Quality Control Technician

Par Health; Village of Hobart (NY); On-site; USD 43,319 - 67,710; Full time

Job summary

Par Health in the Village of Hobart, New York, is seeking a Quality Assurance Analyst to perform analyses of pharmaceutical components while ensuring compliance with industry regulations. The ideal candidate will possess a High School Diploma and relevant experience in laboratory settings.

This position offers a weekday schedule from 8:00 am to 4:30 pm with a competitive salary ranging from $43,319 to $67,710 based on experience.

Qualifications

• Minimum of 1–3 years of experience in a cGMP facility (for Tech III).
• Classroom or work experience in a science-related field (for Tech I).
• Working knowledge of chemistry required (for Tech II).

Responsibilities

• Perform quantitative and qualitative analyses of pharmaceutical components.
• Document all procedures, calculations, and results accurately.
• Set up, calibrate, and operate laboratory equipment.
• Participate in investigations for out-of-specification results.

Skills

Basic arithmetic functions

Reading, writing, and speaking

Basic computer skills

Understanding cGMP and SOP

Problem-solving

Interpersonal skills

Attention to detail

Technical learning ability

Education

High School Diploma or equivalent

Bachelor’s Degree in a science-related field

Associate’s Degree with equivalent experience

Tools

HPLC

GC

Analytical balances

Volumetric glassware

pH Meter

Job description

Why Us

At Par Health, we believe great healthcare is built on getting the essentials right. We’re looking for passionate, talented individuals who share our commitment to improving lives. With 4,000+ team members worldwide, we lead with pride and purpose—prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn’t just our tagline; it’s the higher standard we live by every day.

Job Description Summary

Perform basic, intermediate or advanced quantitative and qualitative analyses of pharmaceutical components, in-process material, finished good product, and/or stability product. Depending on the department to which the incumbent reports, some of the functions listed may not be applicable.

Samples Tested

Perform Basic Analytical Laboratory Tests (e.g., Potency, Purity, Uniformity, Dissolution, Moisture, etc.) in accordance with approved methodology and CGMP, FDA, and DEA regulations.

• Set up, adjust, calibrate and operate laboratory equipment and instruments, as well as any associated software.
• Prepare solutions, solvents, and mobile phases.
• Accurately prepare, collect, weigh, and analyze samples and reference standards, and determine conformance of results to approved specification limits.
• Assist in basic investigations for out-of-specification/out-of-trend results.

Documentation Completed to Standards

Provides accurate and timely documentation of all procedures, calculations, and results.

Department Specific Functions

• LIMS entry, approval, and data release of products.
• Use analytical balances, HPLC, GC, KF Titrator, IR, UV, pH Meter, volumetric glassware.
• Perform wet testing like assay titrations, colorimetric tests, TLC, heavy metals, and sieves.
• Flex skills to other laboratories based on business need.
• Follow established procedures using one's discretion and judgment as to the specific approach or technique.
• Identify/Research new lab supplies and order current lab supplies.
• Identify and implement cost-saving opportunities.
• Sustain laboratory housekeeping and identify improvement opportunities.
• Complete hands‑on and electronic training.
• Participate and lead area huddles or shift meetings.
• Perform other duties as assigned.

QC Tech I

Perform basic wet chemistry, preparation of reagents/solutions, and sample reconciliation following approved methods.

QC Tech II

Experienced at some instrumentation and wet testing.

QC Tech III

Expert in wet chemistry analysis and instrumentation analysis performed by laboratory. Ability to perform some instrument maintenance and troubleshooting chromatography issues. Trainer for areas of proficiency. Perform peer review and release of all products, participate in validations, and execute Gage R&R experiments. Initiate and support Out of Specification, Out of Trend, and Exception Investigations. Identify method improvements and perform change controls. Regularly use communication skills to exchange information, especially technical information within the lab and with other departments.

Education

Minimum Requirements: High School Diploma or equivalent required. Bachelor’s Degree in a science‑related field (Chemistry, Biology) is preferred, or Associate’s Degree with equivalent combination of education, experience, and competencies accepted.

Experience

• Tech I: Classroom or previous work experience in a science‑related field.
• Tech II: Working knowledge of chemistry required.
• Tech III: Minimum 1–3 years of experience in a cGMP facility.

Preferred Skills / Qualifications

• Perform basic functions of arithmetic: add, subtract, multiply and divide all units of measure.
• Perform reading, writing and speaking at a basic level.
• Basic computer skills including Word, Excel and database software.
• Understand and apply cGMP, SOP, and DEA regulations.
• Deal with and solve problems of moderate difficulty.
• Self‑motivated, demonstrate initiative, and make good decisions under pressure.
• Possess sufficient interpersonal skills to function as part of a team.
• Attention to detail and accuracy.
• Learn and apply technical concepts rapidly.

Other Skills / Competencies

• Comply with company policies and procedures.
• Follow safe working practices in the execution of assigned duties.
• Participate in general site and departmental safety initiatives.

Organizational Relationship / Scope

As a QA analyst, you will coordinate with manufacturing and quality assurance teams to ensure product compliance. You will monitor and check work or information and plan and organize time and resources efficiently. You will compare observations of finished work to expected results to find inconsistencies and recommend improvements.

Working Conditions

• The job involves sitting, walking, standing, reaching, talking, hearing, exerting a negligible amount of force continuously and up to 50 pounds of force occasionally.
• Tasks may require standing or moving most of the day; some tasks will involve sitting at a desk/bench while using a computer.
• Requires judging distance and space relationships, identifying colors, focusing up to 20 inches.
• Focus requires mental and visual attention most or all of the time.

Environmental / Atmospheric Conditions

Typical laboratory work environment. Exposure to chemicals, raw materials, and product requires safety precautions and use of lab coat, safety glasses, gloves, dust mask/respirator, safety shoes. Hazards include proximity to chemicals, dust, odors, cleaning solvents, noise, vibration, poor ventilation.

Benefits & Compensation

Day shift Monday–Friday, 8:00 am–4:30 pm. Base pay range $43,319.00–$67,710.00. Bonuses awarded at the Company’s discretion. Relocation assistance not provided. Position not eligible for visa sponsorship. Applicants must be authorized to work in the United States.

EEO Statement

We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provide equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, genetic information, or any other classification protected by law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.