- Bristol Myers Squibb (Bothell, WA)
- …personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Quality Assurance Document Control (QADC) Sr Specialist supports the ... Minimum of 3 years of relevant document control management experience in a cGMP/ FDA regulated...document control management experience in a cGMP/ FDA regulated environment. + Strong communication and customer service… more
- Actalent (Tamarac, FL)
- Document Control Specialist The Specialist - Global Quality & Compliance will create, revise, and manage global quality documentation, including SOPs, ... + 2+ years of experience in Technical Writing or Document Control + Experience in Document...Qualifications + Experience in Regulatory Affairs + Familiarity with FDA regulations + Knowledge of cGMP Work Environment Onsite… more
- Transylvania Vocational Services (Brevard, NC)
- …in management of customer external databases. ESSENTIAL REQUIREMENTS: . Working knowledge as a Document Control Specialist of the following: | Quality Manual ... (QMS) | SQF -Food Safety & Food Quality | Document Control Procedure | Calibration Procedure -...records for all the primary packaging components to ensure FDA compliance. . Head up the Glass & Hard… more
- PCI Pharma Services (Philadelphia, PA)
- …Philadelphia facility. This Quality Management System includes Documentation Control , Investigation and CAPA Management, Training, Internal/External Audits, Customer ... and is responsible for all the upkeep, maintenance and control of all QA related documents. Such documents include...skills. + Basic knowledge of Lean Six Sigma and FDA cGMP's preferred. + Experience in Pharmaceutical industry preferred.… more
- BD (Becton, Dickinson and Company) (Tempe, AZ)
- …Microsoft Word, Excel, and Access. + 2+ years experience in a document control related position, preferably in an FDA and/or regulated environment. + High ... for the revising, formatting, and editing of division documents as requested by document owners. **Job Description** We are **the makers of possible** BD is one… more
- Biomat USA, Inc. (Research Triangle Park, NC)
- …pertaining to shared/impacted processes. + Communicates with Training Department and Document Control to facilitate Center and Corporate training related ... hybrid role based out of our RTP, NC office.** **Summary:** Processes change control requests to ensure that process and documentation changes with the potential to… more
- Eurofins (Louisville, KY)
- …and maintain high standards for product quality and safety. Key Responsibilities: 1. Document Control Management: + Oversee the lifecycle of all QMS ... revision, approval, and archiving on electronic QMS. + Manage and maintain document control processes, ensuring compliance with applicable standards such as… more
- J&J Family of Companies (Wilson, NC)
- Johnson & Johnson is currently seeking a Manufacturing Process Specialist to join our Johnson & Johnson Innovative Medicine Supply Chain organization located in ... potential. At Johnson & Johnson, we all belong. The Manufacturing Process Specialist is a technical expert supporting the manufacturing of biological products both… more
- Integra LifeSciences (Boston, MA)
- …of Integra Boston's Quality Management System under the direction of the Manager of Document Control and Training or Quality Site Leader. **ESSENTIAL DUTIES AND ... duty satisfactorily. Primary responsibilities are to support site change control and document control activities... Control , + Record Control , Change Control + Experience with FDA and/or Notified… more
- Boehringer Ingelheim (Athens, GA)
- …reflect Boehringer Ingelheim's high regard for our employees. The Principal Specialist , Validation manages all phases of higher level, more complex validation ... for assuring compliance of validated systems, process, equipment to current cGMP, FDA , EU, USDA, BIAH and BI corporate requirements. This includes, but is… more
- Envista Holdings Corporation (Pomona, CA)
- …to learn and utilize computer in standard business applications including electronic document control , word processing, spreadsheets and databases. + Must be ... requirements and corporate standards. This involves assuring quality standards ( FDA , ISO, CMDCAS, MDD, MDR, MDSAP and Canadian Medical...assigned, in addition to those identified below + Ensures FDA QSR (GMP), FDA OTC, ISO 13485,… more
- Integra LifeSciences (Boston, MA)
- …incorporation of taught skills and techniques into employees work behavior. + Working with Document Control and platform leads to review document curriculums ... set new standards of care. The Senior Quality Compliance Specialist -Training will create and conduct training programs to...are mapped to the appropriate associate. + Working with Document Control Team, Quality, and Manufacturing Engineering… more
- Catalent Pharma Solutions (Harmans, MD)
- **Lead Specialist , QA Analytical** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission ... treatments for patients annually. Catalent's Harmans/BWI, MD facility is a FDA -licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies. The campus… more
- Edgewell Personal Care (Ormond Beach, FL)
- …+ eBatch Quality Oversight + PLM Change Analyst - backup + Back up for document control , FG review, eBatch characteristics + EQMS Admin for Change Control ... not only confidence but determination. **POSITION TILE** **:** **Quality Systems Specialist ** **DEPARTMENT POSITION IS LOCATED IN** **:** **Ormond Beach** **REPORTS… more
- Catalent Pharma Solutions (Harmans, MD)
- **Manufacturing Specialist ** **Summary:** _Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... of life-enhancing and life-saving treatments for patients annually._ _Our FDA -licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located… more
- Unither Pharmaceuticals (Rochester, NY)
- …control committee meetings, training, and coaching site employees on the change control process. In addition, the Quality Systems Specialist will support ... Quality Systems Specialist Who we are? We are a French...be responsible for the oversight of the site change control system which will include facilitation of the change… more
- BioFire Diagnostics, LLC. (Durham, NC)
- …anticipated to be Friday - Sunday 7:00am - 7:30pm. The Manufacturing Compliance Specialist will focus on Right First Time (RFT) initiatives + Review of manufacturing ... to submission to QA + Provide on the floor document review of batch records and support for Manufacturing...improvement ideas on documentation and processes + Complete change control to ensure that improvement ideas are fully implemented.… more
- Sharing Hope SC (North Charleston, SC)
- Senior Quality Systems Specialist Job Details Job Location Charleston - North Charleston, SC Position Type Full Time Job Shift Day Shift Description Summary The ... Senior Quality Systems Specialist , Quality Systems performs a variety of complex quality specific duties and supports the Quality Systems Department. This role is… more
- MyFlorida (Miami, FL)
- SANITATION AND SAFETY SPECIALIST - 42004478 1 1 1 Date: Jan 21, 2025 The State Personnel System is an E-Verify employer. For more information click on our E-Verify ... Agriculture and Consumer Services Working Title: SANITATION AND SAFETY SPECIALIST - 42004478 1 1 1 Pay Plan: Career...but not limited to, the Food and Drug Administration ( FDA ) and the United States Department of Agriculture (USDA).… more
- Lauridsen Group Inc. (Ankeny, IA)
- …and GMP standards, particularly in bulk pharmaceutical production. + Strong confidentiality, document control , and compliance skills. **Why You'll Love Working ... The Regulatory Affairs Specialist ensures compliance with applicable regulations for new...Quality Management Systems (QMS) is required. + Familiarity with FDA filing requirements such as DMF, NDA, ANDA, MAA… more