At Alamar, we are passionate about enabling our customers to make scientific discoveries that translate into clinical outcomes and benefit patients. Our team is growing quickly as we develop innovative approaches to measure critical protein biomarkers from liquid samples that can enable the earliest possible detection of disease. We believe the next frontier in biology is enabled by measuring proteins at higher sensitivity in highly multiplexed assays at the push of a button, which is something only Alamar can do. As we build our team, we seek collaborative, driven, intellectually curious people committed to solving complex challenges. Our culture rewards accountability and cross functional teamwork because we believe this enables the kind of breakthrough thinking that will accelerate our mission.

Position Description:

We seek a highly motivated Quality Control Analyst II to join our Operations team.  This position will be part of the Quality Control team, supporting all product testing activities from raw materials to finished goods, as well as product stability.  This position will also participate/provide support in data evaluation, troubleshooting, and streamlining processes. Seeking a professional analyst who is a swift learner, resourceful, organized, detail-oriented, and can adapt to shifting priorities in a fast-paced and rapidly growing company, while adhering to established protocols and procedures. All activities will be in compliance with ISO 13485/GMP requirements.

Key Responsibilities:

  • Perform analytical/functional testing for in-process and finished goods on manufactured products.
  • Perform analytical/functional testing on incoming raw materials.
  • Perform product testing to support product stability/dating.
  • Review data and assess against established acceptance criteria.
  • Prepare QC reference test materials per established procedures.
  • Record, track, and maintain QC data in logs and spreadsheets for trending.
  • Revise and update QC testing procedure and documentation for better workflow.
  • Generate data and graphs for trending test results
  • Initiate and participate in nonconformance/deviation and troubleshooting activities
  • Generate Equipment operation and maintenance SOPs.
  • Participate/provide support in streamlining QC workflow

 OCCASIONAL DUTIES AND RESPONSIBILITIES

  • Perform testing on non-routine samples to establish QC specifications.
  • May assist in performing incoming inspection and visual inspection of manufactured products activities.
  • Participate in Test Method Validation

 QUALIFICATIONS

  • A B.S./B.A. in molecular biology, biochemistry, cell biology or related field with 2-3 years of industry laboratory experiences preferability in a Quality Control laboratory.
  • Experience in molecular biology techniques
  • Detail oriented, organized, and efficient
  • Strong team player and can work independently.
  • Excellent verbal and written communication skills
  • Experience working in ISO 13485 and GMP environment preferably in QC processes.

The base salary range for this full-time position is $80,000 - $95,000 + bonus + equity + benefits. Our salary ranges are determined by work location, job-related skills, experience, and relevant education or training. The ranges displayed on each job posting reflect the minimum and maximum target for new hire salaries but are subject to change if the leveling of the role is adjusted.

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