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Experience Level
Entry Level
Qualifications
Associate's degree in a scientific field (or equivalent experience) with a minimum of 2 years of relevant experience; or a Bachelor's degree with at least 1 year of relevant experience; or a Bachelor's degree in Engineering with no prior experience required. Demonstrated ability to apply job skills and company policies to successfully complete assigned tasks. Ability to work on semi-routine assignments while recognizing when deviations from standard practices are necessary. Proficiency in following established procedures for routine tasks, with the ability to seek guidance on new assignments.
About the job
Join AbbVie as a Manufacturing Technician II, where you will play a crucial role in our cGMP manufacturing operations within our biologics production facility. Collaborate with engineers for set-up and calibration tasks while executing rework and quality testing processes for various parts, components, and final materials. Utilize advanced software systems (including LIMS, SAP, and automated control systems) to gather and analyze operational data, enabling real-time adjustments to products and equipment. You will also contribute to the development and refinement of methods and procedures aimed at optimizing the manufacturing process.
Key Responsibilities
Oversee the shipping of finished materials
Manage and maintain inventory levels
Conduct sampling of in-process and raw materials
Operate glass washers and autoclaves
Prepare buffers and media
Prepare equipment for cleaning in place (CIP) and sterilization in place (SIP)
Engage in cell culture processes from vial thaw to production scale
Execute column chromatography and tangential flow filtration
About AbbVie Inc.
About AbbVieAt AbbVie, we are committed to discovering and delivering innovative therapies that address some of the most serious health challenges facing humanity today, while preparing for the medical hurdles of tomorrow. Our impactful work spans several key therapeutic areas, including immunology, oncology, and neuroscience, as well as our esteemed Allergan Aesthetics portfolio. To learn more about our mission and values, please visit www.abbvie.com. Connect with us on LinkedIn, Facebook, Instagram, X, and YouTube.
Role OverviewJoin AbbVie as a Manufacturing Technician II, where you will play a crucial role in our cGMP manufacturing operations within our biologics production facility. Collaborate with engineers for set-up and calibration tasks while executing rework and quality testing processes for various parts, components, and final materials. Utilize advanced software systems (including LIMS, SAP, and automated control systems) to gather and analyze operational data, enabling real-time adjustments to products and equipment. You will also contribute to the development and refinement of methods and procedures aimed at optimizing the manufacturing process.Key ResponsibilitiesOversee the shipping of finished materialsManage and maintain inventory levelsConduct sampling of in-process and raw materialsOperate glass washers and autoclavesPrepare buffers and mediaPrepare equipment for cleaning in place (CIP) and sterilization in place (SIP)Engage in cell culture processes from vial thaw to production scaleExecute column chromatography and tangential flow filtration
About the Role AbbVie is hiring a Scientist II for the Multispecifics Engineering group within Discovery Biotherapeutics in Worcester. This position centers on designing and developing new biotherapeutic solutions that target important healthcare challenges. What You Will Do Apply scientific knowledge to create and advance biotherapeutic candidates Work closely with colleagues from different disciplines to move projects from early concepts through execution Support AbbVie's mission to improve patient outcomes through innovative research
Job Overview:We are looking for a dynamic and collaborative technical leader to spearhead the innovation and development of our lipid nanoparticle (LNP) platform technology. The ideal candidate will engage with cross-functional teams to design and enhance LNPs and tLNP platform technology, supporting our innovative pipeline. This role involves establishing and directing our LNP innovation strategy, focusing on lipid design, chemistry, formulations, and targeted non-viral delivery systems, with a vision towards future product development and pipeline expansion. Key Responsibilities:Act as a scientific and technical authority within the organization, particularly in LNP-based drug delivery systems for nucleic acids.Drive the innovation, development, and optimization of the targeted LNP platform to support programs across various therapeutic areas.Possess an in-depth understanding of lipid and LNP design principles, stability, and scale-up processes, ensuring successful transition of drug product formulation production and purification unit operations from bench to larger scales.Develop LNP-related project plans, timelines, and budget forecasts, ensuring alignment with key stakeholders and organizational objectives.Lead the analysis of complex data sets, clearly communicating findings during internal program meetings, cross-functional reviews, and governance forums.Collaborate extensively with discovery and development teams, including mRNA, antibody, analytical, and process development groups, to propel pipeline initiatives.Oversee the drafting, review, and approval of technical reports pertinent to the function.Manage and mentor a team of over 10 scientists and associates across AbbVie’s East and West Coast sites. 
PurposeWe are looking for a skilled and dedicated Senior Financial Analyst to support our Manufacturing, Engineering, and Contracting Operations at AbbVie’s Biologics Research Center in Worcester, MA. In this pivotal role, reporting directly to the Cost Accounting Manager, you will collaborate with cross-functional leadership teams in Production, Planning & Logistics, Purchasing, R&D, and External Commercial Manufacturing. Your expertise will be essential in managing budgets for various late-stage clinical programs/projects, assisting management with operational spend analysis, and contributing to the Plant's financial planning processes, including Plan, Update, Long Range Plan, and Last Best Estimate. ResponsibilitiesOversee project/program budgets for multiple late-phase clinical programs, conducting variance analysis and delivering actionable insights to management.Collaborate with Finance leadership to manage the Plant's operational expenditures, providing cost center owners with relevant variance analyses and strategic input. Develop comprehensive reporting schedules and models to enhance forecasting accuracy.Support the financial planning cycles of the Plant, including preparation and analysis of operational spend.Execute month-end processes, including inventory reconciliations, booking journal entries, and analyzing manufacturing cost variances.Facilitate everyday business operations, including standard costing of new materials and ensuring the timely completion of manufacturing process orders.Assist in the annual material standard-setting process.Create and implement dashboards and reports necessary for business continuity.
Role Overview AbbVie Inc. is hiring a Scientist II for the Immunopharmacology group in Worcester. This position centers on peptide discovery and research. The scientist will contribute expertise to advance research projects and support the development of new therapeutic solutions.
Join our dynamic and innovative team at AbbVie, where we are dedicated to developing groundbreaking mRNA platforms. As a Scientist II, you will contribute to cutting-edge research and development efforts aimed at advancing therapeutic solutions in a collaborative environment.
Join AbbVie as the Director of External Manufacturing, where you will play a pivotal role in overseeing and enhancing our external manufacturing operations. Collaborating closely with cross-functional teams, you will ensure the highest quality standards and operational excellence are met while driving strategic initiatives that align with our commitment to innovation and patient care.
As the Associate Director of External Manufacturing, you will serve as the primary contact for supplier relationships, overseeing the strategic initiatives, organization, and technical support necessary for the effective management of our designated product supply. This role is pivotal in ensuring that high-quality products are manufactured in compliance with both local and international regulations, while also being delivered on schedule and within budget. You will manage various projects and programs that influence AbbVie, aiming to ensure that our products are cost-effective, marketable, and manufacturable, maximizing profitability throughout their life cycle. Through matrix management of cross-functional teams, you will lead diverse groups without direct authority, providing essential program management support and acting as the primary AbbVie representative for coordinating operations related to existing and new products manufactured by our suppliers.Key Responsibilities:Engage in the negotiation of Manufacturing Service Agreements and amendments, ensuring compliance with their terms.Develop effective planning and material procurement strategies to supply the Third Party Manufacturer (TPM) with necessary materials.Communicate product forecasts to the TPM and agree on manufacturing and delivery timelines. Collaborate with Supply Chain and Planning to ensure supplier delivery aligns with demand forecasts.Contribute to the Financial Operating Plan, Updates, Long Range Planning (LRP), and Standard processes, ensuring financial objectives are met.Coordinate the Steering Committee and ensure that Virtual Operation Teams convene regularly to assess performance and address any issues.Prepare status reports and updates for senior leadership review.In partnership with technical and quality teams, regularly assess process performance, quality trends, and devise improvement plans.Establish governance frameworks, guidelines, and communication channels, ensuring that suppliers have the requisite quality systems in place to meet regulatory standards and follow up on inspection responses.Coordinate with Quality Assurance to conduct annual quality management reviews and periodic audits of the TPM, ensuring timely investigation of deviations and product disposition decisions. Establish performance metrics and monitor them periodically.Develop, implement, and manage programs and projects, focusing on scope, cost, time, resource management, communication, and risk management throughout the project lifecycle.
Join AbbVie, a global biopharmaceutical company dedicated to discovering and delivering innovative medicines to address serious health issues. We are currently seeking a Manufacturing Supervisor I to oversee our manufacturing operations from Wednesday to Saturday, 4 PM to 2:30 AM. In this role, you will be responsible for managing a team of production staff, ensuring compliance with safety and quality standards, and driving operational efficiency. This is an excellent opportunity to contribute to the production of life-changing therapies.
The Manufacturing Supervisor III oversees evening shift operations at AbbVie's Worcester site. This role manages daily manufacturing activities, ensuring products meet quality standards and production runs efficiently. Key responsibilities Lead and direct manufacturing teams during the evening shift Monitor production processes to maintain product quality Ensure compliance with industry regulations and internal procedures Promote efficiency across all manufacturing activities Requirements Experience supervising manufacturing operations Strong understanding of quality standards and regulatory compliance Ability to lead teams and coordinate shift activities Willingness to work the evening shift at the Worcester facility
As the Associate Director of External Manufacturing for Small Molecules at AbbVie, you will play a pivotal role as the primary point of contact for supplier relationships. Your expertise will guide strategic initiatives and provide essential technical support to ensure the smooth management of product supply. You will be responsible for overseeing the manufacturing of high-quality products in adherence to both local and international regulations, ensuring timely delivery in line with established forecasts and budgets.This role encompasses project and program management that directly impacts AbbVie, ensuring that our products remain marketable, manufacturable, and profitable throughout their lifecycle. Leveraging your leadership skills, you will effectively manage cross-functional teams in a matrix environment without direct authority, providing crucial program management support and serving as the main representative for AbbVie in coordinating operations related to existing and new products with suppliers.Key Responsibilities:Lead negotiations for Manufacturing Service Agreements and amendments, ensuring compliance with contract terms.Implement effective planning and material procurement strategies to support TPM needs.Communicate product forecasts to suppliers and collaborate on manufacturing and delivery schedules, ensuring alignment with demand forecasts.Engage in the development of the Financial Operating Plan and ensure financial targets are achieved.Coordinate Steering Committee meetings and ensure the Virtual Operation Teams regularly assess performance and address any issues.Prepare status reports and updates for senior leadership.Collaborate with technical and quality teams to review process performance and implement process improvements.Establish governance and communication protocols, ensuring suppliers maintain necessary quality systems and documentation for regulatory compliance.Coordinate with QA for annual quality management reviews and audits of TPM, ensuring timely investigation of deviations and product disposition decisions.Manage programs/projects, focusing on scope, cost, time, resource management, communication, and risk management through all project phases.
AbbVie is seeking a Business Operations Associate based in Worcester. This position plays a part in supporting daily operations and assists with essential business activities throughout the organization. Role overview The Business Operations Associate works to improve processes and increase efficiency in AbbVie's operations. The role involves collaborating with teams to ensure business functions run smoothly and contribute to the company's healthcare initiatives. Key responsibilities Support day-to-day business operations Assist with process improvement projects Contribute to efforts that drive operational efficiency Location This position is based in Worcester.
AbbVie is hiring a Scientist II for Purification Development in Worcester. This role centers on improving purification processes to advance new therapeutic products. The Scientist II partners with other scientists to support research goals and drive process improvements. Key Responsibilities Develop and refine purification methods for therapeutic products Work with colleagues to troubleshoot and optimize laboratory protocols Use advanced technologies to improve process efficiency and reliability Share scientific expertise in team discussions and project planning Collaboration and Impact This position involves close teamwork with scientists across disciplines. The focus is on applying technical knowledge to solve challenges and enhance purification workflows that support AbbVie's research pipeline.
About the Role AbbVie is seeking a Senior Scientist II with a focus on Immunopharmacology and Peptide Discovery to join the team in Worcester. This position centers on leading research efforts that support the discovery and development of new peptide-based therapeutics. The work directly contributes to advancing AbbVie's drug development pipeline. What You Will Do Lead research projects in immunopharmacology and peptide discovery. Design and execute experiments to identify and characterize novel peptide therapeutics. Apply expertise in immunology and pharmacology to support drug development goals. Collaborate with multidisciplinary teams to move promising candidates forward. Location This position is based in Worcester.
AbbVie Inc. seeks a Principal Data Architect II to join the Biotherapeutics and Genetic Medicine group in Worcester. This position centers on building and maintaining data architecture that supports research and development in biotherapeutics and genetic medicine. Key Responsibilities Collaborate with cross-functional teams to define and document data requirements for projects in biotherapeutics and genetic medicine. Design and implement data architecture solutions that enable research, development, and operational workflows. Use data governance best practices to ensure data integrity and make essential data accessible across platforms. Support the broader data strategy and contribute to the advancement of analytics tools for R&D. Team Focus This group specializes in biotherapeutics and genetic medicine, providing a strong data foundation to drive innovative research.
Join AbbVie as a Principal Research Scientist II, where you will leverage your expertise to drive innovative research projects. Collaborate with a dynamic team of scientists and contribute to groundbreaking advancements in healthcare. This role offers the opportunity to work on complex problems, develop novel solutions, and make a significant impact in the field of research.
AbbVie Inc. seeks a Principal Machine Learning Scientist II for its Biotherapeutics and Genetic Medicine team in Worcester. This role centers on advancing research and development efforts in these fields. Key Responsibilities Use advanced machine learning techniques to drive progress in genetic medicine research projects. Develop and refine new computational approaches that support scientific initiatives in biotherapeutics. Provide subject matter expertise to help shape research strategies and methodologies. Location This position is based in Worcester.
As a Manufacturing Supervisor III, you will leverage your specialized knowledge and extensive experience to oversee a team responsible for the safe and efficient production of our pharmaceutical products. You will lead the team in ensuring compliance with all safety, regulatory, and operational standards, while fostering a culture of excellence in customer service, product quality, and financial performance.Key Responsibilities:Safety: Champion the production safety program, ensuring safety remains a top priority. Conduct safety audits and regularly promote a culture with zero safety incidents.Team Leadership: Effectively deploy team members and delegate tasks to meet production schedules. Conduct regular one-on-ones and performance reviews, ensuring team engagement and timely approvals of attendance records.Operational Excellence: Coordinate shift activities to ensure production schedules are met. Facilitate smooth handovers between shifts for seamless operations.Regulatory Compliance: Ensure adherence to regulatory standards, proactively managing compliance processes including routine checks and addressing any compliance issues promptly.Performance Management: Manage cycle time and change-over improvements, spearheading process improvement initiatives to meet site metrics and expectations.Team Development: Invest in the growth of your team by providing training and opportunities for advancement, with a focus on Key Talent.
AbbVie is seeking a dynamic and experienced Senior Manager of Quality Control (CMC/QC) to join our dedicated team in Worcester. In this role, you will lead quality control initiatives, ensuring compliance with industry regulations while driving continuous improvement in our processes and systems.
AbbVie Inc. seeks an Associate Scientist in Process Development I to join its Worcester team. This entry-level position plays a key role in supporting the development and optimization of therapeutic product processes. The work centers on advancing products through hands-on laboratory efforts and teamwork. Key responsibilities Assist in developing and refining processes for therapeutic products Collaborate with scientists from diverse backgrounds to meet project objectives Build practical laboratory experience in process development Work environment The role is based on-site in Worcester, where close collaboration and daily interaction with the process development team are expected.
Role OverviewJoin AbbVie as a Manufacturing Technician II, where you will play a crucial role in our cGMP manufacturing operations within our biologics production facility. Collaborate with engineers for set-up and calibration tasks while executing rework and quality testing processes for various parts, components, and final materials. Utilize advanced software systems (including LIMS, SAP, and automated control systems) to gather and analyze operational data, enabling real-time adjustments to products and equipment. You will also contribute to the development and refinement of methods and procedures aimed at optimizing the manufacturing process.Key ResponsibilitiesOversee the shipping of finished materialsManage and maintain inventory levelsConduct sampling of in-process and raw materialsOperate glass washers and autoclavesPrepare buffers and mediaPrepare equipment for cleaning in place (CIP) and sterilization in place (SIP)Engage in cell culture processes from vial thaw to production scaleExecute column chromatography and tangential flow filtration
About the Role AbbVie is hiring a Scientist II for the Multispecifics Engineering group within Discovery Biotherapeutics in Worcester. This position centers on designing and developing new biotherapeutic solutions that target important healthcare challenges. What You Will Do Apply scientific knowledge to create and advance biotherapeutic candidates Work closely with colleagues from different disciplines to move projects from early concepts through execution Support AbbVie's mission to improve patient outcomes through innovative research
Job Overview:We are looking for a dynamic and collaborative technical leader to spearhead the innovation and development of our lipid nanoparticle (LNP) platform technology. The ideal candidate will engage with cross-functional teams to design and enhance LNPs and tLNP platform technology, supporting our innovative pipeline. This role involves establishing and directing our LNP innovation strategy, focusing on lipid design, chemistry, formulations, and targeted non-viral delivery systems, with a vision towards future product development and pipeline expansion. Key Responsibilities:Act as a scientific and technical authority within the organization, particularly in LNP-based drug delivery systems for nucleic acids.Drive the innovation, development, and optimization of the targeted LNP platform to support programs across various therapeutic areas.Possess an in-depth understanding of lipid and LNP design principles, stability, and scale-up processes, ensuring successful transition of drug product formulation production and purification unit operations from bench to larger scales.Develop LNP-related project plans, timelines, and budget forecasts, ensuring alignment with key stakeholders and organizational objectives.Lead the analysis of complex data sets, clearly communicating findings during internal program meetings, cross-functional reviews, and governance forums.Collaborate extensively with discovery and development teams, including mRNA, antibody, analytical, and process development groups, to propel pipeline initiatives.Oversee the drafting, review, and approval of technical reports pertinent to the function.Manage and mentor a team of over 10 scientists and associates across AbbVie’s East and West Coast sites. 
PurposeWe are looking for a skilled and dedicated Senior Financial Analyst to support our Manufacturing, Engineering, and Contracting Operations at AbbVie’s Biologics Research Center in Worcester, MA. In this pivotal role, reporting directly to the Cost Accounting Manager, you will collaborate with cross-functional leadership teams in Production, Planning & Logistics, Purchasing, R&D, and External Commercial Manufacturing. Your expertise will be essential in managing budgets for various late-stage clinical programs/projects, assisting management with operational spend analysis, and contributing to the Plant's financial planning processes, including Plan, Update, Long Range Plan, and Last Best Estimate. ResponsibilitiesOversee project/program budgets for multiple late-phase clinical programs, conducting variance analysis and delivering actionable insights to management.Collaborate with Finance leadership to manage the Plant's operational expenditures, providing cost center owners with relevant variance analyses and strategic input. Develop comprehensive reporting schedules and models to enhance forecasting accuracy.Support the financial planning cycles of the Plant, including preparation and analysis of operational spend.Execute month-end processes, including inventory reconciliations, booking journal entries, and analyzing manufacturing cost variances.Facilitate everyday business operations, including standard costing of new materials and ensuring the timely completion of manufacturing process orders.Assist in the annual material standard-setting process.Create and implement dashboards and reports necessary for business continuity.
Role Overview AbbVie Inc. is hiring a Scientist II for the Immunopharmacology group in Worcester. This position centers on peptide discovery and research. The scientist will contribute expertise to advance research projects and support the development of new therapeutic solutions.
Join our dynamic and innovative team at AbbVie, where we are dedicated to developing groundbreaking mRNA platforms. As a Scientist II, you will contribute to cutting-edge research and development efforts aimed at advancing therapeutic solutions in a collaborative environment.
Join AbbVie as the Director of External Manufacturing, where you will play a pivotal role in overseeing and enhancing our external manufacturing operations. Collaborating closely with cross-functional teams, you will ensure the highest quality standards and operational excellence are met while driving strategic initiatives that align with our commitment to innovation and patient care.
As the Associate Director of External Manufacturing, you will serve as the primary contact for supplier relationships, overseeing the strategic initiatives, organization, and technical support necessary for the effective management of our designated product supply. This role is pivotal in ensuring that high-quality products are manufactured in compliance with both local and international regulations, while also being delivered on schedule and within budget. You will manage various projects and programs that influence AbbVie, aiming to ensure that our products are cost-effective, marketable, and manufacturable, maximizing profitability throughout their life cycle. Through matrix management of cross-functional teams, you will lead diverse groups without direct authority, providing essential program management support and acting as the primary AbbVie representative for coordinating operations related to existing and new products manufactured by our suppliers.Key Responsibilities:Engage in the negotiation of Manufacturing Service Agreements and amendments, ensuring compliance with their terms.Develop effective planning and material procurement strategies to supply the Third Party Manufacturer (TPM) with necessary materials.Communicate product forecasts to the TPM and agree on manufacturing and delivery timelines. Collaborate with Supply Chain and Planning to ensure supplier delivery aligns with demand forecasts.Contribute to the Financial Operating Plan, Updates, Long Range Planning (LRP), and Standard processes, ensuring financial objectives are met.Coordinate the Steering Committee and ensure that Virtual Operation Teams convene regularly to assess performance and address any issues.Prepare status reports and updates for senior leadership review.In partnership with technical and quality teams, regularly assess process performance, quality trends, and devise improvement plans.Establish governance frameworks, guidelines, and communication channels, ensuring that suppliers have the requisite quality systems in place to meet regulatory standards and follow up on inspection responses.Coordinate with Quality Assurance to conduct annual quality management reviews and periodic audits of the TPM, ensuring timely investigation of deviations and product disposition decisions. Establish performance metrics and monitor them periodically.Develop, implement, and manage programs and projects, focusing on scope, cost, time, resource management, communication, and risk management throughout the project lifecycle.
Join AbbVie, a global biopharmaceutical company dedicated to discovering and delivering innovative medicines to address serious health issues. We are currently seeking a Manufacturing Supervisor I to oversee our manufacturing operations from Wednesday to Saturday, 4 PM to 2:30 AM. In this role, you will be responsible for managing a team of production staff, ensuring compliance with safety and quality standards, and driving operational efficiency. This is an excellent opportunity to contribute to the production of life-changing therapies.
The Manufacturing Supervisor III oversees evening shift operations at AbbVie's Worcester site. This role manages daily manufacturing activities, ensuring products meet quality standards and production runs efficiently. Key responsibilities Lead and direct manufacturing teams during the evening shift Monitor production processes to maintain product quality Ensure compliance with industry regulations and internal procedures Promote efficiency across all manufacturing activities Requirements Experience supervising manufacturing operations Strong understanding of quality standards and regulatory compliance Ability to lead teams and coordinate shift activities Willingness to work the evening shift at the Worcester facility
As the Associate Director of External Manufacturing for Small Molecules at AbbVie, you will play a pivotal role as the primary point of contact for supplier relationships. Your expertise will guide strategic initiatives and provide essential technical support to ensure the smooth management of product supply. You will be responsible for overseeing the manufacturing of high-quality products in adherence to both local and international regulations, ensuring timely delivery in line with established forecasts and budgets.This role encompasses project and program management that directly impacts AbbVie, ensuring that our products remain marketable, manufacturable, and profitable throughout their lifecycle. Leveraging your leadership skills, you will effectively manage cross-functional teams in a matrix environment without direct authority, providing crucial program management support and serving as the main representative for AbbVie in coordinating operations related to existing and new products with suppliers.Key Responsibilities:Lead negotiations for Manufacturing Service Agreements and amendments, ensuring compliance with contract terms.Implement effective planning and material procurement strategies to support TPM needs.Communicate product forecasts to suppliers and collaborate on manufacturing and delivery schedules, ensuring alignment with demand forecasts.Engage in the development of the Financial Operating Plan and ensure financial targets are achieved.Coordinate Steering Committee meetings and ensure the Virtual Operation Teams regularly assess performance and address any issues.Prepare status reports and updates for senior leadership.Collaborate with technical and quality teams to review process performance and implement process improvements.Establish governance and communication protocols, ensuring suppliers maintain necessary quality systems and documentation for regulatory compliance.Coordinate with QA for annual quality management reviews and audits of TPM, ensuring timely investigation of deviations and product disposition decisions.Manage programs/projects, focusing on scope, cost, time, resource management, communication, and risk management through all project phases.
AbbVie is seeking a Business Operations Associate based in Worcester. This position plays a part in supporting daily operations and assists with essential business activities throughout the organization. Role overview The Business Operations Associate works to improve processes and increase efficiency in AbbVie's operations. The role involves collaborating with teams to ensure business functions run smoothly and contribute to the company's healthcare initiatives. Key responsibilities Support day-to-day business operations Assist with process improvement projects Contribute to efforts that drive operational efficiency Location This position is based in Worcester.
AbbVie is hiring a Scientist II for Purification Development in Worcester. This role centers on improving purification processes to advance new therapeutic products. The Scientist II partners with other scientists to support research goals and drive process improvements. Key Responsibilities Develop and refine purification methods for therapeutic products Work with colleagues to troubleshoot and optimize laboratory protocols Use advanced technologies to improve process efficiency and reliability Share scientific expertise in team discussions and project planning Collaboration and Impact This position involves close teamwork with scientists across disciplines. The focus is on applying technical knowledge to solve challenges and enhance purification workflows that support AbbVie's research pipeline.
About the Role AbbVie is seeking a Senior Scientist II with a focus on Immunopharmacology and Peptide Discovery to join the team in Worcester. This position centers on leading research efforts that support the discovery and development of new peptide-based therapeutics. The work directly contributes to advancing AbbVie's drug development pipeline. What You Will Do Lead research projects in immunopharmacology and peptide discovery. Design and execute experiments to identify and characterize novel peptide therapeutics. Apply expertise in immunology and pharmacology to support drug development goals. Collaborate with multidisciplinary teams to move promising candidates forward. Location This position is based in Worcester.
AbbVie Inc. seeks a Principal Data Architect II to join the Biotherapeutics and Genetic Medicine group in Worcester. This position centers on building and maintaining data architecture that supports research and development in biotherapeutics and genetic medicine. Key Responsibilities Collaborate with cross-functional teams to define and document data requirements for projects in biotherapeutics and genetic medicine. Design and implement data architecture solutions that enable research, development, and operational workflows. Use data governance best practices to ensure data integrity and make essential data accessible across platforms. Support the broader data strategy and contribute to the advancement of analytics tools for R&D. Team Focus This group specializes in biotherapeutics and genetic medicine, providing a strong data foundation to drive innovative research.
Join AbbVie as a Principal Research Scientist II, where you will leverage your expertise to drive innovative research projects. Collaborate with a dynamic team of scientists and contribute to groundbreaking advancements in healthcare. This role offers the opportunity to work on complex problems, develop novel solutions, and make a significant impact in the field of research.
AbbVie Inc. seeks a Principal Machine Learning Scientist II for its Biotherapeutics and Genetic Medicine team in Worcester. This role centers on advancing research and development efforts in these fields. Key Responsibilities Use advanced machine learning techniques to drive progress in genetic medicine research projects. Develop and refine new computational approaches that support scientific initiatives in biotherapeutics. Provide subject matter expertise to help shape research strategies and methodologies. Location This position is based in Worcester.
As a Manufacturing Supervisor III, you will leverage your specialized knowledge and extensive experience to oversee a team responsible for the safe and efficient production of our pharmaceutical products. You will lead the team in ensuring compliance with all safety, regulatory, and operational standards, while fostering a culture of excellence in customer service, product quality, and financial performance.Key Responsibilities:Safety: Champion the production safety program, ensuring safety remains a top priority. Conduct safety audits and regularly promote a culture with zero safety incidents.Team Leadership: Effectively deploy team members and delegate tasks to meet production schedules. Conduct regular one-on-ones and performance reviews, ensuring team engagement and timely approvals of attendance records.Operational Excellence: Coordinate shift activities to ensure production schedules are met. Facilitate smooth handovers between shifts for seamless operations.Regulatory Compliance: Ensure adherence to regulatory standards, proactively managing compliance processes including routine checks and addressing any compliance issues promptly.Performance Management: Manage cycle time and change-over improvements, spearheading process improvement initiatives to meet site metrics and expectations.Team Development: Invest in the growth of your team by providing training and opportunities for advancement, with a focus on Key Talent.
AbbVie is seeking a dynamic and experienced Senior Manager of Quality Control (CMC/QC) to join our dedicated team in Worcester. In this role, you will lead quality control initiatives, ensuring compliance with industry regulations while driving continuous improvement in our processes and systems.
AbbVie Inc. seeks an Associate Scientist in Process Development I to join its Worcester team. This entry-level position plays a key role in supporting the development and optimization of therapeutic product processes. The work centers on advancing products through hands-on laboratory efforts and teamwork. Key responsibilities Assist in developing and refining processes for therapeutic products Collaborate with scientists from diverse backgrounds to meet project objectives Build practical laboratory experience in process development Work environment The role is based on-site in Worcester, where close collaboration and daily interaction with the process development team are expected.
Apr 28, 2026
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