Top 9 quality control associate Jobs in somerset, nj

HTP Analytical QC Associate Scientist
GenScript/ProBio —Piscataway, NJ
- $60,000 - $75,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Analysis skills
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Quality Control Associate, Inbound
The RealReal —Perth Amboy, NJ
- $21 an hour
- Full-time
- Communication skills
- Entry level
- Time management
- Paid parental leave
- Employee stock purchase plan
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Associate Card Auditing Coordinator Crew D
CompoSecure —Somerset, NJ
- $15.38 - $23.54 an hour
- Email
- Basic math
- Office
- Microsoft Office
- Health savings account
- Paid holidays
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14d
Associate Card Auditing Coordinator Crew C
CompoSecure —Somerset, NJ
- $15.38 - $23.54 an hour
- Email
- Basic math
- Office
- Microsoft Office
- Health savings account
- Paid holidays
Quick Apply
14d
QA Associate
ANI Pharmaceuticals —East Windsor, NJ
- $52,000 - $70,000 a year
- Full-time
- 5 years
- Computer literacy
- Mid-level
- Paid holidays
- Disability insurance
1d
Associate Director, Quality Systems & Compliance (Design Controls)
Merck —Rahway, NJ
- $129,000 - $203,100 a year
- Full-time
- Bachelor of Science
- 3 years
- Bachelor's degree
- Paid holidays
- Health insurance
Associate Director, Quality Control
Lantheus Medical Imaging Inc —Springfield, NJ
- $139,000 - $232,000 a year
- Weekends as needed
- Bachelor of Science
- 11+ years
- Bachelor's degree
- Paid parental leave
- Paid holidays
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14d
Quality Assurance Associate (Food Manufacturing)
Nuts.com —Cranford, NJ
- $19.00 - $20.50 an hour
- Overtime
- Computer literacy
- Mid-level
- Organizational skills
- Employee discount
Quality Control Associate
Variety Staffing —Tinton Falls, NJ
- Microsoft Outlook
- Computer literacy
- Driver's License
- Health insurance
- Dental insurance
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HTP Analytical QC Associate Scientist

GenScript/ProBio -
Piscataway, NJ

Quick Apply

Job Details

Full-time
$60,000 - $75,000 a year

Qualifications

Data integrity assurance
Biochemistry
Laboratory safety
Quality control product testing
Sample preparation
Bachelor of Science
Efficiency improvement
High-performance liquid chromatographs
Master's degree in Biochemistry
Protein analysis (analytical chemistry specialty)
Continuous improvement (laboratory quality control method)
Biotechnology
Mid-level
Laboratory equipment calibration
Implementing laboratory quality control protocols
Data integrity and documentation
Collaboration with product development teams
Analysis skills
Biochemical laboratory techniques
Bachelor's degree
Data management
Master of Science
Pharmaceutical analysis
Materials analysis (analytical chemistry specialty)
Laboratory preventive maintenance
Capillary electrophoresis
Polyacrylamide gel electrophoresis
Laboratory information systems (LIS)
Automated liquid handling systems
Bachelor's degree in biochemistry

Full Job Description

About GenScript

GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.

GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.

Genscript is seeking a motivated and detail-oriented HTP Analytical QC Associate Scientist to join our dynamic US Protein Department in Piscataway, New Jersey.

The estimated salary range is $60,000 - $75,000, depending on experience.

Reporting to: Supervisor of HTP Platform
Employment Type: Full-time

Role Description:

We are seeking a detail-oriented and proactive Associate Scientist to join our High-Throughput Protein Analytical QC Laboratory. This role is responsible for performing analytical characterization and quality control testing of recombinant proteins generated from high-throughput production workflows.

The successful candidate will play a critical role in ensuring protein identity, purity, and overall quality through robust analytical methodologies. This position operates in a data-driven and quality-focused environment where accuracy, reproducibility, and data integrity are essential. The ideal candidate will have hands-on experience with protein analytical techniques and familiarity with laboratory data management systems such as ELN, LIMS, or equivalent platforms.

Key Responsibilities:

Perform routine and non-routine analytical and QC testing to evaluate protein identity, purity, and quality attributes.

Execute a range of protein characterization assays, including:

HPLC / UPLC (e.g., SEC, RP, IEX)

Capillary Electrophoresis (CE, iCE/cIEF)

SDS-PAGE

Western blot

LC-MS

Endotoxin assays

Prepare samples, reagents, buffers, and standards in accordance with established protocols and assay requirements.

Perform sample preparation workflows, including use of automated liquid handling systems where applicable.

Analyze, interpret, and document experimental data in ELN, LIMS, or equivalent systems, ensuring compliance with data integrity standards (e.g., ALCOA+ principles).

Support method troubleshooting and optimization, ensuring assay robustness, reproducibility, and consistency across runs.

Maintain laboratory instruments and ensure proper calibration and performance, supporting compliance with quality and safety standards.

Collaborate with cross-functional teams (e.g., protein production, process development) to support project timelines and deliverables.

Contribute to continuous improvement initiatives, including method refinement, workflow efficiency, and data quality enhancement.

Qualifications:

BS or MS in Biochemistry, Analytical Chemistry, Biotechnology, or a related field with 2+ years of relevant experience in protein analytical characterization or QC.

Hands-on experience with protein analytical techniques such as HPLC/UPLC, CE, SDS-PAGE, Western blot, LC-MS, or endotoxin assays.

Familiarity with protein characterization workflows, including purity, aggregation, and identity analysis.

Experience with laboratory data systems (ELN, LIMS, or similar) and strong documentation practices.

Strong attention to detail and commitment to data integrity, accuracy, and reproducibility.

Experience in a CRO/CDMO or regulated QC environment is preferred.

#LI-EB1

#GS

GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.

GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.

Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

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Refine Your Search

quality control associate jobs in somerset, nj

HTP Analytical QC Associate Scientist

Quality Control Associate, Inbound

Associate Card Auditing Coordinator Crew D

Associate Card Auditing Coordinator Crew C

QA Associate

Associate Director, Quality Systems & Compliance (Design Controls)

Associate Director, Quality Control

Quality Assurance Associate (Food Manufacturing)

Quality Control Associate

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