- Merck & Co. (Rahway, NJ)
- …matter expertise -Knowledge of order management, supply chain operations and document control . -#MSJR #eligibleforERP GCSCareer25 #VETJOBS #GCSCareer Current ... High School Diploma with 10+ years equivalent industry experience in Pharmaceutical Clinical Supply (packaging, labeling, logistics and clinical supply inventory… more
- Moderna, Inc. (Norwood, MA)
- …years of experience as a Validation Specialist , Release Technician, QA Specialist , Product Development Associate, Intern - Change Control , or related ... The Role: ModernaTX, Inc. seeks a Sr. Specialist , Manufacturing for its Norwood, Massachusetts location. Here's What You'll Do: Determine root cause of DNA, Drug… more
- Abeona Therapeutics Inc (Cleveland, OH)
- …shift schedule. Performs the following duties with minimal supervision. Process document control requests and issue-controlled forms, logbooks, notebooks, master ... Position Overview The Specialist II, Quality Assuranceperforms routine activities associated with...ensure resolution of and discrepancies that occurred during execution. Control document lifecycle activities, including biennial review… more
- US Tech Solutions (Overland Park, KS)
- …the Compliance Department including audits, internal controls, safety reporting/Pharmacovigilance, document control , training, risk management, vendor risk ... Duration: 05 Months Job Description: This position is for a Compliance Specialist . Compliance is often viewed as behind the scenes; however, Compliance is front and… more
- Genentech, Inc. (Hillsboro, OR)
- …manufacturing processes, equipment and facilities (including engineering changes, document changes, validation documentation, etc.). Where applicable perform ... fields) You have 4-7 years of previous experience in biotechnology or pharmaceutical manufacturing with understanding of cGMP principles.. You have excellent written… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …and losses in the process and build improved efficiency + Under guidance of the Senior QA Specialist Document Control , the QA Specialist - Document ... Quality Assurance Specialist , Document Control Department: QA Manufacturing Location: Monroe, NC START YOUR APPLICATION… more
- Integra LifeSciences (Braintree, MA)
- …improve outcomes. **RESPONSIBILITIES** + Responsible for supporting the maintenance of the document control system during 1st shift. + Day-to-day management of ... and document reconciliation + Serve as a document control reviewer for new and revised...working knowledge preferably in the medical device, diagnostics or pharmaceutical industries. Familiarity with FDA regulations and ISO series… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …research-based pharmaceutical company. POSITION SUMMARY: The Analytical Quality Assurance (AQA) Specialist will work with the Quality Control team to work ... Analytical Quality Assurance Specialist Department: Analytical QA Location: Monroe, NC START YOUR APPLICATION… more
- Regeneron Pharmaceuticals (Rensselaer, NY)
- We are currently looking to fill multiple Change Control Specialist positions. These positions develop strategic plans related to change control and the ... the following: + Craft business plans to independently advances change control initiatives to implement Corrective and Preventative Actions (CAPA's) and process… more
- Unither Pharmaceuticals (Rochester, NY)
- Quality Systems Specialist Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and ... main responsibilities of the position is the oversight of the Rochester Site Change Control systems. The specialist will facilitate the change control … more
- Stryker (Mahwah, NJ)
- …system performance. Key Responsibilities: + Oversee and coordinate the external document control process for monitoring and reviewing regulatory standards ... and Compliance team as a Staff Quality Management Systems specialist . In this role, you will coordinate and support...of contact for audits and inspections related to external document control and compliance. + Track assessments,… more
- Cambrex High Point (Waltham, MA)
- …System (QMS) and GMP operations. This role involves oversight of document control , training compliance, equipment lifecycle documentation, batch record ... System (QMS) to meet regulatory and internal procedural requirements. + Support document control activities including issuance, revision control , archival,… more
- Colorado State University (Fort Collins, CO)
- Posting Detail Information Working TitleQuality Assurance Specialist III Position LocationFort Collins, CO Work LocationPosition is fully in-office/in-person ... Orthopedic Bioengineering Research Laboratory ( OBRL ) are seeking a Quality Assurance (QA) Specialist III to support the CSU Quality Assurance Unit ( QAU ) and… more
- AssistRx (Des Moines, IA)
- …Department, including audits, hotline management, internal controls, pharmacovigilance, document control , training, risk management, business continuity, ... The Vendor Management Specialist at AssistRx is responsible for managing the...and trend analysis. + Monitor changes in healthcare and pharmaceutical regulations and ensure organizational adherence. + Collaborate cross-functionally… more
- Curia (Rensselaer, NY)
- Senior QA Validation Specialist - CSV Systems Engineer Summary: The Senior QA Validation Specialist - CSV Systems Engineer is an integral part of the Curia ... has the power to improve patients' lives with the pharmaceuticals we develop and manufacture. We proudly offer +...Will act as Site System Admin, especially site Quality Control and Manufacturing computerized systems + Generate and execute… more
- Charles River Laboratories (Rockville, MD)
- …a career that you can feel passionate about. **Job Summary** The QA Specialist I - Quality Systems is responsible for supporting Quality Systems, including ... investigation/deviation management, CAPA tracking, Effectiveness Verification, and change control . This position will facilitate the compiling, trending (as… more
- Novo Nordisk (Bloomington, IN)
- …6 weeks paid family medical leave + Free access to Novo Nordisk-marketed pharmaceutical products + Tuition Assistance + Life & Disability Insurance + Employee ... matters. Primary - Drug Product Primary Manufacturing produces sterile pharmaceuticals . The department includes equipment preparation, product formulation, material… more
- Abbott (St. Paul, MN)
- …meet current regulatory requirements and Abbott policies and procedures related to Document Control and control /distribution of current procedures. Support ... Our 114,000 colleagues serve people in more than 160 countries. **Engineering Change Specialist ** **Working at Abbott** At Abbott, you can do work that matters,… more
- Penn Medicine (Philadelphia, PA)
- …adjustments to departmental operations to ensure quantity and ensure quality of pharmaceutical care services. Control pharmaceutical safety while increasing ... documentation are accurate. The individual will monitor, follow up and document corrective actions to ensure complete pharmaceutical compliance. In addition,… more
- Element Materials Technology (Santa Fe Springs, CA)
- …in laboratory activities, equipment and method qualifications review and approval, and document control . Reports to the Quality Supervisor and/or Quality ... **Overview** Element has a current opening for a **Quality Specialist I** to join our growing team in Santa...of SOPs, test methods, protocols, and logbooks through the document control system. + Assist in the… more
