Quality Control Chemist II

Quality Control Chemist II

Position Summary

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 Research Triangle Park (RTP) facility is home to Catalent's Inhalation franchise including product development, clinical and commercial manufacturing for inhalers and Nasal Sprays.

Catalent Pharma Solutions is Morrisville, NC is hiring a Quality Control Chemist II. The Quality Control Chemist II will independently perform work using a variety of methodology.  Experience in a variety of analytical techniques and instrumentation is required.  These may include compendial testing, identification techniques (i.e. FTIR), chromatography, among others.  The Quality Control Chemist II will perform scientific analysis of data and draw reasonable conclusions, follow established methods and protocols, perform initial troubleshooting and investigations as needed, demonstrate leadership skills regarding guiding and training less experienced colleagues and comply with the company safety and operational requirements and procedures requirements.

This is a full-time, salaried role. The core hours are Monday - Friday 8:00AM – 5:00PM

This position is 100% on-site at the Morrisville site.

Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee. 

The Role:

• Execute laboratory activities according in compliance with safety, quality, and regulatory standards. (e.g., GMP, GLP, ICH guidelines)

• Perform secondary review of analytical data generated by peers.

• Assist laboratory technicians as needed with regards to training, scheduling, and troubleshooting.

• Support drafting/reviewing of validation protocols, reports, investigations, or other technical documentation.

• Participate in laboratory improvement projects as assigned.

• Perform all other duties as assigned.

The Candidate:

• Master’s degree in scientific or engineering field and 1+ years related experience (or) Bachelor’s degree in scientific or engineering field and 3+ years related experience (or) Associate’s degree in scientific or engineering field and 6+ years related experience required.

• Experience in testing in a GMP/GXP environment.  Includes an understanding of good documentation skills, data integrity, and compliance.

•  Familiar with compendial testing including USP, EP, and JP compendia.

•  Able to organize workload and complete all required assignments in a timely manner.

• Ability to interpret scientific data and form conclusions as needed and perform critical, scientific analysis of data as needed

• Familiar with or able to learn a variety of analytical instrumentation including operation, maintenance, and troubleshooting.

• Identify and participate in laboratory improvement projects.

• Individual may be required to sit, stand, walk regularly and occasionally lift 0-40 pounds. Specific vision requirements including reading of written documents and the use of computer monitor screen frequently

Why you should join Catalent:

• Defined career path and annual performance review and feedback process 

• Diverse, inclusive culture 

• Positive working environment focusing on continually improving processes to remain innovative

• Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives 

• 152 Hours + 8 paid holidays

• Several Employee Resource Groups focusing on D&I

• Dynamic, fast-paced work environment

• Community engagement and green initiatives 

• Generous 401K match 

• Company match on donations to organizations

• Medical, dental and vision benefits effective day one of employment 

• Tuition Reimbursement – Let u