Quality Control Specialist I

Quality Control Specialist I Employer Boston BioProducts Location Milford, Massachusetts Start date May 1, 2026 View more categories View less categories Discipline Clinical , Clinical Medicine , Quality Required Education Bachelors Degree Position Type Full time Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Send job Job Details Boston BioProducts is looking for a Quality Control Specialist I who will be responsible for in-process testing, quality control testing of final products and raw materials, and maintaining calibration and log data for BBP equipment. The role assists the quality departments in all aspects of conducting quality control testing BBP products. This is a 100% (Mon-Fri) onsite role in Milford, MA - LOCAL

CANDIDATES ONLY

•Direct Applicants ONLY - No Staffing Agencies or Third-Party Recruiters."

Role & Responsibilities:

Maintains a clean and organized work environment, including equipment maintenance and material organization. Maintain calibrations and log data for BBP equipment within the laboratory.

Manage all the samples:

Raw Materials, QC, Stability, and Retain samples in the most retrievable manner Collect and process samples in a timely manner. Performs Environmental monitoring on clean rooms within the facility. Records and documents daily, weekly, and quarterly calibrations using GDP's Monitor in-process control where applicable Assist in conducting quality control testing of Boston Bioproducts' products and raw materials. All findings are interpreted and reported to the Quality Operations Manager and QC Manager. Following GDP and ALCOA+ guidelines, will record results and measurements of calibrations Documents and standard operating procedures (SOP) are managed in a timely fashion and updated to current practices. Assist in maintaining and reporting digital and printed testing results to QC Manager. Assist in maintaining logbooks related to inventory and equipment in the QC laboratory. Assist in maintaining documents and Standard Operating Procedures (SOP) of the Quality Department. Assists in additional duties delegated by the QC Manager. Assists in other duties by the quality department on an as-needed basis.

Qualifications & Requirements:

1-2 years of relevant experience Bachelor's degree in a scientific discipline or equivalent Ability to follow instructions precisely, recognize deviations, and recommend corrective action within the scope of training. Good time management and organizational skills. Demonstrate the ability to multitask and consistently meet deadlines. Familiar with aseptic technique, have a proper understanding of laboratory safety procedures. Good written and verbal communication skills. Ability to communicate effectively with others. Have a detail-oriented work ethic and be familiar with recognized regulations such as ISO and GMP. Ability to troubleshoot within the scope of training. Ability to work well independently and in a team environment. Is computer literate and proficient in MS Word, Excel, and other relevant electronic systems. Must have own, reliable vehicle to drive to Milford, MA (Monday - Friday) Milford does NOT have public transportation Share this job Facebook Twitter LinkedIn Apply now Send job Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Get job alerts Create a job alert and receive personalized job recommendations straight to your inbox. Create alert