Beinheim, Grand Est, France · On-site
Catalent Pharma Solutions est une société américaine, considérée comme le premier fournisseur mondial de technologies avancées d'administration et de développement de solutions pour les médicaments, les produits biologiq…
Skills: Project Management, Product Development, Pharmaceutical Formulation, GMP (Good Manufacturing Practices), Physico-chemical Analysis
Madison, Wisconsin, United States · On-site
Associate Lead I - Biomanufacturing, Compliance Position Summary: Work Schedule: Wednesday – Saturday, 2pm-12am100% on-site (Madison, WI) Catalent, Inc. is a leading global Contract Development and Manufacturing Organiza…
Skills: cGMP Compliance, Deviation Investigations, CAPA, SOP Authoring, Root Cause Analysis
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 Principles, Deviation Investigations, CAPA, SOP Authoring, Root Cause Analysis
Durham, 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
Morrisville, 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
Morrisville, North Carolina, United States · On-site
Operations Technician III Position Summary: Work Schedule: Sunday - Thursday, 10:30pm - 6:00am 100% on-site The Morrisville (MSV) facility is Catalent’s center of excellence for nasal product development and manufacturin…
Skills: cGMP Compliance, SOP Execution, Batch Record Documentation, Equipment Troubleshooting, Data Integrity
Chelsea, Massachusetts, United States · On-site
Job Description Proposal Lead Position Summary: Full time salaried position Onsite based out of our Chelsea, MA location As a key member of the client relationship team, the Proposal Lead is responsible for project manag…
Skills: Project Management, Proposal Generation, Pricing Analysis, Margin Analysis, Stakeholder Management
Beinheim, Grand Est, France · On-site
Localisation :Beinheim, sur site Type de contrat : CDD de 6 mois Pour notre entreprise située à Beinheim à 30min de Strasbourg (67), nous recrutons un(e) Technicien(ne) Contrôle Qualité pour un CDD de 6 mois. Au sein du …
Skills: Physico-chemical Analysis, Sample Management, Quality Control, Documentation, Trackwise
Greendale, Indiana, United States · On-site
Manufacturing Operator Position Summary Work Schedule: 2nd shift 4pm-2:30am 100% based on-site in Greendale, IN Greendale is one of Catalent’s gummy technology development and manufacturing facilities in North America. T…
Skills: Mogul Machine Operation, Troubleshooting, Resource Allocation, Equipment Setup, Quality Inspection
Tampa, Florida, United States · Hybrid
$115k–$200k/yr
Manager, Business Assurance Position Summary: The Manager, Business Assurance will lead critical compliance initiatives. In this role, the Manager, Business Assurance will manage the full SOX 404 compliance process, work…
Skills: SOX 404 Compliance, Internal Controls, Risk Mitigation, Financial Reporting, Internal Audit
Anne Arundel County, Maryland, United States · On-site
$70k–$85k/yr
Facilities Mechanic Position Summary Work Schedule: Night Shift 6pm-6am, Thursday - Saturday and every other Wednesday 100% on-site Catalent, Inc. is a leading global contract development and manufacturing organization (…
Skills: HVAC Maintenance, Utility Systems Operation, Troubleshooting, cGMP, Building Automation Systems
Bridgewater Township, New Jersey, United States · On-site
$70k–$120k/yr
Junior Analyst, Corporate Accounting Position Summary: Full time salaried position Onsite based out of our Bridgewater, NJ location The Junior Analyst, Corporate Accounting supports the company’s accounting and financial…
Skills: Journal Entries, Account Reconciliations, Financial Analysis, US GAAP, Financial Reporting
Madison, Wisconsin, United States · On-site
Associate Lead I - Biomanufacturing, Compliance Position Summary: Work Schedule: Wednesday – Saturday, 2pm-12am100% on-site (Madison, WI) Catalent, Inc. is a leading global Contract Development and Manufacturing Organiza…
Skills: cGMP Compliance, Deviation Investigations, CAPA, SOP Authoring, Root Cause Analysis
Madison, Wisconsin, United States · On-site
Senior Associate - Biomanufacturing, Compliance - Manufacturing Technical Support Position Summary: Work Schedule: Alternating 3/4-4/3 Weekly Schedule, core hours 11pm-10am100% on-site (Madison, WI)On-call rotation requi…
Skills: Biomanufacturing, cGMP Compliance, Technical Writing, Root Cause Analysis, Tech Transfer
Madison, Wisconsin, United States · On-site
Lab Associate - Process Development - Operations Position Summary Shift: Monday – Friday 8:00am – 5:00pm100% on-site Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mis…
Skills: Equipment Maintenance, Solution Preparation, Sample Management, Inventory Management, 5S Organization
Madison, Wisconsin, United States · On-site
Engineer (Facilities) Position Summary: Work Schedule: M-F 8am-5pm100% on-site Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Located in Madison, WI, this facility features…
Skills: Facilities Engineering, HVAC Systems, Process Utilities, Bio-containment Systems, SOP Drafting
Saint Petersburg, Florida, United States · On-site
Finishing Operator Position Summary Work Schedule: Rotating 12-hour shift from 7:00PM to 7:00AM EST, operating on a two-week cycle. Week 1 includes Monday, Tuesday, Friday, Saturday, and Sunday; Week 2 includes Wednesday…
Skills: Quality Inspection, cGMP, Machine Programming, Packaging, Documentation
Saint Petersburg, Florida, United States · On-site
Encapsulation Operator Position Summary Work Schedule: Rotating 12-hour shift from 7 PM to 7 AM EST, operating on a two-week cycle. Week 1 includes Monday, Tuesday, Friday, Saturday, and Sunday; Week 2 includes Wednesday…
Skills: Encapsulation Machine Operation, cGMP Standards, Equipment Troubleshooting, Batch Record Documentation, Quality Control
Madison, Wisconsin, United States · On-site
Specialist I, Quality Assurance Position Summary: Work Schedule: M-F 8am-5pm100% on-site Working for Catalent Biologics is an opportunity to join an entrepreneurial team. Catalent Biologics is making significant investme…
Skills: Supplier Quality Assurance, Auditing, Quality Agreements, CGMPs, Data Integrity
Greendale, Indiana, United States · On-site
Director, Product Development & Technical Services Position Summary: 100% on-site Greendale is one of two gummy technology development and manufacturing facilities in North America. The site has the capability to manufac…
Skills: Product Development, Technical Services, Project Management, Technology Transfer, Process Optimization
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Manage product development projects from active ingredient characterization to formulation design and production supervision. Responsible for technical documentation, laboratory expertise, and maintaining communication with clients in French and English.
Requires a Master's degree in Quality, Engineering, or Pharmacy with a strong understanding of pharmaceutical processes. Candidates must be organized, possess critical thinking skills, and be fluent in English for corporate and client communication.
Catalent Pharma Solutions est une société américaine, considérée comme le premier fournisseur mondial de technologies avancées d'administration et de développement de solutions pour les médicaments, les produits biologiques, les produits de consommation et de santé animale.
Pour notre site situé à Beinheim dans la région de Strasbourg (67), nous recrutons un(e) Chargé.e de Projets en Développement Produit (H/F), dans le secteur Recherche et Développement.
En tant que Chargé.e de Projets, vous aurez à gérer des projets de développement de produits Client et proactifs depuis la caractérisation des principes actifs, jusqu’au design de formulations, de leur procédé de fabrication, et la supervision de leur fabrication dans le respect du cahier des charges techniques, des Bonnes Pratiques de Fabrication et des règles de sécurité. Vous contribuerez au développement technologique de la R&D en explorant des solutions nouvelles (axes de formulation outils de caractérisation, équipements) au travers des projets clients et les programmes d’innovation du groupe.
Gestion documentaire : rédiger/vérifier des procédures, instructions de travail, documentation de production, protocoles et rapports d’études
Expertise technique :
Définition d’études et modes opératoires,
Proposer et supporter des initiatives d’amélioration continue au laboratoire et/ou en production
Participer à la présentation du laboratoire et/ou de la production dans le cadre de visites ou d’audits clients.
Gestion de projets de développement produit :
Planifier, superviser et réaliser des opérations complètes de caractérisation, pré-formulation et de développement de formulation nouvelles,
Superviser et réaliser la mise au point des méthodes de contrôle physico-chimiques de formulations existantes et/ou en cours de développement,
Planifier et assurer le suivi de la bonne réalisation des essais en production.
Assurer la communication aux clients en français ou anglais et proposer, discuter des études à réaliser dans le cadre de projet
Veille technologique et scientifique
Catalent offer des opportunités enrichissantes pour faire avancer votre carrière! Rejoignez le leader mondial du développement et de la production de médicaments et aidez-nous à proposer plus de 7 000 produits qui sauvent et améliorent la vie des patients du monde entier. Catalent est une société internationale passionnante et en pleine croissance où les employés travaillent directement avec des sociétés pharmaceutiques, biopharmaceutiques et de santé grand public de toutes tailles pour faire progresser de nouveaux médicaments, du développement précoce aux essais cliniques et à la mise sur le marché. Catalent produit plus de 70 milliards de doses par an, et chacune sera utilisée par quelqu'un qui compte sur nous. Rejoignez-nous pour faire la différence.
Initiative personnelle. Rythme dynamique. Un travail significatif.
Visitez Catalent Careers pour explorer les opportunités de carrière.
Catalent est un employeur garantissant l'égalité des chances et ne fait aucune discrimination sur la base d'une caractéristique protégée par la législation locale.
Si, en raison d’un handicap, vous avez besoin d'un aménagement raisonnable pour une partie ou plus du processus de candidature ou d'embauche, vous pouvez soumettre votre demande en envoyant un courriel et en confirmant votre demande d'aménagement et en incluant le numéro de poste, le titre et le lieu à [email protected]. Cette option est réservée aux personnes ayant besoin d'un aménagement en raison d'un handicap. Les informations reçues seront traitées par un employé de Catalent aux États-Unis, puis acheminées vers un recruteur local qui fournira une assistance pour assurer une prise en compte appropriée dans le processus de candidature ou d'embauche.
Avis aux représentants des agences et des cabinets de recherche : Catalent Pharma Solutions (Catalent) n'accepte pas les curriculum vitae non sollicités d'agences et/ou de cabinets de recherche pour cette offre d'emploi. Les curriculum vitae soumis à tout employé de Catalent par une agence tierce et/ou une société de recherche sans un accord de recherche écrit et signé valide, deviendront la propriété exclusive de Catalent. Aucuns frais ne seront payés si un candidat est embauché pour ce poste à la suite d'une recommandation non sollicitée d'une agence ou d'un cabinet de recherche. Merci.
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
