Quality Control Analyst (Pharma)**
Quality Control
Middlesex County, NJ, US
Pay Rate Low: 75000 | Pay Rate High: 90000
+ Added - 04/08/2025
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Our client, a dynamic biopharmaceutical company with a global footprint in both R&D and manufacturing, is seeking a QC Analyst to join their growing team.
**Type:** Direct Hire
**Rate:** $75K-$90K (DOE - Multiple levels available)
**Location:** Middlesex County, NJ
**Essential Duties & Responsibilities**
+ Perform analytical testing to support in-process, release, raw materials, and stability programs.
+ Perform both bioassays and chemical analysis.
+ Review, analyze, and report analytical data.
+ Collaborate with internal teams for quality investigations/reporting.
**Qualifications:**
+ Bachelors degree in biology, chemistry, biochemistry, etc. and 3-6+ years of related QC experience.
+ Previous experience in a cGMP laboratory with hands on expertise with techniques such as HPLC with Empower software, cell-based assays (ELISA, SDS-PAGE).
_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_
\#LIDNP
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.
Quality Control
Middlesex County, NJ, US
Pay Rate Low: 75000 | Pay Rate High: 90000
+ Added - 04/08/2025
Apply for Job
Our client, a dynamic biopharmaceutical company with a global footprint in both R&D and manufacturing, is seeking a QC Analyst to join their growing team.
**Type:** Direct Hire
**Rate:** $75K-$90K (DOE - Multiple levels available)
**Location:** Middlesex County, NJ
**Essential Duties & Responsibilities**
+ Perform analytical testing to support in-process, release, raw materials, and stability programs.
+ Perform both bioassays and chemical analysis.
+ Review, analyze, and report analytical data.
+ Collaborate with internal teams for quality investigations/reporting.
**Qualifications:**
+ Bachelors degree in biology, chemistry, biochemistry, etc. and 3-6+ years of related QC experience.
+ Previous experience in a cGMP laboratory with hands on expertise with techniques such as HPLC with Empower software, cell-based assays (ELISA, SDS-PAGE).
_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_
\#LIDNP
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.
Job ID: 488120718
Originally Posted on: 8/5/2025