Operations Technician I

Catalent•Durham, NC

25d•Onsite

About The Position

The Morrisville (MSV) facility is Catalent’s center of excellence for nasal product development and manufacturing, providing end‑to‑end services from early formulation through clinical and commercial production. The site offers comprehensive nasal development capabilities, including analytical support, device selection, spray characterization, and both clinical and commercial scale for unit‑dose, bi‑dose, and multidose nasal products. The Morrisville site also provides development services for dry powder (DPI) and liquid pulmonary products including formulation development and optimization, method services and analytical testing. The Operations Technician I, performs commercial manufacturing of clinical supplies working closely with customers and R&D scientists in the development and scale up of new products and processes. Assists in the scale up of pilot development trials to production processes and is primarily responsible for the manufacture of Pulmonary & Nasal Products, as well will comply with divisional and site Environmental Health and Safety requirements. The Operations Technician I accurately follows manufacturing Master Batch Records (MBRs) and Standard Operating Procedures (SOPs) in accordance with current Good Manufacturing Practices (cGMPs) and with a focus on “right first time” execution. 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.

Requirements

Must have High School Diploma or GED
Must have at least 6 months of pharmaceutical experience OR in lieu of experience, completion of Grads2Work Program, BioWorks certificate program or equivalent required
On an average 8 hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell and lift to 50 pounds
Steel toe/ composite shoes are required to be worn on manufacturing floor
Must be able to wear a respirator
Must have 20/20 vision (with eye correction); Specific vision requirements include inspecting product for defects, reading of written documents, visual troubleshooting of equipment and use of computer monitor screen frequently

Responsibilities

Accurately follows manufacturing Master Batch Records (MBRs) and Standard Operating Procedures (SOPs) in accordance with current Good Manufacturing Practices (cGMPs) and with a focus on “right first time” execution
Prepare and assist in the preparation of all production batch requirements
Review product paperwork to ensure use of proper materials and equipment
Accurately document in real-time as required during all manufacturing processes paying strict attention to detail to ensure data integrity
Following specific cleaning procedures or department cleaning SOP's, clean rooms or equipment as required
Other duties as assigned

Benefits

Defined career path and annual performance review and feedback process
Diverse, inclusive culture
Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
152 hours of PTO + 8 paid holidays
Generous 401K match
Medical, dental and vision benefits
Tuition Reimbursement - Let us help you finish your degree or start a new degree!

Stand Out From the Crowd

Upload your resume and get instant feedback on how well it matches this job.

Upload and Match Resume