Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Apply Offsite

QC Analyst I

Job

Spectraforce

Lexington, MA (In Person)

Full-Time

Posted 6 days ago (Updated 3 days ago) • Actively hiring

Expires 8/4/2026

Review key factors to help you decide if the role fits your goals.
How is this calculated?
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
62
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Position Title:
QC Analyst I Work Location:
Lexington, MA 02421
Assignment Duration:
8
Months Work Arrangement:
Onsite Position Summary Primary duties of this position will focus on the daily lab operations and execution of testing to support manufacturing operations. Testing may include but not limited to samples from drug substance and drug product, manufacturing, stability, raw materials and various protocol studies using test methods. Background & Context This position is expected to maintain operational and GMP readiness of the QC areas. In addition, this position will participate in more complex projects, Operational excellence initiatives and various quality systems.
Discretion:
Work is closely supervised. Follow specific, detailed instructions.
Impact:
Contributions are usually limited to task-related activities. Errors do not typically have major effect on the organization.
Biochemistry Focus:
A280, SOLO
A280, Compedia methods (pH, Moisture, OSMO, Appearance, Subvisible particles), Enzyme Activity assays, DNA, PCR, Free Thiol. Key Responsibilities 80% Testing execution. 10% QC operations support which entails data review, data trending, OE/5S initiative, maintenance of equipment and reagents, reagent prep, lab housekeeping, support for other QC groups if needed. 10% Compliance and quality systems (SOP revisions, input to quality system). Qualification & Experience Bachelor's degree and minimum of 0-2 years related experience.
Desired:
GMP knowledge, work experience. Limited use and/or application of basic principles, theories and concepts. Limited knowledge of industry practices and standards. Position requires critical thinking.
Key Skills:
MS Office, LIMS, SAP, Trackwise, EDMS, Compliance and strong science understanding. Solve routine problems of limited scope and complexity following established policies and procedures. Works on problems of limited scope. Follows standard practices and procedures in analyzing situations of data from which answers can be readily obtained. Builds stable working relationships internally. Contacts are primarily with immediate supervisors, and other personnel in the section or group. Working Conditions & Physical Demands 100% On-site. Limited to no travel expected. Repetitive bendings and reaching to setup and break down equipment. Ability to work around chemicals. Ability to wear personal protective equipment such as gloves, gowning, and respiratory protection in some cases. Ability to walk and stand for periods of time.