Portsmouth, New Hampshire, United States · On-site
Mid level$445M raised
Logistics Specialist II (Day Shift) Training for this position will be held Mon-Fri first shift for first 2 months. Location: The actual location of this job is in Portsmouth, NH. This is a fully site‑based role. Working…
Umzugsunterstützung steht berechtigen Kandidaten und ihren Familien bei Bedarf zur Verfügung. Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist. Wir sind …
As a QC-Analyst you will performs timely testing and analysis of in-process and final product samples in compliance with SOPs and cGMP, ensuring accurate documentation and data integrity. Supports lab operations, sample …
Manufacturing Systems Specialist (Greenwood, SC - Hybrid)
Greenwood, South Carolina, United States · Hybrid
Senior$445M raised
Manufacturing Systems Specialist Location: Greenwood, South Carolina - Hybrid The actual location of this job is in Greenwood, SC. Relocation assistance is available for eligible candidates and their families, if needed.…
Skills: IT/OT Systems Design, C#, C/C++, Python, PLC/HMI/SCADA
Job Title: Associate Director, Nutraceutical Marketing- AMER Location: Morristown, NJ Join Lonza’s Capsules & Health Ingredients team as a Nutraceutical Marketing Associate Director and help shape the future of the nutra…
Quality Supervisor – Cell Therapy Location: This is an on-site position located in Pearland, TX. Available shift: AM Shift, Wednesday – Saturday, 6:00 AM – 4:30 PM, supporting Quality Control operations with weekend shif…
Skills: Quality Control Supervision, cGMP Compliance, Cell-based Assays, ddPCR, ELISA
Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. You will represent Quality Assurance in cross-functional teams,…
Skills: Quality Assurance, GMP Compliance, Drug Product Services, Deviation Management, Change Control
Portsmouth, New Hampshire, United States · On-site
Mid level$445M raised
QA Operations Specialist II - LSA (Dayshift) Location: This is a 1st shift position operating on a 12-hour rotating schedule (7:00 AM – 7:00 PM). The schedule follows a rotating pattern of Monday–Tuesday workdays, Wednes…
Portsmouth, New Hampshire, United States · On-site
Senior+$445M raised
QA Operations Specialist IV - LSA (Nightshift) Location: This is a 3rd shift position operating on a 12-hour rotating schedule (7:00 PM – 7:00 AM). The schedule follows a rotating pattern of Monday–Tuesday workdays, Wedn…
Umzugsunterstützung: Verfügbar für berechtigte Kandidatinnen und Kandidaten sowie deren Familien. Am Standort Visp wird ein Operations Manager Manufacturing (m/w/d) gesucht. In dieser Position bist Du für die Leitung von…
Skills: Production Management, Chemical Manufacturing, API Production, Risk Analysis, GMP
Associate Director, Business Development, Biologics
Portsmouth, New Hampshire, United States · Remote OK
$158k–$205k/yr
Senior+$445M raised
Associate Director, Business Development, Biologics – San Francisco / Bay Area Location: Remotely based out of San Francisco / Bay Area, CA. Note on Travel & Location: This is a field-based, remote position. Candidates m…
Portsmouth, New Hampshire, United States · On-site
Senior$445M raised
QA Operations Specialist III - LSA (Nightshift) Location: This is a 3rd shift position operating on a 12-hour rotating schedule (7:00 PM – 7:00 AM). The schedule follows a rotating pattern of Monday–Tuesday workdays, Wed…
Portsmouth, New Hampshire, United States · On-site
Senior$445M raised
QA Operations Specialist III - LSA (Nightshift) Location: This is a 3rd shift position operating on a 12-hour rotating schedule (7:00 PM – 7:00 AM). The schedule follows a rotating pattern of Monday–Tuesday workdays, Wed…
The QC Analyst will be responsible for Biochemistry Area in the QC Lab to support Lot Release activities What you’ll get An agile career and dynamic working culture in a global life sciences leader. An inclusive and ethi…
Skills: Analytical Testing, cGMP, Data Integrity, ELISA, PCR
Portsmouth, New Hampshire, United States · On-site
Mid level$445M raised
Biotechnologist II – Cell Therapy Location: Portsmouth, NH, USA. Schedule: Day Shift, 7:00 AM – 7:00 PM, Rotational 2-2-3 Pattern (Note: Your first 2-week orientation and training period will be held on the day shift.) N…
Skills: Aseptic Technique, cGMP Regulations, Grade B Cleanroom Processing, Sterile Gowning, Electronic Batch Records
Manufacturing Services Associate I (Days - B shift)
Portsmouth, New Hampshire, United States · On-site
Entry level$445M raised
Today, Lonza is a global leader in life sciences operating across three 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…
Director Operational Excellence & PMO Microbial Operations
Visp, Wallis, Switzerland · On-site
Senior+$445M raised
Director Operational Excellence & PMO – Microbial Operations The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. This role is…
Greenwood, South Carolina, United States · On-site
Senior$445M raised
Job Title Specialty Products Printing Manager Location The actual location of this job is Greenwood, South Carolina, United States. This role leads a multi-shift manufacturing operation focused on printing and finishing …
Skills: Manufacturing Leadership, Production Metrics Monitoring, Budget Management, Process Improvement, Team Coaching
Greenwood, South Carolina, United States · On-site
Entry level$445M raised
Job Title: Printing Operator (Night Shift) Location: Greenwood, South Carolina, USA Join Lonza’s manufacturing team in Greenwood, SC, where you will play a key role in transforming capsules into finished pharmaceutical p…
Operator / Senior Operator Production Support (m/w/d)
Visp, Wallis, Switzerland · On-site
Mid level$445M raised
Der Standort dieser Position ist in Visp, Schweiz. Bei Bedarf steht für berechtigte Kandidaten und ihre Familien Unterstützung beim Umzug zur Verfügung. Was wir Ihnen bieten: Eine agile Karriere und eine dynamische Arbei…
Skills: SOP Compliance, cGMP Guidelines, Production Equipment Operation, Buffer And Media Preparation, Autoclave Operation
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
high school
Medical Insurance, Dental Insurance, Vision Insurance, Paid Time Off
Posted 43d ago
~40 hrs/week
Responsibilities
The Logistics Specialist II manages the receipt, storage, and allocation of API and consumable components using SAP and Syncade. They also support manufacturing by handling domestic and international product shipping and maintaining compliant logbook entries.
Requirements
Candidates must have a high school diploma or equivalent and a valid driver's license. Proficiency in Microsoft Outlook and the ability to learn internal systems is required, with prior manufacturing experience preferred.
Full job description
Logistics Specialist II (Day Shift)
Training for this position will be held Mon-Fri first shift for first 2 months.
Location:The actual location of this job is in Portsmouth, NH.
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 Logistics Specialist II will contribute within team using SAP, Syncade and/or Ship console Systems for receipt, storage, issuance, dispensing and allocations of API and consumable components. Supports Manufacturing in handling & shipping product domestic and internationally.
What you will get:
An agile career and dynamic working culture.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
Medical, dental and vision insurance.
Paid time off.
And much more.
What you will do:
Demonstrates solid understanding of assigned procedures & obtains required qualifications.
Demonstrates an understanding of cGMP’s required in the work environment.
Performs Circular Chart required tasks for assigned area (Installation, Review, Daily monitoring).
Perform Logbook entries/review as required for assigned area.
Performs safe and compliant operation of Class 1,2,3 & 4 for assigned area.
Utilizes DMS and Trackwise for assigned area. Performs SAP and Syncade transactions required for assigned area.
Perform other duties as they are assigned to support department.
What Lonza is looking for:
High school diploma or equivalent or higher level of education
Ability to use Microsoft Outlook, and learn Lonza systems for role requirements
Valid driver’s license
Prior work experience in a manufacturing environment is a plus
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.
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.