Careers

At BioOutsource we are building a world class team and have an interest in talented people. In order to sustain our position as a leading provider of contract testing services, we rely on our employees to deliver. As a result we continually strive to offer our employees an unparalleled level of opportunity and provide an environment that is driven by innovation and high performance.

While our company continues to expand, so does the opportunities available to our employees. If you would relish the opportunity to work in our vibrant, fast-paced and rewarding environment we would like to hear from you.

We fully understand the importance of our service to support our client’s critical testing requirements and as a result continually strive to provide a world class service.

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Sustainability

Growing profitably and acting responsibly towards all stakeholders

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Openness

Driving change and progress internally and externally

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Enjoyment

Working in an energetic and rewarding environment

Quality Auditor

Quality Specialist

Do you have previous experience as a Quality Auditor within the biopharmaceutical industry? Can you perform well in a fast paced environment? Can you work well in a team and also independently on your own initiative? Do you appreciate strong Company values? Then you will fit in well with Sartorius Stedim BioOutsource Ltd.
The post of Quality Specialist is a key supporting role in the Quality Department, reporting to the Quality Team Leader.

What you can look forward to achieving

The Quality Specialist will work closely with the Quality and the Operations team to ensure that the GxP quality systems are adhered to and followed by all staff.
Amongst other duties, tasks will include:
• Performing internal audit functions
• Reviewing and approving study raw data
• Approval of facility and process qualification/validation procedures and documents (facility, equipment, software, materials, personnel, etc.) according to GxP requirements
• Reviewing of Environmental Monitoring results/reports
• Reviewing and approving all laboratory and other GMP, GLP and GCP documentation
• Assessing suppliers
• Assess impact of deviations and provide guidance, support and co-ordination of CAPA
• Review equipment validation documentation

In return we can offer you a competitive salary, a generous benefits package, full on the job training, and significant opportunity for personal growth and development within a rapidly expanding successful CRO.

Skills and experience that you need to bring to our Company:
• A degree in a relevant scientific discipline and/or at least three years Quality experience, preferably within a GMP or GLP environment with an understanding, and experience, of applying EU and US GMP and /or GLP regulations
• Extremely organised approach is required coupled with the ability to influence without authority
• Excellent written and verbal communication skills coupled with the ability to prioritise multiple tasks and have the confidence to challenge existing systems & processes.
• Competent in Word, Excel and PowerPoint

This is a great opportunity to be part of a modern, dynamic business and would offer the right person excellent career development opportunities.

Closing date - 14 Sep 18

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Sites Facilities Manager

Summary
The Newhouse Sites Facilities Manager, reporting to the Operations Director is accountable for the delivery of the site facilities services and equipment management efficiently, on time, within set budgets to GMP / GEP standards whilst providing excellent internal customer service. In addition the role is accountable for materials supply chain and shutdown management at the Newhouse Cell Banking Manufacturing Site.

Key function of this position is to ensure that the Site Facilities, equipment and material supply chain are set up and managed effectively to the appropriate industry and quality standards to ensure continuity of service for internal stakeholders.

Key Responsibilities & Duties
• Responsible for ensuring implementation and adherence to Health & Safety procedures within areas of responsibility
• Responsible for facilities, plant & equipment management budget and management of central services
• Responsible for management and execution of site services such as: HVAC; AHU; Fire Safety provision; Pest Control, Utilities, Waste and Fabric of the building.
• Responsible for facilities security and liaison with site security
• Responsible for facilities, plant and equipment PPM
• Responsible for interface and maintenance of Landlord relationships on the Biocity campus
• Responsible for facilities projects such as expansion, new facilities or office moves
• Responsible for management and review of subcontractor service contracts and subcontractor activities on site
• Responsible for Facility Shutdown Programmes of work for the Newhouse Cell Banking Facility
• Responsible for reporting performance Key Performance Indicators (KPI) to Site Level
• Responsible for personnel training within area of expertise
• Responsible for maintaining GMP / GEP systems where appropriate
• Responsible for presenting to MHRA / Regulatory Bodies / Client Audit within area of expertise
• May be responsible for line management or matrix management of personnel inclusive of personnel performance management
• May contribute to the recruitment process
• Collaborate with all levels of staff at all sites of the company
• Responsible for any other reasonable requests or tasks requested by management

Qualifications / Skills required
• Bachelor’s degree in Facilities Management, Facilities Engineering or related qualification such as project management, business management or construction management.
• working knowledge of electrical and mechanical systems
• Demonstrable knowledge of GMP / GEP in a pharmaceutical setting
• Working Knowledge of the principles and practices of project management
• Working knowledge of financial principles and practices
• Working knowledge of human resource management principles and practices
• Working knowledge of procurement and contracts
• Sound knowledge in health, safety and environmental regulations: IOSH / NEBOSH; Health & Safety at Work preferred
• Experienced in construction, maintenance and all facets of facility operation
• Supervisory experience
• Solid computer and systems knowledge

Desired Competencies

• Communication skills
• Planning and Organisation Skills
• Negotiation Skills
• Problem Analysis
• Decision-Making
• Customer service orientation
• Positive response to change / adaptability

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Quality Control Microbiology Manager

The successful candidate must be able to demonstrate technical excellence in QC processes, understanding and experience in microbial systems inclusive of environmental monitoring and sterility testing requirements for a GMP facility.
Additionally, you will have proven leadership, organisational and communication skills and a proven track record in laboratory systems or process management.
In return we can offer you a competitive salary, a generous benefits package, full on the job training, and significant opportunity for personal growth and development within a rapidly expanding successful CRO.
What you can look forward to:
• Being accountable for the establishment of QC and microbiological services
• Being accountable for day to day QC activities including materials and sample management, retain management, Environmental Monitoring, trending and interpretation of results and performing the functions of QC SME with responsibility as site Microbiologist
• Being accountable for day to day running of the GMP QC laboratory, Microbiology facility and process and equipment qualification
• Being accountable for the cell banking testing programmes to GMP
• Generating project plans and assigning responsibilities & timelines
• Being responsible for the QC & Microbiology team including supervision, delivery of goals and objectives, recruitment, supervision and training and development
• Liaising with clients both internal and external and representing the QC function during audits
• Challenging and improving our existing systems & processes


Skills and experience that you need to bring to our Company:
You will have a Degree, Masters or PhD in a relevant discipline with a proven track record in QC environment with experience of environmental monitoring and sterility testing programmes within a GMP manufacturing facility. Excellent technical knowledge in QC requirements of a GMP facility and microbial systems and sterility testing would be essential.

You will be a driven and motivational leader, with excellent organisational skills, prioritising multiple tasks to ensure on-time project delivery. As well as having the technical insight to problem solve and develop new processes.
An excellent communicator at all levels with the technical insight to troubleshoot and develop new processes is essential.

 

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Client Manager

Client Manager

Do you have project management experience within the biopharmaceutical industry? Can you perform well in a fast paced environment? Can you work well in a team and also independently on your own initiative? Do you appreciate strong Company values? Then you will fit in well with Sartorius Stedim BioOutsource Ltd.

Sartorius Stedim BioOutsource Limited is the world’s fastest growing provider of contract testing services to the biopharmaceutical industry. Our core offering includes a wide range of GMP, GLP and GCP tests to support Biologics and Vaccines therapeutics from their development to release into the market. We are currently recruiting for two Client Managers. Out of hours work may be required from time to time.

In return we can offer you a competitive salary, a generous benefits package and significant opportunity for personal growth and development within a rapidly expanding successful CRO.

What you can look forward to achieving
• Provide a single point of contact for the client
• Define and monitor the project deliverables and client expectations.
• Ensure client service expectations are met (or exceeded) by providing visibility of agreed deliverables (specifications), tracking and monitoring of these deliverables, defining appropriate action(s) required if to get the project back on track when required, providing excellent communication (internal and external) throughout the project.
• Resolving cross-functional issues at a project level.
• Manage internal and external project team relationships.
• Manage project scope and change control where necessary.
• Monitor and report (internal and external) project progress and performance.

Skills and experience you need to bring to our Company
• The successful applicants will be educated at least to degree level in a Scientific Discipline, or comparable experience. Preference is given to degrees in Virology, Molecular Biology, Cell Biology, Immunology, Microbiology.
• Previous experience within a Client Management role, preferably within a GMP or GLP environment
• Previous project management experience is essential
• Experience within a GMP environment is desirable.
• Excellent written and verbal communication skills
• Excellent written and spoken English
• Personable, articulate, and confident communicator
• Excellent organisational skills with ability to manage multiple projects at the same time
• A high level of competence in Microsoft Office (Word, Excel, Powerpoint)
• Flexible and adaptable

Closing Date
3rd September 2018

 

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Analyst – BioAnalytical ADCC/CDC

Do you have experience within the biopharmaceutical industry? Can you perform well in a fast paced environment? Can you work well in a team and also independently on your own initiative? Do you appreciate strong Company values? Then you will fit in well with Sartorius Stedim BioOutsource Ltd.

We are looking for an Analyst to join our ADCC/CDC team. The ADCC/CDC team is an integral part of the larger Bioanalytical department. The department is supported by an Operations Support team and a cell culture team.

In return we can offer you a competitive salary, a generous benefits package and significant opportunity for personal growth and development within a successful CRO.

What you can look forward to
• Performance of laboratory based testing
• Lab housekeeping and stock control
• Work as part of team to ensure the smooth running of the department
• Ensure GxP compliance throughout testing and work with QA to address any potential issues
• Ensure all health & safety regulations are adhered to
Skills and experience that you need to bring to our Company

• A degree in a relevant life science discipline or comparable experience
• Experience in cell-based assays and/or cell culture would be advantagous
• Previous laboratory experience in a GMP/GLP environment is desirable
• Responds well to scientific challenge and applies significant rigor to their own work
• Excellent written and verbal communication skills coupled with the ability to prioritise multiple tasks
• Confidence to challenge existing systems & processes
• Competent in Word, Excel and PowerPoint

 

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Virology Scientist (Biosafety Testing)

Are you an experienced virologist with experience of working in the biosafety testing industry? Can you perform well in a fast paced environment? Can you work well in a team and also independently on your own initiative? Do you appreciate strong Company values? Then you will fit in well with Sartorius Stedim BioOutsource Ltd.

We are seeking a dynamic, results-driven individual with at least 6 years of experience specialising in the area of virology. This role includes responsibility for the co-ordination of all activities relating to virology based projects within the Biosafety department. The job also includes responsibility for operational supervision, line management of other team members and providing technical/scientific expertise as required to ensure operational excellence and to ensure that industry expectations are met according to current regulatory guidelines.


In return we can offer you a competitive salary, a generous benefits package and significant opportunity for personal growth and development within a successful CRO.

What you can look forward to achieving

  • Assisting the leadership of all activities within the virology area of the business and ensuring that activities meet industry standards and regulatory guidelines.
  • Successful co-ordination and completion of all assigned activities relating to virology/gene therapy based projects within the Biosafety department. Resolution of any technical problems affecting virology biosafety assays.
  • Assisting the department head with the following activities: accurate and timely scheduling of all client and internal projects, personnel related activities such as line management of scientists and analysts, recruitment, training and development, disciplinary actions and annual performance delivery.
  • Identification of new opportunities with provision of technical expertise in the areas of virology for any client queries. Preparation and review of proposals, providing costing where required.
  • Functionality as an effective Study Manager/Study Director demonstrating appropriate knowledge of regulatory and GxP requirements and ensuring service first and on-time delivery of all client and internal projects for which responsible.
  • Development and progression of scientific and technical staff through effective training.
  • Provision of operational supervision, technical support and scientific expertise as required for operational excellence and ensuring that industry expectations are met following current regulatory guidelines.

Skills and experience that you need to bring to our company

  • A degree in a relevant scientific discipline
  • At least three years experience within a GMP or GLP environment.
  • At least 6 years experience within the biosafety testing industry or related sector
  • Thorough understanding and experience of applicable EU and US GMP and GLP regulations
  • Line Management Experience
  • Excellent written and verbal communication skills coupled with the ability to prioritise multiple tasks and have the confidence to challenge existing systems & processes
  • Competent in Word, Excel and PowerPoint

 

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Open Applications (BioOutsource)

If you wish to be considered for any forthcoming opportunities please submit your CV and a covering letter including details of the type(s) of role you are interested in and your salary expectations.

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Head of Sales BioOutsource / Cellca, Europe

Sartorius

Our products enable the biopharmaceutical industry to be at the forefront in the development and advancement of treatments for serious diseases. Earning sales revenue of more than 1.4 billion in 2017 our people come from over 60 nations at 50 sites in 33 countries.

For our Sales department we are looking for a Head of Sales in Europe. The position will report directly through Business Development but will work closely with a range of internal stakeholder groups including, Marketing, Technical Support, Operations, Legal, Finance, Process Development and other SSB Sales Groups.

Your tasks
  • Develop and implement a plan to expand our market in Europe through introduction of a range of services/products
  • Identify key clients aligned with the strategic focus of the company and set up a framework to allow your team to develop workable plans to transition target to a client and grow client business through understanding of the clients business programs and objectives
  • Support team to engage at a senior level with customers to negotiate licenses of technology and achieve a successful resolution.
  • Implement a framework to ease liaison between sales, the customer and the functional areas within BioOutsource and Cellca that contribute to the proposal process and ultimately perform the services across geographies.
  • Engage with Senior Stakeholders within the business.
Your profile
  • Bachelor’s Degree or equivalent with relevant practical experience that demonstrates a strong ability and proven competency to work effectively as a Head of Sales within the biopharmaceutical industry.
  • A minimum of 5 years’ relevant industry experience, preferably within a GMP or GLP environment (contract testing experience and or CDMO experience is desirable)
  • A strong understanding of early stage drug development and more specifically experience of working with large molecules and the new wave of biosimilars is desirable including familiarization with global regulatory guidelines.
  • Strong identification with our core values: sustainability, openness, enjoyment
Benefits
  • Participation in the company’s success – Sales Incentive Program
  • Options for further education in personnel management

Driving our future growth requires talented people. Sartorius is a dynamic organization suited to people who want to showcase skills, be recognized for expertise and thrive in a vibrant and innovative environment.

To find out more about Sartorius as an employer, visit us on www.sartorius.com/career

 

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Technische Assistenz (m/w) in der Zelllinienentwicklung (MTA/BTA)

Sartorius

Fachlich macht Ihnen keiner etwas vor, Sie denken über Grenzen hinweg und möchten auch so arbeiten? Zudem sind Sie lieber verantwortlich als nur dabei und schätzen starke Wurzeln und Werte? Dann passen Sie gut zu Sartorius.

Als einer der weltweit führenden Labor-und Pharmazulieferer gestaltet Sartorius dynamische, innovative und stark wachsende Märkte mit. Das 1870 gegründete Unternehmen erzielte im Geschäftsjahr 2017 einen Umsatz über 1,4 Milliarden Euro. Mehr als 7.500 Mitarbeiter sind an den rund 50 Produktions- und Vertriebsstandorten des Konzerns für Kunden rund um den Globus tätig. Der Schwerpunkt der Sartorius Stedim Cellca GmbH liegt in der Entwicklung und im Vertrieb einer zukunftsweisenden Produktionstechnologie basierend auf Zellkulturtechnik für die Herstellung von biopharmazeutischen Proteinen.

Darauf können Sie sich freuen
  • Gemeinsam mit Ihren Kollegen planen und führen Sie den kompletten Prozess der Zelllinienentwicklung für Säugerzellen durch: Angefangen von der Transfektion und Kultivierung, über Fed-Batch Experimente im Schüttelkolben und Bioreaktor, bis hin zum Zellauftau und Zellbankerstellung.
  • Sie dokumentieren die durchgeführten Experimente sorgfältig und gewissenhaft, damit alle Ihre Kollegen auf dem gleichen Wissenstand sind.
  • Sie erstellen eigenständig Präsentationen und technische Berichte, die die Grundlage unserer Kundeninformation darstellen.
Das bringen Sie mit
  • Eine Ausbildung zur Technischen Assistenz haben Sie erfolgreich abgeschlossen und idealerweise haben Sie bereits erste Berufserfahrung in der pharmazeutischen Industrie sammeln können.
  • Sie sind vertraut mit sterilem Arbeiten in der Zellkultur und Sie können durch Ihre theoretischen und praktischen Kenntnisse in der Säugerzellkulturtechnik und Expression rekombinanter Proteine glänzen.
  • Ihre hohe Flexibilität und Einsatzfreude zeigen Sie u.a. durch Ihre Bereitschaft gelegentlich an Wochenenden und Feiertagen zu arbeiten und Sie agieren selbständig und verantwortungsbewusst.
  • Das Lesen und Verfassen von Arbeitsanweisungen und Berichten in englischer Sprache stellt für Sie keine Herausforderung dar. §Sie können sich mit unseren Unternehmenswerten identifizieren: Nachhaltigkeit, Offenheit, Freude

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Technische Assistenz in der Zelllinienentwicklung (MTA/BTA)

Fachlich macht Ihnen keiner etwas vor, Sie denken über Grenzen hinweg und möchten auch so arbeiten? Zudem sind Sie lieber verantwortlich als nur dabei und schätzen starke Wurzeln und Werte? Dann passen Sie gut zu Sartorius.

Als einer der weltweit führenden Labor-und Pharmazulieferer gestaltet Sartorius dynamische, innovative und stark wachsende Märkte mit. Das 1870 gegründete Unternehmen erzielte im Geschäftsjahr 2017 nach vorläufigen Zahlen einen Umsatz über 1,4 Milliarden Euro. Mehr als 7.500 Mitarbeiter sind an den rund 50 Produktions- und Vertriebsstandorten des Konzerns für Kunden rund um den Globus tätig. Der Schwerpunkt der Sartorius Stedim Cellca GmbH liegt in der Entwicklung und im Vertrieb einer zukunftsweisenden Produktionstechnologie basierend auf Zellkulturtechnik für die Herstellung von biopharmazeutischen Proteinen.

Darauf können Sie sich freuen
  • Gemeinsam mit Ihren Kollegen planen und führen Sie den kompletten Prozess der Zelllinienentwicklung für Säugerzellen durch: Angefangen von der Transfektion und Kultivierung, über Fed-Batch Experimente im Schüttelkolben und Bioreaktor, bis hin zum Zellauftau und Zellbankerstellung.
  • Sie dokumentieren die durchgeführten Experimente sorgfältig und gewissenhaft, damit alle Ihre Kollegen auf dem gleichen Wissenstand sind.
  • Sie erstellen eigenständig Präsentationen und technische Berichte, die die Grundlage unserer Kundeninformation darstellen.
Das bringen Sie mit
  • Eine Ausbildung zur Technischen Assistenz haben Sie erfolgreich abgeschlossen und idealerweise haben Sie bereits erste Berufserfahrung in der pharmazeutischen Industrie sammeln können.
  • Sie sind vertraut mit sterilem Arbeiten in der Zellkultur und Sie können durch Ihre theoretischen und praktischen Kenntnisse in der Säugerzellkulturtechnik und Expression rekombinanter Proteine glänzen.
  • Ihre hohe Flexibilität und Einsatzfreude zeigen Sie u.a. durch Ihre Bereitschaft gelegentlich an Wochenenden und Feiertagen zu arbeiten und Sie agieren selbständig und verantwortungsbewusst.
  • Das Lesen und Verfassen von Arbeitsanweisungen und Berichten in englischer Sprache stellt für Sie keine Herausforderung dar. Sie können sich mit unseren Unternehmenswerten identifizieren: Nachhaltigkeit, Offenheit, Freude

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Scientist Product Development

Sartorius Fachlich macht Ihnen keiner etwas vor, Sie denken über Grenzen hinweg und möchten auch so arbeiten? Zudem sind Sie lieber verantwortlich als nur dabei und schätzen starke Wurzeln und Werte? Dann passen Sie gut zu Sartorius.

Als einer der weltweit führenden Labor-und Pharmazulieferer gestaltet Sartorius dynamische, innovative und stark wachsende Märkte mit. Das 1870 gegründete Unternehmen erzielte im Geschäftsjahr 2016 einen Umsatz über 1,3 Milliarden Euro. Mehr als 6.900 Mitarbeiter sind an den rund 50 Produktions- und Vertriebsstandorten des Konzerns für Kunden rund um den Globus tätig. Der Schwerpunkt der Sartorius Stedim Cellca GmbH liegt in der Entwicklung und im Vertrieb einer zukunftsweisenden Produktionstechnologie basierend auf Zellkulturtechnik für die Herstellung von biopharmazeutischen Proteinen.

Darauf können Sie sich freuen

  • Ihr Schwerpunkt ist die Neuentwicklung und Etablierung von Protokollen, die unsere proprietäre Plattform der Zelllinienentwicklung ergänzen und unser Produkt-Portfolio erweitern.
  • Sie planen und bearbeiten selbstständig innovative Entwicklungsprojekte unter Verwendung modernster molekularbiologischen Methoden und innovativen Geräten.
  • Sie evaluieren und etablieren neue Geräte, Prozesse und Methoden und bringen sich aktiv ins Technology Development Team ein.
  • Das Erstellen von Berichten und Präsentationen gehört ebenso zu Ihrem Aufgabengebiet wie Recherchen, die Betreuung von Abschlussarbeiten und die gewissenhafte Dokumentation durchgeführter Experimente.

Das bringen Sie mit

  • Sie haben eine Promotion in Biotechnologie, Biologie oder Biochemie oder einer vergleichbaren naturwissenschaftlichen Fachrichtung. Ebenfalls haben Sie erste Erfahrung als Postdoc als auch in der Industrie sammeln können.
  • Sie verfügen über hervorragende theoretische und praktische Kenntnisse in der Zell- und Molekularbiologie sowie in der Zellkulturtechnik.
  • Sie nehmen die Dinge in die Hand, handeln selbstständig und überzeugen durch eine genaue, strukturierte Arbeitsweise sowie durch Flexibilität, Einsatzfreude und Kreativität
  • Identifikation mit unseren Unternehmenswerten: Nachhaltigkeit, Offenheit, Freude

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Marketing Manager

Sartorius If you live and breathe marketing, we need to talk. We’re looking for a flexible and versatile marketer who will be responsible for the growth of our inbound sales channels.

As one of the world‘s leading laboratory and pharmaceutical equipment providers, Sartorius is actively shaping dynamic, innovative and high-growth markets. Founded in 1870, the company earned sales revenue of more than 1.3 billion euros in 2016. More than 6,900 people work at the Group’s approximately 50 manufacturing and sales sites, serving customers around the globe.

Duties of the Marketing Manager include

  • Developing the marketing strategy and tactics to get the word out about our company and drive qualified traffic to our front door
  • Deploying successful marketing campaigns and own their implementation from ideation to execution
  • Work closely with our application and sales teams to ensure proximity to market
  • Preparing online and print marketing campaigns with a strong focus on digital campaigns
  • Measure and report performance of marketing campaigns, gain insight and assess against goals
  • Working closely with design agencies and assisting with new product launches.

Requirements of the role

  • Bachelor degree in Marketing
  • Proven experience in identifying target audiences and in creatively devising and leading marketing campaigns that engage, educate and motivate
  • Strong analytical and project management skills
  • Experience in Life Science or service industry preferred
  • Confident, dynamic and hands-on personality with the drive to effect change
  • Numerically literate, comfortable working with numbers, making sense of metrics and processing figures with spreadsheets
  • Preferably the position is based in Laupheim, will require up to 30% travel time and can include limited amount of time working at other locations
  • Strong identification with our core values: sustainability, openness, enjoyment

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Team Leader (m/w) im Bereich Product Development

Fachlich macht Ihnen keiner etwas vor, Sie denken über Grenzen hinweg und möchten auch so arbeiten? Zudem sind Sie lieber verantwortlich als nur dabei und schätzen starke Wurzeln und Werte? Dann passen Sie gut zu Sartorius.

Als einer der weltweit führenden Labor-und Pharmazulieferer gestaltet Sartorius dynamische, innovative und stark wachsende Märkte mit. Das 1870 gegründete Unternehmen erzielte im Geschäftsjahr 2015 nach vorläufigen Zahlen einen Umsatz von über 1,1 Milliarden Euro. Rund 6.200 Mitarbeiter sind für den Konzern tätig, der über Produktions- und Vertriebsstandorte in rund 110 Ländern verfügt. Der Schwerpunkt der Sartorius Stedim Cellca GmbH liegt in der Entwicklung und im Vertrieb einer zukunftsweisenden Produktionstechnologie basierend auf Zellkulturtechnik für die Herstellung von biopharmazeutischen Proteinen.

Darauf können Sie sich freuen

  • Sie führen das Team „Product Development“ mit 4-6 Mitarbeitern, welches in unserer Abteilung Technology Development angesiedelt ist.
  • Sie sind unser Hauptansprechpartner für die Entwicklung von neuen Produkten und Services zur Erweiterung der Cellca Plattformtechnologie. Die Koordination, Planung, Betreuung und auch die Umsetzung entsprechender Entwicklungsprojekte liegt in Ihren Händen.
  • Beim Management unseres Patentportfolios sind Ihr Know-How und Ihre Erfahrung gefragt.
  • Das Erstellen von Berichten und Präsentationen gehört ebenso zu Ihrem Aufgabenbereich wie die Durchführung von Datenauswertungen und Recherchen.
  • Zudem bauen Sie die Kooperationen mit universitären und industriellen Partnern weiter aus.

Das bringen Sie mit

  • Sie haben ein Masterabschluss oder Promotion in Biotechnologie, Biologie, Biochemie oder eine vergleichbare Fachrichtung und bringen mindestens 2 Jahre Berufserfahrung vorzugsweise in der Industrie mit.
  • Hervorragende theoretisch und praktische Kenntnisse in der Zellkultur- und Prozesstechnik sowie in der Zell- und Molekularbiologie sind unabdingbar.
  • Ihre Kommunikationsfähigkeit, Ihren Teamgeist und Ihre Führungserfahrung konnten sie idealerweise bereits als Teamleiter unter Beweis stellen.
  • Sie nehmen die Dinge in die Hand, handeln verantwortungsbewusst und überzeugen durch Ihre Flexibilität und Einsatzfreude.
  • Identifikation mit unseren Unternehmenswerten: NACHHALTIGKEIT, OFFENHEIT, FREUDE

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