- Hired by Matrix (Woodcliff Lake, NJ)
- …Services, Fintech, Consumer Goods and Services, Security and Logistics, Pharmaceutical / Biotech, Technology, Automotive, Engineering, and Healthcare. At-a-Glance: ... ready to build your career by joining a global pharmaceutical company? If so, our client is hiring a...company? If so, our client is hiring a Software Validation Quality Consultant. What You'll Do: Work closely with… more
- Aequor (Swiftwater, MN)
- This is a contract position with a global pharmaceutical company. Implementation experience of Lab Information Management System [LIMS] is Required. Position ... Basic - Strong working knowledge of laboratory processes including cGMP's in a pharmaceutical environment - Experience in system testing, validation , and master… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... reconciliation and negotiation of Vendor contracts prior to study termination and contract closure. Manages all aspects of sourcing and negotiating Vendor contracts… more
- Insmed Incorporated (Bridgewater, NJ)
- …stakeholders (therapeutic areas, clinical pharmacology, clinical operations, non-clinical safety, contract research organizations etc.) to build and to execute the ... field.Minimum of 8+ years' post-doctoral experience or equivalent in the pharmaceutical , CRO or related industry within bioanalytical area across various… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... study reports and regulatory submissions, as well as in-house validation of this workPossesses in-depth knowledge of regulatory authority's requirementsTypically… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …trials, clinical development, and regulatory submissions. The position will perform validation of the electronically transmitted external data by ensuring all ... processing, and reporting of diverse external data across DS Programs.Participates in Contract /SOW reviews and MSA discussions of External Vendors by engaging with… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... clinical study reports and regulatory submissions, as well as in-house validation of this work. Possesses in-depth knowledge of regulatory authority's… more
- Merck & Co. (Durham, NC)
- …regulatory requirements.- Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global ... and reviewDirect support of regulatory inspections and auditsDirect support of validation activities and all other associated quality functionsOther duties as… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ... in the treatment of multiple myeloma. Legend Biotech is seeking a CQV Specialist ( Contract Position) as part of the Technical Operations team based in Raritan, NJ.… more
- Eisai, Inc (Exton, PA)
- …and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong ... amount of their time troubleshooting assays, designing future studies, overseeing assay validation and interacting with QA to determine product stability and shelf… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... to address various project needs. The position works closely with contract research organization (CRO) programmers and statisticians and collaborates with internal… more
- Axelon Services Corporation (Libertyville, IL)
- Hybrid Position 50% onsite 50% remote This is a contract . No C2C/NO Corp To Corp Job Description: The Enterprise Systems and IT Service Support position will be ... 21CFR part 11, and good documentation practices. - Knowledge of pharmaceutical , manufacturing and laboratory systems and equipment that support Cell Therapy… more
- On-Board Companies (Warren, NJ)
- …GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation practices.Knowledge of pharmaceutical , ... Equipment Engineer in Warren, NJ! Position Details: Position Type: 12-Month Contract with additional opportunity contingent upon performanceJob Location: Warren, NJ… more
- Sunrise System Inc (Huntington, WV)
- Job Title: Quality Control Engineer II Duration: 18 Months on W2 Contract . Location: Huntington, WV The Senior Quality Engineer I is responsible for working with the ... (this needs to be clearly noted on the resume) Validation Experience Someone with a technical Degree or previous...Assoc.+6 yrs; MS+0 yrs) 2+ Years of experience in Pharmaceutical / Medical Device Industry preferred Project management experience… more
- Nesco Resource (Rensselaer, NY)
- …company in Rensselaer, NY as a MSAT Specialist! This position is a one-year contract ; with potential for extension or permanent hire. A great way to start your ... internship experience preferred! Strong Excel experience needed! Experience in a pharmaceutical /biologics cGMP environment or equivalent preferredA typical day as a… more
- Kelly Services (West Hills, CA)
- Kelly(R) Science & Clinical is seeking a ** Contract Sr. Validation Engineer** at a cutting-edge Therapeutics Company client in the Los Angeles Area. If you're ... DOE ** Contract Length: 2.5-4 months** **Overview** In this role as ** Contract ** **Sr. Validation Engineer,** you'll be providing validation activities… more
- System One (Warminster, PA)
- …manufacturing or OEM environment. + Strong understanding of regulatory requirements for pharmaceutical validation , including FDA 21 CFR Part 11, EU Annex ... Title: Automation Validation Engineer - Pharmaceutical Production Equipment... Production Equipment Location: Warminster, PA Type: 6 Month Contract potential for extension or hire Schedule: Mon-Fri Day… more
- PCI Pharma Services (Bedford, NH)
- … Validation (PV) and Revalidation (RV) in support of cGMP pharmaceutical /medical device contract manufacturing across multiple PCI facilities. These Process ... of equipment qualification, process validation , or cleaning validation is acceptable; QA pharmaceutical experience also..., or cleaning validation is acceptable; QA pharmaceutical experience also preferred. * Validation experience… more
- PCI Pharma Services (Bedford, NH)
- …array of well-defined validation activities in support of cGMP pharmaceutical /medical device contract manufacturing across multiple PCI Pharma facilities. + ... of equipment qualification, process validation , or cleaning validation is acceptable; QA pharmaceutical experience also..., or cleaning validation is acceptable; QA pharmaceutical experience also preferred. + Validation experience… more
- PCI Pharma Services (Philadelphia, PA)
- …validation processes and tasks Validation trends/standards in the pharmaceutical and contract packaging industries Hidden opportunities within existing ... Lead are focused on the qualification of utilities, computer systems, pharmaceutical packaging equipment and validation of the associated processes run… more
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