QC Lab Instrumentation & Methods Specialist

Arcadis; Boston (MA); On-site; USD 65,000 - 85,000; Full time

Job summary

Arcadis is seeking a mid-level Quality Control Analyst to provide fully onsite support for a capital project at a pharmaceutical manufacturing facility in Lexington, Massachusetts.

The QC Analyst will support qualification and implementation of new QC instruments (titrators, density meter, UV spectrophotometers), method transfer and validation, SOP development, analyst training, and GMP documentation. Hands-on GMP lab experience and strong communication skills are preferred.

Qualifications

• Bachelor degree in Engineering, Chemistry, Biochemistry, Pharmaceutical Sciences, Biology, or related field preferred.
• Experience in a QC lab within pharma/biotech or life sciences.
• GMP-regulated environment experience is required or beneficial.
• Hands-on experience with analytical laboratory instruments and testing procedures.
• Experience authoring or revising SOPs and analytical methods.
• Understanding of analytical method validation and method transfer principles.

Responsibilities

• Support qualification and implementation of new QC lab instruments.
• Provide assay support for new titrators and a density meter.
• Support upgrades and qualification activities for UV spectrophotometers.
• Assist with analytical method transfers for new or updated equipment.
• Author, revise, and review SOPs and analytical methods.
• Execute or support analytical method validation activities.
• Perform analytical testing per approved procedures and GMP requirements.
• Prepare, review, and maintain laboratory and qualification documentation.
• Help develop training materials for QC personnel.
• Train analysts on new instruments and methods.
• Ensure qualification, validation, testing and training are properly documented.
• Collaborate with QC, QA, engineering, validation and project stakeholders.

Skills

QC Laboratory

GMP Compliance

Analytical Instruments

SOP Development

Cross-functional teamwork

Education

Bachelor’s degree in a related scientific field

Tools

Titrators

Density meter

UV spectrophotometers

Job description

Arcadis is seeking a mid-level Quality Control Analyst to provide fully onsite support for a capital project at a pharmaceutical manufacturing facility in Lexington, Massachusetts.

The QC Analyst will support qualification and implementation of new QC instruments (titrators, density meter, UV spectrophotometers), method transfer and validation, SOP development, analyst training, and GMP documentation. Hands-on GMP lab experience and strong communication skills are preferred.