Lonza Biologics, Inc.

  Location: Vacaville, California This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. Join Lonza in Vacaville, CA, as a Manufacturing Technician – Bioprocess and be part of a hard-working team dedicated to producing innovative bio-therapeutic medicines. This role offers an ambitious opportunity to collaborate with highly automated production systems and contribute to our world-class operations. At Lonza, we strictly follow cGMP and SOP standards, ensuring our processes meet the highest regulatory requirements. What you will get The full-time base annual salary for this position is expected to range between $43,000 to $69,000 .  In addition, below you will find a comprehensive summary of the benefits package we offer: Performance-related bonus Medical, dental and vision insurance 401(k) matching plan...

  Location: Vacaville, CA This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. The primary responsibility of Instrument Services is to maximize equipment availability for processing by safely maintaining equipment and instrumentation through Calibration, Preventive and Corrective Maintenance.  In support of these activities, Instrument Services provides personnel 24/hours/day, 7 days per week for calibration, maintenance, discrepancy response, contractor oversight, vendor resource management, project support and training.     All Instrument Services Technicians are trained to perform calibration and maintenance in the primary manufacturing support areas and Materials Management, Quality Control Labs, and Utility Operations Work Schedule: Day Shift: 6:00a - 6:30p OR Night Shift 6:00p – 6:30a What you will get...

  Quality Assurance Specialist II - Viral Vector Location: Houston, Texas – Onsite Shift: Sunday through Thursday , 7:00 AM – 3:3 0 PM As a Quality Assurance Specialist II - Viral Vector , you will serve as a key representative of the Quality Assurance organization, ensuring quality and compliance standards are maintained across viral vector and advanced therapy manufacturing operations. This role provides the opportunity to partner closely with Manufacturing, Quality Control, Engineering, and other support functions to support production activities, maintain cGMP compliance, and help deliver life-changing therapies to patients. What you will get: A competitive compensation package. In addition, below you will find a comprehensive summary of the benefits package we offer: Performance-related...

  12-Hour Night Shift | Greenwood, SC At Lonza, people are at the heart of innovation. As a global leader in life sciences, we work every day to develop solutions that improve health and quality of life around the world. When you join Lonza, you become part of a team that values collaboration, accountability, and continuous improvement while providing opportunities to grow your career. We are looking for a Formulations Processor I to join our Manufacturing team in Greenwood, SC. In this role, you will help prepare and process materials used in the production of high-quality capsule products. Your work will directly support safe, efficient operations and help ensure our products consistently meet the highest quality standards. What You'll Do As a Formulations Processor I, you will play an important role in our manufacturing process by: Measuring, weighing, blending, and processing raw materials according to established procedures and quality standards. Monitoring...

  As a Senior Quality Specialist, you will play a key role in ensuring product quality, regulatory compliance, and operational excellence across manufacturing operations. You will support batch release activities, quality record management, product quality evaluations, and quality systems processes while partnering closely with Operations, Engineering, Supply Chain, and Commercial teams. In this position, you will help drive compliance with quality standards, support audit readiness, and contribute to continuous improvement initiatives that ensure the consistent delivery of high-quality products to our customers. What Will You Do Perform batch record review, compliance verification, and product release activities to support business objectives and ensure adherence to quality requirements. Maintain and manage quality records, batch documentation, retained samples, and archival processes in accordance with quality system and regulatory requirements. Evaluate...

  Formulations Processor I 12-hr Shift (Night Shift, D) Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. As a Formulations Processor I , you will support the manufacture of high‑quality formulations at our Greenwood site. You will be part of a dedicated, collaborative team that plays a vital role in ensuring safe, reliable, and compliant capsule production. What you will get Performance-related bonus Medical, dental and vision insurance 401(k) matching plan Life insurance, as well as short-term and long-term disability insurance Employee assistance programs Paid time off (PTO)...

  Manufacturing Supervisor - Cell Therapy Location: Houston, Texas – Onsite Shift: 7 am -7 pm – 12-hour rotating schedule. As a Manufacturing Supervisor in Cell Therapy, you will lead frontline production teams and play a critical role in delivering high-quality, life‑saving therapies under cGMP conditions. This role offers the opportunity to combine people leadership, technical expertise, and cross‑functional collaboration in a fast‑paced, highly regulated manufacturing environment. This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. What you will get: A competitive compensation. In addition, below you will find a comprehensive summary of the benefits package we offer: Performance-related bonus Medical, dental and vision insurance 401(k) matching plan Life insurance, as well as short-term...

  Location: Greenwood, South Carolina Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there is no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses improve people's lives. At Lonza, we respect and protect our people and our environment. Success is achieved because of our people who own their careers, genuinely improve the world around them, and contribute to making a meaningful difference. Join us and be part of a team where your ideas matter and your impact is visible every day. Lonza is seeking an experienced and strategic Associate Director, Supply Chain Warehousing & Distribution to lead and optimize our Americas distribution network from our Greenwood, SC site. This highly visible leadership role is responsible for developing and executing regional logistics and distribution strategies that ensure exceptional...

  The Global Operational Quality Specialist coordinates and drives the consistent execution of Operational Quality Assurance/Quality Control (QA/QC) processes across the global network. The role ensures effective implementation of quality governance, standards, performance monitoring, training, and quality systems through cross-functional collaboration with global and site quality teams. The function supports harmonization of QA/QC practices, coordinates global quality initiatives, monitors execution, and drives timely follow-up of quality actions, risks, and improvement opportunities. The position also facilitates knowledge sharing, strengthens inspection readiness, and promotes sustainable operational quality performance across sites. What you will do Define and maintain the global Quality governance model, including governance structures, KPI/KQI frameworks, reporting processes, and inspection-ready performance management. Coordinate global escalation...

  Today, Lonza is a global leader in life sciences, operating across five continents, Lonza works every day to enable a healthier world. Our greatest scientific solution is talented people working together, devising ideas that help businesses improve lives. In exchange, we empower our employees to own their careers and genuinely make a meaningful difference. We are seeking an experienced Director, Sterility Assurance to provide global leadership for sterility assurance and contamination control across Lonza's sterile manufacturing network. This highly visible role will drive enterprise-wide strategy, governance, and continuous improvement initiatives to ensure world-class biological contamination control and compliance across sterile drug substance and drug product operations. Key Responsibilities Global Sterility Assurance Leadership Develop, implement, and continuously improve biological contamination control strategies addressing viral, bacterial, fungal,...

  Senior Process Engineer – Viral Vector Houston, TX The actual location of this job is in Houston, TX, USA. Relocation assistance is available for eligible candidates and their families, if needed. This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. What you will get: An agile career and dynamic working culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. A variety of benefits dependent on role and location. The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits . The Senior Process Engineer is responsible for leading the support to site operations by ensuring that equipment and related processes are designed and operating to meet the requirements of a regulated manufacturing site.  This role is also...

  As a Senior Quality Engineer, you will play a critical role in driving customer satisfaction, product quality, and continuous improvement across our manufacturing operations. Working closely with customers and cross-functional teams, you will lead quality investigations, support compliance initiatives, and leverage Voice of the Customer (VOC) insights to enhance products, processes, and the overall customer experience. In this highly visible role, you will serve as a trusted quality partner, helping to ensure regulatory compliance, resolve complex quality issues, and drive sustainable improvements that support both business objectives and customer expectations. What Will You Do   Lead customer complaint investigations, root cause analyses, and corrective action processes, ensuring   timely   resolution and effective communication with customers and internal stakeholders.   Drive customer experience improvement through analysis of customer...

  Location: Vacaville, CA This is a fully site based role. Working together in person supports close, real time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. Join Lonza in Vacaville, CA, as a Senior Manufacturing Technician – Bioprocess and be part of a hard-working team dedicated to producing innovative bio-therapeutic medicines. This role offers an ambitious opportunity to collaborate with highly automated production systems and contribute to our world-class operations. At Lonza, we strictly follow cGMP and SOP standards, ensuring our processes meet the highest regulatory requirements. What you will get The full-time base annual salary for this position is expected to range between $ 47,250  to $78,750 .  In addition, below you will find a comprehensive summary of the benefits package we offer: Performance-related bonus Medical, dental and vision insurance 401(k) matching plan...

  Location: Vacaville, California  This is a fully site based role. Working together in person supports close, real time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. Shift leader will foster an environment founded on trust, accountability, and mutual respect and will provide active, visible leadership to maintain and enhance the company's position as a best-in-class, bio-pharmaceutical manufacturer.   What you will get The full-time base annual salary for this position is expected to range between $95,250  to $158,750 .  In addition, below you will find a comprehensive summary of the benefits package we offer: Performance-related bonus Medical, dental and vision insurance 401(k) matching plan Life insurance, as well as short-term and long-term disability insurance Employee assistance programs Paid Time Off Shift hours: 6:30pm-7:30am; Wednesday-Friday and every other...

  Quality Assurance Manager, Operations Location: This position is based in our Portsmouth, NH office. The typical work schedule is Monday through Friday, 8:00 AM–4:30 PM EST. What you will get: Below you will find a comprehensive summary of the benefits package we offer: Performance-related bonus. Medical, dental and vision insurance. 401(k) matching plan. Life insurance, as well as short-term and long-term disability insurance. Employee assistance programs. Paid time off (PTO). Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge. What you will do: We are seeking an experienced Quality Assurance Manager, Operations to lead a team supporting GMP compliance and quality oversight across site operations. This role is responsible for ensuring quality objectives are achieved, supporting cross-functional teams, and promoting a strong culture of quality and continuous...

  Product Development Manager GMP Operations Tampa, FL, USA The actual location of this job is in Tampa, FL. Relocation assistance is available for eligible candidates and their families, if needed.   The Manager, Product Development GMP Operations is a site‑based leadership role supporting early‑phase clinical trial drug product manufacturing and packaging. This position offers the opportunity to design and lead GMP capabilities, guide multidisciplinary teams, and directly contribute to bringing innovative therapies into the clinic. What you will get An agile career with opportunities for growth in a dynamic Product Development environment A collaborative, inclusive, and ethical workplace culture Compensation programs that recognize high performance and leadership impact Competitive medical, dental, and vision insurance coverage Access to Lonza’s learning, development, and leadership programs What you will do: Lead and develop Product Development GMP...

  Quality Assurance Specialist II - Viral Vector Location: Houston, Texas – Onsite Shift: Monday through Friday, 7:30 AM – 4:0 0 PM As a Quality Assurance Specialist II - Viral Vector , you will serve as a key representative of the Quality Assurance organization, ensuring quality and compliance standards are maintained across viral vector and advanced therapy manufacturing operations. This role provides the opportunity to partner closely with Manufacturing, Quality Control, Engineering, and other support functions to support production activities, maintain cGMP compliance, and help deliver life-changing therapies to patients. What you will get: A competitive compensation package. In addition, below you will find a comprehensive summary of the benefits package we offer: Performance-related...

  Quality Assurance Specialist III - Viral Vector Location: Houston, Texas – Onsite Shift: Tuesday through Saturday, 11:00 PM – 8:00 AM As a Quality Assurance Specialist III - Viral Vector , you will serve as a senior representative of the Quality Assurance organization, ensuring quality and compliance standards are maintained across viral vector, cell therapy, and advanced therapy manufacturing operations. This role partners closely with Manufacturing, Quality Control, Engineering, Facilities, and other support functions to provide quality oversight of production activities, support complex quality investigations, maintain cGMP compliance, and help deliver life-changing therapies to patients. You will also provide informal leadership and guidance within the QA team while taking ownership of complex quality issues and continuous improvement initiatives. What you will get: A competitive compensation package. In addition, below you will find a comprehensive...

  Location: Vacaville, California  This is a fully site based role. Working together in person supports close, real time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. Join Lonza in Vacaville, CA, as a Senior Manufacturing Technician – Bioprocess and be part of a hard-working team dedicated to producing innovative bio-therapeutic medicines. This role offers an ambitious opportunity to collaborate with highly automated production systems and contribute to our world-class operations. At Lonza, we strictly follow cGMP and SOP standards, ensuring our processes meet the highest regulatory requirements. What you will get The full-time base annual salary for this position is expected to range between $ 47,250  to $78,750 .  In addition, below you will find a comprehensive summary of the benefits package we offer: Performance-related bonus Medical, dental and vision insurance 401(k) matching...

  Quality Assurance Specialist III - Viral Vector (Second Shift) Location: Houston, Texas – Onsite Shift: Monday through Friday, 3:00 PM – 11:30 PM As a Quality Assurance Specialist III - Viral Vector , you will serve as a senior representative of the Quality Assurance organization, ensuring quality and compliance standards are maintained across viral vector, cell therapy, and advanced therapy manufacturing operations. This role partners closely with Manufacturing, Quality Control, Engineering, Facilities, and other support functions to provide quality oversight of production activities, support complex quality investigations, maintain cGMP compliance, and help deliver life-changing therapies to patients. You will also provide informal leadership and guidance within the QA team while taking ownership of complex quality issues and continuous improvement initiatives. What you will get: A competitive compensation package. In addition, below you will find a...