Company Description Are you looking for an exciting opportunity, a rewarding, enriching, and fulfilling career, and the opportunity to grow to greater levels of success with a company that values you? Then look no further! Join Eurofins PSS: a world class company that is growing by leaps and bounds while making a difference to humanity. At Eurofins PSS, you will gain experience working in state-of-the-art laboratories, and be a part of a team that is dedicated to testing, development, and advancement of life-saving drug products to make the world a healthier and happier place to live in. Our people are our chemistry and we need talented people like you now more than ever. Eurofins PSS is an international life sciences company, providing a unique range of analytical testing services to clients making life and our environment safer, healthier and more sustainable. Eurofins PSS works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Why Eurofins? * A focus on your professional development because your growth is our growth * A chance to step in to the pharmaceutical/biopharmaceutical industry and move up the ladder of success to help you achieve your career goals * Healthy work/life balance, an essential need for employee satisfaction * Excellent benefits such as tuition reimbursement, mentoring and leadership programs, 401k, medical/vision/dental insurance, PTO, and much more! * Opportunity for involvement in several innovative committees surrounding sustainability, equality, development, and much more! Job Description * The Pharmacovigilance Signal Management Sr. Associate will serve as a core member of the safety team and is responsible for performing proactive pharmacovigilance activities to evaluate safety data and signals for marketed products. * This includes performing signal detection and safety management committee activities, contributing to the review of aggregate safety reports, assisting with ad hoc regulatory responses, facilitating signal management process for assigned products (i.e., executing signal detection queries, signal tracking) * Build and maintain technical files within the global signal management system * Utilize technical tools with the Pharmacovigilance suite of software solutions * Provide innovative ideas and solutions to evolving signal detection and signal management landscape Qualifications * B.S. degree required * Other advanced degree (MS, MPH, PhD) in science such as Biology, Epidemiology, Data Analytics, Regulatory Affairs, or related science is preferred. * Minimum 2 years' experience navigating databases and performing queries, exporting data. * Good knowledge of US and EU pharmacovigilance regulatory requirements with experience in interpretation of regulations, guidelines, and policies preferred. * Experience in preparation of regulatory submissions and knowledge of pharmacovigilance practices preferred. * Problem solver with an ability to take ownership for issues and have the ability to suggest opportunities for continuous improvement * High level of competency using Microsoft Office suite - with demonstrated high level competence of working in Microsoft Word, Excel, Power BI * Good organizational skills and attention to detail * Excellent written and verbal communication skills, fluent in English (verbal and written) * Ability to evaluate and synthesize scientific data (analytical thinking) * Team player with ability to function in a cross-functional environment * Self-motivated, able to prioritize and plan effectively, and independently, with minimal supervision * Curious, self-starter with a strong interest in data analysis and patient safety * Pragmatic and agile, with mature business acumen Additional Information * Position is full-time, first-shift. * Candidates currently living within a commutable distance ofKalamazoo MIare encouraged to apply. * What we offer: * Excellent full time