6 Manufacturing jobs in Australia

Manufacturing Engineer

Port Melbourne, Victoria The Boeing Company

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**Job Description**
At Boeing, we innovate and collaborate to make the world a better place. We're committed to fostering an environment for every teammate that's welcoming, respectful and inclusive, with great opportunity for professional growth. Find your future with us.
_At Boeing, we are all innovators on a mission to connect, protect, explore and inspire. From the sea bed to outer space, you'll learn and grow, contributing to work that shapes the world. Find your future with us._
We are seeking a **Manufacturing Engineer** to join our team based in Port Melbourne on a full-time permanent basis. We are looking for motivated individuals driven by the desire to achieve in a high technology industry, someone who will embrace our company's values and is willing to innovate. This position is based 100% onsite.
**Position Responsibilities:**
Depending on the successful candidates' experience and skills, the Manufacturing Engineer will be working in one of the following areas,
+ The production, modification, repair and continuing airworthiness services to support the Department of Defence's Boeing-managed aircraft currently in prototype manufacture, or
+ The production of flight control surfaces for the following commercial aircraft, 787, 737 & 777
In this role you will apply your knowledge and experience to a broad range of designs across the engineering lifecycle, establishing build plans, regulatory compliance, applying lean principles, ensuring first-time quality and corrective action resolution.
Depending on your level of skills and experience and the assigned area, responsibilities may include:
+ Development of Production System Design and build plan documentation
+ Development and execution of digital thread production engineering artifacts
+ Liaise with suppliers to resolve quality related issues / queries
+ Development and implementation of production and tooling methodologies
+ Implement lean principles and technologies
+ Provide guidance on the build and compliance reporting to ensure the production products conform to the product design
+ Resolve technical problems of impact to safety, performance, cost or schedule
+ Conduct analysis to ensure that manufacturing process capability matches requirements and help document producibility best practices
+ Coordinate and implement new engineering principles, theories, advanced technologies and concepts
**Basic Qualifications (Required Skills / Experience):**
+ Tertiary qualifications in Engineering with relevant industry experience. Education specializing in Industrial, Mechanical, Manufacturing, Structural Design Engineering will be highly regarded.
+ Sufficient knowledge and experience of other related engineering disciplines to allow their integration within a design activity
+ Currency in new emerging technologies, and the ability to foster knowledge and abilities in these technologies within the Engineering group
+ Strong verbal and written communication skills
+ Knowledge of continuous improvement and Lean principles and practices highly desirable
Please note that applicants must be Australian Citizens in order to meet Defence security clearance requirements.
Applications for the position will be accepted until 2nd August 2025.
**Additional information:**
This is an Enterprise Agreement position classified as Engineer / Scientist 1B. The successful candidate will be required to complete pre-employment checks and a 3 month probationary period.
**About our benefits:**
+ Work on cutting edge projects
+ Attractive remuneration and annual bonus
+ Additional annual Boeing Day off
+ Access to Boeing Discount Program - an exclusive retail and services discount marketplace
+ Access discounts for health insurance, travel and accommodation
+ Salary packaging options available
+ Health and wellbeing benefits including annual flu vaccinations and Employee Assistance Program
**About us:**
Boeing Aerostructures Australia is Australia's leading designer and manufacturer of composite flight control components for commercial aircraft. We are renowned for our collaborative and supportive working environment and for the high calibre of our people. We are passionate about improving peoples' lives through increasing global mobility with our iconic planes including the production of the 737, 777, 787 and future Airplane Development programs.
At Boeing Aerostructures Australia, we are committed to creating an inclusive and incident and injury free workplace, where employees can realise their career goals and make a positive contribution to Boeing's success.
If this role is you and you're excited by the opportunity to be part of building something amazing, we welcome your application.
Applications for this position will be accepted until **Aug. 04, 2025**
**Export Control Requirements:** This is not an Export Control position.
**Education**
Bachelor's Degree or Equivalent Required
**Relocation**
Relocation assistance is not a negotiable benefit for this position.
**Visa Sponsorship**
Employer will not sponsor applicants for employment visa status.
**Equal Opportunity Employer:**
We are an equal opportunity employer. We do not accept unlawful discrimination in our recruitment or employment practices on any grounds including but not limited to; race, color, ethnicity, religion, national origin, gender, sexual orientation, gender identity, age, physical or mental disability, genetic factors, military and veteran status, or other characteristics covered by applicable law.
We have teams in more than 65 countries, and each person plays a role in helping us become one of the world's most innovative, diverse and inclusive companies. We are proud members of the Valuable 500 ( and welcome applications from candidates with disabilities. Applicants are encouraged to share with our recruitment team any accommodations required during the recruitment process. Accommodations may include but are not limited to: conducting interviews in accessible locations that accommodate mobility needs, encouraging candidates to bring and use any existing assistive technology such as screen readers and offering flexible interview formats such as virtual or phone interviews.
Boeing is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national origin, gender, sexual orientation, gender identity, age, physical or mental disability, genetic factors, military/veteran status or other characteristics protected by law.
This advertiser has chosen not to accept applicants from your region.

Business Development Manager - Manufacturing Capacity Solutions, ANZ

Lane Cove, New South Wales Danaher Corporation

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Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher's ( 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System ( which makes everything possible.
The Business Development Manager - Manufacturing Capacity Solutions, ANZ is responsible for the commercial success of Cytiva's KUBio, FlexFactory, Aseptic Filling, and Hardware Solutions across Australia and New Zealand. The role will also indirectly support FastTrak process development and Validation Service in this same region. This includes developing and deploying strategies, mentoring and leading cross-functional teams, and engaging with and supporting customers across multiple biotherapeutic modalities at various stages of business evolution.
Location: This position reports to the Bioprocessing Leader - Australia & New Zealand. This role is to be based in Brisbane (remote), Sydney (remote), or Melbourne (remote).
What you'll do
+ Lead the commercial discussion with key customers on our overall Cytiva offering, by expertly navigating and collaborating with internal and external stakeholders (product, engineering, operations and commercial teams as well as key technical partners) at both management and engineering levels. Work very closely with internal teams, taking a senior role in driving in-depth commercial discussions with customers in gene and cell therapy manufacturing process design decisions support.
+ Build a strong pipeline of opportunities across the region for Process Development, Flex Factories, Aseptic filling, complex hardware or customized hardware and other services across Asia Pacific.
+ Ensure collaboration in all parts of the Cytiva commercial organization, building internal stakeholders and Account Management synergy to continually increase customer qualification, as well as accelerating the development of sales opportunities.
+ Responsible for driving optimal operating mechanisms to monitor and track progress of opportunities in the pipeline, including design-in initiatives, as well as forecasting performance against Operating Plan.
+ Work directly with the project managers, lead system design engineers, process design engineers and the site implementation team within Enterprise Hardware Solutions to deliver complex FlexFactories, KUBio or Hardware Solutions successfully to Cytiva customers.
Who you are
+ 10+ years' experience in engineering/biopharma.
+ Proven commercial track record in multiple Bioprocessing modalities, with Product Management/Offering/Large deals expertise.
+ Strong manufacturing and engineering knowledge including quality and regulatory understanding of the Bioprocessing modalities, including Gene Therapy and mRNA fields.
+ Proven ability to influence and negotiate internally and with customers.
+ Demonstrated high-level presentation and interpersonal skills; able to communicate and present ideas to customers in a way that produces understanding and impact, and which builds effective partnerships.
Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role
+ Ability to travel - up to 50% of time, within ANZ and internationally
+ Must have a valid driver's license with an acceptable driving record
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
This advertiser has chosen not to accept applicants from your region.

Business Development Manager - Manufacturing Capacity Solutions, ANZ

Dandenong South, Victoria Danaher Corporation

Posted today

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Job Description

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher's ( 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System ( which makes everything possible.
The Business Development Manager - Manufacturing Capacity Solutions, ANZ is responsible for the commercial success of Cytiva's KUBio, FlexFactory, Aseptic Filling, and Hardware Solutions across Australia and New Zealand. The role will also indirectly support FastTrak process development and Validation Service in this same region. This includes developing and deploying strategies, mentoring and leading cross-functional teams, and engaging with and supporting customers across multiple biotherapeutic modalities at various stages of business evolution.
Location: This position reports to the Bioprocessing Leader - Australia & New Zealand. This role is to be based in Brisbane (remote), Sydney (remote), or Melbourne (remote).
What you'll do
+ Lead the commercial discussion with key customers on our overall Cytiva offering, by expertly navigating and collaborating with internal and external stakeholders (product, engineering, operations and commercial teams as well as key technical partners) at both management and engineering levels. Work very closely with internal teams, taking a senior role in driving in-depth commercial discussions with customers in gene and cell therapy manufacturing process design decisions support.
+ Build a strong pipeline of opportunities across the region for Process Development, Flex Factories, Aseptic filling, complex hardware or customized hardware and other services across Asia Pacific.
+ Ensure collaboration in all parts of the Cytiva commercial organization, building internal stakeholders and Account Management synergy to continually increase customer qualification, as well as accelerating the development of sales opportunities.
+ Responsible for driving optimal operating mechanisms to monitor and track progress of opportunities in the pipeline, including design-in initiatives, as well as forecasting performance against Operating Plan.
+ Work directly with the project managers, lead system design engineers, process design engineers and the site implementation team within Enterprise Hardware Solutions to deliver complex FlexFactories, KUBio or Hardware Solutions successfully to Cytiva customers.
Who you are
+ 10+ years' experience in engineering/biopharma.
+ Proven commercial track record in multiple Bioprocessing modalities, with Product Management/Offering/Large deals expertise.
+ Strong manufacturing and engineering knowledge including quality and regulatory understanding of the Bioprocessing modalities, including Gene Therapy and mRNA fields.
+ Proven ability to influence and negotiate internally and with customers.
+ Demonstrated high-level presentation and interpersonal skills; able to communicate and present ideas to customers in a way that produces understanding and impact, and which builds effective partnerships.
Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role
+ Ability to travel - up to 50% of time, within ANZ and internationally
+ Must have a valid driver's license with an acceptable driving record
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
This advertiser has chosen not to accept applicants from your region.

Business Development Manager - Manufacturing Capacity Solutions, ANZ

Brisbane, Queensland Danaher Corporation

Posted today

Job Viewed

Tap Again To Close

Job Description

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher's ( 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System ( which makes everything possible.
The Business Development Manager - Manufacturing Capacity Solutions, ANZ is responsible for the commercial success of Cytiva's KUBio, FlexFactory, Aseptic Filling, and Hardware Solutions across Australia and New Zealand. The role will also indirectly support FastTrak process development and Validation Service in this same region. This includes developing and deploying strategies, mentoring and leading cross-functional teams, and engaging with and supporting customers across multiple biotherapeutic modalities at various stages of business evolution.
Location: This position reports to the Bioprocessing Leader - Australia & New Zealand. This role is to be based in Brisbane (remote), Sydney (remote), or Melbourne (remote).
What you'll do
+ Lead the commercial discussion with key customers on our overall Cytiva offering, by expertly navigating and collaborating with internal and external stakeholders (product, engineering, operations and commercial teams as well as key technical partners) at both management and engineering levels. Work very closely with internal teams, taking a senior role in driving in-depth commercial discussions with customers in gene and cell therapy manufacturing process design decisions support.
+ Build a strong pipeline of opportunities across the region for Process Development, Flex Factories, Aseptic filling, complex hardware or customized hardware and other services across Asia Pacific.
+ Ensure collaboration in all parts of the Cytiva commercial organization, building internal stakeholders and Account Management synergy to continually increase customer qualification, as well as accelerating the development of sales opportunities.
+ Responsible for driving optimal operating mechanisms to monitor and track progress of opportunities in the pipeline, including design-in initiatives, as well as forecasting performance against Operating Plan.
+ Work directly with the project managers, lead system design engineers, process design engineers and the site implementation team within Enterprise Hardware Solutions to deliver complex FlexFactories, KUBio or Hardware Solutions successfully to Cytiva customers.
Who you are
+ 10+ years' experience in engineering/biopharma.
+ Proven commercial track record in multiple Bioprocessing modalities, with Product Management/Offering/Large deals expertise.
+ Strong manufacturing and engineering knowledge including quality and regulatory understanding of the Bioprocessing modalities, including Gene Therapy and mRNA fields.
+ Proven ability to influence and negotiate internally and with customers.
+ Demonstrated high-level presentation and interpersonal skills; able to communicate and present ideas to customers in a way that produces understanding and impact, and which builds effective partnerships.
Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role
+ Ability to travel - up to 50% of time, within ANZ and internationally
+ Must have a valid driver's license with an acceptable driving record
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
This advertiser has chosen not to accept applicants from your region.

AOS & Improvement Expert/Manufacturing, befristet (m/w/d), Hybrid

Takeda Pharmaceuticals

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Job Description

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
**Über die Rolle:**
Als **Improvement Expert** am Standort Industriestraße 131 führen Sie regelmäßige Analysen durch, koordinieren Projekte und kommunizieren mit Kolleg*innen aus unterschiedlichsten Abteilungen. Sie optimieren die Produktivität, sichern die Einhaltung aller Vorgaben (Qualität, Behörden, Ziele) und wahren die Arbeitssicherheit.
Diese Stelle ist auf 8 Monate befristet, mit einer eventuellen Option auf Verlängerung.
**Das bewirken Sie:**
+ Verantwortlich für die Implementierung und Pflege des AOS (Lean Management Systems) und aller zugehörigen Elemente
+ Leitung und Koordination von Continuous Improvement Aktivitäten und Verbesserungsprojekten
+ Erstellung, Aktualisierung und Analyse von Kapazitätsmodellen
+ Zusammenarbeit mit anderen Continuous Improvement Experts der Produktionsbereiche und VertreterIn im Digital Delivery Operational Committee
+ Erarbeitung und Umsetzung von Verbesserungs- und Standardisierungsmaßnahmen
**Das bringen Sie mit:**
+ Abgeschlossene naturwissenschaftliche oder technische Ausbildung (HTL, FH, Universität)
+ Berufserfahrung im Produktionsumfeld und Pharmaerfahrung von Vorteil
+ Erfahrung in der Anwendung von Lean- und Six-Sigma-Tools
+ Ausgeprägte analytische Fähigkeiten und Problemlösungskompetenz
+ Selbstständige, initiative und lösungsorientierte Herangehensweise
+ Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift
**Das bieten wir Ihnen:**
Für diese wichtige und verantwortungsvolle Position beträgt das Mindestgehalt 4.270,14 brutto/Monat. Das tatsächliche Gehaltspaket richtet sich nach Ihrer Berufserfahrung und Qualifikation.
**Weitere Benefits:**
+ Zertifiziertes familienfreundliches Unternehmen (umfassende Wiedereinstiegsmodelle nach der Karenz)
+ Hybrides Arbeiten & flexible Zeiteinteilung wo möglich
+ Weiterbildungs- und -entwicklungsmöglichkeiten
+ Umfassende Trainings- und Fortbildungsprogramme sowie Persönlichkeitsentwicklung und Mentoringprogramm
+ Firmeninterne Job Rotations im In- und Ausland
+ Mitarbeiter*innenempfehlungs- und -anerkennungsprogramme
+ Aktive Teilnahme an Netzwerkgruppen zu verschiedenen Themen (z.B. Diversity, Equity & Inclusion, Nachhaltigkeit)
+ Vielfältige Gesundheits- und Fitnessangebote
+ Kostenlose Impfungen, Psychologische Beratung
+ Firmen-Events & Feste
+ Betriebsrat
+ Betriebsrestaurant zu gestützten Preisen
+ Bilingualer Betriebskindergarten / Betriebliche Kinderbetreuung
+ Gute öffentliche Anbindung
+ Inhouse Fitness & Wellness Center in Wien
Takeda ist seit vielen Jahren ein zertifizierter Top Employer ( und trägt das Zertifikat für "beruf und familie" sowie das Gütesiegel für betriebliche Gesundheitsförderung. Takeda wurde auch mit dem österreichischen Inklusionspreis ausgezeichnet und ist Vorreiter im Bereich der nachhaltigen und verantwortungsvollen Arzneimittelproduktion.
**Empowering our people to shine**
Unter dem Motto "Empowering our people to shine" hat sich Takeda zum Ziel gesetzt, alle Mitarbeiter*innen darin zu unterstützen, ihr Potenzial voll entfalten zu können. Takeda fokussiert ausschließlich auf die Talente und Fähigkeiten, unabhängig von Geschlecht, Alter, kulturelle Herkunft, sexuelle Orientierung, das Leben mit Behinderungen usw.: Wir fördern Vielfalt ( . Bei uns steht Chancengleichheit im Vordergrund, weswegen wir Wert auf einen möglichst barrierefreien Bewerbungsprozesses für Menschen mit Behinderungen legen. Wir bitten Sie daher in Ihrer Bewerbung alle diesbezüglich relevanten Informationen anzugeben.
**Mehr über uns**
Takeda ist ein weltweit führendes, werteorientiertes, forschendes biopharmazeutisches Unternehmen mit Hauptsitz in Japan. Takeda hat sich zum Ziel gesetzt, lebensverbessernde und -erhaltende Arzneimittel für die Behandlung von Menschen mit seltenen und komplexen Erkrankungen zu entwickeln und zu produzieren. Das österreichische Produktportfolio umfasst unter anderem die Bereiche Onkologie, seltene metabolische Erkrankungen, Gastroenterologie und Immunologie. Im Vordergrund steht die Versorgung von Patient*innen, für die keine oder nur wenige Behandlungsmöglichkeiten zur Verfügung stehen. In Österreich findet bei Takeda jeder Prozessschritt für Arzneimittel statt: von der Forschung & Entwicklung, über Plasmaaufbringung und Produktion bis zur Versorgung der Patient*innen. Rund 4.500 Mitarbeiter*innen tragen dazu bei, dass Medikamente aus Österreich in über 100 Länder weltweit gelangen und Patient*innen in Österreich Zugang zu den innovativen Arzneimitteln von Takeda erhalten.
**Mehr über Takeda auf YouTube**
Hier ( geht's zur Takeda YouTube Playlist.
Mehr ( über die Pharma 4.0 bei Takeda.
Mehr ( über Nachhaltigkeit bei Takeda.
Mehr ( über Vielfalt bei Takeda
**Locations**
AUT - Wien - Industriestrasse 131
**Worker Type**
Employee
**Worker Sub-Type**
Fixed Term (Fixed Term)
**Time Type**
Full time
This advertiser has chosen not to accept applicants from your region.

Supervisor Quality Control Mikrobiologie (m/w/d), On Site

Takeda Pharmaceuticals

Posted today

Job Viewed

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Job Description

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
**Über die Rolle:**
Wir suchen eine motivierte, teamfähige Persönlichkeit als Supervisor*in für das Quality Control Mikrobiologie Freigabelabor mit Schwerpunkt mikrobiologisches Umgebungsmonitoring & Wasseranalyse.
**Das bewirken Sie:**
+ Die Führung eines 13-köpfigen Laborteams
+ Sicherstellung der zeitgerechten und effizienten Durchführung von mikrobiologischen In Prozess Kontroll Tests sowie Freigabeanalysen mit Schwerpunkt Umgebungsmonitoring und Wasseranalytik nach GMP Standards
+ Aufrechterhaltung des Laborbetriebes und kontinuierliche Verbesserung der Prozesse und angewandten Testmethoden
+ Bereichsreporting für das Labor, Kapazitätsplanung, Projektplanung, - leitung und -verfolgung
+ Zeitgerechte Implementierung und Validierung von Analysenmethoden, Beschaffung und Qualifizierung von Laborequipment, und Computerized Systems Projekten
+ Repräsentation des Labors gegenüber Behördeninspektionen sowie internen Inspektionen
+ Zusammenarbeit mit lokalen & globalen Schnittstellen, fachliche Beratung von firmeninternen Kunden sowie Kommunikation mit externen Lieferanten.
+ Definition und kontinuierliche Überprüfung von laborspezifischen KPIs sowie Kostenkontrolle im Bereich
+ Bearbeitung von Änderungsanträgen, Abweichungen und Labor-Untersuchungen
+ Fachliche Beurteilung, Erstellung und Genehmigung von Dokumenten (SOPs, Formulare, interne Anweisungen, Gerätedokumentationen, Validierungsdokumente, Untersuchungen, Risikoanalysen, Stellungnahmen.)
**Dafür bringen Sie mit:**
+ Abgeschlossene höhere, chemisch analytische / biologische / mikrobiologische, Ausbildung (Matura oder Studium) mit Berufserfahrung in der pharmazeutischen Industrie (QC/QA) inkl. Führungserfahrung
+ Ausgezeichnete Kenntnisse über Hygienevorgaben, aseptisches Arbeiten sowie mikrobiologische Testverfahren, hohes Maß an Qualitätsbewusstsein.
+ Begeisterung für die Welt der Mikroben, Untersuchung und Bewertung mikrobiologischer Ergebnisse
+ Ausgezeichnete Kenntnisse der GMP-Vorgaben eines pharmazeutischen Qualitätskontrolllabors
+ Sehr gute Kenntnisse im Umgang mit MS-Office und Standard Labor-Software im pharmazeutischen Umfeld (z.B. LIMS, Dokumentationssysteme wie Veeva, Trackwise)
+ Deutsch und Englisch in Wort und Schrift (auf Matura-Niveau)
+ Hohes Maß an Eigenverantwortung und teamübergreifendes, ergebnisorientiertes Arbeiten
+ Kommunikationsstärke, motivierende Persönlichkeit, ausgezeichnetes Stressmanagement, Flexibilität und Empathie
**Das bieten wir Ihnen:**
Für diese wichtige und verantwortungsvolle Position beträgt das Mindestgehalt 4.270,14 brutto/Monat (Vollzeit, KV chem. Industrie). Das tatsächliche Gehaltspaket richtet sich nach Ihrer Berufserfahrung und Qualifikation.
**Weitere Benefits:**
+ Zertifiziertes familienfreundliches Unternehmen (umfassende Wiedereinstiegsmodelle nach der Karenz)
+ Hybrides Arbeiten & flexible Zeiteinteilung wo möglich
+ Weiterbildungs- und -entwicklungsmöglichkeiten
+ Umfassende Trainings- und Fortbildungsprogramme sowie Persönlichkeitsentwicklung und Mentoringprogramm
+ Firmeninterne Job Rotations im In- und Ausland
+ Mitarbeiter*innenempfehlungs- und -anerkennungsprogramme
+ Aktive Teilnahme an Netzwerkgruppen zu verschiedenen Themen (z.B. Diversity, Equity & Inclusion, Nachhaltigkeit)
+ Vielfältige Gesundheits- und Fitnessangebote
+ Kostenlose Impfungen, Psychologische Beratung
+ Firmen-Events & Feste
+ Betriebsrat
+ Betriebsrestaurant zu gestützten Preisen
+ Bilingualer Betriebskindergarten / Betriebliche Kinderbetreuung
+ Gute öffentliche Anbindung
+ Inhouse Fitness & Wellness Center in Wien
Takeda ist seit vielen Jahren ein zertifizierter Top Employer ( und trägt das Zertifikat für "beruf und familie" sowie das Gütesiegel für betriebliche Gesundheitsförderung. Takeda wurde auch mit dem österreichischen Inklusionspreis ausgezeichnet und ist Vorreiter im Bereich der nachhaltigen und verantwortungsvollen Arzneimittelproduktion.
**Empowering our people to shine**
Unter dem Motto "Empowering our people to shine" hat sich Takeda zum Ziel gesetzt, alle Mitarbeiter*innen darin zu unterstützen, ihr Potenzial voll entfalten zu können. Takeda fokussiert ausschließlich auf die Talente und Fähigkeiten, unabhängig von Geschlecht, Alter, kulturelle Herkunft, sexuelle Orientierung, das Leben mit Behinderungen usw.: Wir fördern Vielfalt ( . Bei uns steht Chancengleichheit im Vordergrund, weswegen wir Wert auf einen möglichst barrierefreien Bewerbungsprozesses für Menschen mit Behinderungen legen. Wir bitten Sie daher in Ihrer Bewerbung alle diesbezüglich relevanten Informationen anzugeben.
**Mehr über uns**
Takeda ist ein weltweit führendes, werteorientiertes, forschendes biopharmazeutisches Unternehmen mit Hauptsitz in Japan. Takeda hat sich zum Ziel gesetzt, lebensverbessernde und -erhaltende Arzneimittel für die Behandlung von Menschen mit seltenen und komplexen Erkrankungen zu entwickeln und zu produzieren. Das österreichische Produktportfolio umfasst unter anderem die Bereiche Onkologie, seltene metabolische Erkrankungen, Gastroenterologie und Immunologie. Im Vordergrund steht die Versorgung von Patient*innen, für die keine oder nur wenige Behandlungsmöglichkeiten zur Verfügung stehen. In Österreich findet bei Takeda jeder Prozessschritt für Arzneimittel statt: von der Forschung & Entwicklung, über Plasmaaufbringung und Produktion bis zur Versorgung der Patient*innen. Rund 4.500 Mitarbeiter*innen tragen dazu bei, dass Medikamente aus Österreich in über 100 Länder weltweit gelangen und Patient*innen in Österreich Zugang zu den innovativen Arzneimitteln von Takeda erhalten.
**Mehr über Takeda auf YouTube**
Hier ( geht's zur Takeda YouTube Playlist.
Mehr ( über die Pharma 4.0 bei Takeda.
Mehr ( über Nachhaltigkeit bei Takeda.
Mehr ( über Vielfalt bei Takeda.
**Locations**
AUT - Wien - Lange Allee 24
**Worker Type**
Employee
**Worker Sub-Type**
Regular
**Time Type**
Full time
This advertiser has chosen not to accept applicants from your region.
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