- Kedrion Biopharma (Melville, NY)
- …in hematology, immunology, neurology, and transfusion medicine. **JOB SUMMARY** The Associate Validation Specialist at Kedrion provides technical input to ... and aseptic process introduction into clinical and commercial facilities, the Associate Validation Specialist must integrate and successfully utilize knowledge… more
- Bio-Techne (Minneapolis, MN)
- …- $102,350.00 POSITION SUMMARY The primary responsibilities as a Senior Research Associate in the QC Microbiology team include leading method validations (USP<71>, ... both the Minneapolis and St. Paul sites. As the validation lead for the team, the successful candidate will...of products, general lab duties including stocking, purchasing, receiving, cleaning , and other duties as assigned. This position will… more
- Abbott (Abbott Park, IL)
- …medicines. Our 114,000 colleagues serve people in more than 160 countries. ** Associate Validation Specialist** **About Abbott** Abbott is a global healthcare ... attacks to blood disorders to infectious diseases and cancers. As the ** Associate Validation Specialist** , you'll conduct quality-related activities to deliver… more
- Amneal Pharmaceuticals (Branchburg, NJ)
- …+ Draft Standard Operating Procedure(SOP) for new operational equipment + Supports process validation and cleaning validation by providing product contact ... Description: The Validation Engineer I provides support in performing equipment, facility and utility qualification activity and re-qualification activity to ensure… more
- BioFire Diagnostics, LLC. (Durham, NC)
- …packaging systems etc. In addition provide support to other aspects of validation related to process, test method, software, cleaning , environmental, product, ... of manufacturing equipment and associated computer systems + Associate Degree with 2+ years of validation ...+ Associate Degree with 2+ years of validation experience in implementation and validation of… more
- Lilly (Lebanon, IN)
- …oligonucleotide drug substance manufacturing site. Responsibilities include guiding validation strategy, API commercialization, material selection, and cleaning ... a successful startup into GMP manufacturing operations._ **Responsibilities** The Associate Director - Technical Operations and Commercialization will build and… more
- University of Kansas (Lawrence, KS)
- … validation , and administration, data collection, interviews, data entry, cleaning , transcribing, coding, and analysis;serve as the lead evaluator, evaluation or ... research and evaluation designs, instrument and assessment development, selection, validation , and administration, data collection, entry, cleaning ,… more
- ManpowerGroup (Severn, MD)
- **Job title: Manufacturing Associate ** **Contract on W2** **Onsite from Severn MD 21077** **Pay budget - $25 - $31/hr on W2** **SHIFT - 7AM - 7PM** **REQUIRED** * ... The Manufacturing Associate I performs and documents cGMP activities to support...This involves the operation of process equipment, execution of validation protocols, completion of cGMP documents, creating/ revising cGMP… more
- ManpowerGroup (Severn, MD)
- Job title: Manufacturing Associate Location: Severn, MD - Onsite Duration: 3-6 months SHIFT - 7PM - 7AM (2-2-3 ROTATION) / 7AM - 7PM (2-2-3 ROTATION) ... **Description:** The Manufacturing Associate I perform and documents cGMP activities to support...operations. This involves operation of process equipment, execution of validation protocols, completion of cGMP documents, creating/ revising cGMP… more
- Unither Pharmaceuticals (Rochester, NY)
- Manufacturing Associate - A, B and C Shifts Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that ... Your role Reporting to the Manufacturing Supervisor, The Aseptic Manufacturing Associate is responsible for manufacturing pharmaceutical batches by setting-up, … more
- Fujifilm (Thousand Oaks, CA)
- … cleaning , investigation assistance and continuous improvement plans. The Associate Director will provide guidance to the continuous improvement of Environmental ... workplace, our company, our community, and the world at large. The Associate Director of QC Microbiology will provide strategic, technical, and operational… more
- Takeda Pharmaceuticals (Brooklyn Park, MN)
- …to the best of my knowledge. **Job Description** **Job Title** **: Manufacturing Associate I** **Location** : Brooklyn Park, MN **About the role:** As a ... Manufacturing Associate I, you will perform and document daily manufacturing...units, chromatography systems and fixed/portable vessels) and will execute validation protocols. You will report to the Manufacturing Supervisor.… more
- Lilly (Lebanon, IN)
- …Knowledge of cGMP, applicable global regulatory manufacturing guidance, and the process/ cleaning validation in drug substance pharmaceutical manufacturing are a ... prevent and mitigate variability to deliver a reliable supply of medicine. The Associate Director is primarily responsible to lead TS/MS scientists' team on the… more
- WuXi AppTec (Philadelphia, PA)
- …maintenance of facilities/systems, monitoring, coordination with metrology and validation , managing facilities change controls, troubleshooting equipment processes, ... supporting up-to-dates to as-built engineering drawings and Validation Master Plans, managing external contractors, writing reports and staffing and supervising a… more
- Catalent Pharma Solutions (Harmans, MD)
- We're hiring ** Associate I, Manufacturing** roles to support the cGMP biomanufacturing process for our pharmaceutical manufacturing facility in Baltimore, Maryland. ... doses of life-enhancing and life-saving treatments for patients annually. The ** Associate I, Manufacturing** performs and documents cGMP activities to support… more
- Unither Pharmaceuticals (Rochester, NY)
- Packaging Associate - A, B & C shifts available Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products ... B shift 15% Shift Differential for C shift JOB SUMMARY: The Packaging Associate is responsible for packaging pharmaceutical components and products by setting-up, … more
- System One (Harmans, MD)
- Title: Manufacturing Associate Pay rate $28.35/hr Location: Harmons MD On site daily Schedule: SHIFT 7AM - 7PM (2-2-3 rotation) Duration: 3-6 month possible contract ... HS or GED with 2-4 years' experience GMP Manufacturing experience OR * Associate 's degree in a scientific, engineering or biotechnology discipline with a minimum of… more
- Mentor Technical Group (Juncos, PR)
- …on engineering, regulatory, compliance, calibration, quality, microbial/environmental, technical cleaning , validation , electrical and process automation issues. ... if utility systems, process maintenance, instrumentation/calibration/electrical systems and technical cleaning systems are maintained in compliance with all applicable… more
- Bio-Techne (Minneapolis, MN)
- …SUMMARY We are seeking an experienced and highly skilled Advanced Research Associate to join our Quality Control Microbiology team! The successful candidate will ... inoculation, and membrane filtration. In addition to testing products, the Advanced Research Associate will play a key role in the development and implementation of… more
- Kelly Services (Malvern, PA)
- **Quality Assurance Associate II** Montgomery Country, PA Every day, Kelly Science & Clinical connects professionals with opportunities to advance their careers. We ... are currently interviewing and hiring immediately for an experienced **Quality Assurance Associate II** to join a global pharmaceutical, R&D, and medical device… more