Associate Scientist in Process Development I

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.

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.

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.

AbbVie Inc. seeks an Aseptic Product Quality Manager to oversee the quality and safety of aseptic products at the Worcester site. This position leads a team focused on implementing quality assurance protocols and upholding industry standards throughout the manufacturing process. Role overview This manager ensures that aseptic production meets strict quality and safety requirements. The role involves guiding a team, monitoring compliance, and supporting a culture where quality and continuous improvement are priorities. What you will do Lead a team responsible for quality assurance in aseptic manufacturing Implement and maintain protocols to ensure product safety and compliance Drive ongoing improvements in manufacturing processes Promote a culture of quality and excellence across operations Requirements Experience in aseptic product quality management or related field Knowledge of industry standards and regulatory compliance Leadership skills to guide and develop a quality-focused team

Join AbbVie, a global biopharmaceutical company, as the Associate Director of Procurement Leadership. In this pivotal role, you will be responsible for leading procurement strategies that drive operational efficiency and enhance our overall supply chain. Your expertise will play a crucial part in ensuring that we not only meet our business goals but also maintain our commitment to quality and integrity.

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

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 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.

Join AbbVie, a global biopharmaceutical leader, as a Senior Manufacturing Execution Systems (MES) Engineer. In this critical role, you will enhance and manage our MES solutions, ensuring optimal production processes and compliance within our manufacturing facilities. Your expertise will drive operational excellence and innovation, aligning with our mission to deliver transformative medicines.

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.

Role Overview AbbVie Inc. is hiring a Director of Program Management in Worcester. This leader guides cross-functional teams to deliver programs that strengthen the company’s product portfolio. The Director manages planning, execution, and delivery for major initiatives, keeping projects aligned with AbbVie’s broader strategy. Key Responsibilities Lead and coordinate teams across departments to achieve program goals Oversee program planning, timelines, and execution Ensure all initiatives support AbbVie’s strategic objectives Promote strong collaboration among stakeholders and departments

Join our dynamic healthcare team as the Director of Nursing for the Operating Room at dstaff in Worcester, Massachusetts. In this pivotal role, you will oversee nursing operations, ensuring the highest standards of patient care and safety are met. You will lead and mentor a dedicated team of nursing professionals while collaborating with surgeons and other healthcare staff to optimize operating room efficiency and patient outcomes.

The Director of Operations will play a pivotal role in enhancing the delivery of exceptional care within our outpatient specialty pharmacy program. This position requires integrated support across various stakeholders, including healthcare providers, clinical staff, hospital administration, pharmacy partners, and vendors. You will proactively identify growth opportunities and conduct cost-benefit analyses to assess the feasibility of new initiatives. Your leadership will guide a team of pharmacy patient liaisons across multiple specialties, ensuring seamless access to outpatient prescriptions for our patients. You will oversee daily operations with hospital partners, ensuring overall financial performance, while collaborating with functional leadership to optimize processes and improve operational efficiencies.

FIELD ASSOCIATE - WORCESTER AREA ABOUT THE ROLE Join our dynamic team at Doorstead as a Field Associate in the Worcester area. This contracted hourly role (1099 position) centers around two key responsibilities: facilitating property showings and conducting evaluations. Key Responsibilities: Conduct property showings to prospective tenants and clients.Perform detailed property evaluations and assessments.Utilize mobile applications for evaluations and deliver high-quality photographic documentation.Maintain open and effective communication with team members and clients. IDEAL CANDIDATE Possesses a valid real estate license or property inspection certificate (REQUIRED).Experience in real estate showings, property management, home evaluations, or appraisals is preferred.Exceptional verbal and written communication skills.Meticulous attention to detail.A collaborative team player with a proactive growth mindset.Willingness to travel frequently within the local area.Proficient in using mobile applications and smartphone photography.Displays a professional demeanor with a positive attitude. TECHNICAL REQUIREMENTS Must have reliable transportation.Smartphone capable of running our mobile-friendly evaluation tool and capturing high-quality photos.

Join the dynamic team at gopuff as an Operations Associate in Worcester, where your enthusiasm and dedication will play a pivotal role in our operations. Working directly with a Site Leader, you will handle a variety of essential tasks, including the picking and packing of items, receiving products, and collaborating with our partner drivers. At gopuff, we deliver everyday essentials to our customers around the clock, rain or shine. We are on the lookout for innovative thinkers and passionate individuals ready to transform the retail landscape. If you love snacks and thrive in a fast-paced environment, we want you on our team!

Join our dynamic team at Sika AG as a Sales Associate. In this role, you will be responsible for assisting customers, driving sales, and building lasting relationships. If you are passionate about delivering excellent customer service and have a knack for sales, we want to hear from you!

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. 

Join our dynamic team as a Part-Time Retail Data Collection Associate at Crossmark! In this role, you will be responsible for collecting valuable data from retail environments, ensuring that our clients receive accurate and up-to-date information to drive their business decisions. This is an excellent opportunity for individuals looking to gain experience in retail analytics while working flexible hours.

AbbVie Inc. seeks a Global Process Engineer specializing in biologics for its Worcester location. This role focuses on enhancing manufacturing processes to strengthen both quality and operational efficiency across AbbVie's worldwide biologics operations. Key responsibilities Refine and optimize biologics manufacturing processes to improve efficiency and reliability Support the introduction of new process innovations Contribute to maintaining high standards of quality in production Role focus This position plays a central part in advancing biologics manufacturing methods, with an emphasis on continuous improvement and global impact. The work directly supports AbbVie's commitment to quality and innovation in biopharmaceutical production.

Join our dynamic team as a Data Collection Associate at Crossmark! This part-time role is perfect for individuals seeking to gain valuable experience in data collection and analysis. You will contribute to various projects by gathering and organizing essential data, ensuring accuracy and efficiency.