Large

At Revvity, we understand how important and intertwined the work we do is to our people and our communities around the globe. Our aim is to foster a culture of collaboration, engagement, innovation, and inclusion, and ensure our employees are supported with the resources needed to assist with their professional and personal growth, while enabling them to work as their best selves. All team members are encouraged to play an active role in creating an inclusive workforce and giving back to their communities on their own, as well as through company-sponsored volunteer events.
 

Science & Healthcare

Revvity

Expanding the boundaries of human potential through science

You need an LL.M. or JD, 6+ years in life sciences law, IP expertise, strong communication skills, project management, and fluency in English and German.

You will provide commercial legal counsel, draft and negotiate agreements, advise on employment law, support M&A activities, and enhance contracting processes within the Life Sciences team.

Legal

Cambridge

<div>
 Revvity is seeking a full-time attorney to work within its legal department, supporting the Licensing &amp; Technology organisation within the Life Sciences segment. This attorney will primarily focus on supporting the Licensing &amp; Technology business by handling complex licensing agreements related to collaboration agreements with large pharmaceutical companies.
 While the primary responsibility will involve providing legal support to the Licensing &amp; Technology business, including its Bioproduction business located at our Cambridge, UK office, the attorney will also support other areas within the Life Sciences organisation, such as the Reagents and Platforms businesses, as needed. Additionally, this position will handle general employment and labour law matters within the EU, as required.
 This attorney will help manage risk while working collaboratively with business colleagues to find practical and creative solutions to various legal matters. The legal department’s responsibilities include, but are not limited to, drafting and negotiating a broad range of commercial agreements, providing practical legal advice to the Life Sciences organisation, supporting and negotiating complex licensing agreements, offering employment and labour law advice to HR in the EU, and supporting various departmental and cross-functional projects and initiatives.
 We seek a highly motivated, independent individual who thrives in a high-volume, dynamic environment with rapidly shifting priorities.
 
 Duties and Responsibilities:
 <ul>
 <li>Support and provide day-to-day counsel to the business on general commercial matters by collaborating with business partners at all levels of management to effectively balance minimising legal risk while enabling the execution of strategic business objectives.</li>
 <li>Draft, review, and negotiate a variety of commercial agreements, including but not limited to confidentiality, material transfer, professional services, procurement, and other general customer and supplier agreements.</li>
 <li>Draft, review, and negotiate a variety of complex licensing and collaboration agreements for the Licensing &amp; Technology business, with an initial focus on Horizon’s Bioproduction business. While this role primarily supports the Licensing &amp; Technology business, it is part of the Life Sciences legal team and will support other businesses within the Life Sciences organisation, such as Reagents and Platforms.</li>
 <li>Provide practical, sound employment and labour law advice to the HR team in the EU, as required.</li>
 <li>Support M&amp;A activities for the Life Sciences organisation.</li>
 <li>Work collaboratively with other members of the legal department and assist as needed.</li>
 <li>Create, improve, and/or update form agreements and processes to enhance aspects of contracting procedures and ensure alignment of contract terms with Revvity’s policies and standards.</li>
 <li>Perform other related duties as assigned or requested as knowledge of the business and legal skills evolve.</li>
 </ul>
 
 Required Qualifications:
 <ul>
 <li>LL.M., JD, or equivalent degree in law with a focus on intellectual property or life sciences law.</li>
 <li>Licensed to practise law in any jurisdiction.</li>
 <li>A minimum of 6+ years of transactional/commercial experience, ideally within the gene therapy, pharmaceutical, or broader life sciences sector.</li>
 <li>Strong understanding of intellectual property law, including patents, trademarks, and trade secrets.</li>
 <li>Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse stakeholders.</li>
 <li>Ability to determine risk exposure and advise the business in a practical manner, balancing legal risks with business needs.</li>
 <li>Fluent in English (both written and spoken).</li>
 </ul>
 
 Preferred Qualifications:
 <ul>
 <li>Strong project and process management skills, with the ability to prioritise and handle multiple projects and a wide range of tasks.</li>
 <li>Customer-focused and solutions-oriented approach to delivering contract management services to internal customers.</li>
 <li>Strong analytical and creative troubleshooting skills.</li>
 <li>Excellent judgement and personal and professional maturity and integrity.</li>
 <li>Understanding of German law, as part of the Licensing &amp; Technology business is based in Germany.</li>
 <li>Fluent in German (both written and spoken).</li>
 </ul>
 
 Additional Information:
 <ul>
 <li>This position may be remote or, depending on location, based at a local in-country Revvity office.</li>
 <li>Travel: &lt;5%.</li>
 </ul>
 
 LI-EMEA
</div>

Revvity is seeking a full-time attorney to work within its legal department, supporting the Licensing & Technology organisation within the Life Sciences segment. This attorney will primarily focus on supporting the Licensing & Technology business by handling complex licensing agreements related to collaboration agreements with large pharmaceutical companies.
 While the primary responsibility will involve providing legal support to the Licensing & Technology business, including its Bioproduction business located at our Cambridge, UK office, the attorney will also support other areas within the Life Sciences organisation, such as the Reagents and Platforms businesses, as needed. Additionally, this position will handle general employment and labour law matters within the EU, as required.
 This attorney will help manage risk while working collaboratively with business colleagues to find practical and creative solutions to various legal matters. The legal department’s responsibilities include, but are not limited to, drafting and negotiating a broad range of commercial agreements, providing practical legal advice to the Life Sciences organisation, supporting and negotiating complex licensing agreements, offering employment and labour law advice to HR in the EU, and supporting various departmental and cross-functional projects and initiatives.
 We seek a highly motivated, independent individual who thrives in a high-volume, dynamic environment with rapidly shifting priorities.
 
 Duties and Responsibilities:
 
 Support and provide day-to-day counsel to the business on general commercial matters by collaborating with business partners at all levels of management to effectively balance minimising legal risk while enabling the execution of strategic business objectives.
 Draft, review, and negotiate a variety of commercial agreements, including but not limited to confidentiality, material transfer, professional services, procurement, and other general customer and supplier agreements.
 Draft, review, and negotiate a variety of complex licensing and collaboration agreements for the Licensing & Technology business, with an initial focus on Horizon’s Bioproduction business. While this role primarily supports the Licensing & Technology business, it is part of the Life Sciences legal team and will support other businesses within the Life Sciences organisation, such as Reagents and Platforms.
 Provide practical, sound employment and labour law advice to the HR team in the EU, as required.
 Support M&A activities for the Life Sciences organisation.
 Work collaboratively with other members of the legal department and assist as needed.
 Create, improve, and/or update form agreements and processes to enhance aspects of contracting procedures and ensure alignment of contract terms with Revvity’s policies and standards.
 Perform other related duties as assigned or requested as knowledge of the business and legal skills evolve.
 
 
 Required Qualifications:
 
 LL.M., JD, or equivalent degree in law with a focus on intellectual property or life sciences law.
 Licensed to practise law in any jurisdiction.
 A minimum of 6+ years of transactional/commercial experience, ideally within the gene therapy, pharmaceutical, or broader life sciences sector.
 Strong understanding of intellectual property law, including patents, trademarks, and trade secrets.
 Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse stakeholders.
 Ability to determine risk exposure and advise the business in a practical manner, balancing legal risks with business needs.
 Fluent in English (both written and spoken).
 
 
 Preferred Qualifications:
 
 Strong project and process management skills, with the ability to prioritise and handle multiple projects and a wide range of tasks.
 Customer-focused and solutions-oriented approach to delivering contract management services to internal customers.
 Strong analytical and creative troubleshooting skills.
 Excellent judgement and personal and professional maturity and integrity.
 Understanding of German law, as part of the Licensing & Technology business is based in Germany.
 Fluent in German (both written and spoken).
 
 
 Additional Information:
 
 This position may be remote or, depending on location, based at a local in-country Revvity office.
 Travel: <5%.
 
 
 LI-EMEA

Senior Corporate Counsel - Revvity

United Kingdom

Senior Corporate Counsel

You must manage sample collection, segregation, centrifugation, quality checks, registration, barcoding, and maintain Excel records efficiently and accurately.

You will receive, segregate, and check sample quality and quantity, centrifuge samples, register and barcode them, and maintain Excel sheets for sample management.

Science

Logistics

Chennai

<ul>
 <li>Receiving Samples through courier &amp; local collection centers</li>
 <li>Segregating the samples - departments wise</li>
 <li>Centrifuging the samples</li>
 <li>Sample quality &amp; quantity checking</li>
 <li>Partially separating query forms</li>
 <li>Samples registration (FTS-Serum &amp;DBS, QD, ST, NBS) initially under supervision.</li>
 <li>Barcoding the samples</li>
 <li>Maintaining the excel sheet for sample boxes</li>
</ul>


 Receiving Samples through courier & local collection centers
 Segregating the samples - departments wise
 Centrifuging the samples
 Sample quality & quantity checking
 Partially separating query forms
 Samples registration (FTS-Serum &DBS, QD, ST, NBS) initially under supervision.
 Barcoding the samples
 Maintaining the excel sheet for sample boxes


Executive Accession- Temporary - Revvity

Executive Accession- Temporary

You need a BS in STEM, 7+ years in web front-end dev, proficiency in HTML5, CSS3, TypeScript, JavaScript, and experience with frameworks like React or Angular. Strong communication and leadership skills are essential.

You will analyze business needs, guide UI development, provide technical leadership, improve software processes, establish CI/CD pipelines, and collaborate with UX and product teams.

Software Engineering

IT & Cybersecurity

Hamburg

Revvity is manufacturer of scientific instruments, reagents, and software to drive innovations in human and environmental health around the world. Here in Hamburg, we are developing complex life-science solutions, including instruments and software, to help our customers around the world, from academic and business environments, with their challenging objectives. To strengthen our international and diverse R&D Application Software Team in Hamburg, we are looking for Principal Frontend Software Engineer (m/w/d) who will contribute to the development of efficient and reusable Web-based UI, collaborate with UX design team, and provide technical leadership to the UI development team, utilizing modern technologies and tools. You will: * Analyse and translate business needs into the efficient and reusable Web applications, UI components and elements; contribute to project and release planning in collaboration with management and engineering teams, develop appropriate technical and architectural project documentation. * Coordinate and guide Web-based UI development to ensure architectural and technology consistency of software solutions, enabling efficient maintainability, re-usability, and modularity across cross-platform environments. * Provide technical leadership to the international and diverse team of UI developers, enabling their efficient collaboration and communications within the team and across organization. * Contribute to continuous improvement of software engineering processes, including automation and standardization of development activities and tools. In collaboration with the team, establish efficient CI/CD pipeline for cross-platform software development and automation of daily routines such as testing, documentation and packaging. * In close collaboration with UX design team, product management and project stakeholders proactively participate in UX design process. Basic Qualifications: * BS in STEM (science, technology, engineering, mathematics) or equivalent * 7+ years of software engineering in Web-based front-end development * Confident level of English in speaking and writing * Knowledge of Scrum-based software development * Proficiency in HTML5, CSS3, TypeScript and JavaScript Preferred Qualifications (in addition to Basic Qualifications): * 10+ years of experience in Web-based front-end development. * 2+ years of technical team leadership. * Strong knowledge of OOP and UX/UI design processes, principles, and patterns. * Strong expertise in such frameworks as React, Angular, Vue.js, Flutter, Bootstrap. * Proven track record in development of scalable and reliable REST API. * Strong communication, negotiation, and presentation skills. * Knowledge of CI/CD practices and tools based on Git and GitHub. * Experience in UI test automation and knowledge of UI test automation tools and frameworks. * Knowledge of C# and Python would be a big plus. * Experience with high-performance 3D imaging and large image rendering is an advantage. Revvity is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, or veteran status or any other characteristics protected by applicable law. Revvity is committed to a culturally diverse workforce.

Revvity is manufacturer of scientific instruments, reagents, and software to drive innovations in human and environmental health around the world. Here in Hamburg, we are developing complex life-science solutions, including instruments and software, to help our customers around the world, from academic and business environments, with their challenging objectives. To strengthen our international and diverse R&D Application Software Team in Hamburg, we are looking for Principal Frontend Software Engineer (m/w/d) who will contribute to the development of efficient and reusable Web-based UI, collaborate with UX design team, and provide technical leadership to the UI development team, utilizing modern technologies and tools.You will: * Analyse and translate business needs into the efficient and reusable Web applications, UI components and elements; contribute to project and release planning in collaboration with management and engineering teams, develop appropriate technical and architectural project documentation. * Coordinate and guide Web-based UI development to ensure architectural and technology consistency of software solutions, enabling efficient maintainability, re-usability, and modularity across cross-platform environments. * Provide technical leadership to the international and diverse team of UI developers, enabling their efficient collaboration and communications within the team and across organization. * Contribute to continuous improvement of software engineering processes, including automation and standardization of development activities and tools. In collaboration with the team, establish efficient CI/CD pipeline for cross-platform software development and automation of daily routines such as testing, documentation and packaging. * In close collaboration with UX design team, product management and project stakeholders proactively participate in UX design process.      Basic Qualifications: * BS in STEM (science, technology, engineering, mathematics) or equivalent * 7+ years of software engineering in Web-based front-end development * Confident level of English in speaking and writing * Knowledge of Scrum-based software development * Proficiency in HTML5, CSS3, TypeScript and JavaScript      Preferred Qualifications (in addition to Basic Qualifications): * 10+ years of experience in Web-based front-end development. * 2+ years of technical team leadership. * Strong knowledge of OOP and UX/UI design processes, principles, and patterns. * Strong expertise in such frameworks as React, Angular, Vue.js, Flutter, Bootstrap. * Proven track record in development of scalable and reliable REST API. * Strong communication, negotiation, and presentation skills. * Knowledge of CI/CD practices and tools based on Git and GitHub. * Experience in UI test automation and knowledge of UI test automation tools and frameworks. * Knowledge of C# and Python would be a big plus. * Experience with high-performance 3D imaging and large image rendering is an advantage.      Revvity is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, or veteran status or any other characteristics protected by applicable law. Revvity is committed to a culturally diverse workforce.

Principal Frontend Software Engineer (m/w/d) - Revvity

Revvity is manufacturer of scientific instruments, reagents, and software to drive innovations in human and environmental health around the world. Here in Hamburg, we are developing complex life-science solutions, including instruments and software, to help our customers around the world, from academic and business environments, with their challenging objectives. To strengthen our international and diverse R&amp;amp;D Application Software Team in Hamburg, we are looking for Principal Frontend Software Engineer (m/w/d) who will contribute to the development of efficient and reusable Web-based UI, collaborate with UX design team, and provide technical leadership to the UI development team, utilizing modern technologies and tools.&lt;br&gt;&lt;br&gt;You will:&lt;br&gt;&lt;br&gt;&lt;ul&gt;&lt;li&gt;Analyse and translate business needs into the efficient and reusable Web applications, UI components and elements; contribute to project and release planning in collaboration with management and engineering teams, develop appropriate technical and architectural project documentation.&lt;/li&gt;&lt;li&gt;Coordinate and guide Web-based UI development to ensure architectural and technology consistency of software solutions, enabling efficient maintainability, re-usability, and modularity across cross-platform environments.&lt;/li&gt;&lt;li&gt;Provide technical leadership to the international and diverse team of UI developers, enabling their efficient collaboration and communications within the team and across organization.&lt;/li&gt;&lt;li&gt;Contribute to continuous improvement of software engineering processes, including automation and standardization of development activities and tools. In collaboration with the team, establish efficient CI/CD pipeline for cross-platform software development and automation of daily routines such as testing, documentation and packaging.&lt;/li&gt;&lt;li&gt;In close collaboration with UX design team, product management and project stakeholders proactively participate in UX design process.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Basic Qualifications:&lt;br&gt;&lt;br&gt;&lt;ul&gt;&lt;li&gt;BS in STEM (science, technology, engineering, mathematics) or equivalent&lt;/li&gt;&lt;li&gt;7+ years of software engineering in Web-based front-end development&lt;/li&gt;&lt;li&gt;Confident level of English in speaking and writing&lt;/li&gt;&lt;li&gt;Knowledge of Scrum-based software development&lt;/li&gt;&lt;li&gt;Proficiency in HTML5, CSS3, TypeScript and JavaScript&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Preferred Qualifications (in addition to Basic Qualifications):&lt;br&gt;&lt;br&gt;&lt;ul&gt;&lt;li&gt;10+ years of experience in Web-based front-end development.&lt;/li&gt;&lt;li&gt;2+ years of technical team leadership.&lt;/li&gt;&lt;li&gt;Strong knowledge of OOP and UX/UI design processes, principles, and patterns.&lt;/li&gt;&lt;li&gt;Strong expertise in such frameworks as React, Angular, Vue.js, Flutter, Bootstrap.&lt;/li&gt;&lt;li&gt;Proven track record in development of scalable and reliable REST API.&lt;/li&gt;&lt;li&gt;Strong communication, negotiation, and presentation skills.&lt;/li&gt;&lt;li&gt;Knowledge of CI/CD practices and tools based on Git and GitHub.&lt;/li&gt;&lt;li&gt;Experience in UI test automation and knowledge of UI test automation tools and frameworks.&lt;/li&gt;&lt;li&gt;Knowledge of C# and Python would be a big plus.&lt;/li&gt;&lt;li&gt;Experience with high-performance 3D imaging and large image rendering is an advantage.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Revvity is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, or veteran status or any other characteristics protected by applicable law. Revvity is committed to a culturally diverse workforce.&lt;br&gt;&lt;br&gt;

Principal Frontend Software Engineer (m/w/d)

You need a science degree, 3+ years in a lab, experience with techniques like flow cytometry and ELISA, sterile cell culture skills, and strong organization and documentation abilities.

You will test products, perform aseptic cell culture, analyze data, maintain lab safety, assist with troubleshooting, support process improvements, train others, and manage additional projects as needed.

Research & Development

San Diego

BioLegend, Inc. (a Revvity, Inc. Company) develops world-class, cutting-edge antibodies and reagents for biomedical research, manufactured in our state-of-the-art facility in San Diego, CA. Our mission is to accelerate research and discovery by providing the highest quality products at an outstanding value, along with superior customer service and technical support. Our product expertise covers a diverse set of research areas including Immunology, Neuroscience, Cancer, Stem cells, and Cell Biology. Job Summary At BioLegend we are dedicated to commercializing high quality reagents to support the research community for legendary discoveries. The Associate for BioLegend’s Quality Control group will test products such as antibodies and proteins in the following application(s): flow cytometry, immunohistochemistry, western blotting, ELISA, multiplex immunoassays and/or functional bioassays. The candidate will perform all aspects of the assays following SOPs and ISO requirements. Additional responsibilities include culturing mammalian cell lines, isolating primary cells, and maintaining laboratory equipment and supplies. The candidate will assist with troubleshooting, efficiency and process improvement projects, and creation and modification of SOPs. The associate will generate and present data summaries, provide ETAs, and help train others on specific protocols. We are looking for a highly motivated person who loves science and wants to be part of a dynamic and fast paced team. Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * Perform testing of products in a timely manner * Perform aseptic cell culture * Isolate primary cells and tissues * Perform data analysis and document results * Maintain a safe and clean laboratory * Assist with troubleshooting projects, generate data summaries * Support efficiency and process improvement projects * Train others on specific laboratory protocols * Other projects or responsibilities as may be required. Minimum Qualifications – Education And Experience * Bachelor’s degree in a scientific discipline * Experience with some of the following applications: flow cytometry, western blotting, Immunoprecipitation, bioassays, ELISA and IHC/ICC is a big plus. * >3 years working experience in a laboratory environment * Familiarity with basic lab equipment and knowledge of lab safety protocols Preferred Qualifications – Education And Experience * Experience in sterile cell culture technique * Excellent organization, communication, and problem-solving skills * Proven ability to multi-task * Excellent documentation skills The base salary range for this full-time position is $28-$29.80/hour. This range reflects the minimum and maximum target for a new hire in this position. The base pay actually offered to the successful candidate will take into account internal equity, work location, and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process. Please note that base pay is only one part of our total compensation package and is determined within a range. This range allows for the successful candidate to have an opportunity to progress within the position and develop at our company. This base pay range does not take into account bonuses, equity, or other benefits which may be applicable and are dependent on the level and position offered. Work Environment & Physical Demands - Lab While performing the duties of this job, the employee regularly works in a laboratory environment with occasional data entry on a computer. Occasional exposure to a warehouse environment. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to use hands and fingers to handle, feel, or operate objects, tools or controls, and reach with hands and arms. The employee is frequently required to stand, talk and hear.

BioLegend, Inc. (a Revvity, Inc. Company) develops world-class, cutting-edge antibodies and reagents for biomedical research, manufactured in our state-of-the-art facility in San Diego, CA. Our mission is to accelerate research and discovery by providing the highest quality products at an outstanding value, along with superior customer service and technical support. Our product expertise covers a diverse set of research areas including Immunology, Neuroscience, Cancer, Stem cells, and Cell Biology.Job SummaryAt BioLegend we are dedicated to commercializing high quality reagents to support the research community for legendary discoveries. The Associate for BioLegend’s Quality Control group will test products such as antibodies and proteins in the following application(s): flow cytometry, immunohistochemistry, western blotting, ELISA, multiplex immunoassays and/or functional bioassays. The candidate will perform all aspects of the assays following SOPs and ISO requirements. Additional responsibilities include culturing mammalian cell lines, isolating primary cells, and maintaining laboratory equipment and supplies. The candidate will assist with troubleshooting, efficiency and process improvement projects, and creation and modification of SOPs. The associate will generate and present data summaries, provide ETAs, and help train others on specific protocols. We are looking for a highly motivated person who loves science and wants to be part of a dynamic and fast paced team.Essential FunctionsReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * Perform testing of products in a timely manner * Perform aseptic cell culture * Isolate primary cells and tissues * Perform data analysis and document results * Maintain a safe and clean laboratory * Assist with troubleshooting projects, generate data summaries * Support efficiency and process improvement projects * Train others on specific laboratory protocols * Other projects or responsibilities as may be required.         Minimum Qualifications – Education And Experience * Bachelor’s degree in a scientific discipline * Experience with some of the following applications: flow cytometry, western blotting, Immunoprecipitation, bioassays, ELISA and IHC/ICC is a big plus. * >3 years working experience in a laboratory environment * Familiarity with basic lab equipment and knowledge of lab safety protocols         Preferred Qualifications – Education And Experience * Experience in sterile cell culture technique * Excellent organization, communication, and problem-solving skills * Proven ability to multi-task * Excellent documentation skills         The base salary range for this full-time position is $28-$29.80/hour. This range reflects the minimum and maximum target for a new hire in this position. The base pay actually offered to the successful candidate will take into account internal equity, work location, and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.Please note that base pay is only one part of our total compensation package and is determined within a range. This range allows for the successful candidate to have an opportunity to progress within the position and develop at our company. This base pay range does not take into account bonuses, equity, or other benefits which may be applicable and are dependent on the level and position offered.Work Environment & Physical Demands - LabWhile performing the duties of this job, the employee regularly works in a laboratory environment with occasional data entry on a computer. Occasional exposure to a warehouse environment.The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.While performing the duties of this job, the employee is regularly required to use hands and fingers to handle, feel, or operate objects, tools or controls, and reach with hands and arms. The employee is frequently required to stand, talk and hear.

Quality Control Associate II - Revvity

BioLegend, Inc. (a Revvity, Inc. Company) develops world-class, cutting-edge antibodies and reagents for biomedical research, manufactured in our state-of-the-art facility in San Diego, CA. Our mission is to accelerate research and discovery by providing the highest quality products at an outstanding value, along with superior customer service and technical support. Our product expertise covers a diverse set of research areas including Immunology, Neuroscience, Cancer, Stem cells, and Cell Biology.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Job Summary&lt;br&gt;&lt;br&gt;&lt;/strong&gt;At BioLegend we are dedicated to commercializing high quality reagents to support the research community for legendary discoveries. The Associate for BioLegend’s Quality Control group will test products such as antibodies and proteins in the following application(s): flow cytometry, immunohistochemistry, western blotting, ELISA, multiplex immunoassays and/or functional bioassays. The candidate will perform all aspects of the assays following SOPs and ISO requirements. Additional responsibilities include culturing mammalian cell lines, isolating primary cells, and maintaining laboratory equipment and supplies. The candidate will assist with troubleshooting, efficiency and process improvement projects, and creation and modification of SOPs. The associate will generate and present data summaries, provide ETAs, and help train others on specific protocols. We are looking for a highly motivated person who loves science and wants to be part of a dynamic and fast paced team.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Essential Functions&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.&lt;br&gt;&lt;br&gt;&lt;ul&gt;&lt;li&gt;Perform testing of products in a timely manner&lt;/li&gt;&lt;li&gt;Perform aseptic cell culture&lt;/li&gt;&lt;li&gt;Isolate primary cells and tissues&lt;/li&gt;&lt;li&gt;Perform data analysis and document results&lt;/li&gt;&lt;li&gt;Maintain a safe and clean laboratory&lt;/li&gt;&lt;li&gt;Assist with troubleshooting projects, generate data summaries&lt;/li&gt;&lt;li&gt;Support efficiency and process improvement projects&lt;/li&gt;&lt;li&gt;Train others on specific laboratory protocols&lt;/li&gt;&lt;li&gt;Other projects or responsibilities as may be required.&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Minimum Qualifications – Education And Experience&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Bachelor’s degree in a scientific discipline&lt;/li&gt;&lt;li&gt;Experience with some of the following applications: flow cytometry, western blotting, Immunoprecipitation, bioassays, ELISA and IHC/ICC is a big plus.&lt;/li&gt;&lt;li&gt;&amp;gt;3 years working experience in a laboratory environment&lt;/li&gt;&lt;li&gt;Familiarity with basic lab equipment and knowledge of lab safety protocols&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Preferred Qualifications – Education And Experience&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Experience in sterile cell culture technique&lt;/li&gt;&lt;li&gt;Excellent organization, communication, and problem-solving skills&lt;/li&gt;&lt;li&gt;Proven ability to multi-task&lt;/li&gt;&lt;li&gt;Excellent documentation skills&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;em&gt;The base salary range for this full-time position is &lt;/em&gt;$28-$29.80/hour&lt;em&gt;. This range reflects the minimum and maximum target for a new hire in this position. The base pay actually offered to the successful candidate will take into account internal equity, work location, and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process. &lt;br&gt;&lt;br&gt;&lt;/em&gt;&lt;em&gt;Please note that base pay is only one part of our total compensation package and is determined within a range. This range allows for the successful candidate to have an opportunity to progress within the position and develop at our company. This base pay range does not take into account bonuses, equity, or other benefits which may be applicable and are dependent on the level and position offered.&lt;br&gt;&lt;br&gt;&lt;/em&gt;&lt;strong&gt;Work Environment &amp;amp; Physical Demands - Lab&lt;br&gt;&lt;br&gt;&lt;/strong&gt;While performing the duties of this job, the employee regularly works in a laboratory environment with occasional data entry on a computer. Occasional exposure to a warehouse environment.&lt;br&gt;&lt;br&gt;The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.&lt;br&gt;&lt;br&gt;While performing the duties of this job, the employee is regularly required to use hands and fingers to handle, feel, or operate objects, tools or controls, and reach with hands and arms. The employee is frequently required to stand, talk and hear.

Quality Control Associate II

You must have a degree in Life Science (Biomedical/Medical Genetics preferred), experience in an NABL-accredited lab, and goal-oriented with an understanding of process flow and TAT.

You will culture samples, prepare karyograms, train junior staff, analyze data, ensure TAT compliance, maintain instruments, and follow SOPs and GLP while managing urgent cases.

Healthcare

<div>
 <div>
 Job Description –Cytogeneticist/Senior Cytogeneticist
 
 About us: Revvity is an international developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world’s greatest health challenges. We have deep experience in our field, having been part of Revvity’s 85-year history, and are excited for our future as a dedicated life sciences &amp; diagnostics business. Our diverse team of 11,000+ colleagues from around the globe are vital to our success and the reason we’re able to push boundaries in pursuit of better human health.
 
 Site – India
 Business Unit - Diagnostic Laboratory Operations
 
 Purpose of the main job
 Technical work related to processing of various samples for cytogenetic study
 Main responsibilities
 <ul>
 <li>Culturing different samples for karyotyping. Expertise in checking confluence of cells for long term cultures.</li>
 <li>Harvesting, slide preparation, capturing of images and preparing karyograms.</li>
 <li>Pre-finalizing of reports</li>
 <li>2nd day Processing of samples for FISH and analysis</li>
 <li>Train the junior staff in different techniques</li>
 <li>Data analysis, and report entry in LIMS</li>
 <li>First level authorization of reports</li>
 <li>Routinely follow the Samples from receipt to reporting and storage and ensure TAT compliance.</li>
 <li>Prepare daily or monthly reports as needed for the number of samples processed, reported and cancelled.</li>
 <li>Takes ownership of the processes and tasks handed over – maintenance of Instruments and follow the calibration of instruments and pipettes.</li>
 <li>Keep track of ILC samples for audit purpose.</li>
 <li>Keep track of cases that are urgent.</li>
 <li>Keep track of completed cases for critical alerts</li>
 <li>Take responsibility for following quality SOPs and GLP.</li>
 </ul>
 
 <h1 class="jobSectionHeader"> REQUIRED COMPETENCE</h1>
 Education - Graduate/Postgraduate in Life science, preferably in Biomedical genetics /Zoology/ Medical genetics/Applied Genetics/ Human Genetics.
 Required work experience related to position 
 Junior Cytogeneticist – Fresher or 1 – 2 years of experience
 Senior Cytogeneticist - 3 to 5 years of experience
 
 Special requirements / Skills / Attributes
 </div>
 Experience in an NABL accredited Cytogenetic laboratory
 
 <h1 class="jobSectionHeader"> Competency Required</h1>
 Strategic Perspective:
 <ul>
 <li>Successfully complete individual goals settings.</li>
 <li>Ensure proper process flow and TAT for different tests in order to remain competitive in the lab service business.</li>
 </ul>
</div>



 
  Job Description –Cytogeneticist/Senior Cytogeneticist
  
   About us: Revvity is an international developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world’s greatest health challenges. We have deep experience in our field, having been part of Revvity’s 85-year history, and are excited for our future as a dedicated life sciences & diagnostics business. Our diverse team of 11,000+ colleagues from around the globe are vital to our success and the reason we’re able to push boundaries in pursuit of better human health.
  
   Site – India
   Business Unit - Diagnostic Laboratory Operations
  
  Purpose of the main job
  Technical work related to processing of various samples for cytogenetic study
  Main responsibilities
  
   Culturing different samples for karyotyping. Expertise in checking confluence of cells for long term cultures.
   Harvesting, slide preparation, capturing of images and preparing karyograms.
   Pre-finalizing of reports
   2nd day Processing of samples for FISH and analysis
   Train the junior staff in different techniques
   Data analysis, and report entry in LIMS
   First level authorization of reports
   Routinely follow the Samples from receipt to reporting and storage and ensure TAT compliance.
   Prepare daily or monthly reports as needed for the number of samples processed, reported and cancelled.
   Takes ownership of the processes and tasks handed over – maintenance of Instruments and follow the calibration of instruments and pipettes.
   Keep track of ILC samples for audit purpose.
   Keep track of cases that are urgent.
   Keep track of completed cases for critical alerts
   Take responsibility for following quality SOPs and GLP.
  
  
   REQUIRED COMPETENCE
   Education - Graduate/Postgraduate in Life science, preferably in Biomedical genetics /Zoology/ Medical genetics/Applied Genetics/ Human Genetics.
   Required work experience related to position 
  Junior Cytogeneticist – Fresher or 1 – 2 years of experience
  Senior Cytogeneticist - 3 to 5 years of experience
  
  Special requirements / Skills / Attributes
 
 Experience in an NABL accredited Cytogenetic laboratory
 
  Competency Required
  Strategic Perspective:
 
  Successfully complete individual goals settings.
  Ensure proper process flow and TAT for different tests in order to remain competitive in the lab service business.
 



Revvity

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