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Cell Therapy Analytical Development Scientist Onsite

  • ... Posted on: Sep 20, 2024
  • ... Stage Solutions Inc
  • ... Summit, New Jersey
  • ... Salary: Not Available
  • ... Full-time

Cell Therapy Analytical Development Scientist Onsite   

Job Title :

Cell Therapy Analytical Development Scientist Onsite

Job Type :

Full-time

Job Location :

Summit New Jersey United States

Remote :

No

Jobcon Logo Job Description :

Cell Therapy Analytical Development Scientist (Onsite, Summit, NJ)

We are looking for a Cell Therapy Analytical Development Scientist for a Global pharmaceutical Company. The focus of this role is to perform and interpret RT-qPCR/PCR, flow cytometry, cell-based potency, and other analytical assays with moderate supervision and to execute GLP analytical tests to support process characterization testing of the lentiviral vector and cell therapy drug product samples.

This is a 40-hour per-week, 12-month contract (extensions possible), 100% onsite role in Summit, NJ (The candidate must be able to work onsite 5 days a week).

This is a W2 role as a Stage 4 Solutions employee. Health benefits and 401K are offered.

  • Perform experiments using the following methodologies: PCR, RT-qPCR, flow cytometry, mammalian cell culture, Luminex, MSD, and ELISA.
  • With moderate supervision design and execute analytical experiments of moderate complexity.
  • Perform data analysis, summarize and report experimental results
  • Document/review laboratory work in notebooks that is detailed, accurate, timely, and in compliance with Good Lab Practices/Good Documentation Practices requirements.
  • Collaborate with the QC and Process Development teams to advance analytical and development projects.
  • Ensure proper operation and perform routine maintenance of all laboratory equipment.

Requirements:

  • 4+ years of work experience in Cell Therapy Analytical Development
  • Experience executing GLP analytical tests to support process characterization testing of the lentiviral vector and cell therapy drug product samples
  • Experience with PCR and/or flow cytometry and/or mammalian cell culture
  • Experience working in a regulated (GLP/GMP) environment (Preferred)
  • Assay development, especially cell-based potency assays (Preferred)
  • Assay qualification/validation experience (Preferred)
  • Assay Technology Transfer (TT) experience (Preferred)
  • Bachelor's degree in Molecular & Cellular Biology, Immunology, or related discipline

Please submit your resume to our network at (please apply to the Cell Therapy Analytical Development Scientist (Onsite, Summit, NJ) role).


Please feel free to forward this project opening to others who may be interested.

Stage 4 Solutions is an equal-opportunity employer. We celebrate diversity and are committed to providing employees with an inclusive environment that is free of discrimination and harassment. All employment decisions are based on the job requirements and candidates' qualifications, without regard to race, color, religion/belief, national origin, gender identity, age, disability, marital status, genetic information, or other applicable legally protected characteristics.

Compensation: $49/hr to $50/hr

Jobcon Logo Position Details

Posted:

Sep 20, 2024

Employment:

Full-time

Salary:

Not Available

Snaprecruit ID:

SD-CIE-e20f048706b23d3fd158f0799752bc048e39f5a18755bf0e9857d475eabebc7f

City:

Summit

Job Origin:

CIEPAL_ORGANIC_FEED

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Cell Therapy Analytical Development Scientist (Onsite, Summit, NJ)

We are looking for a Cell Therapy Analytical Development Scientist for a Global pharmaceutical Company. The focus of this role is to perform and interpret RT-qPCR/PCR, flow cytometry, cell-based potency, and other analytical assays with moderate supervision and to execute GLP analytical tests to support process characterization testing of the lentiviral vector and cell therapy drug product samples.

This is a 40-hour per-week, 12-month contract (extensions possible), 100% onsite role in Summit, NJ (The candidate must be able to work onsite 5 days a week).

This is a W2 role as a Stage 4 Solutions employee. Health benefits and 401K are offered.

  • Perform experiments using the following methodologies: PCR, RT-qPCR, flow cytometry, mammalian cell culture, Luminex, MSD, and ELISA.
  • With moderate supervision design and execute analytical experiments of moderate complexity.
  • Perform data analysis, summarize and report experimental results
  • Document/review laboratory work in notebooks that is detailed, accurate, timely, and in compliance with Good Lab Practices/Good Documentation Practices requirements.
  • Collaborate with the QC and Process Development teams to advance analytical and development projects.
  • Ensure proper operation and perform routine maintenance of all laboratory equipment.

Requirements:

  • 4+ years of work experience in Cell Therapy Analytical Development
  • Experience executing GLP analytical tests to support process characterization testing of the lentiviral vector and cell therapy drug product samples
  • Experience with PCR and/or flow cytometry and/or mammalian cell culture
  • Experience working in a regulated (GLP/GMP) environment (Preferred)
  • Assay development, especially cell-based potency assays (Preferred)
  • Assay qualification/validation experience (Preferred)
  • Assay Technology Transfer (TT) experience (Preferred)
  • Bachelor's degree in Molecular & Cellular Biology, Immunology, or related discipline

Please submit your resume to our network at (please apply to the Cell Therapy Analytical Development Scientist (Onsite, Summit, NJ) role).


Please feel free to forward this project opening to others who may be interested.

Stage 4 Solutions is an equal-opportunity employer. We celebrate diversity and are committed to providing employees with an inclusive environment that is free of discrimination and harassment. All employment decisions are based on the job requirements and candidates' qualifications, without regard to race, color, religion/belief, national origin, gender identity, age, disability, marital status, genetic information, or other applicable legally protected characteristics.

Compensation: $49/hr to $50/hr

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