Winchester, Kentucky, United States · On-site
Quality Control Analyst Position Summary Typical working hours are Monday-Friday 3 PM - 11:30 PM. This position is 100% on-site in Winchester, Kentucky. Catalent’s Winchester location is the flagship US manufacturing loc…
Skills: Analytical Testing, Dissolution, Titration, Polarimetry, Loss on Drying
Chelsea, Massachusetts, United States · On-site
$24/hr–$26/hr
Pharmaceutical Technician I Position Summary: Work Schedule: 2/2/3 Work Schedule - 6:00am to 6:00pm100% on-site The Chelsea facility is Catalent’s global Center of Excellence for spray dry dispersion and Dry Powder Inhal…
Skills: GMP Manufacturing, Equipment Operation, Cleaning and Sanitization, Batch Documentation, Material Handling
Chelsea, Massachusetts, United States · On-site
$24/hr–$26/hr
Pharmaceutical Technician I Position Summary: Work Schedule: 2/2/3 Work Schedule - 6:00am to 6:00pm100% on-site The Chelsea facility is Catalent’s global Center of Excellence for spray dry dispersion and Dry Powder Inhal…
Skills: GMP Manufacturing, Equipment Operation, Cleaning and Sanitization, Batch Documentation, Material Handling
Chelsea, Massachusetts, United States · On-site
$24/hr–$26/hr
Pharmaceutical Technician I Position Summary: Work Schedule: 2/2/3 Work Schedule - 6:00pm to 6:00am100% on-site The Chelsea facility is Catalent’s global Center of Excellence for spray dry dispersion and Dry Powder Inhal…
Skills: GMP Manufacturing, Equipment Operation, Cleaning and Sanitization, Batch Documentation, Material Handling
Clark County, Kentucky, United States · On-site
Pharmaceutical Technician Position Summary Typical working hours will be 6 PM-6 AM 2-2-3 schedule This role is 100% on-site in Winchester, Kentucky. Catalent’s Winchester location is the flagship US manufacturing locatio…
Skills: Weighing, Mixing, Processing Raw Materials, cGMP Compliance, SOP Adherence
Limoges, Nouvelle-Aquitaine, France · On-site
Localisation : Limoges, sur site Type de contrat : CDI Horaire : 3x8 en semaine, possible astreinte dans l’année Le poste Le département technique assiste, supporte et participe au bon déroulement des activités de produc…
Skills: Preventive Maintenance, Corrective Maintenance, Industrial Maintenance, Mechanical Engineering, Electrical Engineering
Madison, Wisconsin, United States · On-site
Manager - Manufacturing Sciences & Technology (Upstream Technology Transfer) Position Summary: Work Schedule: Monday – Friday, core hours 8am-5pm100% on-site (Madison, WI) Catalent, Inc. is a leading global Contract Deve…
Skills: Upstream Tech Transfer, Mammalian Cell Culture, GMP Manufacturing, Process Modeling, Change Management
Anne Arundel County, Maryland, United States · On-site
$145k–$165k/yr
Manager, QA Batch Disposition Position Summary: Work Schedule: Monday – Friday, 8am – 5pm. 100% on-site Catalent is a leading global CDMO partnering with pharma and biotech innovators to accelerate development and delive…
Skills: QA Batch Disposition, cGMP Compliance, People Leadership, Batch Record Review, Quality Management Systems
Morrisville, North Carolina, United States · On-site
Operations Technician I Position Summary: Work Schedule: Sunday - Thursday, 10:30pm to 6:00am (3rd Shift) 100% on-site The Morrisville (MSV) facility is Catalent’s center of excellence for nasal product development and m…
Skills: Manufacturing, cGMP, Master Batch Records, Standard Operating Procedures, Data Integrity
Kansas City, Missouri, United States · On-site
Associate Scientist II, Molecular and Cellular Biology Position Summary Shift: Monday – Friday 8am-5pm 100% on-site Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose miss…
Skills: Mammalian Cell Culture, Sterile Technique, In Vitro Cell-Based Assays, ELISA, qPCR
Anne Arundel County, Maryland, United States · On-site
$165k–$185k/yr
Sr. Manager, Quality Position Summary: Work Schedule: Monday – Friday, 8am – 5pm. 100% on-site Catalent is a leading global CDMO partnering with pharma and biotech innovators to accelerate development and delivery of lif…
Skills: Quality Assurance, Quality Control, GMP Compliance, Plasmid DNA Manufacturing, CAPA
Strathroy-Caradoc, Ontario, Canada · On-site
Pharmaceutical Packaging Operator Position Summary Work Schedule: 12 hour rotating continental shifts (Days and Nights) This position is 100% on-site at the Strathroy site. This position is located in Strathroy, Ontario,…
Skills: Material Handling, Equipment Setup, Sanitation, Quality Checks, Product Inspection
Durham, North Carolina, United States · On-site
Operations Technician III Position Summary: Work Schedule: Monday - Friday, 2:00pm - 10:30pm 100% on-site The Morrisville (MSV) facility is Catalent’s center of excellence for nasal product development and manufacturing,…
Skills: cGMP Compliance, SOP Execution, Batch Record Documentation, Equipment Troubleshooting, Data Integrity
Madison, Wisconsin, United States · On-site
Associate - Biomanufacturing, Downstream/mRNA Position Summary: Work Schedule: 6am-4pm (Sunday-Wednesday or Wednesday–Saturday shift availability)100% on-site Catalent, Inc. is a leading global Contract Development and M…
Skills: Downstream Purification, mRNA Production, In-vitro Transcription, Chromatography, Tangential Flow Filtration
Madison, Wisconsin, United States · On-site
Senior Associate - Biomanufacturing, Downstream/mRNA Position Summary: Work Schedule: 2pm-12am (Sunday-Wednesday or Wednesday–Saturday shift availability)100% on-site Catalent, Inc. is a leading global Contract Developme…
Skills: Downstream Purification, mRNA Production, In-vitro Transcription, Chromatography, Tangential Flow Filtration
Madison, Wisconsin, United States · On-site
Senior Associate - Biomanufacturing, Downstream/mRNA Position Summary: Work Schedule: 6am-4pm (Sunday-Wednesday or Wednesday–Saturday shift availability)100% on-site Catalent, Inc. is a leading global Contract Developmen…
Skills: Downstream Purification, mRNA Production, In-vitro Transcription, Chromatography, Tangential Flow Filtration
Madison, Wisconsin, United States · On-site
Associate - Biomanufacturing, Downstream/mRNA Position Summary: Work Schedule: 10pm-8am (Sunday-Wednesday or Wednesday – Saturday shift availability)100% on-site$5,000 sign-on bonus offered Catalent, Inc. is a leading gl…
Skills: Downstream Purification, mRNA Production, In-vitro Transcription, Chromatography, Tangential Flow Filtration
Madison, Wisconsin, United States · On-site
Senior Associate - Biomanufacturing, Downstream/mRNA Position Summary: Work Schedule: 10pm-8am (Sunday-Wednesday or Wednesday–Saturday shift availability)100% on-site$5,000 sign-on bonus offered Catalent, Inc. is a leadi…
Skills: Downstream Purification, mRNA Production, In-vitro Transcription, Chromatography, Tangential Flow Filtration
Madison, Wisconsin, United States · On-site
Associate - Biomanufacturing, Downstream/mRNA Position Summary: Work Schedule: 2pm-12am (Sunday-Wednesday or Wednesday – Saturday shift availability)100% on-site Catalent, Inc. is a leading global Contract Development an…
Skills: Downstream Purification, mRNA Production, In-vitro Transcription, Chromatography, Tangential Flow Filtration
Madison, Wisconsin, United States · On-site
Associate Lead I - Biomanufacturing, Compliance Position Summary: Work Schedule: Sunday – Wednesday, 2pm-12am100% on-site (Madison, WI) Catalent, Inc. is a leading global Contract Development and Manufacturing Organizati…
Skills: cGMP Compliance, Deviation Investigations, CAPA, SOP Authoring, Root Cause Analysis
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Perform high-quality analytical testing and data generation in accordance with global pharmacopeia guidelines. Maintain accurate records, calibrate lab instrumentation, and write standard operating procedures.
Requires a Bachelor's degree in a scientific field or equivalent experience in a material testing laboratory. Preference is given to candidates with 2+ years of experience in quality, laboratory, or chemical manufacturing roles.
Typical working hours are Monday-Friday 3 PM - 11:30 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.
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
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.
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 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 [email protected]. 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.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to [email protected] for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Championing the missions that matter™. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) and trusted partner to pharma, biotech, and consumer health companies worldwide. We put patients first in everything we do, helping people live better and healthier lives through every product we help develop, manufacture and deliver. With over 1,000 active development programs at any given time, we launch over 100 new products and line extensions annually. Catalent has supported half of all FDA approvals over the past decade, and our teams working at over 40 global sites help us produce over 60 billion doses every year. Our strength lies in our people: teams across our more than 40 sites and thousands of passionate scientists and technicians who bring expertise in development sciences, delivery technologies, and multi-modality manufacturing. What unites us is our commitment to championing our partners’ missions as our own, anticipating customer needs, solving complex challenges and ultimately making a difference in the lives of patients across the globe. At Catalent, you will be able to directly have an impact, solving problems and ensuring excellence for our customers. Our focus on delivering meaningful outcomes alongside our customers means your work directly impacts millions of people around the world. Join us in championing the missions that matter. Catalent is headquartered in Tampa, Florida, with over 40 global sites. Visit www.catalent.com to learn more.
Offices: 101 E Kennedy Blvd, Tampa, Florida 33602, US · 14 Schoolhouse Road, Somerset, NJ 08873, US · Frankland Road, Blagrove, Swindon, Wiltshire SN5 8YG, GB · 4-9-17 Akasaka, Minato-ku, Tokyo 107-0052, JP · 160 Pharma Dr, Morrisville, NC 27560, US
Championing the missions that matter™. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) and trusted partner to pharma, biotech, and consumer health companies worldwide. We put patients first in everything we do, helping people live better and healthier lives through every product we help develop, manufacture and deliver. With over 1,000 active development programs at any given time, we launch over 100 new products and line extensions annually. Catalent has supported half of all FDA approvals over the past decade, and our teams working at over 40 global sites help us produce over 60 billion doses every year. Our strength lies in our people: teams across our more than 40 sites and thousands of passionate scientists and technicians who bring expertise in development sciences, delivery technologies, and multi-modality manufacturing. What unites us is our commitment to championing our partners’ missions as our own, anticipating customer needs, solving complex challenges and ultimately making a difference in the lives of patients across the globe. At Catalent, you will be able to directly have an impact, solving problems and ensuring excellence for our customers. Our focus on delivering meaningful outcomes alongside our customers means your work directly impacts millions of people around the world. Join us in championing the missions that matter. Catalent is headquartered in Tampa, Florida, with over 40 global sites. Visit www.catalent.com to learn more.
Offices: 101 E Kennedy Blvd, Tampa, Florida 33602, US · 14 Schoolhouse Road, Somerset, NJ 08873, US · Frankland Road, Blagrove, Swindon, Wiltshire SN5 8YG, GB · 4-9-17 Akasaka, Minato-ku, Tokyo 107-0052, JP · 160 Pharma Dr, Morrisville, NC 27560, US
