Validation Engineer Salary at Dmp Technologies BETA

Why Precision for Medicine? Welcome to the forefront of innovation in cutting edge patient treatments! We are thrilled to present an incredible opportunity to join our high performing organization. As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the standards of excellence. Our dynamic team is composed of vibrant professionals who are passionate about delivering high quality work for our partners and changing the lives of patients across the globe. If you are driven by innovation, thrive in a fast-paced environment, love to travel and are ready to make a real impact, then Precision for Medicine, Manufacturing Solutions wants you to join our team. Who Are We? We are Precision for Medicine, Manufacturing Solutions, the leading advanced therapy technical operations consulting company in the life science industry. As a Patient Focused, People First delivery team, we are committed to advancing manufacturing to achieve

Job Title: Validation Engineer, Temperature Control Mapping Location: Framingham, MA Duration: 6 + months contract JOB DESCRIPTION Our client is a small biotechnology company based in Framingham, MA that provides development, manufacturing and services. Primarily focusing on upstream manufacturing of the recombinant proteins. Responsibilities: Execute TCU Mapping Protocols: Perform and document temperature mapping activities to ensure TCUs meet regulatory and operational standards. Protocol Support: Assist with validation protocols, ensuring adherence to internal and regulatory requirements. Data Collection & Analysis: Support data collection and preliminary analysis of TCU mapping results to inform validation reporting and quality control. Collaborate and Learn: Work under the mentorship of a senior engineer and receive guidance from an experienced leader preparing for a supervisory role. Ensure Compliance: Help maintain compliance with GMP, safety, and internal quality standards in a

Job Description Job Description Our client is a growing contract manufacturing. They just acquired their 4th building. There are approx 250 employees. They truly put an emphasis on their people and are very family oriented feel in terms of their culture. Job Description: Performs diverse tasks focused on equipment and facility change controls, training, and validation (IQ/OQ/PQ/PV) to maintain compliance with GMP standards and customer requirements. Ensures that validation protocols and reports are executed promptly, keeping manufacturing equipment and facilities in a validated state. Location: Anaheim, CA Pay: $70k-$80k/yr, depending on experience Direct Hire Key Responsibilities: Lead validation programs covering equipment, processes, cleaning, and facility requirements. Develop and update internal procedures to meet regulatory and quality standards. Ensure thorough documentation and completion of recording forms, inspections, and procedures. Work cross-functionally to facilitate acc

Job Description Job Description Pharma-Bio Serv, a global consulting firm headquartered in Puerto Rico, has been dedicated exclusively to providing services to the largest biotechnology & bio-engineering companies within the regulated industry for 30 years. Since our inception, our services have resulted in a project experience level and personnel resource base ranking among the highest worldwide. Currently, we are gathering a pool talent for future Validation Engineer opportunity to provide onsite services in Duluth, GA. Duties may include: Develop and execute validation plans and protocols for various projects. Qualify equipment, processes, and utilities. Write and prepare validation protocols. Maintain project validation oversight. Review and troubleshoot SOPs and equipment/system failures. Collaborate with Engineering, QA, IT, and Production. Requirements: Bachelor’s Degree or equivalent experience. Local candidate or able to relocate by January 2025. Previous experience with R&D d

The Opportunity: Avantor, a Global Fortune 500 company is looking for a dedicated Process/ Validation Engineer to optimize our Biopharma Production organization. This Devens, MA role is full-time, on-site. If you have lean manufacturing/ process experience – let’s talk! Minimum Education Requirement: Bachelor's degree Required Experience (4+ yrs): Managing the optimization of resources and processes in compliance with company policies/procedures. Writing SOPs and training documents to establish standard work and develop initial documents for new processes and systems. Troubleshooting equipment and hardware Managing data through data collection, modeling, and analysis Managing data through cost/benefit analysis, process mapping and/or problem analysis. With lean manufacturing practices and the Toyota Production System (TPS; TPMS). With six sigma process improvement methods (Green Belt preferred) Performs other duties as assigned. Preferred Experience: Conducting risk assessments (IE: PF

Responsibilities: Review qualification requirements for any new instrument, equipment and process with system owner and cross-functional teams. Prepare protocols and reports related to equipment/system/utility qualification (IQ/OQ/PQ), calibrations, engineering, process, packaging, and cleaning validations. Preparation and review of associated procedures, change controls, standard operating procedures, validation master plans, etc. Execute protocols and related activities associated with validating equipment/ systems/ utilities/ processes, transferring new products/ processes from R&D to manufacturing, and executing process/documentation improvements. Perform statistical analysis for process monitoring. Initiate and investigate protocol deviations, events, exceptions, and coordinate follow up with QA. Initiate, follow-up, close out and implementation of corrective and preventive actions. Co-ordinate activities related to risk management and preparation of quality risk management and ri

Job Description Job Description Hello, We are hiring validation engineer. If you are interested send your resume. Support the Validation Manager by ensuring effective implementation and maintenance of the Validation program. Serve as a Validation subject matter expert (SME) and track/report action plan status/completion as it relates to validation systems improvement efforts. Responsible for the writing of and the execution of project and system qualifications, validation, and re-qualifications/periodic reviews. Develops validation plans, qualification protocols, compiles and analyzes data, drafts summary reports, and reviews validation documentation to ensure that system are qualified in accordance with applicable regulatory agencies, clients and Client specifications/requirements. Highly experienced with equipment and/or computer system validation. Able to assess deviations that affect validation with minimal assistance. Able to work with minimal assistance on moderate Corrective Act

Job Description Job Description McKenna Labs, a manufacturer of personal care products, is currently seeking a Validation Engineer to perform highly diversified duties that focus on change controls of equipment/facility, training, and validation activities related to IQ/OQ/PQ/PV. Ensures that validation protocols and reports are performed in a timely basis and any equipment and facility used for manufacturing is maintained in a validated state to meet all GMP requirements and customer requirements. Responsibilities Supports conformance to regulatory requirements and generates internal documents to establish company procedures. Responsible for the overall Validation Program including but not limited to equipment, process, cleaning, or facility validations. Supports product lifecycle review initiatives to ensure product quality, safety, and integrity is maintained. Ensures that recording forms, inspections, and procedures are properly completed and documented. Interfaces cross-functional