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Pharma Biotech Validation Jobs

178 jobs

The primary mission of the Genentech Research & Early Development (gRED) organization is to discover and rigorously assess promising molecule candidates for viable therapeutic benefits. The gRED Development Sciences division’s core mission is to translate scientific hypotheses into therapeutic possibilities by enabling the discovery and development of safe and effective therapeutics at optimal dos...

Please no third party candidates. No sponsorships available. Only apply if you can work on a W2 basis. Technical Writer Duties: Play an integral role on the Enterprise Manufacturing Intelligence System Project Team Create and revise IT strategy documents, IT system technical documents (System-level User Requirements, Design Specifications, Hardware Specifications) , flowcharts, diagrams, and d...

Description The primary mission of the Genentech Research & Early Development (gRED) organization is to discover and rigorously assess promising molecule candidates for viable therapeutic benefits. The gRED Development Sciences division’s core mission is to translate scientific hypotheses into therapeutic possibilities by enabling the discovery and development of safe and effective therapeutics a...

Business Systems Analyst - Pharma / Biotech Requisition ID-00438588 Description The primary mission of the Genentech Research & Early Development (gRED) organization is to discover and rigorously assess promising molecule candidates for viable therapeutic benefits. The gRED Development Sciences division’s core mission is to translate scientific hypotheses into therapeutic possibilities by enabl...

Planet Pharma is working with a client in Minneapolis, MN to hire Medical Device Reporting Specialists for a contract that will start out at 6 months, but may extend.Looking for entry level knowledge of the clinical trials industry. There is a job fair on 9-10 for interested candidates and you MUST be able to attend. Must be able to pass a background check and drug screen.Please apply here or emai...

With 30 years of experience in the CRO/pharma industry and more than 13,000 employees worldwide, PPD's lab services units continue to flourish. PPD continues to recognize our employees as the cornerstone of our success and strive to provide a supportive environment that offers exciting opportunities for skills enhancement. Our cutting-edge technologies, real time analytics and superior training dr...

Job Title: Clinical Data Manager I (2 openings) Working Arrangement:Onsite at large pharma in Northern NJ Duties: Responsible for providing timely and prefessional ongoing quality management of clinical trial data by identifying errors/inconsistencies in CRF data and ensuring their resolutions in order that databases can be declared clean and locked according to strict performance standards. Rev...

Job Title: Clinical Data Manager (2 openings) Working Arrangement:Onsite at large pharma in Northern NJ Initial Duration:6 months with the option to be extended Duties: Responsible for providing timely and professional ongoing quality management of clinical trial data by identifying errors/inconsistencies in CRF data and ensuring their resolutions in order that databases can be declared clean a...

Lead Clinical Data Manager (Onsite in MD, Permanent Salaried, Relocation Assistance Provided)Position Summary:* Provides DM leadership and subject matter expertise to the study team(s) and is responsible for overseeing and managing all DM activities for the study. * Serves as an ad hoc member of the study team(s) and is accountable for all DM-related communications, specifications, and documentat...

Senior Validation Specialist – High Growth Opportunity One of our top clients, a leading biopharmaceutical company, is seeking an experienced Sr. Validation Specialist to be part of their mid-west team. This financially stable, high growth, company is looking for a Validation expert with 7+ years of biotech/pharma experience with a minimum of 3 years in validation. The individual will develop an...

Hi All, Just posting an update in regards to the Computer System Validation position I have with a major pharma located in MA. My client is now looking for a consultant who has at least 2 years of CSV experience (within pharma/biotech domain) and who has a general knowledge of GxP regulations. The responsibilities are closer to that of a lead position, so this would be a great opportunity for a c...

Description Perform and supportKansas City, MOsite validation activities and support Quality Assurance functions: Researches, writes and executes qualification protocols and supporting documents for equipment, instruments, utilities and processes Researches, writes and executes environmental protocols using Kaye Validator and data loggers Researches and writes periodic reviews for all qualifie...

Description Under the direction of the Technical Validation Director the Senior Technical Manager will be accountable for leading teams and performing validation activities such as Commissioning and Qualification, Performance Qualification (PQ) / Cleaning Validation (CV) / Process Validation (PV) and Revalidation (RV). • Able to collaborate with both plant and all network organizations seamlessl...

Validation Engineer I Requisition ID-2970152437 Description Under the direction of theTechnical Validation Manager, the Validation Engineer II will be accountablefor validation activities such as Performance Qualification (PQ) / CleaningValidation (CV) / Process Validation (PV) and Revalidation (RV) activities. Able to collaborate with both plant and corporate organizations seamlessly. Is con...

CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Validation Engineer Cambridge, MA Full-Time $70,000 - $90,000 Apply Apply Validation Engineer Cambridge, MA Full-Time $70,000 - $90,000 Apply Job Details We are a rapidly growing Pharma Company that is located right outside of Boston We are looking to expand our dynamic Validation team. We are currentl...

Sr. Business Analyst Validation Assessment Foster City, CA (local/onsite) 6 months + project Looking for a Senior Business Analyst to support system validation assessment to include requirements gathering from key stakeholder groups. -Assessment partner Computer System Validation Assessment. -Domain experience for computer validation. -Strong Business Analysis, requirements gathering, scope...

Research Scientist Are you a research scientist? Are you interested in participating in client communications regarding expectations and requirements for successful projects? Do you enjoy troubleshooting analytical instruments and method performance? If so, I have an opportunity for you! My client is a leading global CRO proving drug discovery, management services, and development partnered with ...

Our client in the North Bay is looking for a Device Validation Engineer to join their growing team! Responsibilities: Responsible for writing and reviewing design verification test protocols/reports Execution of design verification test protocols for functional and stability testing for drug delivery devices Manage test sample inventory Responsible for statistical analysis of test data Will ...

We at PharmMed Solutions Inc. specialize in placing contract/permanent employees in Pharmaceutical/Medical Device/Biotech companies in the field of quality, validation, and engineering. We currently have a Validation Engineer opportunity with a consumer pharma client in NY/NJ area. See below for job description. This position does not offer relocation package, however it offers competitive salary,...

Email job to a friend Remove Saved Job Save Job Printer Quick ApplyApply via Email Pharma Search Partners Technology Transfer Supervisor Responsible for assisting with and/or coordinating the transfer and implementation of projects and technology from development groups to the plant manufacturing site. Responsible for designing manufacturing procedures for new or modified products. Responsi...