Catalent

Head of Production - Finishing / Abteilungsleiter Pharmazeutische Produktion (f/m/d)

Catalent  •  Eberbach, DE (Onsite)  •  1 month ago
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Job Description

Catalent Pharma and Consumer Health (PCH) is a fast-growing business within Catalent Pharma Solutions that delivers innovative technologies to improve patient and consumer treatments. Its offerings include Softgel, Liquid-Filled Hard Shell, Liquid in Bottle, Zydis® ODT, and a broad range of solid dose technologies across Rx, OTC, VMS, and topical products.

Working at Catalent PCH means joining a diverse, experienced team developing prescription therapies for serious diseases such as cancer, autoimmune, cardiovascular, metabolic, and neurological disorders, as well as leading consumer products including pain relief, cough and cold, vitamins, and cosmetics in patient-friendly dosage forms.

Head of Production - Finishing (f/m/d)

I. Purpose of the Position

Lead and manage a GMP-compliant production area with approximately 100 employees operating in 24/5 and 24/7 shift systems for visual inspection, bulk packaging, blister packaging, printing and additional treatments of the products like coating and hardening. Ensure adherence to all regulatory requirements and Catalent’s global quality standards while fostering a culture of Patient First and strong customer orientation. Drive continuous improvement through Lean Management principles, optimize processes for efficiency, and maintain the highest standards of product quality and safety.

II. Responsibilities

  • Provide leadership and strategic direction for the production area under GMP conditions.
  • Ensure compliance with all applicable regulations, SOPs, and quality standards.
  • Manage and develop a team of approximately 100 employees across multiple shifts (24/5 and 24/7).
  • Implement and sustain Lean Management principles to improve efficiency and reduce waste.
  • Ensure timely and accurate production to meet customer requirements and delivery schedules.
  • Foster a Patient First mindset and customer-focused culture throughout the team.
  • Monitor production KPIs and initiate corrective actions as needed.
  • Coordinate with Quality Assurance, Supply Chain, and other departments to ensure seamless operations.
  • Drive digitalization and process optimization projects within the production area.
  • Ensure proper training and qualification of staff for GMP compliance.
  • Prepare and manage budgets, resources, and capacity planning.
  • Handle audits and inspections from regulatory authorities and customers.
  • Take on special projects and tasks as assigned by senior management.

III. Requirements Profile

Education & Experience:

  • University degree in Pharmacy, Chemistry, Engineering, or related field; advanced degree preferred.
  • Several years of experience in pharmaceutical or GMP-regulated production environment.
  • Proven leadership experience managing large teams in a shift-based operation.
  • Experience with Lean Management and continuous improvement methodologies.
  • Strong understanding of GMP regulations and compliance requirements.

Technical Competencies:

  • In-depth knowledge of production processes in a GMP environment.
  • Familiarity with digital tools and systems for production management.
  • Ability to analyze KPIs and implement data-driven improvements.
  • Understanding of quality assurance and regulatory requirements.

Personal Competencies:

  • Strong leadership and people management skills.
  • Acting like a change manager
  • High customer orientation and commitment to Patient First principles.
  • Excellent communication and decision-making abilities.
  • Ability to work under pressure and manage complex operations.
  • Strategic thinking combined with hands-on problem-solving skills.

Language Skills:

  • Fluent in German and English (written and spoken).

Additional Requirements:

  • Willingness to work in a dynamic, shift-based environment.
  • Openness to digital innovation and continuous learning.
  • Intercultural competence and experience in international settings.

Catalent bietet Möglichkeiten, Ihre Karriere voranzutreiben! Werden Sie Teil des globalen Marktführers in der Entwicklung von Darreichungsformen von Medikamenten und helfen Sie uns, Patienten auf der ganzen Welt über 7.000 lebensrettende und lebensverbessernde Produkte anzubieten. Catalent ist ein spannendes und wachsendes internationales Unternehmen, dessen Mitarbeiter direkt mit Pharma-, Biopharma- und Consumer-Health-Unternehmen jeder Größe zusammenarbeiten, um neue Medikamente von der frühen Entwicklung über klinische Studien bis hin zur Marktreife zuentwickeln. Catalent produziert mehr als 70 Milliarden Dosen pro Jahr und jede davon wird von jemandem verwendet, der auf uns zählt. Machen Sie mit uns den Unterschied.

Persönliche Initiative. dynamisches Tempo. Bedeutungsvolle Arbeit.

Besuchen Sie, Catalent Careers um Karrieremöglichkeiten zu entdecken.

Catalent ist ein Arbeitgeber für Chancengleichheit und diskriminiert nicht aufgrund von Merkmalen, die durch lokale Gesetze geschützt sind.

Wenn Sie aufgrund einer Behinderung für einen Teil des Bewerbungs- oder Einstellungsverfahrens angemessene Vorkehrungen benötigen, können Sie Ihre Anfrage per E-Mail senden und Ihre Anfrage nach einer Unterkunft bestätigen und die Stellennummer, den Titel und den Standort an DisabilityAccommodations@catalent.com angeben. Diese Option ist Personen vorbehalten, die aufgrund einer Behinderung eine Unterkunft benötigen. Die erhaltenen Informationen werden von einem US-amerikanischen Catalent-Mitarbeiter verarbeitet und dann an einen lokalen Personalvermittler weitergeleitet, der Unterstützung bietet, um eine angemessene Berücksichtigung im Bewerbungs- oder Einstellungsverfahren sicherzustellen.

Hinweis für Vertreter von Agenturen und Personalberatungen Catalent Pharma Solutions (Catalent) akzeptiert keine unaufgefordert eingesandten Lebensläufe von Agenturen und/oder Personalberatungen für diese Stellenausschreibung. Lebensläufe, die einem Catalent-Mitarbeiter von einer Drittagentur und/oder einer Personalberatung ohne gültige schriftliche und unterzeichnete Beauftragung vorgelegt werden, gehen in das alleinige Eigentum von Catalent über. Es wird keine Gebühr gezahlt, wenn ein Kandidat für diese Position aufgrund einer unaufgeforderten Empfehlung einer Agentur oder einer Suchfirma eingestellt wird. Vielen Dank.

Catalent

About Catalent

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.

Industry
Chemicals & Materials
Company Size
10,000+ employees
Headquarters
Tampa, Florida
Year Founded
Unknown
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