Quality Control Analyst

Aequor

Framingham (MA)

On-site

USD 45,460 - 48,216

Full time

14 days+

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Job summary

A technology solutions company is seeking a Quality Control Analyst I in Framingham, MA. The role requires 3 years of QC experience, including GDP and ALCOA knowledge. The analyst will execute quality testing procedures and participate in implementing new technologies. The position is contractual until November 2026 with a possibility for extension.

Qualifications

3 years' experience as a QC Analyst.
Must have GDP with ALCOA experience.
Experience with quality testing procedures.

Responsibilities

Perform operations necessary for quality testing.
Implement new technology within quality control.
Conduct data review and preliminary evaluation of results.

Skills

Quality Control

Data Analysis

Laboratory Skills

Tools

Perkin Elmer Spectrometer LAMBDA 365+

Job description

This range is provided by Aequor. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base Pay Range

$33.00/hr - $35.00/hr

Direct message the job poster from Aequor

Sr US Recruiter at Aequor Information Technologies Pvt. Ltd

Job Title- Quality Control Analyst I

Location: Framingham, MA 01701

Duration: Contract till Nov 2026 with possibility to extend

Notes 1-3: 3 years’ experience as a QC Analyst. QDCI (Quality, Delivery, Cost and Innovation) daily meetings to review schedules, testing, assay assigned (80% of time in lab), and data packet. Must have GDP with ALCOA experience (Attributable, Legible, Contemporaneous, Original and Accurate). Experience with Perkin Elmer Spectrometer LAMBDA 365+

Job Description

1st Shift: Perform operations necessary for quality testing and plays a role in implementing new technology within quality control. At more senior levels, provide an investigative or technological orientation in designing, executing, interpreting and validating quality procedures and test methods. Complete routine testing of raw materials, in-process and final products in accordance with SOPs for product release and validation. Aid in the development of test methods. Conduct data review and preliminary evaluation of results. Solve problems using limited predetermined options such as repeating the assay when parameters are not met to determine the cause, etc. Provide input to the technical composition of operating documentation. Work is closely supervised. Follows standard practices to obtain solutions. Contribute to the completion of routine technical tasks. Failure to achieve results can normally be overcome without serious effect on schedules and programs. Contacts are primarily with immediate supervisor and other personnel in the section or group.. Years of Experience: 0 - 3 Years