Novartis

Compensation

Full Description

:::Please note: This is a temporary contractor opportunity at Novartis ::: Novartis touches the lives of a tenth of the world’s population. Every role here, regardless of contract type, makes an impact on human life! Novartis US partners with external managed service provider Magnit Global to offer engaging temporary contractor opportunities like this, to those who are looking for flexibility in their career while looking to gain new skills and experiences providing services to an inclusive global medicines company. Click here to learn more about Magnit www.magnitglobal.com Ready to work with/through Magnit at Novartis? Please read on... We are seeking a detail-oriented and experienced Validation Engineer Contractor to support the qualification of laboratory equipment in compliance with cGMP and regulatory standards. The contractor will be responsible for executing qualification protocols (IQ/OQ/PQ), preparing documentation, and ensuring equipment is fit for its intended use in a pharmaceutical quality control environment. Key Responsibilities: Develop, review, and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols. Collaborate with cross-functional teams (QC, QA, Engineering, Validation) to ensure timely and compliant equipment qualification. Prepare and maintain User Requirement Specifications (URS) and Design Qualification (DQ) documentation. Ensure all qualification activities are documented accurately and meet FDA, EMA, and ICH guidelines. Support investigations and deviations related to equipment performance. Assist in change control processes related to equipment upgrades or replacements. Maintain traceability and data integrity throughout the qualification lifecycle. Qualifications: Bachelor’s degree in Engineering, Life Sciences, or related field. Minimum 3 years of experience in equipment qualification within a GMP-regulated pharmaceutical or biotech environment. Strong understanding of Good Manufacturing Practices (GMP) and Good Engineering Practices (GEP). Experience with laboratory instruments (e.g., HPLC, GC, incubators, autoclaves) and manufacturing equipment. Proficiency in writing and reviewing technical documentation. Excellent organizational and communication skills. Preferred Skills: Experience with computer system validation (CSV) and data integrity principles. Ability to work independently and manage multiple priorities. Location: Millburn, NJ (Onsite) Pay Rate: $45/hr - $56.81/hr based on experience and qualifications (W2 Only) Contract: 6+-month Health, dental, vision, 401k Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? EEO Statement: The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accommodation: If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to Magnit at directsourceproteam@prounlimited.com.