Role Overview
ARx Pharma is hiring a entry-level Quality Control Chemist I. This is a full-time role in Glen Rock. Part of ARx Pharma's Qa hiring, posted 3 days ago. Full responsibilities, required qualifications, and the apply link are listed in the description below.
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Job Description
Job Summary
Provide analytical support and data generation for daily chemistry testing activities related to raw materials, in- process and finish products. Perform all testing in a timely and accurate manner in accordance with approved GMP documents (test methods, Specifications, SOPs).
Chemist I
Essential Functions:
- Inspects components, products and/or processes to ensure conformance with standards.
- Executes laboratory procedures for sample preparation
- Performs materials analysis of substantial variety & complexity using ARx test methods, compendia methods, specifications with minimal supervision.
- Ensure all analytical operations comply with cGMPs & ARx procedures and all laboratory experiments are properly documented in notebook and are in accord with regulatory requirements.
- Provide support to routine USP water and environmental testing.
- Works with minimal supervision/direction in expediting completion of laboratory assignments.
- Abide by the ARx Laboratory Chemical Hygiene Plan and other safety policies. Maintains a safe and clean work environment, notifying the supervisor of unsafe practices, conditions, or acts; L-II takes on increasing responsibility for surfacing and implementing improved safety practices.
- Responsible for following all applicable waste handling procedures.
Additional Responsibilities:
- Completes required paperwork / documentation accurately, neatly and in a timely manner.
- Responsible for the proper disposal of hazardous waste into the proper labeled containers and drums.
- Performs other duties and responsibilities as assigned.
- Make identifiable and substantial contributions to continuous improvement. Performs all duties consistent with established ARx guideline consistent with all regulatory requirements. Actively complies with and endorses Department and Company objectives.
Job Specifications:
- BS (or higher) degree in Chemistry, Microbiology, or closely related discipline and 0-2 years lab experience (preferably pharmaceutical GMP) or requires high school education and 5 years minimum lab experience (preferably pharmaceutical GMP).
- Knowledgeable in the application of various analytical techniques such as chromatography and spectroscopy; thermal analysis and wet chemistry techniques desired.
- Basic knowledge and understanding of scientific principles involved in the performance of analytical test methods.
- Ability to efficiently utilize time (coordinate several assignments concurrently).
- Ability to read and interpret documents such as test methods and procedure manuals.
- Knowledge of requirements for maintaining proper laboratory
otebook documentation
- Must have above average computer skills and knowledge; specially in the operational use of analytical equipment have a computer interface.
- Ability to perform basic mathematical functions and apply basic concepts such as mean and standard deviation.
- Good communication skills (verbal and written).
- Excellent interpersonal skills.
- Requires common physical characteristics and abilities, such as above average agility and dexterity; physical exertion such as long periods of standing, recurring bending, crouching, stooping, stretching, reaching or similar activities should be expected.
- Work environment involves moderate risks or discomforts requiring special safety precautions, will be required to use personal protective equipment.
Physical Demands:
Sitting: 67-100%/day
Standing: 67-100%/day
Walking: 67-100%/day
Kneeling: 1-33%/day
Reaching: 1-33%/day
Overhead Reaching: 1-33%/day
Crawling: Never
Twist/Pivot at Waist: 1-33%/day
Bending: 1-33%/day
Upward Gaze: 1-33%/day
Downward Gaze: 1-33%/day
Squat: 1-33%/day
Balance: Rarely
Light Grasping: 1-33%/day
Heavy Grasping: Rarely
Fine Motor: 1-33%/day
Foot Pedal: Rarely
Hand Controls: 34-66%/day
Frequently Asked Questions
How do I apply for the Quality Control Chemist I position at ARx Pharma?
Use the Apply button above to submit your application directly to ARx Pharma. Most applications take less than 5 minutes if your resume and contact details are ready, and you'll be routed to the employer's official application system to finish.
Where is the Quality Control Chemist I position at ARx Pharma located?
This position is based in Glen Rock. ARx Pharma has not indicated remote or hybrid options for this role, so candidates should plan for on-site work.
What does a Quality Control Chemist I at ARx Pharma earn?
ARx Pharma has not disclosed a salary range in this posting. Many employers share specifics later in the interview process; you can also ask during a recruiter screen if compensation transparency is important to you.
When was the Quality Control Chemist I role at ARx Pharma posted?
This role was posted on June 19, 2026 (3 days ago). It's still listed as actively hiring; we re-confirm openings against the source system multiple times per day and remove closed roles.
Is the Quality Control Chemist I role at ARx Pharma entry-level?
Yes. This is an entry-level position. Strong candidates typically have 0-2 years of relevant work experience, internships, or significant project work. Read the full description for any specific qualification requirements ARx Pharma has listed.
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