Senior Research Associate
October 21, 2021
Senior Research Associate - Scientific
Location: Frederick Maryland USA
Frederick Maryland United States
Job Type: Regular Full-time
Division: Precision for Medicine
Business Unit: Specialty Lab Services
Requisition Number: 443
Position Summary
Reliably performs and provides bioanalysis services for commercial clients using Softmax or MSD benchwork software and analyzing data in Prism and Excel. May also perform critical reagent production, plate based assays and DNA/RNA extraction. Duties also include recording and reporting results, preparation of samples and reagent solutions, and maintenance of equipment.
Essential functions of the job include but are not limited to:
Qualifications
Minimum Required:
Other Required:
Preferred:
Location: Frederick Maryland USA
Frederick Maryland United States
Job Type: Regular Full-time
Division: Precision for Medicine
Business Unit: Specialty Lab Services
Requisition Number: 443
Position Summary
Reliably performs and provides bioanalysis services for commercial clients using Softmax or MSD benchwork software and analyzing data in Prism and Excel. May also perform critical reagent production, plate based assays and DNA/RNA extraction. Duties also include recording and reporting results, preparation of samples and reagent solutions, and maintenance of equipment.
Essential functions of the job include but are not limited to:
- Maintains instrument and reagent inventory per SOPs
- Conducts immunological assays including ADA, PK or Potency assay, as well as cytokine measurement etc
- Independently plans and conducts bioassays various scales and for different customers
- Performs QC analyses to ensure that results meet specifications. Monitors assays and trouble shoots, as appropriate
- Performs research and development activities to support new product development. Performs new assay development as needed
- Assists Scientists to modify and re-optimize current assays or procedures to address changing technologies or the introduction of new assays
- Completes all paperwork completely and accurately for QA/QC and GLP purposes using Good Documentation Practices (GDP) and updates computer tracking systems, as required
- Operates equipment such as spectrophotometer, MSD plate reader, Quanterix, or Nanostring and performs processes in accordance with SOPs
- Assists in the training of new and existing laboratory staff in accordance with SOPs
- Drafts and/or edits SOPs as needed, to include validation documents for new equipment, new documents and other quality documents
- Evaluates opportunities for revision of SOPs and makes necessary recommendations to improve efficiency and quality
- Organizes data prior to submission. Ensures lab maintenance activities and equipment calibration is performed according to schedule
- Plans for raw material requirements, maintenance of appropriate inventory of reagents and submission of purchase orders
- Maintains a clean and safe lab environment
- Carry out other duties/projects as assigned
Qualifications
Minimum Required:
- Bachelor's Degree (Biology, Chemistry or Life Sciences) or equivalent combination of education and experience
- 4 years' relevant laboratory experience or equivalent combination of education and experience
Other Required:
- Previous experience with ELISA, MSD or Quanterix based platform or Nanostring.
- Requires good attention to detail, excellent documentation skills and willingness to work well in a group environment
- Ability to interact and function in a highly productive work environment
- Ability to work independently
- Must be proficient using Microsoft office, specifically with Excel
- Ability to lift and carry between 1-15 lbs.; Ability to lift up to 50 lbs. overhead with assistance; frequently required to sit, grasp, and use right/left finger dexterity; May be exposed to a cold freezer environment (Freezer temperatures range between -20ºC -196ºC)
- Must be able to read, write, speak fluently and comprehend the English language
Preferred:
- Substantial ligand binding assay experience
- Prior experience in a GLP or GMP or GCLP environment