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About GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a leading global biotechnology group founded in 2002. With a strong presence across North America, Europe, Greater China, and Asia Pacific, we specialize in four key areas driven by our cutting-edge gene synthesis technology: Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.At GenScript, we are dedicated to our vision of becoming the most reliable biotech company worldwide, enhancing the health of both humanity and nature through biotechnology.Unlock Your Potential with the Gen-X Program at GenScript!We at GenScript Biotech are excited to introduce the Gen-X Program, an initiative aimed at cultivating exceptional talent in life sciences. We are searching for innovative and bright individuals to join our vibrant team.About GenScriptFounded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotech and healthcare by equipping researchers and companies with essential tools for developing groundbreaking treatments and products. With over 5,700 employees, we have proudly served more than 200,000 customers across over 100 countries and regions, all guided by our mission to make people and nature healthier through biotechnology.Discover more at: https://www.genscript.comProgram OverviewThe Gen-X Program is meticulously crafted to transform high-potential Ph.D. and MBA candidates into the leaders of tomorrow, fostering a cross-functional mindset, strategic business insight, and innovation-driven leadership.

Join Credera, a pioneering global consulting firm that integrates transformative consulting skills, extensive industry expertise, AI, and technical proficiency to enhance customer experiences and drive growth across diverse sectors. We are constantly adapting our services to align with the future needs of organizations and adhere to contemporary best practices. Our distinct global approach offers customized solutions, reshaping some of the most impactful brands and entities worldwide.Our workforce, the core of our organization, is driven by a passion for making a significant difference in the lives of our clients, colleagues, and communities. This enthusiasm influences how we allocate our time, resources, and talents. We are proud of our commitment to our people and the recognition we've received globally. Visit our employer awards page for more details: https://www.credera.com/awards-and-recognition

At Credera, we are a global consulting firm that merges transformational consulting prowess with deep industry insights, AI innovation, and technology expertise to create exceptional customer experiences and drive accelerated growth across diverse sectors. We are committed to evolving our services to adapt to the future needs of organizations while upholding modern best practices. Our unique global approach ensures tailored solutions that transform leading brands and organizations around the globe.Our employees are the heartbeat of our company, driven by a passion for making a significant impact on our clients, colleagues, and communities. This dedication shapes how we allocate our time, resources, and talents. Our commitment to our people and our work has garnered global recognition. For more information, please visit our employer awards page: https://www.credera.com/awards-and-recognition

Credera is a distinguished global consulting firm that merges transformational consulting expertise, profound industry insights, AI capabilities, and technology proficiency to foster exceptional customer experiences and drive rapid growth across diverse sectors. We are committed to evolving our services to align with the future needs of organizations while embodying modern best practices. Our distinctive global perspective allows us to offer customized solutions that transform some of the most influential brands and organizations across the globe.Our employees are the heartbeat of our firm, passionately dedicated to making a significant impact on our clients, colleagues, and communities. This commitment fuels how we allocate our time, resources, and talents. Our dedication to our people and the quality of our work has garnered global recognition. Explore our accolades on our awards page.

Join Our Team as an Indirect Procurement Lead!At GenScript, we are seeking a dynamic and experienced Indirect Procurement Lead focused on Capital Expenditures (CapEx) and construction projects. This role will be pivotal in driving strategic sourcing initiatives that align with our organizational objectives and enhance value across our operations.Your Role: You will oversee the entire source-to-pay procurement process, manage project execution, ensure compliance with company protocols, and assess vendor performance. The position will require you to negotiate contracts, identify cost-saving opportunities, and monitor key performance indicators related to cost savings, delivery, compliance, and quality.Collaboration is key as you will work closely with cross-functional teams, act as the primary contact for legal and internal stakeholders, and champion procurement compliance and continuous improvement. Additionally, you will support our vision of making humans and nature healthier through biotechnology.

About GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a leading global biotechnology company established in 2002, with a strong presence across North America, Europe, Greater China, and the Asia Pacific region. Our business spans four key domains leveraging cutting-edge gene synthesis technology, including Life Science Contract Research Organization (CRO), enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.At GenScript, we are dedicated to our vision of becoming the world's most trusted biotechnology company, enhancing the health of humans and nature through our innovative biotechnological solutions.Key ResponsibilitiesSynthesize targeted genes as per departmental protocols to meet customer requirements.Conduct a range of experimental procedures including PCR, Ligation Transformation, Bacterial Inspection, Plasmid Construction, and Quality Inspection.Perform data analysis and evaluate results to ensure accuracy.Strictly adhere to safety and production management regulations while independently conducting experiments involving Gene Synthesis, Vector Construction, Gene Mutation, Plasmid Extraction, Sequence Analysis, Sequencing, PCR & qPCR, and Reagent Preparation.Timely report any production issues and collaborate with the team to resolve them.Ensure proper handover of experimental tasks and conduct a basic analysis of any unfinished experiments.Complete additional tasks as assigned by supervisors.

About GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a leading global biotechnology organization founded in 2002. With a strong presence in North America, Europe, Greater China, and Asia Pacific, GenScript specializes in several key areas driven by its cutting-edge gene synthesis technology. These areas include Life Science CRO operations, enzyme and synthetic biology products, biologics development and manufacturing, and innovative cell therapy solutions.GenScript is dedicated to its mission of becoming the world's most trusted biotech company, enhancing the health of both humanity and nature through innovative solutions.Key ResponsibilitiesProtein ExpressionConduct resuscitation, passage, transfection, and culture of mammalian cells, including HEK293 and CHO.Perform data analysis and processing of cell culture experiments, including the preparation of experimental records and reports.Operate bioreactors and centrifuges, and prepare necessary buffers and reagents.Formulate and update standard operating procedures (SOPs) while summarizing and solidifying work experiences.Manage laboratory instruments, ensuring maintenance as required.Complete other tasks as assigned by the supervisor.Protein PurificationPurify mammalian recombinant antibodies and proteins using techniques such as affinity chromatography, ion-exchange chromatography, and size exclusion chromatography.

About GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a leading global biotechnology group dedicated to advancing human health and environmental sustainability through innovative biotechnology solutions. Established in 2002, GenScript has cultivated a robust global footprint across North America, Europe, Greater China, and the Asia Pacific region. Our diverse offerings are anchored in our pioneering gene synthesis technology, which spans four primary sectors: Life Science CRO operations, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.At GenScript, we are passionately committed to becoming the most trusted biotechnological partner worldwide, enhancing health and wellness for people and nature alike through our cutting-edge biotechnology advancements. Job Responsibilities:Assist in processing and confirming shipping documentation for logistics operations.Support the preparation and maintenance of shipping documents and customs declarations.Contribute to data entry and record-keeping for daily order processing and shipping tasks.Assist in organizing picking, packing, and shipping procedures.Help monitor and update data related to inbound and outbound shipments.Support tracking of freight costs and assist in data analysis.Communicate with internal teams to ensure logistics align with production and inventory needs.Assist in basic coordination with freight forwarders and customs brokers.Help organize and maintain compliance documentation for import and export operations.Assist in preparing transaction data for audits.

About GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a leading global biotechnology company established in 2002. With a strong international presence spanning North America, Europe, Greater China, and Asia Pacific, GenScript specializes in gene synthesis technology and operates in four primary sectors: Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.At GenScript, we are dedicated to our vision of becoming the most trusted biotech partner in the world, enhancing health for humanity and nature through innovative biotechnology solutions.Position: Procurement InternLine Manager: Procurement SpecialistKey Responsibilities:Assist in daily procurement operations, including tracking purchase requests and preparing Request for Quotations (RFQs) for vendors.Facilitate the generation and follow-up of purchase orders (POs) using SAP software.Organize and maintain procurement documentation, such as contracts and supplier records.Support vendor management initiatives, including the setup of new vendor accounts in SAP.Communicate with vendors to monitor order fulfillment and delivery status.Contribute to contract and supplier management by drafting basic procurement contracts and coordinating with legal teams.Ensure compliance with contract terms regarding delivery timelines, quality standards, and payment conditions.Collaborate with internal departments, including Quality Assurance, logistics, and global procurement, to effectively address supplier-related issues.Collect and aggregate procurement data to support decision-making and reporting processes.

At Credera, we are a global consulting firm dedicated to merging transformational consulting with deep industry expertise, AI, and technology to enhance customer experiences and drive growth across various sectors. Our commitment to innovation ensures that we adapt our services to meet the evolving needs of modern organizations, showcasing best practices while delivering tailored solutions that positively impact some of the most influential brands worldwide. Our employees, who are the heart of our organization, are driven by a passion for making a significant impact on our clients, colleagues, and communities. This dedication influences how we allocate our time, resources, and talents. Our global recognition for our commitment to our workforce and our work is a testament to our culture. For details, please visit our employer awards page: https://www.credera.com/awards-and-recognition

About GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a leading global biotechnology company founded in 2002, renowned for its innovative gene synthesis technology. With a strong global presence spanning North America, Europe, Greater China, and the Asia Pacific, GenScript is committed to enhancing the health of humanity and nature through biotechnology.Our mission is to be the most reliable biotech company globally, striving to improve lives through advanced biotechnological solutions.Key ResponsibilitiesConduct concentration tests, SDS-PAGE, Western blot analysis, HPLC, and endotoxin testing on protein samples.Summarize, analyze, and process experimental data, identifying and addressing unqualified data, while maintaining comprehensive experimental records.Formulate and update standard operating procedures (SOPs), documenting and refining work experiences.Manage laboratory instruments and perform necessary maintenance as required.Complete additional tasks assigned by the supervisor.

Credera is a leading global consulting firm that combines transformative consulting capabilities with deep industry insights, artificial intelligence, and cutting-edge technology expertise to craft exceptional customer experiences and drive accelerated growth across various sectors. Our commitment to innovation ensures that we continuously adapt our services to align with the evolving needs of organizations worldwide, reflecting modern best practices. Through our unique global approach, we deliver tailored solutions that transform some of the most influential brands and organizations around the globe.At Credera, our employees are the cornerstone of our success. We are passionate about making a significant impact on our clients, colleagues, and communities. This passion fuels how we allocate our time, resources, and talents. Our dedication to our team and their work has earned us global recognition. To learn more about our accolades, please visit our employer awards page.

About GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a leading global biotechnology company dedicated to improving health through innovative solutions. Since our inception in 2002, we have established a robust presence across North America, Europe, Greater China, and Asia Pacific. Our core competencies encompass a wide range of services, including life science contract research, enzyme and synthetic biology products, biologics development, manufacturing, and advanced cell therapies.At GenScript, we are driven by our vision to be the most trusted biotech partner globally, committed to enhancing the health of individuals and the environment through our biotechnological advancements.Key ResponsibilitiesExecute experiments while analyzing and processing data, and identifying inconsistencies.Engage in various research activities, including cell culture, protein purification, concentration testing, SDS-PAGE, Western blot analysis, endotoxin testing, HPLC, and LC-MS analysis of protein samples.Set up experiments, manage sample processing, and maintain detailed experimental documentation.Contribute to multiple R&D projects as a key member of the project team.Ensure meticulous documentation of all experimental records.Participate in routine laboratory maintenance tasks, including 5S organization, stocktaking, replenishment of consumables, and regular equipment checks to ensure operational efficiency.Adhere to all safety protocols and standard operating procedures to maintain a safe working environment.Complete additional tasks as assigned by the supervisor.Key RequirementsDiploma or Bachelor’s degree in a relevant field, such as Life Sciences or Biotechnology.Strong analytical skills and attention to detail.Ability to work effectively both independently and as part of a collaborative research team.Familiarity with laboratory safety practices.

At Credera, we are a global consulting firm that integrates transformational consulting with deep industry expertise, cutting-edge AI, and advanced technology solutions to create exceptional customer experiences and drive substantial growth across a variety of sectors. We are committed to adapting our services to align with the evolving needs of modern organizations while embodying best practices. Our distinctive global approach enables us to deliver customized solutions, transforming leading brands and organizations around the world.Our team members, the heart of our organization, are dedicated to making a significant impact on our clients, colleagues, and communities. This commitment informs how we allocate our time, resources, and talents. We take pride in our dedication to our employees, which has been acknowledged internationally. Explore our accolades on our awards page.

About GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a pioneering global biotechnology group, established in 2002. With a robust global footprint, GenScript operates across North America, Europe, Greater China, and the Asia Pacific region. Our core business focuses on four major categories led by our cutting-edge gene synthesis technology, including Life Science Contract Research Organization (CRO) services, enzyme and synthetic biology products, biologics development and manufacturing, and advanced cell therapy solutions.At GenScript, we are dedicated to our vision of becoming the most trusted biotechnology company globally, enhancing health for people and nature through innovative biotechnological solutions.Job Title: SAP Engineer (MM/WM/PP/SD)Location: Pennington, NJThe salary range for this role is approximately $110,000 - $120,000, commensurate with experience.Position SummaryGenScript is on the lookout for a skilled SAP Engineer with extensive hands-on experience with SAP MM, WM, PP, and SD modules to enhance our SAP application framework. This role necessitates profound functional expertise combined with solid business acumen, particularly in WM and PP.Key ResponsibilitiesOversee daily operations, maintenance, and administration of SAP MM/WM/PP/SD modules.Lead or assist in rollout projects and continuous improvement initiatives related to MM/WM/PP/SD.Ensure master data integrity and compliance within MM/WM/PP/SD; adhere to Standard Operating Procedures (SOPs).Collect business requirements, draft functional specifications, organize testing (UT, IT, UAT), and monitor post-go-live adoption.

Credera is a distinguished global consulting firm that merges transformational consulting capabilities with profound industry knowledge, cutting-edge AI, and technology expertise. Our mission is to deliver exceptional customer experiences and drive accelerated growth across diverse industries. We are committed to evolving our services to meet the future needs of organizations while adhering to modern best practices. Our distinctive global approach enables us to provide customized solutions that transform leading brands and organizations worldwide.Our employees are the heartbeat of our company, fueled by a passion for making a meaningful impact on clients, colleagues, and communities. This drive shapes our investments of time, resources, and talent. Our dedication to our people and work has garnered global recognition. For more details, please visit our employer awards page: https://www.credera.com/awards-and-recognition

At Credera, a leading global consulting firm, we merge transformational consulting capabilities with profound industry expertise, AI, and technology to craft exceptional customer experiences and drive accelerated growth across diverse sectors. Our commitment to innovation ensures that we continuously adapt our services to meet the evolving needs of organizations worldwide, adhering to modern best practices. We take pride in our unique global approach, offering tailored solutions that significantly impact some of the most influential brands and organizations globally.Our employees are the heartbeat of Credera, fueled by a passion to create a meaningful impact on our clients, colleagues, and communities. This dedication shapes how we allocate our time, resources, and talents. Our unwavering commitment to our team and our work has earned us global recognition. Explore our accolades on our awards and recognition page.

About GenScript: GenScript Biotech Corporation (Stock Code: 1548.HK) is a leading global biotechnology group founded in 2002, with a robust presence across North America, Europe, Greater China, and the Asia Pacific region. We specialize in four main business areas driven by our cutting-edge gene synthesis technology, including Life Science CRO operations, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is dedicated to its vision of being the most trusted biotech company globally, committed to enhancing human and environmental health through innovative biotechnology.Job Overview: As a Laboratory Supervisor, you will lead and oversee daily laboratory operations, ensuring efficiency and accuracy in all processes. This role requires a solid background in laboratory practices, alongside significant experience in team management. The ideal candidate will be adept at setting clear team objectives, developing performance assessment criteria (PBC/KPI), and motivating the team to meet their goals.

Credera is a leading global consulting firm that merges transformative consulting capabilities with profound industry knowledge, AI, and technology expertise. We strive to enhance customer experiences and foster rapid growth across diverse industries. Our commitment to evolution allows us to continuously adapt our services to the demands of modern organizations, embodying best practices that are reflective of today’s market. Our distinct global strategy delivers customized solutions, enabling the transformation of some of the world’s most influential brands and organizations.Our dedicated team members are the cornerstone of our success, driven by a passion for making a significant impact on our clients, colleagues, and communities. This enthusiasm informs how we allocate our time, resources, and talents. Our commitment to our people and our work has garnered global recognition. To learn more about our accolades, please visit our employer awards page: https://www.credera.com/awards-and-recognition

Join the Modera Wealth Management Team! At Modera Wealth Management, we pride ourselves on being an independent, fee-only advisory firm dedicated to positively transforming our clients' financial lives through detailed financial planning and strategic investment management. As a rapidly growing firm, we offer extensive career development opportunities from entry-level positions to ownership roles. Since our inception in 1983, we have committed ourselves to providing personalized client service with a unique blend of professional expertise and a welcoming approach. We have expanded to over 200 employees across 19 offices on the East Coast, managing assets exceeding $15 billion for over 6,000 clients, including individuals, families, and businesses. Position Overview: We are seeking a dynamic Planning Associate to support our lead advisors at our Westwood, NJ office. Key Responsibilities: Assist Lead Advisors in delivering exceptional client service during various client interactions, including the onboarding of new assets. Ensure timely and accurate completion of tasks while managing multiple projects and keeping the team informed of progress. Help prepare materials for client meetings. Draft Investment Policy Statements and asset allocation reports for clients. Communicate effectively with clients and their legal and financial representatives, both verbally and in writing. Attend client meetings, assisting with documentation and follow-up actions. Demonstrate a collaborative spirit by helping with visitor inquiries, answering phones, and scheduling meetings as necessary. Long-term Duties and Responsibilities: Conduct comprehensive client interviews to collect personal financial data and establish planning objectives. Create detailed financial plans that encompass investment strategies, tax considerations, retirement and estate planning, executive compensation, risk management, cash flow, and education funding. Support clients in implementing their financial plans. Participate in client meetings to assist the primary relationship manager. Review and interpret investment allocation trading reports. Collaborate with the client service team to facilitate and oversee client service activities. Be open to occasional travel as required.