Pharmaceutical Quality Control Associate
2 weeks ago
Catalent is seeking a Quality Control Associate to support our Supplier Audits program in Greenville, N.C. As a Quality Control Associate, you will be responsible for conducting system-based audits and risk assessments for Supplies Audits and Internal Quality Systems.
Key responsibilities include:
- Performing external supplier audits (Desktop, Virtual or On-Site) per schedule, communicating findings and ensuring CAPA plans are appropriate to address the findings.
- Ensuring Supplier Audit Team members are properly qualified and assigning their roles and responsibilities; training staff to conduct or assist with audits and risk assessments.
- Participating in Regulatory Inspections and assisting Inspection Readiness Teams with inspection preparation, including walkthroughs and gathering of documentation, per inspection agenda as required.
- Assisting with the generation of the Internal Audit Schedule, preparation and execution of Internal Quality Audits of Catalent systems / subsystems.
- Participating in process improvement projects and investigations, as required.
This role requires a strong understanding of cGMPs and experience working in a Quality Auditing function. The ideal candidate will have a Bachelor's degree in a technical field and at least 6 years of professional experience in the pharmaceutical industry, with 3 years of experience in a Quality Auditing function.
The salary range for this position is $80,000 - $110,000 per year, depending on experience.
Benefits include competitive medical benefits, 152 hours of PTO + 8 Paid Holidays, dynamic work environment, and opportunities for career growth and development.
],-
Pharmaceutical Manufacturing Associate
1 month ago
Greenville, North Carolina, United States Catalent Inc Full timeAbout the Role: We are seeking a skilled Pharmaceutical Manufacturing Associate to join our team at Catalent Inc. As a key member of our oral solid dosage (OSD) manufacturing department, you will play a critical role in ensuring the quality and compliance of commercial batches.Key Responsibilities:Assemble, disassemble, clean, and store manufacturing...
-
Pharmaceutical Operations Manager
5 days ago
Greenville, North Carolina, United States Catalent Inc Full timeKey Job ResponsibilitiesAs a Pharmaceutical Operations Manager at Catalent Inc., you'll lead a team of professionals responsible for manufacturing, packaging, and labeling commercial products and clinical trial materials. Your expertise will ensure seamless execution of production schedules, quality control, and regulatory compliance. Key responsibilities...
-
Pharmaceutical Development Manager
1 week ago
Greenville, North Carolina, United States Disability Solutions Full timeAbout UsDisability Solutions is a global leader in the development and delivery of pharmaceuticals, with a strong presence in the field of analytical chemistry. Our state-of-the-art facility in Greenville, N.C. features cutting-edge equipment and technologies, and our team of experts is dedicated to delivering high-quality results.Job DescriptionThis is an...
-
Pharmaceutical Process Specialist
1 week ago
Greenville, North Carolina, United States Disability Solutions Full timeAbout the RoleAs a Pharmaceutical Operator II with Catalent, you will play a vital part in developing and optimizing suitable formulations and processes for our clients. This position requires a strong understanding of pharmaceutical manufacturing and a commitment to quality and compliance.Responsibilities- Assist in the development and optimization of...
-
Pharmaceutical Technologist
7 days ago
Greenville, North Carolina, United States Disability Solutions Full timeCompany OverviewCatalent is a global leader in the development and manufacturing of pharmaceuticals. Our Greenville, N.C. facility specializes in end-to-end solutions for oral solid dosage forms, with a focus on quality and compliance.
-
Pharmaceutical Analytical Chemist Position
1 month ago
Greenville, North Carolina, United States Catalent Inc Full timeCatalent Inc is a global leader in the drug development and delivery industry. Our team at the Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms.Salary$110,000 - $140,000 per yearAbout the JobWe are seeking a Senior Analytical Chemist to perform routine and non-routine analytical testing in support of...
-
Pharmaceutical Project Coordinator
1 week ago
Greenville, North Carolina, United States Disability Solutions Full timeJob DescriptionThe Associate Scientist serves as a primary point of contact with clients regarding pharmaceutical development and clinical manufacturing project activities. Responsibilities include supporting these activities in supervision, process development, clinical trial batch manufacturing, packing, and documentation.Organize multiple responsibilities...
-
Greenville, North Carolina, United States Catalent Inc Full timeAbout Catalent IncCatalent is a global company with high growth and market presence. We specialize in pharmaceutical drug development and manufacturing for patients worldwide.Our TeamWe have over 7,000 life-saving products and work directly with pharma companies to bring medicines from early development to the market. Our goal is to advance new treatments...
-
Pharmaceutical Operations Specialist
7 days ago
Greenville, North Carolina, United States Disability Solutions Full timeAbout Our CompanyCatalent is a global drug development and delivery leader specializing in integrated formulation development, analytical services, commercial manufacturing and packaging.Our Greenville, N.C. facility features cutting-edge technology and infrastructure supporting numerous projects simultaneously.Job Requirements:Associate degree in Life...
-
Pharmaceutical Development Professional
7 days ago
Greenville, North Carolina, United States Disability Solutions Full timeJob Overview">This entry-level position is an exciting opportunity for a recent graduate or undergraduate student to join our team at Catalent as a Pharmaceutical Development Intern. The selected candidate will work closely with our experienced professionals to assist in project execution, ensuring the development and manufacturing of new treatments for...
-
Quality Assurance Specialist
2 weeks ago
Greenville, North Carolina, United States Disability Solutions Full timeCatalent, a leading global partner for the pharmaceutical industry, is seeking a talented Validation Engineer II to join their team in Greenville, N.C. This exciting opportunity offers a chance to work on end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and...
-
Pharmaceutical Production Supervisor
1 month ago
Greenville, North Carolina, United States Catalent Inc Full timeCatalent Inc is a leading global provider of development and manufacturing services for the pharmaceutical industry.With over $100M in recent investments, our state-of-the-art facility in Greenville, N.C. offers fit-for-scale capacity with potent handling capabilities ideal for orphan or targeted drug development.We are committed to a Patient First culture...
-
Quality Assurance Specialist
1 week ago
Greenville, North Carolina, United States Disability Solutions Full timeOverviewCatalent is a leading global partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Our mission is to help people live better, healthier lives by advancing new medicines from early development to clinical trials and to the market.SalaryThe estimated annual salary for this position is...
-
Control Panel Quality Engineer
6 days ago
Greenville, South Carolina, United States Panelmatic Inc. Full timeJob Overview: Control Panel Quality EngineerWe are seeking a highly skilled Control Panel Quality Engineer to join our team at Panelmatic Inc. This role requires a strong background in electrical inspection and testing, with excellent problem-solving skills and attention to detail.About the Job:Develop and implement quality control measures to ensure the...
-
Pharmaceutical Chemist
7 days ago
Greenville, South Carolina, United States PAI Holdings LLC Full timeJob OverviewWe are seeking a skilled Pharmaceutical Chemist to join our team at PAI Holdings LLC.Key ResponsibilitiesAnalyze drug substances, drug products, and/or stability samples using approved laboratory monographs/specifications, Standard Operating Procedures, and USP/NF methodologies to ensure quality and compliance requirements are met.Perform...
-
Quality Assurance Internship
2 weeks ago
Greenville, North Carolina, United States Disability Solutions Full timeAbout UsCatalent is a leading partner for the pharmaceutical industry in development and manufacturing of new treatments for patients worldwide.Our Greenville facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including formulation development, analytical services, commercial manufacturing, and packaging.We are committed to a...
-
Pharmaceutical Operations Coordinator
2 weeks ago
Greenville, South Carolina, United States Prisma Health Full timeKey Responsibilities:Performing technical pharmacy functions in Ambulatory Pharmacy, Inpatient Pharmacy, Pharmaceutical Research Center, or Drug Policy Program.Inventory management for controlled substances, purchasing, and maintaining records.Mentorship of new pharmacy technicians and interns, and supporting education and training of pharmacists and...
-
Quality Assurance Specialist
7 days ago
Greenville, North Carolina, United States Disability Solutions Full timeAbout the Role$61,000 - $82,000 per year (Estimated Salary)The Laboratory Analyst position plays a crucial role in supporting pharmaceutical products by performing routine non-chromatographic analytical testing.This position ensures data integrity, adheres to applicable safety, quality, and regulation requirements, and follows standard operating procedures...
-
Quality Assurance Manager Compliance
2 weeks ago
Greenville, South Carolina, United States PAI Holdings LLC Full timeAbout the RoleWe are seeking an experienced Quality Assurance Manager - Compliance to join our team. In this role, you will be responsible for managing the change control program, including change initiations, reviews, approvals, and closure of changes. You will also create and maintain electronic databases for tracking change activities.A bachelor's degree...
-
Research Development Associate
7 days ago
Greenville, North Carolina, United States Disability Solutions Full timeAssociate Scientist Role OverviewCatalent's Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms.This state-of-the-art facility features fit-for-scale capacity with potent handling capabilities and has had over $100M of investments in recent years.The Associate Scientist serves as a primary point of contact...