What are the responsibilities and job description for the Quality Control Analyst position at Meet Life Sciences?
Job Title: Scientist II, Analytical Development / Quality Control
Location: Watertown, MA
Job Summary:
The Scientist II will support analytical development and quality control activities for nucleic acid and microbiome-based platforms. This role focuses on method development, validation, and tech transfer in a cGMP environment, while driving data analysis, problem-solving, and continuous improvement.
Key Responsibilities:
- Plan and execute analytical development and tech transfer activities in a cGMP setting.
- Design and perform experiments to support assay development, validation, and stability programs.
- Develop, optimize, and qualify analytical methods, including sequencing and release assays.
- Analyze complex data, interpret results, and prepare technical reports and presentations.
- Support implementation of 21 CFR Part 211-compliant systems and processes.
- Collaborate cross-functionally with Manufacturing, Quality, and external partners.
- Monitor processes, ensure timely project delivery, and contribute to continuous improvement initiatives.
- Participate in recruiting and mentoring technical staff.
Qualifications:
- Bachelor’s degree with 6 years of experience in assay development and validation.
- Strong knowledge of cGMP environments and analytical technologies.
- Experience with method development, tech transfer, and stability-indicating assays.
- Proven ability to design experiments, analyze data, and solve complex problems.
- Excellent communication skills and ability to manage multiple priorities in a fast-paced environment.