Analytical Scientist

Astrix Inc.; Cranbury Township (NJ); On-site; USD 52,000 - 62,000; Full time

Job summary

Astrix Inc. is seeking an Analytical Scientist to join our pharmaceutical manufacturing team in New Jersey.

The candidate will perform routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods, or stability samples, ensuring compliance with SOPs and regulatory requirements. The role involves designing and validating analytical methods (including HPLC for cleaning verification) and preparing Certificates of Analysis and analytical reports.

Qualifications

• 2 years hands-on method development experience with 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.

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.

Skills

HPLC method development

cGMP knowledge

Regulatory standards awareness

Education

Bachelor's in Chemistry-related discipline

Job description

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.