with Quality Assurance policies and procedures, cGMPs, SOPs,...alignment with QA policies + Reviewing completed records and batch sheets and working with… more
- Catalent Pharma Solutions (St. Petersburg, FL)
- ** Quality Assurance Documentation Specialist **...using computer to create and revise batch records (including in electronic batch record ... safety of every patient, consumer and Catalent employee. The Quality Assurance Documentation Specialist is... documentation and electronic systems such as the electronic batch record system and electronic weigh and… more
- Abeona (Cleveland, OH)
- JOB TITLE SPECIALIST I, QUALITY ASSURANCE -...of a cGMP Operation for production processes relating to batch record review and release from start to ... Quality Operations or above Ladder Level 2 DESCRIPTION Position Overview The Specialist I, Quality Assurance performs routine activities associated with… more
- ManpowerGroup (Cambridge, MA)
- …Pharmaceutical QA Specialist to join their team. As a QA Specialist , you will be part of the Quality Assurance department supporting various ... which will align successfully in the organization. **Job Title:** Pharmaceutical QA Specialist **Location:** Cambridge, MA **Pay Range:** $50-55 per… more
- Novo Nordisk (West Lebanon, NH)
- …specifications and procedures + Releases product based on Quality Assurance record review and approval by QA Manager + Performs regular internal audits ... QA signature authority on the review of individual batch records , supporting test records ... QA presence on the manufacturing floor. Relationships Quality Assurance . Essential Functions + Reviews all… more
- Merck (De Soto, KS)
- **Job Description** **Position Description:** The Quality Assurance Specialist role is responsible for providing guidance and support to implement, execute, ... Manufacturing Practices (GMP), GxP Validation, Management Process, Personal Initiative, Policy Development, Quality Assurance ( QA ), Quality Control (QC),… more
- Kelly Services (Fort Washington, PA)
- ** Quality Assurance Specialist ** Kelly(R) Science & Clinical is seeking a Quality Assurance Specialist for our client a top consumer product ... office and other systems to improve business effectiveness + Exposure to electronic batch records and/or other automated processes/systems (labs). + Basic SAP or… more
- Abbott (Des Plaines, IL)
- …products and processes, which adds value to the business. The primary function of the Quality Specialist is to assist in maintaining the quality system. ... + Reviews GMP related documentation for compliance such as batch records and associated data related to...complaint logs to identify and report recurring issues to quality assurance management and product development. Collaborate… more
- Novo Nordisk (Clayton, NC)
- …& other documentation. Perform Self Audits (in conjunction with line of business (LoB)), Quality Assurance ( QA ) presence & process confirmation on shop floor ... with stakeholder. Relationships Senior Manager, Quality Assurance . Essential Functions . Ensure site...documentation for Quality approval - components/raw material, batch records , change control requests, deviations, … more
- System One (Pittsburgh, PA)
- … QA Document Specialist to manage critical documentation and support quality assurance within a cutting-edge GMP environment. You'll create and manage ... SOPs, batch records , and controlled documents using an electronic ...requirements. + Deviation and Out-of-Specification (OOS) Support: Assist the Quality Assurance ( QA ) team in… more
- Sanofi Group (Swiftwater, PA)
- **Job Title:** Quality Assurance Specialist **Location** : Swiftwater, PA **About the Job** We deliver 4.3 billion healthcare solutions to people every year, ... knowledge of documentation review, deviation investigation, contamination control, disinfection, quality assurance , aseptic processing, cGMPs and regulatory… more
- Lilly (Concord, NC)
- …want to miss! Responsibilities: The Quality Assurance Floor Support Specialist is responsible for providing QA oversight to GMP operations. The role ... startup, commissioning and qualification of the Concord site. The QA Floor Support Specialist will demonstrate teamwork...+ Review and approve GMP documentation such as electronic batch records , logbooks, etc. + Troubleshoot and… more
- Catalent Pharma Solutions (Harmans, MD)
- …lives. The ** Specialist , QA ** is responsible for providing Quality Assurance support for GMP Manufacturing of master/working cell banks, biological ... consumer, and Catalent employee.** **The Role:** + Provides dedicated QA quality floor oversight of GMP operations...revise GMP documentation such as Standard Operating Procedures, Master Batch Record review and SMP's + Compile… more
- Sanofi Group (Framingham, MA)
- …to protect people from infectious diseases and bring hope to patients and their families. Quality Assurance ( QA ) Operations is responsible for quality ... to ensure cGMPs are adhered to during manufacturing operations. Quality Assurance Operations is responsible for providing...QA review deviations + Provide off-hour support for batch record and logbook issuance + Represent… more
- Catalent Pharma Solutions (Harmans, MD)
- …The Sr. Specialist , QA -OTF is responsible for providing Quality Assurance support for GMP Manufacturing of master/working cell banks, biological ... consumer and Catalent employee. **The Role:** + Provides dedicated QA quality floor oversight of GMP operations...revises GMP documentation such as Standard Operating Procedures, Master Batch Record review and SMP's; compile deviations… more
- Actalent (Delaware, OH)
- Quality Assurance Specialist INTERESTED CANDIDATES MAY SEND UPDATED RESUMES TO: JGASSER @ ACTALENTSERVICES.COM OR TEXT JENNA TO SETUP A PHONE INTERVIEW: 419. ... 980. 5823 Job Description We are seeking a dedicated Quality Assurance Specialist to ensure...change requests for formula, process, or specification based on quality metrics. + Develop methods to eliminate batch… more
- Catalent Pharma Solutions (Chelsea, MA)
- **Document Control Specialist - Quality Assurance ** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing ... in North America. Catalent Pharma Solutions is hiring a QA Document Control Specialist who is responsible...of master documents (including but not limited to SOPs, Batch Records , Test Methods, Protocols, Reports, Specifications,… more