Analytics Senior Associate Scientist II

Catalent Pharma Solutions • Kansas City, MO

1d • Onsite

About The Position

Analytics Senior Associate Scientist II Position Summary Shift: Monday – Friday 8am-4:30pm 100% on-site Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. The Analytics Senior Associate Scientist II performs work that is varied and that may be somewhat difficult in character but usually involves limited responsibility. Some evaluation, originality or ingenuity is required. Follows established protocols and work plans. May be assisted by laboratory technicians/assistants. Comply with divisional and site Environmental Health and Safety requirements.

Requirements

• Bachelor's degree in related life science or physical science field required.
• 4+ years related work experience preferred.
• Master's degree in related life science or physical science field required.
• 2+ years related work experience preferred.
• Proactively address work issues at both an individual and a team level
• Ability to process, maintain, and interpret data
• Basic understanding of instrument operations and troubleshooting skills in multiple techniques
• Written and verbal communication skills with internal and external customers
• Well organized and ability to multitask as well as efficient time management

Responsibilities

• Execute laboratory work plans/schedules developed with input from a supervisor or senior team member.
• Sample types include in-process, release or stability. Techniques include HPLC, GC, Karl Fischer, Disintegration, Friability, Hardness, and appearance.
• Under direction, may perform method development, validation, and transfer activities.
• Maintain accurate and high quality laboratory documentation in accordance with regulatory guidance and Site SOPs
• May draft technical documents such as methods or certificate of analysis
• Performs parallel review of laboratory documentation and may become qualified to perform technical review of documents for accuracy, thoroughness and regulatory compliance
• Assists in execution of efficiency improvement projects with guidance
• Trains others on laboratory techniques

Benefits

• Competitive medical benefits and 401K
• 152 hours PTO + 8 Paid Holidays
• Dynamic, fast-paced work environment
• Opportunity to work on Continuous Improvement Processes
• Catalent offers rewarding opportunities to further your career!
• Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world.
• Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
• Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us.
• Join us in making a difference. personal initiative. dynamic pace. meaningful work.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level