Die Clemens GmbH, part of Avantor, sucht eine geeignete & qualifizierte Person als R&D Electronics Engineer (m/w/d). Bereichern Sie unser dynamisches Team, um an der Spitze der technologischen Innovation in unserem hochmodernen Forschungs- und Entwicklungssektor tätig zu werden. Ziel der Stelle ist es eine stetige Weiterentwicklung der bestehenden Geräteserien sowie eine erfolgreiche Umsetzung der Kundenprojekte zu gewährleisten.

Was die Clemens GmbH, part of Avantor bietet

• Sinnhafte & innovative Tätigkeit: Unsere Produkte und Dienstleistungen haben einen tiefgreifenden Einfluss auf das Leben der Menschen, und das gilt auch für Ihren Beitrag. Unsere Mission ist inspiriert von der Verbesserung des Lebens für alle Menschen!
• Wachstumschancen: bei uns bekommen Sie die Möglichkeit, neue Fähigkeiten zu erlernen und Ihre Karriere vom ersten Tag an selbst zu bestimmen.
• Eine Kultur des Respekts und der Zusammenarbeit: Sie werden Teil eines innovativen Teams, das den Wandel vorantreibt und nach Spitzenleistungen strebt.
• Produktivität und Erholung gehen bei uns Hand in Hand: Wir bieten 30 Tage bezahlten Urlaub & sehr gute Vereinbarkeit von Arbeit und Privatleben.

Ihre Aufgabenbereiche:

• Erstellung der Elektronikarchitektur in der Konzeptphase
• Auslegung elektronischer und elektromechanischer Komponenten
• Erstellung von Schaltplänen & Platinenlayouts
• Interdisziplinäre Zusammenarbeit mit  den Kollegen aus dem Maschinenbau, der Software- und der Optikentwicklung, um nahtlose Integrationen zu gewährleisten
• Planung und Koordinierung der Herstellung elektronischer Komponenten für Prototypen
• Inbetriebnahme von Funktionsmustern und Prototypen
• Verifizierung und Validierung von elektronischen und elektromechanischen Komponenten
• Verantwortlicher Ansprechpartner bei Abweichungen in der Serienproduktion von elektronischen und elektromechanischen Komponenten, bei Bauteilabkündigungen und Recherche nach Alternativbauteilen

Was Sie mitbringen:

• Abgeschlossenes Studium im Bereich Elektrotechnik, Elektronik oder vergleichbare Qualifikation (Bachelor/Master) und/oder langjährige Erfahrung in einem vergleichbaren Beruf im Bereich der Elektronik
• Umfangreiche Kenntnisse in der elektronischen Schaltungsentwicklung, Mess-, Steuerungs- und Regelungstechnik, Signalverarbeitung, Elektronik und Computertechnik
• Gute Kenntnis von Sicherheitsstandards, Regulierungen und Umweltschutzanforderungen
• Erfahrung mit Mikrocontrollern, Embedded Software Systems und Signalverarbeitung sowie Programmierkenntnisse in C, C++ oder Python sind von Vorteil, aber nicht zwingend erforderlich
• Starke analytische Fähigkeiten und Problemlösungskompetenz sowie die Charaktereigenschaften eines Teamplayers – denn nur gemeinsam können wir Innovationen auf höchstem Maß vorantreiben!
• Gute Deutsch- und Englischkenntnisse in Wort und Schrift

Das Team

Die Clemens GmbH ist ein innovatives Technologieunternehmen auf nachhaltigem Wachstumskurs. Wir entwickeln und produzieren Geräte und Komponenten für die Branchen Medizintechnik und Life Sciences. Unsere technisch anspruchsvollen Lösungen werden in Laboren und Forschungszentren weltweit eingesetzt. Darüber hinaus bieten wir mit einer top-modernen Maschinenausstattung Electronic Manufacturing Services (EMS) auf höchstem Niveau. Kundenzufriedenheit, hohe Innovationskraft und exzellente Qualität stehen bei uns an erster Stelle. Wir sind sowohl nach ISO 9001 als auch nach ISO 13485 zertifiziert, was unser Engagement für Spitzenleistungen unterstreicht.

Nun, als Teil von Avantor können die anspruchsvollen Produkte und hochmodernen Fertigungskapazitäten von Clemens mit dem Angebot von Avantor für kritische Laborautomatisierungsabläufe, dessen globaler Reichweite und der Leidenschaft für das Erreichen wissenschaftlicher Durchbrüche kombiniert werden.

Werden Sie Teil unseres Teams von engagierten Fachleuten, die komplexe Herausforderungen mit intelligenten Lösungen lösen.

Warum Avantor?

Trauen Sie sich, Karriere zu machen. Schließen Sie sich unserem globalen Team von mehr als 14.000 Mitarbeitern an, die mit ihrer Leidenschaft für Entdeckungen und ihrer Entschlossenheit, Herausforderungen zu meistern, unermüdlich die lebensverändernde Wissenschaft voranbringen.

Unsere Arbeit verändert das Leben der Menschen zum Besseren. Sie bringt neue Behandlungen und Therapien für Patienten auf den Markt und gibt einem Krebsüberlebenden die Chance, seine Tochter vor den Traualtar zu führen. Sie ermöglicht medizinische Geräte, die einem kleinen Jungen helfen, zum ersten Mal im Leben die Stimme seiner Mutter zu hören. Ergebnisse wie diese schaffen unbegrenzte Möglichkeiten für Sie, Ihre Talente einzubringen, neue Fähigkeiten zu erlernen und Ihre Karriere bei Avantor weiterzuverfolgen.

Wir helfen Ihnen unbeirrt auf diesem Weg durch unsere vielfältige, gleichberechtigte und integrative Kultur, die personalisierte Lernerfahrungen beinhaltet, um Ihre berufliche Entwicklung und Ihren Erfolg zu fördern. Bei Avantor können Sie es wagen, über sich hinauszuwachsen und zu sehen, wie die Auswirkungen Ihrer Beiträge die Wissenschaft in Bewegung setzen, um eine bessere Welt zu schaffen. Bewerben Sie sich noch heute!

#LI-Hybrid #career #growth #AvantorSetsScienceInMotion

Disclaimer:

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.

Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science.
 
The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor.
 
We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today!

EEO Statement:

We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law.

If you need a reasonable accommodation for any part of the employment process, please contact us by email at recruiting@avantorsciences.com and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.

We will use the personal information that you have submitted to us in order to consider your application for the relevant role.
 

Your privacy is important to us. Please click here for our Privacy Policy which explains the purposes for which we will use your personal information and the ways in which we will handle and retain your information. It also explains the rights you have in relation to your information, and how to contact us with any queries or requests.

3rd Party Non-Solicitation Policy:

By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation.

• This position involves working with R&D engineers on the development and qualification of the Thermal printer products and systems.
• The Test Engineers will be responsible for executing all aspects of the test and qualification process for printer products, including executing test plans, documenting test results, assisting in troubleshooting of issues, and coordinating testing with in-house, out-source and driving the project to be delivered in time with high quality.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

• Actively participate in Scrum teams and work with other The SQA engineers to test the printer under test.
• Learn to analyze and decompose printer systems and assist in the development of strategies to test at system level.
• Strong commitment to quality software engineering best practices and the Scrum methodology.
• Communicate and file reports on issues encountered during testing. Perform basic troubleshooting and feedback to SQA engineers with detail of issue.
• Support ad-hoc test requests from the R&D Engineers.

KNOWLEDGE, SKILLS, AND ABILITIES:

1. Degree in Electronics or Computer disciplines.
2. Minimum 4-5 years’ experience with at least one full project lifecycle SQA experience.
3. Experience in testing Printer or other Electro-Mechanical product is preferred.
4. Experience in Software Quality Assurance Methodologies.
5. Independent and goal-oriented.
6. Strong teamwork, communication and interpersonal skills

Highlights:

• Fortune 500 MNC
• Permanent job opportunity
• Great remuneration & benefits
• Great career progression

Responsibilities:

• Establish and maintain relationships with local research institutions and collaborate on projects.
• Develop recycled additive manufacturing (AM) technology and develop specification for new AM powder.
• Need to keep track and understand the research progress in the field of sustainable materials.
• Manage multiple projects and maintain good communication channels both internally and externally

Requirements:

• PhD in materials science (metal, prefer Titanium/Aluminum/Stainless Steel
• Familiar in the production of AM powder production
• Familiar with metal AM printing technology (preferably metal laser bed powder fusion)
• At least 3 years of relevant research or work experience

HOW TO APPLY:

Interested applicants, please click on “Apply Now” and send your latest resume to dicksern@trustrecruit.com.sg and provide the below details in your resume.

• Last drawn salary
• Expected salary
• Notice period
• Reason for leaving

We regret only shortlisted candidates will be notified.

Important Note: Trust Recruit Pte Ltd is committed to safeguarding your personal data in accordance with the Personal Data Protection Act (PDPA).

Please read our privacy statement on our corporate website www.trustrecruit.com.sg.

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EA License No: 19C9950

EA Personnel: Lim Dick Sern (Dick Sern)

EA Personnel Reg No: R22106832

Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Group revenues in 2022 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.com

Every day, our products improve the lives of millions of people around the world. We’re hugely proud of this, which is why we’re transforming our business to reach millions more. Join us on our journey to #ForeverCaring as a Front End R&D Engineer, and you’ll drive progress that really means something.

 

About the Role

Reporting to the Director of Front End Innovation for Ostomy Care within the Technology and Innovation organization the Front End R&D Engineer will serve as project lead/manager and/or specialist. They will interface with marketing, clinical, and users to initiate and run Front end projects to feed into Convatec's product development pipeline.

Key Responsibilities

Self:

• Closely partner with Clinical, Marketing, and Design teams to understand unmet needs in the therapy space and translate these into prototype designs with clear market differentiation.   Develop a deep understanding of the patient journey through discussions with users, patients, payers, and providers.
• Develop a deep understanding of our current product portfolio and how it fits in context vs. other offerings on the market
• Partner with internal and external resources to proactively identify a variety of creative/innovative technical solutions to those needs
• When needed drive the preparation toward a research showcase or similar milestone. Provide technical input too.  
• Use leading front-end Innovation practices and stages of the new product development (IDEAL) to mature ideas/projects to Research showcase.
• Understand and balance opportunities and constraints of reimbursement, market access, and environment factors as well as manufacturability and financial targets.
• Work with partners, including key opinion-leading customers, universities, design partners, contract research organizations, testing laboratories, tech incubators and startup companies.
• Stay abreast of trends in the field, including awareness of competitors’ new product introductions and development activities.
• Lead and undertake the IP and technology mapping activities for projects.
• Have a flexible approach and fill roles in teams when needed. Be the mortar that holds the small teams together
• Have an open and including approach to Innovation – Be the hub that allows us to leverage the whole organization
• Take responsibility for specific areas (technical, user, medical) and grow the knowledge including the relevant build/facilitate building of e.g test rigs, prototypes, and models. ID labs/ parts that can accelerate development in the area.
• Scope, plan, and execute front-end projects

Others:

• Provide project management of a small project team if required
• Work effectively and proactively engage with key stakeholders to manage expectations and deliver on commitments; Understand needs and requirements across multiple functions, manage relationships to ensure effective execution.
• Work collaboratively across the organization and support colleagues to achieve shared goals and objectives.
• Ensure diligent and effective handover
• Strive to prioritize building of strong teams. Seek help and input on fostering strong teams

Business:

• Understands and can explain their role within T&I and the wider organization.
• Understands and can articulate the T&I strategy and key initiatives within ostomy car
• Role models behaviors appropriate to our values.
• Maintain compliance with HSE regulations
• Maintain compliance with QMS.

Principal Contacts:

• Internal: R&D, Marketing, Design, Clinical
• External: Vendors, Contractors, Suppliers

About You

Key Education, Experience & Competencies

• Master's degree in a science or engineering field, or equivalent experience

Experience:

• At least 3 years of experience in innovation and/or product development
• Experience in a regulated medical device industry
• Evidence of taking part in several development projects
• Good understanding of design control and regulatory control for Medical devices
• Have a working understanding of reimbursement systems in key countries.
• General understanding of the use and manufacture of Ostomy devices

• Ability to plan and execute effectively and systematically
• Able to utilize MS Office effectively
• Excellent interpersonal skills
• Effective time management
• Leadership style that promotes and supports a collaborative working environment.
• Laboratory or prototyping skills/experience
• Basic project management skills

Location:

• Lexington, MA (Greater Boston area) - hybrid or onsite

Travel Requirements:

• None

 

Our transformation will change your career. For good. You’ll be pushed to think bigger and aim for excellence. Your ideas will be heard, and you’ll be supported to bring them to life. There’ll be challenges. But, stretch yourself and embrace the opportunities, and you could make your biggest impact yet. This is stepping outside of your comfort zone. This is work that’ll move you.

#LI-MH1

#LI-Hybrid

 

Beware of scams online or from individuals claiming to represent Convatec

A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.

If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com.

Equal opportunities

Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.

Notice to Agency and Search Firm Representatives

Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Already a Convatec employee?

If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!

Use the Pharmacy Wellsky stock control computer system. To assist with stock control including the investigation of any discrepancies. As determined by the Lead Technicians supervise occasional visitors to the department, ensuring security, safety, and confidentiality is always maintained during the visit. To co-ordinate and prioritise workflow relating to cancer chemotherapy, parenteral nutrition, CIVAS, other non-cytotoxic products, non-sterile manufacturing, and radiolabelled kits under direction of senior technicians. This will include worksheet generation, calculations, raw material assembly and labelling. To prepare cancer chemotherapy for intrathecal use according to Department of Health guidelines, Local Trust policy and departmental procedures. To complete the initial check of cytotoxic, non-cytotoxic, CIVAS and parenteral nutrition batches prior to compounding. This will be achieved by completing and achieving the Pharmacy Workforce Development South Pre and In-Process Checking accreditation. To supervise senior assistant technical officers, assistant technical officers, and students within the pharmacy technical services unit. To Train and carry out competency assessments for senior assistant technical officers, assistant technical officers, rotational technicians under the guidance and direction of senior technicians. To carefully follow all standard operating procedures and work instructions to ensure that all products are made safely and efficiently in accordance with Good Manufacturing Guidelines. To assist with the preparation of draft documents pertaining to new products and procedures under guidance and supervision of senior technicians. To participate in production of clinical trials products completing all necessary documentation as required by the study protocols.

Responsibilities & Duties:

• To be able to operate equipment and electrical systems independently. Primary focus of equipment: GCMS, HPLC, MPAES, FTIR, CVS, IC, ICP-OES, Welting Angle.
• To maintain control on the use of equipment.
• To be able to troubleshoot simple operational problem with the equipment.
• To be able to interpret results of equipment when used for evaluation and/or failure analysis and report accordingly
• To maintain proper documentation for all projects involved in compliance with ISO 9001, ISO 14001 and ISO 17025.
• To communicate with internal and external customers on requirements and expectations
• To maintain records of service – PM and breakdown.
• To communicate with vendors for support in the upkeep of equipment.
• To make improvements in operational requirements when the need arises.
• Provide support for experiments conducted by Manager / Senior Engineer(R&D)
• To carry out any other tasks required by the Company and Superiors

Qualification:

• Min Diploma in related field (Electrical, Chemistry, Physics, Mechanical Engineering)
• Fresh graduates are welcome to apply
• Candidate without any relevant experience will be consider as training will be provided
• Proficient in MS Office (Word, Excel, PowerPoint)
• Familiar with the requirements of ISO 9001, ISO 14001 and ISO 17025

Job Description

Filiale de notre division Santé Animale, Allflex Livestock Intelligence est le leader mondial de la conception, du développement, de la fabrication et de la fourniture de solutions d’identification, de monitoring et de traçabilité des animaux. Nos solutions basées sur la gestion des données sont utilisées par les éleveurs, les organisations d’élevage ainsi que les États pour gérer des centaines de million d’animaux dans le monde. En mettant à la disposition des éleveurs des informations claires et concrètes, nos solutions leur permettent de décider et d’agir rapidement pour garantir le bien-être, la santé et la traçabilité de leurs animaux afin de faciliter une production optimale pour une alimentation sûre, saine et durable.

Nous recherchons pour notre site de Vitré en Bretagne, un Ingénieur Développement pour le développement de nouveaux produits innovants pour l’identification animale.

Description

En tant qu’Ingénieur Développement vous aurez en charge la création de produits nouveaux et innovants depuis l’idéation jusqu’à l’industrialisation

La responsabilité inclut les modifications et améliorations des produits existants et il est attendu que vous établirez et maintiendrez des relations de sous-traitance afin d’augmenter la capacité d’exécution.

Vous traiterez les problématiques associées aux demandes d’agrément. Vous tiendrez à jour la documentation technique et serez activement impliqué dans la veille technologique des produits concurrents et des process.

L’ingénieur développement est force de proposition afin de réduire le temps de mise sur le marché et du temps de développement, de production et des coûts.

Vous participerez au processus d’homologation des nouveaux produits

Le poste implique de nombreuses interactions avec divers services au niveau du groupe (achats, production, Industrialisation, Qualité…)

Profil

• Ingénieur mécanique et/ou plasturgiste

• Expérience dans un département R&D, idéalement dans les très grandes séries

• Expérience dans le management de plusieurs projets en simultané, sous-traitants en parallèle.

• Expérience dans le développement de produits multi-matériaux (Plastique, métal, verre…)

• Expérience dans une entreprise multiculturelle.

• Expérience en spécifications techniques de produits et demandes de solution.

• Excellente compétence technique avec le désir d’aller dans le détail afin d’atteindre les besoins client

• A l’aise avec AMDEC, Analyse fonctionnelle, Lean, 8D

• Habitué de la CAO (idéalement Solid Edge)

• Bonne communication verbale et écrite

• Français et Anglais technique impératif (oral/ecrit)

Savoir faire

• Connaissance de la simulation numérique

• Connaissances des matières plastiques, de la mécanique

• Expérience dans le marquage, marquage à chaud, gravures

• Expérience dans le moulage de grandes séries

• Expérience dans le moule TPU

• Expérience dans le milieu agricole ou santé animale.

Savoir être

• Motivé et indépendant, bonne gestion du temps et des priorités

• Motivé et à l’aise dans le travail d’équipe

• Capacité à innover et force de proposition

Current Employees apply HERE

Current Contingent Workers apply HERE

Secondary Language(s) Job Description:

As a ‘Development Engineer” you will oversee the creation of new and innovative product lines from the initial ideation cycle through to complete development cycle and industrialization.

The responsibility includes modifications and improvements of existing identification products, and it is expected that you will establish and maintain contractor relations to increase the capacity of execution.

You will resolve issues regarding the agreement compliances. You will be responsible for keeping all the technical information current as well as being an active contributor in watching the competition and keeping up with new processes.

The Development Engineer is also a source of proposals contributing to the reduction of the time to market and the reduction of development, and production, costs.

You participate in the compliance and the homologation of the new products.

This position involves interactions with several departments globally including, , Purchasing, Production, Industrialization, Quality.

Key requirements

• Mechanical and/or Plastic Engineer.

• A minimum of 10 years of experience in R&D department, ideally in high series productions,

• Demonstrated experience of leading multiple projects, subcontractors, in parallel

• Demonstrated experience with developing products with multiple elements & materials (plastic + metal + Glass + …)

• Experience working with multi-national cultural environment

• Experience in documenting product specifications and solutions requirements

• Strong technical competence with ability to dive into small details to properly balance product attributes with customer needs

• Experienced with the FMECA, Functional analysis, Lean, 8D, methodologies.

• Familiar with CAD design (ideally with Solid Edge).

• Excellent verbal/written communication and presentation skills

• Fluent French and technical orientated English

Advantages

• Knowledge in mechanical simulated environments.

• Good knowledge of plastic materials, mechanics.

• Experience of leading groups of developers

• Experience in labelling, hot stamping, engraving…

• Experience in high series injection molding process.

• Experience in TPU molding.

• Experience in agriculture and/or animal health

Personal Characteristics

• Self-motivated and independent with good time and priorities management skills

• Diligent and methodical.

• Highly motivated individual and excellent team player.

• Able to innovate, bringing forward improvement proposals.

Search Firm Representatives Please Read Carefully 
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

 

R&D Software Engineer

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

We seek a proactive, skilled, and enthusiastic Software Engineer to fulfil an entirely new and unique role at our Slough site, to enhance our Biologics Research and Development (R&D). The ideal candidate would have a demonstrated expertise in developing and implementing software solutions to automate laboratory processes. You will achieve this by creating, implementing, and managing easy-to-use lab software solutions and user interfaces to link with our new automation systems within Biologics R&D.

This will be a vital component in forming the first basis of in-house automation on our site and so you will work closely with our lab scientists, bioinformaticians, as well as our other newly-created appointment, the R&D Automation Engineer, who will be your counterpart on the hardware side.

Key responsibilities:

• Engage directly with laboratory scientists and other stakeholders to comprehend challenges and requirements, and to propose and/or implement robust software applications accordingly.
• Identify, Design, develop, and implement easy-to-use software solutions and user interfaces for both new and existing robotic equipment, integrated systems, and liquid handling platforms to automate laboratory processes, including data acquisition and reporting.
• Provide technical support and training to laboratory staff on the use of automation software and systems, troubleshooting issues and optimizing performance as needed.
• Integrate laboratory instruments, such as liquid handling systems, robotic arms, and analytical instruments, with software solutions to enable seamless data exchange and process automation
• Adapt, tailor, and maintain both new and existing robotic equipment, integrated systems, and liquid handling platforms to facilitate the automation of laboratory processes.
• Collaborate with cross-functional teams, including IT, bioinformatics, and quality assurance, to align automation efforts with overall business objectives and regulatory requirements.
• Document software designs, implementation details, and validation protocols in accordance with company standards and regulatory guidelines
• Demonstrate familiarity with Biopharma 4.0 digitalization initiatives.
• Participate in required Lonza training programs.
• Willing to travel to other Lonza sites within the UK and Europe, accounting for approximately 10% of working time

Key requirements:

• Possess an MSc in Bioengineering, Computer Engineering or other relevant discipline.
• Demonstrated depth of proficiency and experience in laboratory automation
• Proficient programming skills in Python, Java ,SQL with a focus on automation and software development.
• Experience of automation integration of hardware into data infrastructure, scheduling systems, cloud infrastructure and other analytical and data visualization tools.
• Strong understanding of laboratory automation platforms, including liquid handling systems, robotic arms, and integrated software solutions.
• Experience with LIMS/ELN systems
• Proven track record of innovation and experience in leading interdisciplinary hardware/software automation projects
• Proven track record of innovation and experience in leading complex technology projects
• Excellent communication and presentation abilities to a diverse audience

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

#LI-IG1

 

R&D Automation Engineer

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

We seek a proactive, skilled, and enthusiastic Automation Engineer to fulfil an entirely new and unique role at our Slough site, to enhance our research, development, and analytical capacities. You will achieve this by identifying, creating, implementing, and managing state-of-the-art lab automation platforms and technologies in Biologics R&D. This will be the first basis of in-house automation on our site and will work closely with our lab scientists, bioinformaticians, as well as our other newly-created appointment, the R&D Software Engineer, who will be your counterpart on the software side.

If you are someone who brings expertise in multiple commercially accessible automation equipment, liquid handling systems, and robotic arms, coupled with experience in integrating laboratory systems, then we would love to see what you can do!

Key responsibilities:

• Engage directly with laboratory scientists, bioinformaticians, IT personnel, and other stakeholders to comprehend challenges and requirements, and to propose or implement automation solutions accordingly.
• Adapt, tailor, and maintain both new and existing robotic equipment, integrated systems, and liquid handling platforms to facilitate the automation of laboratory processes.
• Serve as a subject matter expert (SME) in automation, robotics, and laboratory systems integration.
• Supervise the installation, validation, and qualification of equipment to ensure performance meets standards.
• Ensure adherence to security and operational standards by managing documentation and collaborating with local engineering groups, health and safety offices, and other relevant entities.
• Demonstrate familiarity with Biopharma 4.0 digitalization initiatives.
• Participate in required Lonza training programs.
• Willing to travel to other Lonza sites within the UK and Europe, accounting for approximately 10% of working time

Key requirements:

• Possess an MSc in Bioengineering, Robotics, Computer Engineering or other relevant discipline.
• Demonstrated depth of proficiency and experience in laboratory automation
• Ability in programming and development, ideally using one of the following laboratory automation software/hardware and liquid handlers: Hamilton Vantage/STAR line, Tecan Fluent/Evo
• Hands-on experience integrating and programming third-party automation hardware such as robotic arms and plate readers.
• Proficient programming skills in Python or another object-oriented language relevant to automation.
• Proven track record of innovation and experience in leading complex technology projects
• Excellent communication and presentation abilities to a diverse audience

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

#LI-IG1

Key Responsibilities:

• The design verification engineer is expected to check, test, and gate the product design for both performance and reliability.
• Draft a test plan to cover each feature in product spec, certification requirement, and customer application.
• Support on DFMEA documentation draft and maintenance.
• Test products' electrical & mechanical performance and reliability with lab equipment such as multi-meter, integrating sphere, oscilloscope, and environmental chamber.
• Testing equipment management & maintenance.
• Follow up on the quality issues found and verify the effectiveness of corrective action.
• Give quality input during the early design stage to avoid potential quality issues.
• Update & deliver the test reports to the project lead and define the quality level of R&D stages.
• Work with QA to ensure the design quality can be delivered to the next phase.

Requirements:

• Bachelor’s in Electronic Engineering, computer science, or relevant majors.
• At least 8 years of design, testing, or quality experience.
• Experience in power electronics product testing and understanding of electronic product schematics is required.
• Operation experience with basic electronic equipment like oscilloscope, multimeter, power supply, and load are required.
• Knowledge or experience in electronic design, design quality, MCU, FW testing & appliances is preferred.
• Able to travel overseas.
• Familiar with UL standards will be an added advantage.
• Proficient in English and chinese to liase with HQ counterpart

Key Responsibilities:

• The design verification engineer is expected to check, test, and gate the product design for both performance and reliability.
• Draft a test plan to cover each feature in product spec, certification requirement, and customer application.
• Support on DFMEA documentation draft and maintenance.
• Test products' electrical & mechanical performance and reliability with lab equipment such as multi-meter, integrating sphere, oscilloscope, and environmental chamber.
• Testing equipment management & maintenance.
• Follow up on the quality issues found and verify the effectiveness of corrective action.
• Give quality input during the early design stage to avoid potential quality issues.
• Update & deliver the test reports to the project lead and define the quality level of R&D stages.
• Work with QA to ensure the design quality can be delivered to the next phase.

Requirements:

• Bachelor’s in Electronic Engineering, computer science, or relevant majors.
• At least 5 years of design, testing, or quality experience.
• Experience in power electronics product testing and understanding of electronic product schematics is required.
• Operation experience with basic electronic equipment like oscilloscope, multimeter, power supply, and load are required.
• Knowledge or experience in electronic design, design quality, MCU, FW testing & appliances is preferred.
• Able to travel overseas.
• Familiar with UL standards will be an added advantage.
• Proficient in English and chinese to liase with HQ counterparts.

Key Responsibilities:

• The design verification engineer is expected to check, test, and gate the product design for both performance and reliability.
• Draft a test plan to cover each feature in product spec, certification requirement, and customer application.
• Support on DFMEA documentation draft and maintenance.
• Test products' electrical & mechanical performance and reliability with lab equipment such as multi-meter, integrating sphere, oscilloscope, and environmental chamber.
• Testing equipment management & maintenance.
• Follow up on the quality issues found and verify the effectiveness of corrective action.
• Give quality input during the early design stage to avoid potential quality issues.
• Update & deliver the test reports to the project lead and define the quality level of R&D stages.
• Work with QA to ensure the design quality can be delivered to the next phase.

Requirements:

• Bachelor’s in Electronic Engineering, computer science, or relevant majors.
• At least 3 years of design, testing, or quality experience.
• Experience in power electronics product testing and understanding of electronic product schematics is required.
• Operation experience with basic electronic equipment like oscilloscope, multimeter, power supply, and load are required.
• Knowledge or experience in electronic design, design quality, MCU, FW testing & appliances is preferred.
• Able to travel overseas.
• Familiar with UL standards will be an added advantage.
• Proficient in English and chinese to liase with HQ counterparts.

Job Description Summary

Do you thrive in environments where strategic thinking meets hands-on problem-solving? If so, then this is your chance to make a transformative impact at BD.
As Director, R&D, Product Development, you will become the architect of our future, shaping the materials science function and capability across diverse business platforms within our $4B+ business unit (BU). You will lead a dynamic team of experts, advancing the BU’s innovation agenda and shaping the future of a broad, global portfolio of drug, device, combination products, where materials science innovation is critical to sustained market leadership.
Beyond a leadership opportunity, it's a chance to be a catalyst for change. You will be entrusted with optimizing the existing portfolio, leveraging your deep technical and product development expertise to identify and implement improvements that enhance performance, sustainability, and cost-effectiveness. Simultaneously, you will be a visionary leader, empowered to build a strong, collaborative R&D team, fostering a culture of continuous learning, and pushing the boundaries of what's possible.
You will be a strategic thought partner, collaborating across business platforms, the corporation, and the external ecosystem, to infuse materials science advances throughout our operations and portfolio.

Job Description

We are the makers of possible 

 

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities. 

 

We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us. 

BD Medical is an ~$9B segment consisting of three Business Units (Medication Delivery Solutions, Medication Management Solutions and Pharmaceutical Systems) arising from the merger of BD, CareFusion and CR Bard. The Medication Delivery Solutions (MDS) business is a ~$4B business for the BD Medical Segment and is made up of 4 fully integrated, cross-functional business platforms (i.e., Peripheral Intravascular Catheters, Advanced Access Devices, Infusion Preparation & Delivery, Catheter Care & Injection Systems).

Role Overview:

Do you thrive in environments where strategic thinking meets hands-on problem-solving? If so, then this is your chance to make a transformative impact at BD.

As Director, R&D, Product Development, you will become the architect of our future, shaping the materials science function and capability across diverse business platforms within our $4B+ business unit (BU). You will lead a dynamic team of experts, advancing the BU’s innovation agenda and shaping the future of a broad, global portfolio of drug, device, combination products, where materials science innovation is critical to sustained market leadership.

Beyond a leadership opportunity, it's a chance to be a catalyst for change.  You will be entrusted with optimizing the existing portfolio, leveraging your deep technical and product development expertise to identify and implement improvements that enhance performance, sustainability, and cost-effectiveness. Simultaneously, you will be a visionary leader, empowered to build a strong, collaborative R&D team, fostering a culture of continuous learning, and pushing the boundaries of what's possible.

You will be a strategic thought partner, collaborating across business platforms, the corporation, and the external ecosystem, to infuse materials science advances throughout our operations and portfolio.

The position is based in Franklin Lakes, NJ.

Primary Responsibilities

Portfolio Leadership & Innovation:

• Set the material strategy for multiple businesses to ensure compliance to an ever-changing regulatory landscape and work with the businesses to convert the strategy to an implementable roadmap.
• In partnership with business platforms, lead the development and implementation of a comprehensive sustainability strategy and roadmap.
• Think strategically and partner with business platforms to develop a clear vision for the future of the portfolio, addressing business’ growth and profitability aspirations.
• Ensure timely and robust delivery of the product development portfolio, driving execution across functions and sites and ensuring effective and compliant commercialization of new products.
• Integrate sustainability principles into all stages of the product development process, from material selection to manufacturing and end-of-life considerations.
• Manage intellectual property portfolio related to the assigned portfolio.
• Stay informed about emerging technologies and market trends, anticipating future needs and driving innovation in the medical device materials landscape.

People & Organization Development:

• Build and lead a diverse, high-performing expert organization with expertise in diverse material areas such as materials science, chemistry, and engineering.
• Be the voice of the materials function across the organization.
• Cultivate a culture of innovation, collaboration, and continuous learning, fostering talent development and empowering team members to reach their full potential.
• Champion diversity, equity, and inclusion within the team and foster a collaborative and respectful work environment.
• Implement talent development programs and identify opportunities for team members to grow and advance their careers.

Collaboration & Relationship Building:

• Foster a collaborative environment, partner closely with cross-functional teams within BU platforms to ensure business continuity and successful commercialization of new solutions.
• Collaborate with sustainability experts within BD to ensure alignment with broader company goals and contribute to industry-wide sustainability initiatives.
• Build strong relationships with internal and external stakeholders, including academic institutions, research partners, and industry leaders.

Qualifications:

This role requires a seasoned leader with deep expertise in materials science, a passion for bringing differentiated and sustainable solutions to market and a strong commitment to people development and collaboration.

• PhD in Chemistry, Materials Science, or related field.
• 10+ years of experience (preferred) in R&D leadership with a proven track record of success in product development, in a regulated environment, preferably in medical devices.
• Demonstrated experience in leading and developing high-performing, geographically and culturally diverse teams.
• Strong communication, collaboration, and relationship building skills, with the ability to influence and build trust across various departments and organizations.
• Strategic thinking and problem-solving skills, with the ability to translate scientific concepts into practical applications.
• Passion for medical device innovation and a commitment to sustainability principles.
• Strong knowledge of intellectual property protection and experience in managing patent portfolios (preferred).
• Experience with regulatory requirements and processes relevant to medical devices (a plus).

For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.

Why Join Us?

A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It’s also a place where we help each other be great, we do what’s right, we hold each other accountable, and learn and improve every day.

You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time. And through the organization’s investment in BD University, you will continually level up your tech skills and expertise.

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place. 

To learn more about BD visit https://bd.com/careers

Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

Primary Work Location

USA NJ - Franklin Lakes

Additional Locations

Work Shift

Key Responsibilities:

• Develop and maintain server-side application logic.
• Implement data storage solutions with Redis.
• Manage messaging systems with Message Brokers.
• Collaborate with front-end developers to integrate user-facing elements with server-side logic.
• Collaborate with AI developers to integrate AI modules.
• Write reusable, testable, and efficient code.
• Design and implement low-latency, high-availability, and performance applications.
• Implement security and data protection measures.
• Integrate data storage solutions and third-party services.
• Implement an email notification system for abnormal events.
• Develop and maintain microservices architecture.
• Implement and manage CI/CD processes.
• Manage and deploy applications on Kubernetes.
• Troubleshoot, debug and upgrade software.
• Write technical documentation.

Requirements:

• Proven more than 8 years of experience as a Software Engineer or similar role in software development.
• Proficiency in using Redis and Message Brokers.
• Experience in implementing email notification systems.
• Strong knowledge of server-side languages.
• Experience in microservices architecture project development.
• Proficiency in DevOps and familiarity with CI/CD processes.
• Familiarity with Kubernetes.
• Familiarity with front-end languages (e.g., HTML, JavaScript, and CSS).
• Degree in Computer Science, Statistics, or a relevant field.

New Product Development

• Proceeds development according to implement plan
• Makes functional specification
• Proceeds electrical, or firmware design
• Plans and proceeds prototype model evaluation and prepare evaluation to reports.

Re-design of Products

• Supports Lead Engineer to estimate return and investment.
• Proceed re-design according to implementation plan.
• Proceeds electrical, mechanical or firmware design.
• Plans and proceeds prototype model evaluation and prepare evaluation report.
• Makes up product manufacturing standard.

Technical Support

• Prepares technical information for parts localize and price negotiation.
• Supports production line if necessary according to superior’s direction.
• Supports parts faculty/investigation according to superior’s direction.

Requirements:

• Bachelor of Mechanical Engineering or its equivement.
• Experience in analog or digital electrical hardware design
• Entry level are welcome to apply.

Electronics Manufacturing Industry

East/Bedok

5 days work week

Interested Applicants, kindly email your detailed resume to hr@tempserv.com.sg

Tempserv Pte Ltd

License No: 06C3745

Tel: 62226441

Attention: Audris Teo / EA Personnel No: R1102063