CQV Engineer Salary at Msd Ltd BETA

Company Description It's more than a job. It's a passion. Doka is one of the world's leading companies for developing, manufacturing and distributing formwork solutions for use in all fields of the construction sector. The Doka Group is a company of the Umdasch Group and employs more than 7,000 people in over 70 countries. Job Description Summary Of Position: The Engineering Group Leader is accountable for technical planning, forming projects, managing multiple projects and may manage engineering teams consisting of Technicians and Senior Technicians. This individual provides strong leadership, technical direction and ensures that team members are continually trained in Doka formwork systems. Ensures that the team represents the proper use of Doka concrete forming equipment for customers. The Engineering Group Leader provides technical assistance to the sales department from the project design stage to project inception and completion. Responsibilities: Determines and plans technical s

Impel Talent is exclusively supporting a confidential hiring project for a leading global pharmaceutical company undergoing rapid expansion. With over £100 million invested in state-of-the-art greenfield and brownfield projects across the US, and the EU, we are seeking an experienced Senior CQV Engineer to lead commissioning, qualification, and validation activities for a refurbishment project within New Jersey. This is a high-impact role that will play a critical part in delivering cutting-edge pharmaceutical facilities that meet the highest regulatory standards. Key Responsibilities ?? Lead CQV activities for facilities, equipment, and utilities, ensuring compliance with cGMP, FDA, and industry regulations. ?? Manage commissioning, qualification, and validation of complex engineering projects, ensuring operational efficiency and compliance. ?? Collaborate with cross-functional teams to ensure GMP and HSE requirements are met from design to execution. ?? Develop installation, commissi

Impel Talent is exclusively supporting a confidential hiring project for a leading global pharmaceutical company undergoing rapid expansion. With over £100 million invested in state-of-the-art greenfield and brownfield projects across the US, and the EU, we are seeking an experienced Senior CQV Engineer to lead commissioning, qualification, and validation activities for a refurbishment project within New Jersey. This is a high-impact role that will play a critical part in delivering cutting-edge pharmaceutical facilities that meet the highest regulatory standards. Key Responsibilities ?? Lead CQV activities for facilities, equipment, and utilities, ensuring compliance with cGMP, FDA, and industry regulations. ?? Manage commissioning, qualification, and validation of complex engineering projects, ensuring operational efficiency and compliance. ?? Collaborate with cross-functional teams to ensure GMP and HSE requirements are met from design to execution. ?? Develop installation, commissi

Job Description Job Description CONSTRUCTION PROJECT MANAGER Are you a collaborator ready to play a critical role in implementing strategic initiatives? Do you enjoy organizing project timelines and have a meticulous eye for detail? If so, we are looking for you to join our exceptional team as our Construction Project Manager! WHO WE ARE We’re Genesis AEC – an award-winning architecture, engineering, construction management, and CQV firm and a leader in the life sciences industry. Ranked #5 in Pharmaceutical Design by ENR magazine, we’re designing and constructing facilities that advance worldwide health. We’re proud to contribute to our clients’ success, earning honors that include a 2021 ISPE Facility of the Year (FOYA) award and an ENR Mid-Atlantic’s Best Manufacturing Project award for our work at the National Institutes of Health. Our culture is based on inclusion, one where all identities, backgrounds, and perspectives are embraced. When you’re on our team, you’ll find you are su

Job Description PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients' success, and you can be a part of our team's achievements. Employing a global team of skilled professionals and experts that span across strategically located offices in North America, Europe, Asia and the Middle East, we are proud of the roles we have fulfilled to help our clients achieve success. The Experience With operations spanning the globe and featuring a multi-cultural team, PSC Biotech® is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture

Job Description: At IPS, we are global leaders in developing innovative solutions for the consulting, architecture, engineering, project controls, procurement, construction management, and CQV of technically complex facilities, primarily in the life sciences industry. We are looking for a dedicated Construction Lean Specialist to join our talented team at our office located in Somerset, New Jersey. As a Lean Implementation Specialist, you will play a crucial role in ensuring the successful execution of projects within our firm. Your primary focus will be on optimizing project workflows, enhancing collaboration among various stakeholders, and coaching the implementation of various Lean Design and Construction tools and principles, such as the Last Planner System (LPS). If you have experience with implementing and coaching Lean and a passion for driving efficiency, this role is perfect for you! LPS Implementation and Oversight: Lead the adoption and integration of the Last Planner System

Title: Equipment Validation Specialist Job #: 61532-1 Primary Recruiter: Jane Bautista Pay Rate: $60.00-$63.00/Hour # of Openings: 1 Priority: B Position Type: 1 Year Contract Location: Summit, NJ, United States minimum 50% onsite Purpose and Scope of the Position The Compliance Specialist, Equipment Commissioning & Qualification, supports the successful operation of facility, laboratory, and business functions at multi‐use sites through interaction with internal team members and peer‐level customers as well as external service providers. The incumbent in this individual contributor role ensures the compliance of equipment and the ECQ group with local, global, and regulatory guidelines. The incumbent will perform periodic reviews of equipment, policies and procedures, gap analysis where required, and small-scale projects to complete departmental objectives. Required Competencies- Knowledge, skills, and abilities • Advanced knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR

Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap – Right Talent – Right Time – Right Place – Right Price and acting as a Career Coach to our consultants. Company: One of Our Clients Description: Title: Lab Operations Technician Location: Summit, NJ Duration: 12+ Months (Extendable) This role is 100% ONSITE Work Schedule: Mon - Fri, Business Hours Key Responsibilities Equipment Maintenance & Calibration • Manage, schedule, and escort vendors for equipment repair, calibration, and maintenance. • Review vendor contracts to ensure service adherence and cost-effectiveness. • Most equipment managed includes pipettes, centrifuges, shakers, welders (training provided). Consumables & Inventory Man