Validation Specialist Salary at Bsp Pharmaceuticals Srl BETA

Job Description Job Description Job Description: Cleaning Validation Expertise: The primary responsibility of the Cleaning Validation Specialist is to develop, execute, and oversee cleaning validation protocols for pharmaceutical solid, semi solid, liquid, cream and gel equipment and processes. Develop and implement cleaning Standard Operating Procedure for new equipment. Perform risk assessments to identify critical cleaning parameters and potential residues. Design and execute sampling plans to verify cleaning effectiveness. Analyze and interpret cleaning validation data using statistical methods. Author technical reports and present findings to cross-functional teams. Collaborate with production, quality assurance, and production departments to optimize cleaning processes. Ensure compliance with cGMP regulations and company standards for cleaning validation. Troubleshoot and investigate cleaning-related issues in manufacturing. Train personnel on proper cleaning techniques and valid

Job Description Job Description Job Title: Project Validation Specialist III Location (On-site, Remote, or Hybrid?): Anasco, PR (onsite) Contract Duration: Contract until 12/31/2025 Description: Support European Union Medical Device Regulation (EU MDR) and Design History File (DHF) improvement program Añasco, PR for the Tissue Technologies (TT) Product Families. The incumbent will be supporting the following activities to ensure conformance with EU MDR for technical filing of TT products manufactured at Añasco, included in the EU MDR and Design History File (DHF) improvement program: Data Gathering – Participate in the discovery and compilation of required documentation to be evaluated. Gap Assessments – Support assessment of all manufacturing documentation such as product device master record (drawings, specifications, bill of materials, production router/instructions, procedures, labeling), process flow charts, incoming inspections, in-process inspections, final inspections, validati

Job Description Job Description We are seeking a Validation Specialist to become an integral part of our team! You will develop and execute software test plans in order to identify software issues. Responsibilities: Devise and implement test strategies that adequately assess all software aspects Investigate and recreate reported defects Work with other engineers to troubleshoot and resolve coding issues Track and document all testing defects and resolutions Participate in the design and development for test automation and support Qualifications: Previous experience in software development, quality assurance, or other related fields Knowledge of Java, Python, or other programming languages Familiarity with relational databases such as MySQL, Oracle, and SQL Server Strong root-cause analysis skills Deadline and detail-oriented Company Description Group Technology of Trumbull, Inc. is located in Shelton, CT and Group Technology of Trumbull, Inc. operates in the Staffing industry. Company

Job Description Job Description At Safari Circuits, we believe our drive for a family-like culture makes a positive impact on our team and the quality of products we produce. We manufacture Printed Circuit Board Assemblies (PCBAs) for the global electronics market. We are a growing business, and we meet the stringent regulatory demands of medical, military, and defense fields. Founded in 1985, Safari Circuits provides world-class electronics development and manufacturing services to our customers and has a proven track record of creating stability within our ever-growing team. We are ready to shape a stronger future for our company and invest in your success. Job Summary The PPAP – Validation Specialist will work with customers (internal and external) to develop documentation for products produced by Safari Circuits. Responsibilities Include: Generate PPAP documentation for new programs, transfers, or engineering changes as required, including submittal of customer PPAP’s and maintaini

Job Description Job Description Experience and Skills: 4 years of experience in automation validation, change controls, and troubleshooting. Proficiency in source code review, batch recipe development, and documentation. Familiarity with formulation and filling line systems and auxiliary equipment. Educational Qualifications: A Bachelor’s degree in Engineering (Electrical, Mechanical, or Chemical), Computer Science, or a related field is required. Training and Compliance: Completion of required training programs to perform assigned tasks. Thanks Suchi suchi@vastekgroup.com Company Description Vastek Inc is managed by a group of dedicated professionals having rich experience of over years in Healthcare, IT consulting and staffing. We are a certified minority owned, Small business company head quartered out of San Diego, with coverage all across United States, Canada, Mexico, Italy and India. We specialize in Engineering, Validation, Regulatory, IT and NON-IT related areas primarily focu

Primary responsibility is to provide/lead validation services required for the successful delivery of IT & Automation projects. Provide validation & technical support through the preparation, execution, data analysis, & report writing for IV, OV & PV protocols. Ownership of Change Requests (CR’s) related to project validation responsibilities. Perform compliance & technical reviews/approvals of protocols & protocol data. Author project quality masterplans (PQMP’s), validation plans (VPL’s), & other key validation documentation. Author & execute assigned IV, OV & PV protocols for direct impact systems/processes per approved timeframes. Requires no guidance & direction to complete these goals & needs no coaching on technical competencies for goal obtainment. Serves as a source of expertise in the group for validating new systems. Ensure compliance of validation protocols executed are aligned with local, corporate & regulatory regulations. Lead validation failure investigations & non-conf

Join Kelly FSP as a Instrument Validation Specialist on site with our client in West Point, PA! Instrument Validation Specialist – Level I Primary responsibilities include, but are not limited to: Manage equipment assets at multiple locations Gain a working knowledge of laboratory equipment to facilitate with troubleshooting and/or communicate with the vendor/ service engineer to identify resolutions Participate in computer system validation activities associated with new or upgraded equipment or software packages. Originate and progress Deviations and Change Control records. Perform and document investigations and assist in developing and implementing CAPA plans Contribute to new SOP drafting, implementation, and revisions. Represent the laboratory on all aspects of laboratory equipment during audits. Ensure compliance with all regulatory requirements (cGMP), internal policies and procedures. Customer focused mindset with the ability to communicate adequately (verbally/writing) to all

Quality Chemical Laboratories (QCL), a leading Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of Computer System Validation Specialist. Responsibilities: Performs and leads computer system validation projects related to authoring and executing validation documentation for laboratory instruments/equipment and systems according to the ISPE GAMP 5 Validation Life Cycle. Documentation includes Computer System Validation Plan, Risk Assessment, IQ, OQ, PQ, Test Scripts, Summary reports, Requirements Traceability Matrix (RTM), Periodic Review of Computer Systems, and Data Integrity Assessment. Track and resolve deviations/exceptions during qualification activities. Work with company management to implement changes and upgrades to computer systems Work with vendors on purchasing and planning for new lab equipment/software upgrades, review vendor protocols/design specifications Communicate Computer System Validation approache