Scientist II

Ourvita is the largest Europe-based CDMO for food supplements, with a strong global presence. Backed by over 3,000 dedicated professionals worldwide, we pride ourselves on a customer‑centric approach and a culture built on expertise, resilience, service quality, and consumer insight—working together to create innovative and impactful solutions. Our vision is to make high‑quality health and medical products accessible whenever and wherever they are needed, transforming lives and advancing healthcare globally. Through our commitment to development, distribution, and strategic partnerships, we strive to deliver excellence across the entire value chain. We are currently seeking a skilled and experienced Scientist II to join our team and contribute to this mission. Job Summary The Scientist II position is responsible for the development of new formulations, researching new raw materials, in‑process and stability testing, coordinating analytical testing and scale‑up to production. This position also provides leadership to Development Scientists and Technicians. Your responsibilities will include: Develops new product formulations and changes to current formulations, improving client and Ourvita products. Utilizes new technology and innovation to develop new product ideas. Provides regular updates on project progress to leader. Makes recommendations to the R&D Director for creating efficiencies in the product formulation and development process, as well as with the department. Acts as a technical leader for the manufacture of pilot and qualification batches with supporting documentation, batch records, and protocols. Writes validation protocols and assists with validation activities as a technical leader. Performs scale‑up of production formulations, recommend procedures, product handling, specialized equipment, etc. Mentors, coaches and develops Scientist and Technician positions. Consistently answers questions from staff within the department and outside of the department as they relate to R&D. Performs process testing to ensure product performance, manufacturability, stability etc. Leads the coordination of required documentation for master formulas, blending and tableting or filling records. Interacts with appropriate departments on new products/projects. Oversee the setting of raw material and product specifications in cooperation with Quality. Writes protocols and summary reports for development activities. Writes/reviews paper formulas for initial cost estimate based on customer requests. Works with Client Services to provide formulation samples to customers with appropriate follow‑up. Investigates production problems dealing with formulation, blending and tableting. Other Duties and Responsibilities: Understand and adhere to Good Manufacturing Practices. Safety Protocol: Stop any observed unsafe acts and obey facility safety rules and procedures. Correct or report any observed safety hazards. Support safety policies and programs. This list of duties and responsibilities is not all‑inclusive and may be expanded to include other duties and responsibilities, as deemed necessary from time to time. Qualifications: Education / Experience / Certifications: Bachelor’s degree in Chemistry, Biology, Food Science or related science. 5 years of experience in a product development role within a dietary supplement, pharmaceutical or dry food manufacturing company. 3 years development experience with powders or solid dosage forms. Effervescent experience a plus. Skills Required: Knowledge of scientific development principles and language. Knowledge of CFR Title 21, Part 111 and 101 regulations. Solid knowledge and understanding of GMPs and FDA regulations. Ability to think creatively and demonstrate the use of new technology and innovation in development. Ability to recognize problems and establish a plan for solving the problem. Strong attention to detail. Self‑motivated, self‑starter with a demonstrated desire to coach and mentor others. Excellent verbal and written communication skills to maintain and develop working relationships across functional areas. Ability to maintain accurate, legible and complete documentation. Computer proficiency and working knowledge of the Microsoft Office Suite. Benefits At Ourvita, we are committed to providing our employees with a supportive and engaging work environment that fosters growth and development. We offer competitive market pay, annual bonus, and a benefits package including: Medical, Dental, and Vision coverage Basic Life, Accidental Death and Dismemberment (AD&D), Short Term Disability (STD) at no cost to employees Holiday pay and Paid Time Off (PTO) Opportunities for advancement Fitness discounts Tuition Reimbursement If you are a motivated and skilled Scientist II with a passion for excellence, we encourage you to apply today and join our dynamic team at Ourvita. #J-18808-Ljbffr Ourvita