Qureos Mentor

Lonza

<div><h1 class="jobSectionHeader">Diagnostics Technician &ndash; QMA</h1>
Location: Greenwood, SC
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.
As a Diagnostics Technician (QMA) based in Greenwood, SC, you will help ensure product quality and operational excellence in our capsule manufacturing facility. You will support continuous production flow, perform in‑process quality checks, and uphold safety and compliance standards.<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>
Access to our global benefits: https://www.lonza.com/careers/benefits</li></ul><h2 class="jobSectionHeader">
What you will do</h2><ul><li>
Change feed tanks to maintain continuous material supply for capsule manufacturing.</li><li>
Perform in‑process inspections and make disposition decisions.</li><li>
Measure and record capsule dimensions and weights.</li><li>
Conduct routine sampling and metal detector checks.</li><li>
Enter inventory and quality data using tablets and handheld scanners.</li><li>
Monitor SCADA systems and respond promptly to alarms.</li><li>
Support continuous flow through basic troubleshooting at the HCM.</li></ul><h2 class="jobSectionHeader">
What we are looking for</h2><ul><li>
High school diploma or GED.</li><li>
Ability to work 12‑hour shifts, including weekends and holidays.</li><li>
Attention to detail and comfort using precision measurement tools.</li><li>
Ability to lift, push, or pull up to 50 lbs and use step ladders.</li><li>
Basic computer skills.</li><li>
Reliable on‑site attendance and commitment to quality and safety.</li><li>
Flexibility to support different duties as needed.</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>

Diagnostics Technician - QMA

<div>QC Analyst IV &ndash; Environmental Monitoring
Location: Portsmouth, NH, USA.
As a QC Analyst IV, you are a Subject Matter Expert (SME) and a primary technical lead for the Environmental Monitoring team. This senior role is critical for maintaining the microbial control strategy of our multi-modal facility. You will be responsible for leading complex investigations, driving continuous improvement projects, and ensuring our EM program remains in a permanent state of compliance with global regulatory standards.
Schedule: Day Shift, Monday &ndash; Friday, 8:00 AM &ndash; 5:00 PM
What You&rsquo;ll Get<ul><li>
Technical Leadership: Act as a lead for the EM department, influencing site-wide quality culture and operational strategy.</li><li>
Audit Frontline: Represent the EM program as a Subject Matter Expert during internal and external regulatory inspections (FDA, EMA, etc.).</li><li>
Advanced Project Ownership: Lead the implementation of new technologies, such as rapid microbiological methods or paperless data systems.</li><li>
Comprehensive Benefits: Medical, dental, vision, 401(k), and performance-based incentives. Our full list of global benefits: lonza.com/careers/benefits.</li></ul>
What You&rsquo;ll Do<ul><li>
Technical SME Ownership: Serve as the technical lead for the site&rsquo;s EM and Utility monitoring programs. Provide high-level guidance on sampling plans, risk assessments, and the qualification of new cleanrooms.</li><li>
Complex Investigations: Lead and author high-complexity environmental excursion investigations. Utilize root cause analysis (RCA) tools to identify systemic issues and implement effective CAPAs.</li><li>
Data Trending &amp; Strategy: Perform advanced analysis of environmental and utility data. Identify long-term trends and present findings to site leadership and the Quality Council to drive proactive contamination control.</li><li>
Regulatory &amp; Audit Excellence: Prepare, review, and defend EM data and procedures during regulatory audits. Ensure all department SOPs and sampling protocols meet current Annex 1 and global cGMP expectations.</li><li>
Mentorship &amp; Coaching: Provide advanced technical training and mentorship to Level I, II, and III analysts. Foster a culture of technical excellence and &quot;Right First Time&quot; performance.</li><li>
Continuous Improvement: Identify and execute Lean Laboratory initiatives to increase efficiency, reduce lead times, and enhance data integrity across the EM program.</li><li>
Review &amp; Approval: Act as a final technical reviewer for complex laboratory records, validation protocols, and summary reports.</li></ul>
Who We&rsquo;re Looking For<ul><li>
Education: Bachelor&rsquo;s degree (BS) in a Life Sciences discipline (Microbiology, Biology, or related field) is required.</li><li>
Experience: 5&ndash;10 years of advanced experience in Quality Control Microbiology or Environmental Monitoring within a cGMP manufacturing environment is required.</li><li>
Technical Mastery: * Expert-level knowledge of cleanroom classifications (Grade A&ndash;D) and aseptic processing.<ul><li>
Deep understanding of global regulatory requirements (FDA, EMA, ICH) for environmental and utility monitoring.</li><li>
Proficiency in utilizing Laboratory Information Management Systems (LIMS) and data trending software.</li></ul></li><li>
Leadership Attributes: A proven track record of leading projects, managing timelines, and influencing cross-functional teams without direct authority.</li><li>
Communication: Exceptional technical writing skills and the ability to present complex scientific data clearly to senior management and auditors.</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 lead the standard of excellence in QC? Apply now.</div>

QC Analyst Level IV - Environmental Monitoring

<div>QC Analyst I &ndash; Analytical (Cell Therapy, Night Shift)
Location: Portsmouth, NH, USA.
As a QC Analyst I on our Cell Therapy Analytical team, you are responsible for the high-precision testing that confirms the safety and potency of personalized medicines. Working on the night shift, you provide the critical data needed to move patient treatments forward. This is a foundational role for a scientifically minded individual who wants to master complex analytical methods in a fast-paced, high-stakes environment.
Schedule &amp; Shift<ul><li>
Shift: Night Shift (8:00 PM &ndash; 6:30 AM)</li><li>
Days: Wednesday through Saturday (4-day, 10-hour schedule)</li><li>
Orientation: Your first 2 weeks of training will be held on the day shift.</li><li>
Differentials: This role includes competitive night and weekend shift pay.</li></ul>
What You&rsquo;ll Get<ul><li>
Specialized Technical Training: Master foundational analytical techniques (such as Flow Cytometry, ELISA, or qPCR) used in the release of cell-based therapies.</li><li>
Direct Impact: Your work directly verifies that a patient&rsquo;s custom treatment is safe and effective before it reaches them.</li><li>
Predictable Balance: The 4x10 schedule offers three consistent days off per week.</li><li>
Full Lonza Benefits: Medical, dental, vision, 401(k), and performance-based incentives. Our full list of global benefits: lonza.com/careers/benefits.</li></ul>
What You&rsquo;ll Do<ul><li>
Analytical Testing: Perform routine analytical assays to support in-process, lot release, and stability testing for Cell Therapy products.</li><li>
Aseptic Handling: Maintain the highest standards of sterility when handling sensitive biological samples to ensure data integrity and prevent contamination.</li><li>
Data Recording: Document all results in real-time, following Good Documentation Practices (GDP) and ensuring 100% compliance with cGMP standards.</li><li>
Lab Support: Assist in the maintenance of laboratory equipment, the preparation of reagents, and ensuring the lab remains in an audit-ready state.</li><li>
Collaborative Quality: Work closely with your night shift team to meet manufacturing deadlines and participate in clear, detailed shift handovers.</li><li>
Problem Recognition: Learn to identify and escalate any results that deviate from expected ranges, supporting the team in maintaining total process control.</li></ul>
What We&rsquo;re Looking For<ul><li>
Education: Associate&rsquo;s or Bachelor&rsquo;s degree in a Scientific Discipline (Biology, Chemistry, Biochemistry, or related field) is required.</li><li>
Experience: This is an entry-level (Level I) role. We are looking for individuals with strong foundational lab skills, whether from an academic setting or prior industry experience.</li><li>
Technical Aptitude: A strong desire to learn complex analytical instrumentation and laboratory computer systems (LIMS).</li><li>
Attention to Detail: The ability to follow detailed Standard Operating Procedures (SOPs) with 100% accuracy.</li><li>
Reliability: Ability to consistently work the 8 PM &ndash; 6:30 AM schedule and contribute to a high-performing night team.</li><li>
Attributes: Self-motivated, positive attitude, and a deep commitment to the patient-first mission of Cell Therapy.</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 start your career in QC? Apply now.</div>

QC Analyst I - Analytical (Nights)

<div>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.
As an Assistant Manager &ndash; Operational Quality, you will lead the on-site QA function supporting capsule manufacturing operations. You will ensure real-time GMP compliance across IPQA, validation, batch review and release, deviation and CAPA management, document control, and SAP master data governance. This role plays a critical leadership position in maintaining regulatory readiness and driving quality excellence within operations.
What you&rsquo;ll get<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>
Opportunities to lead a QA team in a regulated GMP manufacturing environment.</li></ul>
The full list of our global benefits can be found at: 
https://www.lonza.com/careers/benefits
What you&rsquo;ll do<ul><li>
Lead the IPQA team to ensure real-time GMP compliance during capsule manufacturing operations, including line clearance, in-process controls, documentation review, sampling, and AQL inspections.</li><li>
Provide on-floor quality decision-making during deviations and critical manufacturing activities.</li><li>
Own and govern the Validation Master Plan (VMP) and ensure execution of equipment qualification (IQ/OQ/PQ) and process validation activities.</li><li>
Review and approve validation protocols and reports in alignment with GxP, WHO-GMP, and Schedule M requirements.</li><li>
Ensure timely batch record review, disposition, and release readiness.</li><li>
Lead deviation investigations, perform robust root cause analysis, and ensure effective CAPA implementation and closure.</li><li>
Oversee control sample management and document control systems (WOPs, validation records, electronic documentation).</li><li>
Ensure SAP master data governance (item codes, BOMs, material attributes) is accurate and compliant with approved procedures.</li><li>
Compile and review Annual Product Quality Reviews (APQR), analyze trends, and recommend continuous improvement initiatives.</li><li>
Support audits and inspections (customer, regulatory, third-party), ensuring documentation readiness and compliance responses.</li><li>
Drive quality improvement initiatives and support Operational Excellence programs.</li></ul>
What we&rsquo;re looking for<ul><li>
Bachelor&rsquo;s degree in pharmacy (B. Pharm) or relevant life sciences discipline.</li><li>
Experience in Quality Assurance within a regulated pharmaceutical or life sciences manufacturing environment.</li><li>
Strong knowledge of cGMP, GDP, ICH guidelines, and regulatory compliance standards.</li><li>
Proven experience in IPQA, qualification &amp; validation, deviation/CAPA management, and batch review.</li><li>
Experience leading teams in a manufacturing environment (direct people management preferred).</li><li>
Demonstrated analytical, documentation, and problem‑solving skills.</li><li>
Ability to make sound quality decisions in real-time production environments.</li><li>
Effective communication skills in English and Hindi.</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 around the world &mdash; and making a meaningful difference.</div>

Assistant Manager - Operational Quality

Join Lonza and explore 4   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.

Lonza

About Company

Diagnostics Technician - QMA

QC Analyst Level IV - Environmental Monitoring

QC Analyst I - Analytical (Nights)

Assistant Manager - Operational Quality