Qureos Mentor

Lonza

<div>QC Analyst I - Environmental Monitoring (2nd Shift)
Location: Portsmouth, NH, USA. The actual location of this job is in Portsmouth, NH, USA.
Join our Quality Microbial Control team on a specialized Sunday &ndash; Wednesday (1:00 PM &ndash; 11:30 PM) shift. In this role, you will support our 2k asset by performing critical environmental and utility monitoring, ensuring our manufacturing environment meets the rigorous standards required for life-saving drug production.
What you will get:<ul><li>
An agile career and dynamic working culture.</li><li>
An inclusive and ethical workplace.</li><li>
Competitive salary and performance-based bonuses.</li><li>
401(k) matching plan.</li><li>
Competitive compensation programs that reward high performance.</li><li>
Comprehensive medical, dental, and vision insurance.</li></ul>
Access to our full list of global benefits: https://www.lonza.com/careers/benefits
What you will do:<ul><li>
Execute routine test samples for In-Process, Lot Release, and Stability studies to support the 2k asset production schedule.</li><li>
Support the monitoring and sampling of critical utilities and HVAC systems throughout the facility to ensure a state of microbial control.</li><li>
Apply Data Integrity principles in all aspects of work, ensuring compliance with Lonza policies and cGMP standards.</li><li>
Work on assignments that are semi-routine in nature, recognizing and escalating deviations from accepted practices as required.</li><li>
Utilize laboratory computer systems and Microsoft Office (Word, Excel) to accurately record and report high-quality results.</li><li>
Take personal responsibility for safety and maintain a &quot;Quality First&quot; mindset, notifying management of any potential GMP deficiencies or process deviations.</li><li>
Act as an engaged member of the Microbial Control team, maintaining a positive attitude and ensuring all tasks are completed accurately and on time.</li></ul>
What we are looking for:<ul><li>
High School Diploma or equivalent is required. An Associate&rsquo;s Degree in Microbiology, Biochemistry, or a related Science field is preferred.</li><li>
Strong ability to interpret data and follow complex instructions within defined procedures and practices.</li><li>
A desire to learn from experience and treat errors as opportunities for professional growth.</li><li>
Commitment to adherence to cGMPs and the ability to exercise sound judgment to determine appropriate actions.</li><li>
Strong verbal and written communication skills, necessary for reporting and collaborating within a shift-based team.</li><li>
Ability to work the assigned Sunday &ndash; Wednesday, 1:00 PM &ndash; 11:30 PM shift, arriving on time and maintaining focus on manufacturing demands.</li></ul>
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone&rsquo;s ideas, big or small, have the potential to improve millions of lives, and that&rsquo;s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you&rsquo;re ready to help turn our customers&rsquo; breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.</div>

QC Analyst Level I - Environmental Monitoring (2nd Shift)

<div>
 United States, Morristown (New Jersey)
 
 
 Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there&rsquo;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&rsquo;s the kind of work we want to be part of.
 
 
 
 Reporting to the Head of Indirect Tax and Global Trade, the Head of Global Trade is responsible for setting the strategic direction and overseeing the operational execution of global trade and tariff compliance across all jurisdictions, with a particular focus on the U.S. and Europe.
 
 This expert-level role ensures full regulatory compliance, drives cost‑optimization opportunities, and supports alignment with Lonza&rsquo;s global supply chain and tax strategies in a complex, high‑stakes environment.
 
 
 Sitting at the intersection of finance, supply chain/operations, and legal/regulatory, the role requires extensive collaboration across these and other key functions. The Head of Global Trade leads and develops a small global team of trade specialists (4&ndash;6 direct reports, including two GG13 roles based in the US and Europe), with a strong emphasis on upskilling, leadership development, and change management.
 
 
 The ideal candidate brings a deep theoretical and practical understanding of international trade regulations and tariff compliance&mdash;particularly within the US and European contexts&mdash;paired with strong business acumen, ability to communicate with key stakeholders, and the ability to grow and mentor a high‑performing specialist team.
 
 
 This role may be based in Morristown, NJ; Portsmouth, NH; or Manchester, UK.
 
 
 
 Key Responsibilities
 
 
 
 
 Strategic Leadership
 
 
 
 <ul>
 <li>
 Develop, implement and maintain a global trade strategy
 </li>
 <li>
 Ensure compliance with laws and regulations and adherence to strategy
 </li>
 <li>
 Serve as a key advisor to senior leadership on trade-related risks and opportunities in a fast changing and complex environment with increasing tariff barriers
 </li>
 <li>
 Collaborate with internal stakeholders, including finance, legal, regulatory affairs, and operations, to ensure trade and customs aspects are well understood and considered.
 </li>
 <li>
 Monitor changes in trade and customs legislation and assess their impact on Lonza, incl. cost reduction / risk mitigation options
 </li>
 <li>
 Drive complex and typically cross functional trade-related projects, ensuring delivery on time and on budget
 
 
 </li>
 </ul>
 
 Operational Execution
 
 
 
 <ul>
 <li>
 Conduct risk assessments to identify potential compliance issues and implement corrective actions.
 </li>
 <li>
 Oversee implementation of trade technology platforms, drive automation and promote adoption of AI-based tools.
 </li>
 <li>
 Oversee audits, training, and day-to-day compliance operations performed by the trade team.
 
 
 </li>
 </ul>
 
 Team Leadership
 
 
 
 <ul>
 <li>
 Foster a highly performing global trade team by setting clear directions, coaching team members, and promoting collaboration, transparency, continuous learning and development opportunities.
 </li>
 <li>
 Drive organizational development through talent planning, succession strategies, and cross-functional collaboration.
 
 
 </li>
 </ul>
 
 Key Skills
 
 
 
 <ul>
 <li>
 Strong theoretical and practical knowledge of international trade regulations and customs compliance; in-depth experience with US trade regulations and practice is a strong plus
 </li>
 <li>
 Ability to think and act strategically while being able to execute on operational deliverables
 </li>
 <li>
 Business acumen; experience pertaining to the CDMO, Pharmaceutical or Chemical industry is a plus.
 </li>
 <li>
 Ability to build strong relationships with stakeholders at all levels of the organization in achievement of goals
 </li>
 <li>
 Strong people leadership skills; proven ability to build and develop a highly performing trade organization across various countries
 </li>
 <li>
 Thrives in a global company with strong US and Swiss / European footprint. Prior working experience in several countries is a plus
 </li>
 <li>
 Excellent analytical, problem-solving, and decision-making skills
 </li>
 <li>
 Strong communication, project management and collaboration skills
 </li>
 <li>
 Affinity with technology solutions
 
 
 </li>
 </ul>
 Compensation for the role will depend on a number of factors, including the successful candidate&rsquo;s qualifications, skills, competencies, experience, and job-related knowledge. Full-time employees receive a comprehensive benefits package including performance-related bonus, medical and dental coverage, 401k plan, life insurance, short-term and long-term disability insurance, an employee assistance program, paid time off (PTO), and more.
 
 
 Every day, Lonza&rsquo;s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
 
 
 People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
 
 
 Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
 
 
 Reference: R74684
 
 
 Apply
</div>

Head of Global Trade

<div>Computer Systems Validation Engineer
Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.
The Computer Systems Validation (CSV) Engineer will, as an individual contributor, identify and implement industry best practices through an extensive industry network and detailed knowledge of applicable regulations. During the scoping portion of these improvement projects the person in this role will work with other experienced members of the CSV team to identify roadblocks and additional efficiencies. Additional day to day tasks will include risk assessing systems, reviewing change requests and test scripts, drafting protocols and initiating and reviewing GMP documentation revisions.
What you will get:<ul><li>
Competitive salary and comprehensive benefits package.</li><li>
Opportunities for career development and advancement.</li><li>
Supportive and collaborative team environment.</li><li>
Access to cutting-edge technology and tools.</li><li>
Commitment to employee well-being and safety.</li><li>
Inclusive workplace culture.</li><li>
Recognition and reward for your contributions.</li></ul>
Access to our full list of global benefits: https://www.lonza.com/careers/benefits
What you will do:<ul><li>
Lead efforts between internal customers and CSV to ensure assigned activities are prioritized, communicated in an effective and timely manner, and completed on time.</li><li>
Accountable for maintaining full knowledge of Lonza's policies/procedures, 21 CFR Part 11, Data Integrity, ICH Q7A requirements and GAMP and the underlying principles of each.</li><li>
Perform all aspects of Quality Systems Management (QSM) processes (Change Control, Deviation, Corrective and Preventable Actions) as well as Validation Maintenance of computerized systems.</li><li>
Participate in audits and inspections as a Subject Matter Expert.</li><li>
Own, revise and maintain computer systems validation SOPs (Standard Operations Procedures).</li><li>
Function as CSV SME in Inspections and Audits.</li><li>
Mentor and train junior members of the department.</li></ul>
What we are looking for:<ul><li>
Bachelor&rsquo;s degree required, preferred in computer science, engineering, or other sciences.</li><li>
Minimum of 7 years of experience working with automation and/or computerized system validations.</li><li>
Minimum 2 years&rsquo; experience with Controls Automation, Process Control Systems, Distributed Systems, Manufacturing Execution Systems (MES) required, DeltaV preferred.</li><li>
Prior experience leading or managing projects beneficial.</li><li>
CAPAs and deviations experience desired.</li><li>
Biotech/Pharma/Medical Device/Medical or biologics industry experience required.</li><li>
Ability to work independently and meet deadlines successfully.</li></ul>
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone&rsquo;s ideas, big or small, have the potential to improve millions of lives, and that&rsquo;s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you&rsquo;re ready to help turn our customers&rsquo; breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.</div>

Computer Systems Validation Engineer

<div>Associate Director, Aseptic Operations
Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families.
The Associate Director of Aseptic Operations is responsible for maintaining superior quality and GMP standards across all operational areas. Key duties include directing deviation management to ensure investigations are completed accurately and on schedule. The role also involves analyzing operational trends to implement holistic, long-term process improvements. Additionally, the incumbent leads the development of training strategies focused on technical skills and aseptic behaviors like gowning and interventions. Finally, they provide aseptic stewardship by contributing to the design and enhancement of facility infrastructure to ensure sterility.
What you will get:<ul><li>
Competitive salary and comprehensive benefits package</li><li>
Opportunities for career development and advancement</li><li>
Supportive and collaborative team environment</li><li>
Access to cutting-edge technology and tools</li><li>
Commitment to employee well-being and safety</li><li>
Inclusive workplace culture</li><li>
Recognition and reward for your contributions</li></ul>
Access to our full list of global benefits: https://www.lonza.com/careers/benefits
What you will do:<ul><li>
Lead the deviation management and aseptic training teams, overseeing staffing, performance, and continuous development to maintain a motivated workforce.</li><li>
Own end-to-end deviation management to ensure on-time, &quot;right-first-time&quot; closures that align with batch release schedules.</li><li>
Spearhead quality improvement projects to strengthen the site&rsquo;s quality culture and proactively reduce the frequency of deviations.</li><li>
Manage complex root cause analyses and implement effective CAPAs to enhance process performance and verify long-term efficacy.</li><li>
Collaborate with cross-functional stakeholders and Quality Assurance to drive record completion and meet critical production deadlines.</li><li>
Oversee all GMP-relevant training for the asset, focusing on reducing &quot;door-to-floor&quot; time and improving training effectiveness.</li><li>
Partner with site leadership to identify training gaps and develop a comprehensive GMP Training Plan aligned with the latest industry trends</li></ul>
What we are looking for:<ul><li>
Bachelor&rsquo;s Degree required in Life Sciences, Pharmacy, Engineering or related field.Six Sigma/Lean or similar process improvement certification is preferred.</li><li>
8+ years of experience in a GMP-regulated industry, preferably in QA, QC, or Manufacturing.</li><li>
At least 5 years in a quality role and/or role related to aseptic manufacturing.</li><li>
Strong knowledge of regulatory requirements (FDA, EMA, ICH, WHO) and quality standards (GMP, ISO).</li><li>
Experience with electronic quality management systems (e.g., TrackWise, Veeva, MasterControl).</li><li>
Strong experience supporting regulatory inspections (e.g., FDA, MHRA, EMA).</li><li>
Knowledge of risk management and change control processes.</li></ul>
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone&rsquo;s ideas, big or small, have the potential to improve millions of lives, and that&rsquo;s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you&rsquo;re ready to help turn our customers&rsquo; breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.</div>

Associate Director, Aseptic Operations

<div><h1 class="jobSectionHeader">UCII Operator</h1>
Greenwood, South Carolina 
2nd Shift: 3:00pm&ndash;1:00am (Monday&ndash;Thursday)
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there&rsquo;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&rsquo;s the kind of work we want to be part of.
Based at our Greenwood UC‑II&reg; manufacturing site, you will support daily production activities that help maintain safe, high‑quality operations. You&rsquo;ll play a hands‑on role in producing materials that support our customers and ultimately consumers worldwide.<h2 class="jobSectionHeader">
What you will get
</h2><ul><li>An agile career and dynamic working culture.</li><li>
An inclusive and ethical workplace.</li><li>
Compensation programs that recognize high performance.</li><li>
Medical, dental, and vision insurance.</li><li>
The full list of our global benefits can also be found at https://www.lonza.com/careers/benefits.</li></ul><h2 class="jobSectionHeader">
What you will do</h2><ul><li>
Receive, prepare, and process raw materials following EHS, Quality, and GMP procedures.</li><li>
Operate automated production equipment and CIP controls through the DeltaV DCS platform.</li><li>
Perform milling and packaging of finished goods.</li><li>
Complete accurate production, quality, EHS, and maintenance documentation.</li><li>
Use SAP for operational tasks and production tracking.</li><li>
Conduct basic equipment upkeep and support site maintenance activities.</li><li>
Participate in training and continuous improvement efforts to enhance safety, quality, and performance.</li></ul><h2 class="jobSectionHeader">
What we are looking for</h2><ul><li>
High school diploma or GED.</li><li>
Experience in industrial or food processing environments preferred.</li><li>
Ability to read, write, and understand English.</li><li>
Ability to perform basic math functions without a calculator.</li><li>
Ability to use a calculator for percentages, averages, and conversions.</li><li>
Strong attention to detail and ability to follow precise instructions.</li><li>
Ability to meet all physical and PPE requirements of the role.</li></ul>
Every day, Lonza&rsquo;s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.</div>

Technician, Diagnostics

<div>Senior Administrative Assistant
Location: This position is based in our Walkersville, MD office. The typical work schedule is Monday through Friday, 8:00 AM&ndash;5:00 PM EST.
What you will get:
The full-time base annual salary for this position is expected to range between $62,000 to $100,000. In addition, below you will find a comprehensive summary of the benefits package we offer:<ul><li>
Performance-related bonus.</li><li>
Medical, dental and vision insurance.</li><li>
401(k) matching plan.</li><li>
Life insurance, as well as short-term and long-term disability insurance.</li><li>
Employee assistance programs.</li><li>
Paid time off (PTO).</li></ul>
Compensation for this role will be determined by the candidate&rsquo;s qualifications, skills, experience, and relevant knowledge.
What you will do:
The Senior Administrative Assistant provides comprehensive support to the ADS US Operations Growth Project leadership team and additional ADSLT members in the US, including the Global Head of Sales. This role is essential to maintaining efficient operations, facilitating clear communication, and supporting the successful execution of key initiatives.
Primary responsibilities include managing complex calendars, coordinating domestic and international travel, handling expense reporting, organizing meetings, and preparing reports and presentations. The role also involves supporting special projects from initiation to completion and requires strong technical proficiency, excellent research skills, and the ability to manage multiple priorities. A high level of professionalism, discretion, and sound judgment is critical, particularly when handling confidential and time-sensitive matters under pressure.<ul><li>
Completes a broad variety of administrative tasks, which requires extreme confidentiality.</li><li>
Organize events, guest visits and welcome visitors to the site.</li><li>
Arranging complex, detailed travel plans, itineraries, reservations, presentation creation/review, and agendas and compiling documents for meetings.</li><li>
Assisting with pre-, during, and post-meeting action items follow-up.</li><li>
Manages the schedules of Leadership Team and other senior leaders.</li><li>
Researches, prioritizes, and follows up on incoming issues and concerns addressed to the executives, including those of a sensitive or confidential nature, determining the appropriate course of action or response.</li><li>
Works closely and effectively with the executives, keeping them well informed of upcoming commitments and responsibilities, following up appropriately.</li><li>
Prioritize conflicting needs; handle matters expeditiously, and proactively, and follow through on projects to successful completion, often with deadline pressures.</li><li>
Prepares and supports communications to various stakeholders, including ones that require great confidentiality and sensitivity.</li><li>
Supports expense management and orders supplies and materials as needed.</li><li>
Files and organizes documents in electronic systems.</li><li>
Supports and asks for support from other administrative assistants.</li><li>
Perform other duties as assigned.</li></ul>
What we are looking for:<ul><li>
Advanced proficiency in Microsoft 365 (PowerPoint, Word, Excel, Teams, and related applications).</li><li>
Strong comfort with modern communication tools, including video creation platforms and social media management tools.</li><li>
Exceptional organizational skills with the ability to prioritize multiple competing demands while maintaining attention to detail.</li><li>
Strong interpersonal and relationship-building skills across diverse stakeholder groups.</li><li>
Sound problem-solving abilities, including the capacity to analyze information, exercise judgment, and implement effective solutions.</li><li>
Excellent written and verbal communication skills.</li><li>
Demonstrated proactive mindset with strong decision-making capabilities.</li><li>
High emotional intelligence and professional maturity.</li><li>
Commitment to quality, accuracy, and continuous improvement.</li><li>
Ability to work independently while also contributing effectively as part of a team.</li><li>
Proven discretion in handling confidential information and adaptability in a fast-paced environment.</li><li>
Demonstrated ability to meet deadlines and achieve high-performance goals.</li><li>
Forward-thinking approach with the initiative to identify opportunities and propose solutions.</li></ul>
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone&rsquo;s ideas, big or small, have the potential to improve millions of lives, and that&rsquo;s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you&rsquo;re ready to help turn our customers&rsquo; breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.</div>

Senior Administrative Assistant

Join Lonza and explore 6   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.