Analytical Scientist
Most applications go out cold — see where you stand first. No sign-up to start.
Don't just apply. Show up ready.
Olive works from this exact posting — no sign-up to start.
At a glance
Requirements
Credentials this posting asks for.
Job overview
Astrix Technology is hiring an Analytical Scientist. Astrix Technology seeks an Analytical Scientist to perform routine and non‑routine chemical analyses of raw materials, in‑process goods, finished products, and environmental samples for a pharmaceutical manufacturing company in Cranbury, New Jersey.
Key focus areas include Conduct and document chemical analyses for raw materials, in‑process goods, and finished products, Design, validate, and resolve issues with analytical methods, including HPLC for cleaning verification, and Collect and analyze equipment cleaning validation samples.
Important skills include cGMPs, Pharmacopeia, USP, EP, Regulatory Standards, and 21 CFR Part 210/211/820. Preferred (not required): Chemical Analyses, Analytical Method Design, Analytical Method Validation, and Equipment Cleaning Validation Sample Collection.
Skills & qualifications
Skills
Qualifications
Full job description
Analytical Scientist
Laboratory
Cranbury, New Jersey, US
- Added - 03/08/2026
Pay Rate Low: 38 | Pay Rate High: 45
Pay Rate Low: 38.00 | Pay Rate High: 45.00
We are seeking an Analytical Scientist to join a reputable pharmaceutical manufacturing company to conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods, or stability samples.
** No Relocation, No C2C Candidates**
Pay: Up to $45/hour.
RESPONSIBILITIES:
-
Conduct and document chemical analyses for raw materials, in-process goods, and finished products.
-
Design, validate, and resolve issues with analytical methods, including HPLC for cleaning verification.
-
Collect and analyze equipment cleaning validation samples.
-
Prepare Certificates of Analysis, analytical reports, and maintain lab documentation.
-
Peer-review records and support OOS or OOT investigations as per SOPs.
-
Ensure compliance with SOPs, cGMPs, and regulatory requirements.
-
Assist with environmental monitoring and other tasks as assigned.
QUALIFICATIONS:
-
2 years hands-on method development experience (HPLC)
-
Knowledge of cGMPs, pharmacopeia (USP, EP), and regulatory standards (21 CFR Part 210/211/820, ISO).
-
Bachelor’s in Chemistry-related discipline with 2+ years of analytical lab experience.
This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
INDBH
#LIR-AR1
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
You've read the whole posting — now see how you match it.