Quality Control Analyst

Catalent Pharma Solutions; Winchester (VA); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Tuition Reimbursement

401K match

PTO + 8 holidays

Career growth opportunities

Job summary

Catalent Pharma Solutions in Winchester, KY is seeking a Quality Control Analyst to perform day-to-day analytical testing in a 100% on-site lab.

You will generate and interpret data, write reports, and help maintain accurate records while adhering to USP/NF/EP guidelines.

Qualifications

• The Candidate Bachelor’s degree in a scientific field required (Chemistry or Biology preferred).
• Alternate degrees in a non-scientific field may be accepted with at least 2 years of relevant experience in a material testing laboratory.
• 2+ years in Quality, Laboratory, Clinical, or Chemical manufacturing role preferred.
• Assisting with others and lifting heavy containers as needed.

Responsibilities

• Perform efficient/reliable/high quality analytical testing in accordance with USP/NF/EP/JP/FCC/etc. or customer supplied guidelines.
• Typical testing may include Dissolution, Titration, Polarimetry, Loss on Drying, Viscosity, Residue on Ignition, Heavy Metal Content, FTIR, HPLC, and GC, etc.
• Maintain accurate written records of all analysis performed.
• Accurately interpret and effectively communicate analytical results and issues.
• Schedule daily tasks in an organized and efficient manner.
• Calibrate and maintain lab equipment and instrumentation.
• Responsible for operating in a safe manner, must be familiar with basic laboratory and chemical hygiene practices
• Perform peer review of analytical testing and write up.
• Write SOPs on an as needed basis.
• Other duties as required in support of Catalent Pharma Solutions high performance.

Skills

Analytical testing

Laboratory records

Safety compliance

Data reporting

Education

Bachelor's degree in a scientific field

Tools

HPLC

GC

FTIR

Dissolution

Titration

Polarimetry

Loss on Drying

Viscosity

Residue on Ignition

Heavy Metal Content

Job description

Quality Control Analyst Position Summary

Typical working hours are on E shift (6 AM- 6 PM Saturday - Monday, every other Tuesday from 6 AM - 2:30 PM) This position is 100% on-site in Winchester, Kentucky. Catalent’s Winchester location is the flagship US manufacturing location for large scale oral dose forms, with integrated analytical and development services. With 28 years of expertise in product development, technology transfers and commercial manufacturing, and roots in industry-leading Glatt technology.

The Quality Control Analyst performs the basic and critical experimental work of day-to‑day analysis, including generation and analysis of data. The Quality Control Analyst works “hands on” in an analytical lab that requires analytical testing, computer operating, record keeping, and report writing abilities.

Responsibilities

• Perform efficient/reliable/high quality analytical testing in accordance with USP/NF/EP/JP/FCC/etc. or customer supplied guidelines.
• Typical testing may include Dissolution, Titration, Polarimetry, Loss on Drying, Viscosity, Residue on Ignition, Heavy Metal Content, FTIR, HPLC, and GC, etc.
• Maintain accurate written records of all analysis performed.
• Accurately interpret and effectively communicate analytical results and issues.
• Schedule daily tasks in an organized and efficient manner.
• Calibrate and maintain lab equipment and instrumentation.
• Responsible for operating in a safe manner, must be familiar with basic laboratory and chemical hygiene practices
• Perform peer review of analytical testing and write up.
• Write SOPs on an as needed basis.
• Other duties as required in support of Catalent Pharma Solutions high performance.

Qualifications

• The Candidate Bachelor’s degree in a scientific field required (Chemistry or Biology preferred).
• Alternate degrees in a non-scientific field may be accepted with at least 2 years of relevant experience in a material testing laboratory.
• 2+ years in Quality, Laboratory, Clinical, or Chemical manufacturing role preferred.
• Assisting with other personnel with lifting of liquid containers and all objects of greater than 50 lbs.
• Operating safely in a dynamic environment which includes mobile and fixed equipment and changing conditions while completing job tasks that range from simple to complex and/or multi-tasking.

Why You Should Join Catalent

• Several Employee Resource Groups focusing on D&I.
• Tuition Reimbursement – Let us help you finish your degree or earn a new one!
• Generous 401K match.
• 152 hours accrued PTO + 8 paid holidays.
• 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.
• Visit Catalent Careers to explore career opportunities.
• 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 Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [e-mail]. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

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.