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Neurotech Pharmaceuticals, Inc. · 2 hours ago

QC Scientist

Cumberland, RI

Full-time

Onsite

Senior Level

6+ years exp

Neurotech Pharmaceuticals, Inc. is a private biotech company focused on developing transformative therapies for chronic eye diseases. The QC Scientist Technical Services will lead the planning and execution of quality control activities, ensuring the integrity and traceability of testing materials while collaborating with cross-functional teams to support method development and product characterization.

Biotechnology

Responsibilities

Oversee daily scheduling, prioritization, and execution of QCTS activities supporting QC Analytical operations

Lead the creation, qualification, and maintenance of reference standards, assay controls, and test reagents in compliance with GMP requirements

Ensure appropriate documentation, lifecycle management, and traceability of all QCTS materials

Collaborate closely with the QC Analytical, Commercial Sciences, and Process Development teams to support method development, method optimization, and transfer activities

Support new product development and characterization testing through technical expertise and resource management

Author, review, and approve technical documents including SOPs, protocols, reports, and investigations

Serve as a subject matter expert (SME) for analytical reagents, control systems, and reference material management

Train and mentor QCTS staff to ensure consistent performance, technical competency, and adherence to cGMP and GDP practices

Partner with Quality Assurance to ensure inspection readiness and continuous improvement of laboratory systems

Drive operational excellence by identifying and implementing process improvements in material management, documentation, and testing workflows

Qualification

GMP complianceAnalytical developmentBioassay executionMethod developmentTechnical writingLeadershipProblem solvingCross-functional collaboration

Required

Bachelor's or Master's degree in Biology, Biochemistry, Biotechnology, or related scientific discipline

6–10 years of progressive laboratory experience within Quality Control or Analytical Development, preferably in a biologics, cell therapy, or gene therapy environment

Demonstrated expertise in bioassay execution, analytical reagent management, and method lifecycle support

Proven leadership experience, with the ability to coordinate multidisciplinary teams and projects

Strong understanding of GMP, GLP, and data integrity requirements

Excellent technical writing, organizational, and communication skills