Become an Expert!

CordenPharma is one of the leading Full-Service Global CMOs in today’s pharmaceutical industry, employing highly trained experts in multiple facilities across Europe and the US.

Because team work is the basis for success, we are constantly looking for qualified employees to join our team of experts.

Please review our current list of job offerings and reply to the respective links below each for more information or to submit an application.

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Pharmaziepraktikum - CordenPharma Plankstadt

Internship, CordenPharma Plankstadt

Seit mehreren Jahren bieten wir Pharmaziestudenten/-innen die Möglichkeit ein vielseitiges und interessantes Praktikum gemäß Approbationsordnung in unserem Unternehmen zu absolvieren. Sie lernen in sechs Monaten die vielfältigen Berufsmöglichkeiten eines Apothekers in der Pharmaindustrie kennen und erhalten einen Überblick über die Anforderungen und Aufgaben bei der Entwicklung, Herstellung und Prüfung von Arzneimitteln. Im Rahmen des Praktikums lernen Sie die Bereiche Pharmazeutische Entwicklung, Analytische Entwicklung, Produktion, Qualitätssicherung und Qualitätskontrolle näher kennen und können hierbei auch an aktuellen Projekten aktiv mitarbeiten.

QA Specialist - Peptisyntha

Full-time, Brussels, BE

The Quality Assurance Specialist will be working as part of the Quality Assurance team on site ensuring products are manufactured, stored and packaged in accordance with cGMP. He / she will also support the development of GMP training packages and delivery of training.                                                                                                     

Chemielaboranten - CordenPharma Plankstadt

Full-Time, Exempt, CordenPharma Plankstadt

Ihre Aufgabe: Durchführung von Prüfungen nach festgelegten Methoden an Rohstoffen, Wirkstoffen und Fertig- arzneimitteln innerhalb der Qualitätskontrolle (HPLC, U(H)PLC, GC, IR/NIR, Identitätsnachweise (nasschemisch), Zerfallszeiten, Partikelgrößenverteilung, Titrationen aller Art, Wirkstofffreisetzung,
DC, Trockungsverluste/Sulfatasche); Durchführung von Gerätewartungen und Kalibrierungen; GMP-gerechte Dokumentation der durchgeführten Arbeiten.

Scientist (m/w) Formulierungsentwicklung - CordenPharma Plankstadt

Full-Time, Exempt, Plankstadt, Germany

Für den Bereich Entwicklung fester Darreichungsformen suchen wir zum nächstmöglichen Zeitpunkt - zunächst befristet auf zwei Jahre - einen Scientist (m/w) Formulierungsentwicklung. Ihre Aufgaben: Koordination aller Aktivitäten in der Pharmazeutischen Entwicklung, insbesondere sorgen Sie für
einen reibungslosen Ablauf der Zusammenarbeit mit der analytischen Entwicklung; Erstellung von Versuchsplänen nach Vorgabe der Entwicklungsziele; die Entwicklung erfolgt nach
QbD/ICHQ8 und Q9 Standards.

Senior Chemical Process Engineer - Job 1610 - CordenPharma Colorado

Full-Time, Exempt, Boulder, Colorado, USA

The Senior Chemical Process Engineer targets Complex Small Molecules, Peptides, and Highly Actives for Active Pharmaceutical Ingredients. Performs research and development activities for the purpose of designing/improving a process or technology and provides process engineering support for manufacturing processes in assigned group or plant through proactive problem prevention and troubleshooting as well as identifying and implementing process improvements. Provides leadership and project management to work groups on large scale projects and technology transfers.

Laboratory Assistant Analytical Development - CordenPharma Plankstadt

Full-time, Plankstadt, Germany

Für den Bereich Analytische Entwicklung suchen wir zum nächstmöglichen Zeitpunkt
- befristet auf 15 Monate - Chemielaborant (m/w) Analytische EntwicklungIhre Aufgaben: Durchführung und Bewertung der Analytik im Rahmen der Entwicklung, Optimierung und Validierung von analytischen Prüfmethoden; Durchführung der Analytik im Rahmen der Produkt- und Prozessentwicklung sowie der zugehörigen Stabilitätsstudien; Durchführung von Gerätewartungen und Kalibrierungen.

Teamleiter (m/w) Pharmazeutische Entwicklung - CordenPharma Plankstadt

Full-Time, Exempt, Plankstadt, Germany

Für den Bereich Pharmazeutische Entwicklung suchen wir zum nächstmöglichen Zeitpunkt einen Teamleiter (m/w) Pharmazeutische Entwicklung. Ihre Aufgabe: Leitung von Entwicklungsprojekten und Steuerung aller Entwicklungstätigkeiten entsprechend dem Stand der pharmazeutischen Technologie (Quality by Design driven Development); Verantwortung der inhaltlichen und qualitativen Steuerung der Projekte: Entwicklung von festen Darreichungsformen für Kunden von Phase I bis Phase III der klinischen Prüfung.

Leiter (m/w) Standort- / Werkscontrolling - CordenPharma Plankstadt

Full-Time, Exempt, Plankstadt, Germany

Wir suchen zum nächstmöglichen Zeitpunkt einen Leiter (m/w) Standort- / Werkscontrolling. Ihre Aufgabe: Verantwortung für die Planung, das monatliche Managementreporting nach IFRS; sowie alle relevanten Zahlen der Produktionsstätte; Enge Zusammenarbeit mit dem Shared Service Center der Gruppe und dessen Steuerung hinsichtlich deren Leistungserbringung; Personalverantwortung für zwei Mitarbeitern; Durchführung der Liquiditätsplanung und  des Cash Forecasts sowie Optimierung des
Working Capitals.

Senior Analytical Chemist Oligonucleotide - Job 1617 - CordenPharma Colorado

Full-Time, Exempt, Boulder, Colorado, USA

The Senior Analytical Chemist Oligonucleotide is responsible for developing and testing oligonucleotide analytic methods to characterize, troubleshoot, optimize and control the oligonucleotide process and materials. Performs analytical research and development activities for the purpose of designing/improving an oligonucleotide manufacturing process or technology, as well as producing clinical trial batches by performing the following duties.

Quality Control Manager - CordenPharma Latina

Full-Time, Exempt, Latina, Italy

The Quality Control Manager is responsible to guarantee compliance with all quality standards concerning with sampling, specification, testing, and with the organization, documentation and release procedures which ensure that the necessary and relevant tests are actually carried out and the materials are not released until the quality is judged to be satisfactory. Guarantee that all parameters related to the quality and stability of the products are regularly checked following validated methods, in alignment with quality requirements and regulatory dossiers. The Quality Control Manager is reporting to Quality Operations Director.

Master I&E Technician - Job 1622 - CordenPharma Colorado

Full-Time, Exempt, Boulder, Colorado, USA

The Master I&E Technician reviews equipment and instrument design information, specifies new/replacement instruments, is part of a project team to evaluate equipment and designs, determines spare part needs, and coordinates the work of others. A Master level Technician also develops calibration and operational check procedures and is proficient on access and replacement of control systems (PLC, DCS I/O). This position requires the employee to stand in for the Lead as needed.

Chemical Operator - Job 1623 - CordenPharma Colorado

Full-Time, Non-Exempt, Boulder, Colorado, USA

The Chemical Operator is responsible for the safe manufacture of pharmaceutical chemicals and intermediates. Performs various unit operations on raw materials and intermediates according to written manufacturing procedures and SOPs. Prepares equipment for maintenance. Hands-on operation of process equipment and material handling. Maintains a consistent high level of housekeeping. Displays initiative in completing assigned tasks and ability to think ahead to prepare for the next steps in a chemical process.  Displays high level of attention to detail and accuracy in work.  

NPI Engineer - CordenPharma Latina

Temporary Contract, Latina, Italy

Gestire le attività di valutazione, realizzazione e modifiche di impianti, sistemi ed apparecchiature legate ai nuovi prodotti attraverso la gestione dei relativi progetti nei tempi e budget previsti.

Production Manager - CordenPharma Caponago

Full-time Permanent, Caponago, Italy

The Production Manager is responsible to assure the organization of the units Production, Inspection and Packaging, in order to guarantee the realization of the productive plans; to coordinate the update of the production schedules being considered the business plans and the levels of stock; to plan the necessary requirements of labor and machinery for the realization of the same plan; to manage the activities for the technological innovation and of process for the total improvement of the effectiveness and the efficiency of the production.

Q.A. Validation Manager - CordenPharma Caponago

Full-time Permanent, Caponago, Italy

Within Q.A. Department, in accordance with GMPs and corporate procedures, the Q.A. Validation Manager plans, supervises, inspects and approves the validation activities on equipments, processes, products, materials and computerized systems. He/she guarantees the management of Change Control System and the drafting/review of validation protocols and reports. The Q.A. Validation Manager also ensures the technical support to all functions of the plant for the evaluation of GMPs’ aspects and collaborates with the HSE Department in order to guarantee an high security level for equipments and technical systems. The person reports to Q.A. Manager and has to coordinate the Q.A. Validation and Change Control Team.