Portsmouth, New Hampshire, United States · On-site
Mid level$445M raised
QC Analyst III, Analytical - Large Scale Allogenic Manufacturing Location: Portsmouth, NH, USA. Schedule: Monday - Friday, 0800-1700 We are seeking an advanced laboratory professional to join our Quality organization in …
Portsmouth, New Hampshire, United States · On-site
Mid level$445M raised
QC Analyst II, Analytical – Large Scale Allogenic Manufacturing Location: Portsmouth, NH, USA. Schedule: Monday – Friday, 0800 - 1700 We are seeking a laboratory professional to join our Quality organization in Portsmout…
Security Supervisor Tampa, FL 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 tal…
Skills: Physical Security Management, Access Control Systems, CCTV Monitoring, Incident Response, DEA Regulations Compliance
Microbiology – QC Technologist Location: Slough Shift Pattern: Every Weekend is required for this role. You will join our QC Microbiology team, where you will help ensure the quality and safety of our products through es…
Skills: Microbiological Testing, Environmental Monitoring, GMP, cGMP, Good Documentation Practices
Ibex® Solutions (www.ibex.lonza.com) ist ein modularer Komplex für die Entwicklung und Herstellung von biologischen Produkten. Unternehmen können damit auf eine Komplettlösung zugreifen, dabei an Schnelligkeit gewinnen u…
Der Standort dieser Position ist in Visp, Schweiz. Bei Bedarf steht für berechtigte Kandidaten und ihre Familien Unterstützung beim Umzug zur Verfügung. Dies ist eine onsite Position. Die persönliche Zusammenarbeit vor O…
Skills: cGMP Guidelines, Mammalian Cell Culture, Buffer and Media Preparation, Autoclave Operation, Troubleshooting
Senior Manager, Data Scientist (AI/ML & GenAI) Location: Hyderabad, India This is an office‑first role. Working together in person supports close, real‑time collaboration and team alignment, enabling us to deliver our be…
Senior Program Manager (CGT) The actual location of this job is in Singapore. This critical role partners closely with our customers to successfully deliver programs. As a Senior Program Manager, you will be responsible …
Skills: Program Management, Customer Relationship Management, Project Planning, Cross Functional Leadership, Data Integrity
Concur & Card Application Lead Location: San Jose, Costa Rica Join Lonza in a global role where you will own and evolve our SAP Concur Expense platform and Corporate Card Program. This is an exciting opportunity to drive…
Skills: SAP Concur, Corporate Card Program Management, Expense Management, Financial Controls, Process Automation
Portsmouth, New Hampshire, United States · On-site
Senior$445M raised
Facilities Suite Maintenance Mechanic, Level III Location: Portsmouth, NH. The shift schedule will be from 6am-6pm: Sunday-Tuesday week 1, Sunday-Wednesday week 2… The first 3 months of training will be during M-F: 8-4:3…
R&D Purification Scientist Slough, United Kingdom 12 Month Fixed Term Contract Join a cutting-edge R&D team at Lonza, where you will help advance next-generation purification technologies. This is an exciting laboratory-…
Skills: Downstream Processing, Chromatography, Filtration, Data Analysis, Process Optimisation
Portsmouth, New Hampshire, United States · Remote OK
Senior+$445M raised
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,…
Payroll Payments & Accounting Specialist (EMEA) Location: Hyderabad This is an office‑first role. Working together in person supports close, real‑time collaboration and team alignment, enabling us to deliver our best wor…
Quality Assurance Supervisor – Night Shift Location: This is an on-site position located in Pearland, TX. Available shift: 5:00 pm to 2:00 am Monday through Friday The Quality Assurance Supervisor - Night Shift will over…
Skills: Quality Assurance, cGMP Compliance, Team Leadership, Batch Record Review, Deviation Management
Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist. Wir sind in der Wissenschaft tätig, jedoch gibt es keine Zauberformel dafür, wie wir die Arbeit angehen…
The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Lead a high-impact MSAT team through a demanding CAPEX growth projec…
Skills: People Leadership, Sterile Fill & Finish, MSAT, Technology Transfer, Process Performance Qualification
Senior IT Solution Expert – SAP PP/MM Location: Hyderabad, India The actual location of this job is in Hyderabad, India. Join Lonza as a Senior IT Solution Expert – SAP PP/MM, where you will play a key role in delivering…
Skills: SAP PP, SAP MM, MES Integration, Production Planning, Inventory Management
Job Title: Quality Assurance Operations Specialist Location: Verviers Relocation assistance is provided for the successful candidate. The role: The Quality Assurance (QA) Operations Specialist is an experienced professio…
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
Full-time
bachelor degree, postgraduate degree
Medical Insurance, Dental Insurance, Vision Insurance, Paid Time Off
Posted 50d ago
~40 hrs/week
Responsibilities
Execute complex cGMP release testing using biological and immunological assays while leading method validations and analytical transfers. Manage laboratory investigations, OOS events, CAPAs, and provide technical training to junior QC personnel.
Requirements
Requires a Bachelor's degree in Biochemistry, Biology, or a related science with 3-4+ years of QC experience in a cGMP biomanufacturing environment. Must possess technical mastery of flow cytometry, PCR, and cell culture maintenance.
Full job description
QC Analyst III, Analytical - Large Scale Allogenic Manufacturing
Location: Portsmouth, NH, USA.
Schedule: Monday - Friday, 0800-1700
We are seeking an advanced laboratory professional to join our Quality organization in Portsmouth, NH, as an Analyst III, QC Analytical. Operating under general supervision, this senior bench-based role executes critical cGMP release testing, handles method validation protocols, and drives complex laboratory investigations.
What will you get?
An agile career and dynamic working culture
An inclusive and ethical workplace
Compensation programs that recognize high performance
Medical, dental and vision insurance, as well as PTO and more
Advanced cGMP Release Testing: Execute complex biological, immunological, and cell-based testing—specifically utilizing flow cytometry, ELISA, PCR assays, cell culture, and cell counting—ensuring total compliance with internal SOPs, USP, and EP guidelines to support on-time in-process control and final product release.
Assay Transfer & Method Validation: Actively spearhead analytical method transfers, qualifications, and validation protocols, including onboarding new methodologies and configuring advanced laboratory instrumentation.
Data Review & Verification: Review raw laboratory records, data calculations, and execution logs for absolute accuracy, protocol compliance, and strict adherence to Good Documentation Practices (GDP).
Investigation & OOS Ownership: Lead comprehensive Out-of-Specification (OOS) and laboratory deviation investigations, leveraging root-cause analysis tools to address complex non-conformances with minimal support.
CAPA & Change Control Management: Author, edit, and coordinate corrective and preventive actions (CAPAs) and detail structured Change Controls to promote compliance and continuous laboratory improvement with minimal support.
Document Architecture: Develop, modify, and sustain standard operating procedures (SOPs), master forms, and test records to match evolving industry expectations and site improvements.
Peer Training & Floor Leadership: Deliver hands-on, on-the-job training for junior QC personnel, reviewing data packets, modeling strong work ethics, and escalating critical laboratory anomalies to management as needed.
What we’re looking for:
Experience: 3-4+ years of direct Quality Control laboratory experience within a cGMP biomanufacturing or regulated clinical testing setting is required.
Technical Mastery: Proven, hands-on experience performing cell culture maintenance, immunophenotyping panels via flow cytometry, PCR amplification, and standard immunological assay techniques.
Systems & Digital Compliance: Familiarity with Laboratory Information Management Systems (LIMS), enterprise data management applications, and quality systems software (such as TrackWise) is highly preferred.
Investigation Savvy: Demonstrated ability to independently lead laboratory event investigations, formulate root-cause theories, and write clear, logical technical summaries.
Education: Bachelor’s Degree in Biochemistry, Biology, or a closely related technical science discipline is required. A Master’s Degree in a scientific discipline is preferred.
Soft Skills: Superior written and oral communication skills, a solutions-focused team attitude, and the personal initiative required to navigate multiple testing demands and overcome performance roadblocks without routine reminders.
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’s ideas, big or small, have the potential to improve millions of lives, and that’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’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
Related keywords
cGMPQuality ControlAnalytical ChemistryBiomanufacturingFlow CytometryELISAPCRCell CultureUSPEPGDPLIMSTrackWiseOOSCAPAChange Control
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.
Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.
For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.
Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.
For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.