Quality Specialist Salary at Profol Gmbh BETA

With a legacy spanning more than 100 years, our client is a respected innovator in the animal health space—delivering trusted, high-quality solutions that support the health of pets, livestock, and equine companions. Their dedication to excellence and continuous innovation has made them a go-to partner for veterinarians, producers, and pet owners alike. We are seeking a Quality Specialist to help uphold their rigorous quality standards. In this critical role, you'll audit contract manufacturers, collaborate with cross-functional teams, and play an active part in ensuring product integrity from development to delivery. If you're passionate about quality and animal well-being, this is your opportunity to make a real impact! Responsibilities: Audit contract manufacturers to ensure compliance with quality, regulatory, and company standards. Build strong supplier relationships to promote transparency and continuous improvement. Develop and implement SOPs, validation systems, and quality pro

Stratasys is a world leader in 3D printing! Stratasys is leading the global shift to additive manufacturing with innovative 3D printing solutions for industries such as aerospace, automotive, consumer products and healthcare. Through smart and connected 3D printers, polymer materials, a software ecosystem, and parts on demand, Stratasys solutions deliver competitive advantages at every stage in the product value chain. The world's leading organizations turn to Stratasys to transform product design, bring agility to manufacturing and supply chains, and improve patient care. Stratasys Direct Manufacturing (SDM) is seeking a Quality Specialist to perform detailed product inspections using various tools. The role involves developing and maintaining internal quality systems to ensure compliance with customer and regulatory standards. The Quality Specialist will also manage the Document Control process, ensuring documents and procedures are regularly reviewed, updated, and stored. Additional

The Science team at Russell Tobin & Associates is supporting a world-class organization that has an opening for “Quality Specialist” Duties: Support client's separation efforts with a focus on product rebranding, ensuring timely delivery. Update quality documentation, ensuring compliance and task closure. Identify and streamline processes to reduce duplication and improve efficiency. Develop and execute testing protocols and generate related reports for rebranding. Manage and update quality-owned documents, creating review/update plans. Assist Rebranding Program Leaders with project prioritization and task management. Track task progress and escalate issues related to quality, resources, or timelines. Requirements: Bachelor’s degree in a technical or quality field. 3+ years of experience in Medical Device/Drug Quality. Proven risk management experience. Additional Information: Location: (Hybrid) Maplewood, MN Duration: 12 months Rate: $30–$35/hr. on W2 Must be authorized to work in the

**The Opportunity** This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. + Reporting compliance status data to operational quality management + Collaborate with center management in the development and implementation of continuous improvement plans + Collaborate with Assistant Manager of Quality (AMQ), to be able to represent the center during internal and external audits, responds to questions, and may stop operations, including shipments to address quality concerns + Responsible for coordinating and managing training activities, policies and processes at the center level. You will report to the Assi

**Job Description Summary** This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. Reporting compliance status data to operational quality management Collaborate with center management in the development and implementation of continuous improvement plans Collaborate with Assistant Manager of Quality (AMQ), to be able to represent the center during internal and external audits, responds to questions, and may stop operations, including shipments to address quality concerns Responsible for coordinating and managing training activities, policies and processes at the center level ? **Job Description** **1**

Description Home Search Jobs Job Description Quality Specialist Contract: Wilson, North Carolina, US Salary Range: 40.00 - 45.00 | Per Hour Job Code: 360159 End Date: 2025-04-19 Days Left: 3 days, 3 hours left Apply About the Role: We are seeking a Specialist, Quality Assurance to join our team. The ideal candidate will be responsible for supporting batch record management, generating batch conformance documentation, completing batch record reviews, supporting investigations, compiling data for audits and inspections, developing SOPs, and other Quality Assurance functions as needed. The Specialist must demonstrate leadership, critical thinking, and the ability to work independently to ensure timely and reliable completion of job responsibilities. Pay Range: $40 - $45 Responsibilities: - Retrieve and track site Batch Records Prepare Certificate of Compliance (CoC) and Certificate of Analysis (CoA) Assist with document retention and reconciliation Support tracking and processing of tende

Job Description Job Description Responsibilities: Supports corrective Action Boards with suppliers, lead escape management activities and validate root Cause and Corrective Actions. Perform detailed product inspections on in-process and finished goods, including but not limited to First Article Inspections. Qualified in performing Coordinate Measuring Machine (CMM) functions for Zeiss Contura machine. Qualified in programming, writing and editing CMM programs, either manually or using software, to ensure the machine can perform automated measurements. Document characteristics of products accurately and with technical detail. Initiate quality notifications for any non-conforming products. Requirements: Apply quality assurance procedures and requirements to the inspection of hardware and to document reviews. Identify any potential quality issues early and help to prevent their occurrence. Communicate effectively to other Client personnel any quality issues needing resolution. Flexibility

Who we are Klein Marine Systems is the world's leading side scan sonar manufacturer and we are immensely proud of where we are and how we got here. We are currently undergoing a remarkable period of transformation, making now an incredibly exciting time to join our team. We are searching for dynamic, technically skilled individuals who are passionate about their work to join us in Newburyport, MA. In return, you will have the opportunity to be part of the world's leading side scan sonar enterprise: contributing to significant advancements in our technologies and operations. Unleash your potential with a rewarding career If you possess a visionary mindset, a knack for solving complex challenges, and a burning desire to make a genuine impact on the world, explore our job opportunities. Seize the opportunity to unleash your courage and contribute to a more connected, smarter, and brighter future. We are seeking a highly motivated Quality Specialist to execute and maintain our Quality Mana