- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QA Validation Specialist III as part of the Quality team based in Raritan, ... NJ. Role OverviewThe QA Validation Specialist role is an exempt level...and qualification activities for equipment, systems , computer systems , and processes within a cell therapy manufacturing… more
- Aequor (Thousand Oaks, CA)
- …best work alongside other innovative, driven professionals in this meaningful role. Role: Specialist Manufacturing , New Product Introduction Let's do this! At we ... responsible for the introduction of new products into the manufacturing plant. This " Specialist Manufacturing "...New Product Introduction Lead within the New Product Introduction, Manufacturing Execution Systems , and Digital team at… more
- Omni Inclusive (Summit, NJ)
- …CSV lifecycle. The Specialist will be responsible for ensuring the validation of the S12 Enterprise Manufacturing Execution System (EMES), and applications ... onsite days with manager and be available onsite when manager requests) The Specialist works cross-functionally to execute validation activities and prepare … more
- Merck & Co. (Rahway, NJ)
- …company's Research Laboratories Division is seeking applicants for a Metrology and Validation Specialist position available at the Rahway, New Jersey research ... facility. The Metrology and Validation Specialist will work as part of...beneficial.-Demonstrated commitment to diversity and inclusion-Experience with IT, computerized systems , software and applicationsExperience leading a team for a… more
- Merck & Co. (Durham, NC)
- …with validation documentation and execution Experience with SAP Experience with Manufacturing Execution Systems (MES) Experience with Delta V Ability to ... Job DescriptionThe Maurice R. Hilleman Center for Vaccine Manufacturing is located in Durham, NC. This state-of-the-art facility established in 2004, manufactures… more
- New York Blood Center Inc (Rye, NY)
- …approves validation studies for critical processes, equipment, and computer systems to assure that they will consistently perform as expected. Qualifies outside ... Connect with us on Facebook, X, Instagram, and LinkedIn. Responsibilities The Quality Specialist II works to ensure the quality and safety of products and services… more
- Scientific Protein Laboratories (Waunakee, WI)
- …(APIs). SPL has an exciting opportunity to join the team as a Manufacturing Documentation and Compliance Specialist . This position supports manufacturing ... manufacturing personnel. Assist in the execution and documentation of manufacturing protocols (eg, qualification, validation , process studies). Participate in… more
- Planet Pharma (Newbury Park, CA)
- …of and experience with processes involved in quality analytical labs, validation , manufacturing , quality assurance, process development and distribution. 8. ... 32-42/hr *depending on experience Summary: Under general direction, functions as the Specialist Quality Control working at the Corporate QC Center. Description: Job… more
- American Packaging Corporation (Columbus, WI)
- …continue propelling our shared success into the future. Customer Account Specialist LOCATION: Columbus, WI SUMMARY: To professionally and effectively communicate ... internal customer by accurately and efficiently processing information by means of systems and procedures. REPORTS TO: Customer Service Manager ESSENTIAL DUTIES AND… more
- LanceSoft (Northridge, CA)
- Job Title: Sr Manufacturing Engineer Location: 18000 Devonshire Street Northridge California 91325 Duration : 12+ Months with possible FTE Pay: $60/hr. to $65/hr. ... Electrical, Mechanical or Biomedical Engineering Line Verification Process Development process validation statistical knowledge Nice to Have: Prior experience in a… more
- Michael Page (Hicksville, NY)
- Quality Manager- Aerospace Manufacturing - Hicksville, NY Join a business with over a 50 year history in the market About Our Client My client is a privately held, ... family-founded specialist in advanced coatings and finishing services based in...Coordinate with metallurgical lab and inspection teams for product validation and release. MPI does not discriminate on the… more
- Planet Pharma (Newbury Park, CA)
- …transactional/tactical tasks to ensure performance execution across the external manufacturing network. * Manufacturing operations: Ensure accuracy and completion ... High school diploma / GED and 10 years of Manufacturing experience OR Associates degree and 8 years of...of cGMP principles, FDA and other regulatory guidelines, and validation principles. 2+ years of project management experience leading… more
- LanceSoft (North Haven, CT)
- …author closing reports, update specifications and technical documentation. Leads successful validation of packaging systems for medical devices. Identify and ... Practices (GMPs), and may support prototype line development in manufacturing facilities/plants. Specialist Career Stream: Typically an individual contributor… more
- Staff Icons LLC (San Diego, CA)
- …Team, safety, cGMP and Quality Plan. Responsibilities Adheres to current good manufacturing practices (cGMP) guidelines. Adheres to CUA, AABB, FDA, and other ... the available data. Ability to work with a variety of temperature monitoring systems and effectively deal with equipment situations that arise. Assist with the… more
- Legrand North America (Uniontown, PA)
- …manufacturing technologies through software and hardware system construction, validation , data collection, operator training, technical support and maintenance. ... automated manufacturing equipment Validate functionality of software and hardware systems prior to deployment or following updates under direction and guidance… more
- AbbVie (North Chicago, IL)
- …Pharmaceutical experience strongly preferred. + 6+ years of overall experience in Manufacturing , Quality or Engineering including 4 major validation subjects (eg ... to plan, and complete tasks associated with commissioning, qualification and validation of new and modified equipment, facilities, utilities, product, processes… 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 ... especially site Quality Control and Manufacturing computerized systems + Generate and execute validation documents,...working in a cGMP regulated industry specific to computer systems validation + Validation experience… more
- Unither Pharmaceuticals (Rochester, NY)
- Computer Systems Validation Specialist Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that ... Functional and Design Specifications. If completed by an external company, the computer systems validation (CSV) specialist will be responsible for obtaining… more
- Kedrion Biopharma (Melville, NY)
- …a critical role in ensuring the compliance and reliability of computerized systems across our GxP operations, including manufacturing and laboratory ... _Kedrion is looking for a_ **_Validation Specialist - Computer Systems_** _to join our team...GAMP 5 standards._ **_Job Role and Responsibilities_** + _Lead validation projects for GxP systems -authoring and executing… more
- Catalent Pharma Solutions (Harmans, MD)
- …house 8 CGMP manufacturing suites and cold storage warehousing. The **Lead Specialist , QA - Validation & Quality Engineering** is responsible for providing ... **Lead Specialist , QA Validation & Engineering** Catalent...Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture,… more
