The Opportunity
Conduct quality control testing on products and materials
Analyze test results and report deviations
Ensure compliance with GMP and regulatory standards
Document quality control procedures and findings
Assist in troubleshooting and root cause analysis
Who You Are
• 0–5 years of experience
• Strong problem-solving skills
• Excellent communication abilities
• Knowledge of industry best practices
ADQC Associate I The job responsibility within the PTCC Analytical Development & Quality Control US Testing Group is to perform biochemical/immunological and cell-based assays in support of clinical and to-be-marketed products. The candidate will support process development, product characterization, stability, and lot release testing with established procedures in a cGMP environment.
Responsibilities include, but are not limited to, routine execution of sample preparation and testing, compliance review and release of assay data (electronic and paper-based), preparing reagents, presenting results, and monitoring assay quality. Expectations include Good Documentation Practices, demonstrating ALCOA principles, data integrity, routine lab maintenance, and following EHS safety practices.
Qualifications:
B.S. in Biological Sciences with 1-5 years of relevant laboratory experience
Hands-on experience with performing immunological or cell-based assays including ELISA, PCR, cell killing, and flow cytometry assays
Experience with aseptic cell culturing is required
Ability to work independently as well as with a team, handle multiple projects, demonstrate initiative while maintaining exceptional attention-to-detail
Demonstrate effective verbal and written communication skills
Ability to work in a fast paced environment
Required proficiency in computer applications, data management, and electronic documentation systems.
Prior experience with Benchling, Client FACSDiva/FACSLyric, and FlowJo along with GxP-compliant systems such as global SoftMax Pro, Single LIMS, and Veeva QMS is highly preferred.
Experience with laboratory testing preferred
Working Model: Fully On-site (Lab Based)
Interview Format: Two Round (1 - virtually; 2 - on-site)
Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.
Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
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Conduct quality control testing on products and materials
Analyze test results and report deviations
Ensure compliance with GMP and regulatory standards
Document quality control procedures and findings
Assist in troubleshooting and root cause analysis
Who You Are
• 0–5 years of experience
• Strong problem-solving skills
• Excellent communication abilities
• Knowledge of industry best practices
ADQC Associate I The job responsibility within the PTCC Analytical Development & Quality Control US Testing Group is to perform biochemical/immunological and cell-based assays in support of clinical and to-be-marketed products. The candidate will support process development, product characterization, stability, and lot release testing with established procedures in a cGMP environment.
Responsibilities include, but are not limited to, routine execution of sample preparation and testing, compliance review and release of assay data (electronic and paper-based), preparing reagents, presenting results, and monitoring assay quality. Expectations include Good Documentation Practices, demonstrating ALCOA principles, data integrity, routine lab maintenance, and following EHS safety practices.
Qualifications:
B.S. in Biological Sciences with 1-5 years of relevant laboratory experience
Hands-on experience with performing immunological or cell-based assays including ELISA, PCR, cell killing, and flow cytometry assays
Experience with aseptic cell culturing is required
Ability to work independently as well as with a team, handle multiple projects, demonstrate initiative while maintaining exceptional attention-to-detail
Demonstrate effective verbal and written communication skills
Ability to work in a fast paced environment
Required proficiency in computer applications, data management, and electronic documentation systems.
Prior experience with Benchling, Client FACSDiva/FACSLyric, and FlowJo along with GxP-compliant systems such as global SoftMax Pro, Single LIMS, and Veeva QMS is highly preferred.
Experience with laboratory testing preferred
Working Model: Fully On-site (Lab Based)
Interview Format: Two Round (1 - virtually; 2 - on-site)
Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.
Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.