Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Apply Offsite

Tishcon Corp.

Quality Control Analyst

Pay: $57,000–$64,000/yr

Posted: 2 weeks ago

Location: Westbury, NY (Onsite)

Last Updated: 6 days ago

Hours: Full-Time

Expires: 10/1/2026

Career Insights for Quality Control Analyst

See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.

Scorecard

Based on New York data

Review key factors to help you decide if this role fits your goals. How is this calculated?

Were these scores useful?

What they do

A Quality Control Analyst, in the biotech and medical device industries, works in laboratories performing biological, microbiological, and chemical tests on products and materials. Responsible for calibrating equipment, inspecting products, processing and testing materials, and reporting results. May work in other production environments to monitor and improve quality and efficiency in production systems and products.

$69,465 / year median in New York

-13% projected decline

Explore Career

Job Description

Company Overview Tishcon Corp is a reputable contract manufacturer and product formulation company with over a decade of experience. We specialize in developing innovative products across multiple delivery systems, including capsules, vegetarian capsules, tablets, and softgels. Operating under NSF cGMP certified guidelines with two FDA-registered facilities, we are dedicated to maintaining the highest quality standards in manufacturing. Overview We are seeking a detail-oriented and proactive Quality Control (QC) Analyst to join our dynamic team. Responsible for performing routine analytical testing of raw materials, in-process blends, finished products, and stability samples using advanced laboratory instrumentation while ensuring compliance with quality standards and laboratory procedures. Key Responsibilities

Perform routine analytical testing on raw materials, in-process blends, finished products, and stability samples.
Operate and maintain laboratory instruments including KF titrator, FTIR, HPLC, UPLC, and UV/Visible Spectrophotometers.
Conduct assay analysis of fat-soluble vitamins including Vitamin A, Vitamin D, Vitamin E, and Vitamin K2.
Conduct assay analysis of water-soluble vitamins including B Vitamins, Vitamin C, Biotin, N-Acetyl Cysteine (NAC), Folic Acid, and related compounds.
Analyze food supplement ingredients including Curcuminoids, Alpha Lipoic Acid, Piperine, Royal Jelly, Coenzyme Q10, Ubiquinol, L-Carnitine, Silibinin, Quercetin, Rutin, and similar products using HPLC, UPLC, and UV/Visible spectroscopy.
Document test results accurately and maintain laboratory records in accordance with quality procedures.
Follow Good Laboratory Practices (GLP), laboratory safety standards, and applicable regulatory requirements.
Assist in instrument calibration, troubleshooting, and preventive maintenance activities.

Preferred Qualifications/Skills:

Bachelor's degree in chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field.
Minimum 2 years' experience with Laboratory instruments i.e. KF, FTIR, HPLC/UPLC, UV-Vis analytical testing and laboratory documentation
Analytical testing like Blend, Assay, Impurity, LOD, Titration
Worked in the QC Laboratory environment (i.

e. GLP, GDP, ALCOA++) Join us to be part of a thriving organization where your expertise directly impacts product excellence! We are committed to fostering a collaborative environment that values precision measurement, regulatory compliance, and continuous improvement—empowering you to grow your career while ensuring the highest quality standards in every product we deliver.

Pay:

$57,000.00 - $64,000.00 per year

Benefits:

401(k) 401(k) matching Dental insurance Flexible spending account Health insurance Life insurance Vision insurance

Work Location:

In person