Intern - Quality Operations

Job Description

When you are part of the team at Thermo Fisher Scientific, you’ll do important work. You’ll have the opportunity to grow and learn in a culture that empowers your development. We have built an inclusive, global environment that values the power of diverse talent, backgrounds, and experiences to drive speed, efficiency, innovation, and growth.\n\nOur internship program will give you a chance to get real world business experience and build your network before graduation. We are seeking an upbeat, responsible intern to join our growing organization. In this position, you will learn the ins-and-outs of our daily routines and procedures. You will focus on learning how our organization runs and will gain valuable insight that can further your interest in your chosen career field. This position has many opportunities to offer!\n\nCustomers throughout the globe rely on our extensive range of products and services—from next-generation instruments to everyday lab essentials to life-saving medicine. If you desire to be a part of a world-class team, Thermo Fisher Scientific can provide you with the opportunity to work in quality assurance to produce products that enable our customers to make the world healthier, cleaner and safer.\n\nSummary of Internship\nInternship positions provide an opportunity for students to get hands-on experience in a quality environment. In detail, the position allows to learn manufacturing process and equipment cleaning strategies specifically on Continued Process Verification (CPV) approach in the production of sterile pharmaceutical forms in the pharmaceutical industry. Participate in ensuring periodic cleaning verification, as per SOPs and regulatory requirements.\n\nAcquire information from other departments to define process validation strategy, as well as collaborating with company functions to define actions to be carried out, as per company procedures.\n\nApproach validation of the manufacturing processes (applying \"Lifecycle approach\" Stage 2 Process Qualification and Stage 3 Continued Process Verification), cleaning procedures and APS/Media Fill, collaborating with other departments in the operational activities envisaged by the Protocols\n\nEssential Functions:\nBecome familiar with EU regulations regarding the required statements for the site’s manufactured products\nCollaborate with team members in production and quality to build robust documentation to support Continued Process Verification (CPV) approach in the production of sterile pharmaceutical forms in the pharmaceutical industry\nQualifications:\nStrong desire and motivation to develop a career in manufacturing/operations\n\nteam building skills\nAbility to learn, be mentored, and improve\nInterest in working with hands and having experience using hand-tools may be beneficial\nThermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.\n\nAt Thermo Fisher Scientific, each one of our 100,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer. Apply today!