Assoc. Director of Support Operations (m/f/d) Jetzt bewerben
Assoc. Director of Support Operations (m/f/d)

Assoc. Director of Support Operations (m/f/d)

Werthenstein Vollzeit 72000 - 84000 € / Jahr (geschätzt) No home office possible
Jetzt bewerben
MSD

Auf einen Blick

  • Aufgaben: Lead support teams in biotech manufacturing, ensuring excellence in operations and material management.
  • Arbeitgeber: Join a research-driven biopharmaceutical company dedicated to innovative medicine and vaccine solutions.
  • Mitarbeitervorteile: Enjoy international relocation opportunities, VISA sponsorship, and a commitment to diversity and inclusion.
  • Warum dieser Job: Be part of a dynamic team that values diverse ideas and fosters breakthrough innovations in healthcare.
  • Gewünschte Qualifikationen: Requires a degree in science or engineering and 8+ years in GMP-regulated environments.
  • Andere Informationen: Position includes travel requirements of 10% and is open until 01/10/2025.

Das voraussichtliche Gehalt liegt zwischen 72000 - 84000 € pro Jahr.

Job Description

Assoc. Director of Support Operations (m/f/d)

The Biotech facility embeds the latest technologies into the early stage clinical pipeline, helping to refine these technologies for inclusion into the late-stage and commercial launch of programs. By integrating leading-edge technology with a dynamic, activity-based workspace, the facility will support seamless connection and collaboration within and across teams and functions. Schachen Biotech provides Biologics Drug Substance manufacturing for Early Phase Clinical Supply and Technology Innovation implementation into the pipeline.

The Assoc. Director of Support Operations (m/f/d) will be a member of the Biotech Manufacturing Leadership team, reporting to the Head of Manufacturing. The successful candidate will lead the support teams including Material management in the GMP shop floor area, Solution Supply execution and a team of delivering excellence in the Manufacturing Operations Organization. This person will be a key stakeholder in the maintenance of the multiproduct strategy and will have a leadership role in the introduction of new processes, materials, and technologies to the facility as well as transfer of processes out.

Key Responsibilities:

  • Leading a team engaged in both day-to-day production execution and strategic activities aimed at improving the time-to-clinic.
  • Overseeing the coordination efforts for Material Weight and Dispense, Solution Supply execution to meet Drug Substance Manufacturing Execution (Process Operations) requirements of New Product Introduction (NPI) schedule.
  • Management of the team for Operational Excellence, Technology Excellence, Innovation Excellence and Business Excellence which includes hiring and building team capabilities to meet the facility’s operational requirements.
  • Overseeing the material management activities for the GMP areas, interfacing with the Supply Chain team and warehouse team and establishing standards for business processes associated with materials such as Kanban and VMI.
  • Embedding a culture that aligns with the Ways of Working and is committed to both facility and site priorities.
  • Overseeing production planning and associated activities, integrated with the Multiproduct platform.
  • In partnership with the Assoc. Director of Process Operations, championing the implementation of the lights-out manufacturing philosophy.
  • Ensuring operational readiness in cross-functional partnership with other key stakeholders, as required by each Tech Transfer program to the facility.
  • As applicable to Solution Supply and Weigh and Dispense, accountable for the management of the Production Alarm System, Sample Management Processes, Change approver for MES, Delta V Recipes, and material BOMs.
  • Deploying manufacturing and associated release standards in compliance with the company’s Quality Manual and collaborating with network partners for a common approach.
  • Developing future breakthrough business solutions, initially leveraging existing resources in the company’s network to reduce overall effort and risk.
  • Collaborating across the network on sharing best practices and lessons learned.

Education, Skills, and Experience:

  • Degree level qualification in science or engineering, with People Manager Experience.
  • Demonstrated experience (8 years minimum) in a GMP-regulated biological drug substance manufacturing environment.
  • Possess a deep understanding of a manufacturing/operational GMP environment.
  • Delta V and MES knowledge and experience an advantage.

We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

Employee Status:

Regular

Relocation:

International

VISA Sponsorship:

Yes

Travel Requirements:

10%

Job Posting End Date:

01/10/2025

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

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Assoc. Director of Support Operations (m/f/d) Arbeitgeber: MSD

At Schachen Biotech, we pride ourselves on being an exceptional employer that fosters a culture of innovation and collaboration. Our dynamic, activity-based workspace is designed to support seamless connections across teams, while our commitment to employee growth ensures that you will have ample opportunities to develop your skills and advance your career in the biopharmaceutical industry. With a focus on diversity and inclusion, we believe that great ideas come from diverse perspectives, making our facility not just a workplace, but a community dedicated to making a meaningful impact on global health.
MSD

Kontaktperson:

MSD HR Team

StudySmarter Bewerbungstipps 🤫

So bekommst du den Job: Assoc. Director of Support Operations (m/f/d)

Tip Number 1

Familiarize yourself with the latest trends and technologies in GMP-regulated environments. This knowledge will not only help you understand the role better but also demonstrate your commitment to staying updated in a rapidly evolving field.

Tip Number 2

Network with professionals in the biotech industry, especially those who have experience in support operations or manufacturing. Engaging in conversations can provide insights into the company culture and expectations, which can be invaluable during interviews.

Tip Number 3

Prepare to discuss your leadership style and how you have successfully managed teams in the past. Highlight specific examples where you improved operational excellence or implemented new processes, as these are key aspects of the role.

Tip Number 4

Understand the company's mission and values deeply. Be ready to articulate how your personal values align with theirs, especially regarding innovation and collaboration, as this will show that you are a good cultural fit for the team.

Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Assoc. Director of Support Operations (m/f/d)

Leadership Skills
Operational Excellence
Material Management
GMP Compliance
Process Improvement
Project Management
Cross-Functional Collaboration
Delta V Knowledge
MES Experience
Supply Chain Management
Production Planning
Change Management
Problem-Solving Skills
Team Building
Communication Skills

Tipps für deine Bewerbung 🫡

Understand the Role: Make sure to thoroughly read the job description for the Assoc. Director of Support Operations position. Highlight key responsibilities and required skills that align with your experience.

Tailor Your CV: Customize your CV to reflect your relevant experience in GMP-regulated environments, leadership roles, and any specific technologies mentioned, such as Delta V and MES.

Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also demonstrates your understanding of the company's mission and how you can contribute to their goals in biopharmaceutical innovation.

Highlight Team Leadership Experience: Emphasize your experience in managing teams and driving operational excellence. Provide examples of how you've successfully led projects or initiatives in previous roles.

Wie du dich auf ein Vorstellungsgespräch bei MSD vorbereitest

Understand the GMP Environment

Make sure you have a solid grasp of Good Manufacturing Practices (GMP) as they relate to biological drug substance manufacturing. Be prepared to discuss your experience in this area and how it aligns with the company's operational standards.

Showcase Leadership Experience

Highlight your previous leadership roles, especially in managing teams within a manufacturing context. Discuss specific examples where you successfully led initiatives that improved operational excellence or introduced new processes.

Familiarize Yourself with Delta V and MES

If you have experience with Delta V and Manufacturing Execution Systems (MES), be ready to talk about it. If not, do some research on these systems and be prepared to explain how you would approach learning and implementing them in your role.

Emphasize Collaboration Skills

Since the role involves cross-functional partnerships, be prepared to discuss how you've effectively collaborated with other teams in the past. Share examples of how you’ve contributed to a culture of inclusivity and innovation in your previous positions.

Assoc. Director of Support Operations (m/f/d)
MSD Jetzt bewerben
MSD
  • Assoc. Director of Support Operations (m/f/d)

    Werthenstein
    Vollzeit
    72000 - 84000 € / Jahr (geschätzt)
    Jetzt bewerben

    Bewerbungsfrist: 2027-01-14

  • MSD

    MSD

    50 - 100
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