Lonza
QC Technical Services Analyst II
US - Portsmouth, NH · Mid
Sponsorship not specifiedDetected 27 days ago
Supply ChainLogisticsGMPCommunicationCollaborationTime Management
About the role
- QC Technical Services Analyst II - Large Scale Allogeneic (LSA) Project Location: Portsmouth, NH, USA.
- Schedule: Monday - Friday, 8:00 AM - 5:00 PM Note on shift transition: As production ramps up and scales, this schedule will transition to a 4x10 alternative work week.
- The final shift assignment will be determined by production output timelines, moving to either Sunday - Wednesday (7:00 AM - 5:30 PM) or Wednesday - Saturday (7:00 AM - 5:30 PM).
Responsibilities
- Controlled Document Governance: Issue controlled-copy prints of active SOPs, Test Methods, and master assay execution forms. Coordinate periodic inventory reviews to maintain adequate bench-side stocks while archiving completed quality records.
- GMP Documentation & Authorship: Create, revise, and review localized cGMP laboratory documentation, logbooks, and material tracking protocols in strict compliance with data integrity regulations.
- Cross-Functional Communication: Proactively interface with cross-functional partners in Manufacturing (MFG), Supply Chain (SC), and broader Quality Control (QC) units to align sample delivery milestones with testing timelines.
- Physical Requirements: Routine ability to handle ultra-low temperature environments (freezers/cold rooms), comfortably walk the production and lab footprint, maintain compliance during sterile cleanroom gowning blocks, and occasionally lift up to 50 lbs.
- Manage the long-term archival placement of retain samples.
- Coordinate periodic inventory reviews to maintain adequate bench-side stocks while archiving completed quality records.
Requirements
- Proactive, "go-getter" attitude: Strong sense of personal ownership, urgency, and the initiative required to drive projects to a successful conclusion.
- Soft Skills: Strong written and oral communication skills, a collaborative team-player mindset, and the professional flexibility required to manage ambiguity and adapt to shifting project prioritization timelines.
- ability to make independent compliance decisions using defined internal practices, company policies, and historical data baselines.
- 1-3 years of direct experience within a cGMP Quality Control laboratory, regulated pharmaceutical manufacturing inventory, or clinical repository setting is required.
Nice to have
- High School Diploma or equivalent is required.
- A Bachelor's Degree in Chemistry, Computer Systems, Biology, or a related technical science field is highly preferred.
Compensation
- Compensation programs that recognize high performance
Benefits
- https://www.lonza.com/careers/benefits.
- Medical, dental and vision insurance, as well as PTO and more
- Education: High School Diploma or equivalent is required.
Company info
- What we're looking for:
This listing is sourced directly from Lonza's careers page and normalized into a canonical job model.