QC Technical Services Analyst II - Sample Logistics & Docs

Lonza; Portsmouth (VA); On-site; Confidential; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

PTO

Job summary

Lonza is seeking a QC Technical Services Analyst II to support the Large Scale Allogeneic (LSA) project in Portsmouth. You will own sample logistics, inventory control, and core cGMP documentation, ensuring right-first-time testing and strict data integrity while interfacing with Manufacturing, Supply Chain, and QC teams.

The role requires 1–3 years in a cGMP lab or regulated setting, with a focus on quality systems, chain-of-custody, and aseptic methods.

Qualifications

• Experience in a cGMP laboratory or regulated pharmaceutical inventory.
• Understanding of quality systems and data integrity principles.
• Familiarity with chain-of-custody tracking and controlled documents.
• Aseptic validation concepts and cleanroom workflows.
• Strong written and verbal communication; ability to manage ambiguity.

Responsibilities

• Manage sample receipt, login, and temperature-controlled storage tracking.
• Oversee long-term archival and annual inventories of retain samples.
• Issue controlled-copy prints of SOPs, test methods, and master forms.
• Create and revise cGMP documentation, logbooks, and material tracking protocols.
• Collaborate with Manufacturing, Supply Chain, and QC to align sample timelines.

Skills

Quality systems

Chain-of-custody

Cleanroom documentation

Aseptic validation

Communication skills

Time management

Education

High School Diploma or equivalent

Bachelor's in Chemistry

Bachelor's in Biology

Bachelor's in Computer Systems

Job description

Lonza is seeking a QC Technical Services Analyst II to support the Large Scale Allogeneic (LSA) project in Portsmouth. You will own sample logistics, inventory control, and core cGMP documentation, ensuring right-first-time testing and strict data integrity while interfacing with Manufacturing, Supply Chain, and QC teams.

The role requires 1–3 years in a cGMP lab or regulated setting, with a focus on quality systems, chain-of-custody, and aseptic methods.