QC Scientist: Pharma Quality Control & Analytical Excellence

Ardena; New Jersey; Vor Ort; USD 85.000 - 120.000; Vollzeit

Benefits dieser Stelle

Competitive salary

401(k) match

Paid holidays

Medical insurance

Dental insurance

Vision insurance

Career development

Zusammenfassung

Ardena, a Somerset, New Jersey-based CDMO/CRO, is seeking a Scientist – Quality Control to join the Quality Control team. The role focuses on analytical testing of raw materials, in-process materials, finished products, and stability samples in a GMP-regulated lab.

You will analyze data, investigate deviations, and prepare technical reports while collaborating with QA, Manufacturing, and Regulatory teams to ensure quality and timely project delivery.

Qualifikationen

• Requires GMP-regulated lab experience and pharmaceutical development exposure.
• Strong analytical chemistry knowledge and chromatographic skills.
• Experience with HPLC, GC, dissolution, and wet chemistry techniques.
• Proficient with CDMS, LIMS, ELN and related lab software.
• Excellent written and verbal communication; capable of multi-tasking.

Aufgaben

• Perform analytical testing of materials and products to support development and manufacturing.
• Document results with complete, compliant laboratory records and reports.
• Interpret data, investigate deviations, and communicate findings to teams.
• Operate and maintain laboratory instrumentation and software per GMP.
• Collaborate with QA, Regulatory, and Manufacturing to meet project timelines.

Kenntnisse

Analytical Chemistry

GMP Experience

HPLC

LIMS

Documentation

Communication

Ausbildung

Associate's degree in Chemistry

Bachelor's degree in Chemistry

Tools

CDMS

ELN

Dissolution Systems

LC (HPLC)

GC

Jobbeschreibung

Ardena, a Somerset, New Jersey-based CDMO/CRO, is seeking a Scientist – Quality Control to join the Quality Control team. The role focuses on analytical testing of raw materials, in-process materials, finished products, and stability samples in a GMP-regulated lab.

You will analyze data, investigate deviations, and prepare technical reports while collaborating with QA, Manufacturing, and Regulatory teams to ensure quality and timely project delivery.