Biologist (1-3 years)
- Employer
- Joulé
- Location
- Branchburg, New Jersey, US
- Salary
- Competitive
- Closing date
- Aug 4, 2024
View more
- Sector
- Academic / Research
- Field
- Conservation science
- Discipline
- Other
- Salary Type
- Salary
- Employment Type
- Full time
You need to sign in or create an account to save a job.
Title: Research Associate Biochemistry
Location: Branchburg, NJ
Schedule: M-F 8-5, 1 hour lunch
Type: Contract
Responsibilities:
Conduct routine and non-routine analyses of in-process materials, raw materials, environmental/water samples, finished goods and stability samples by appropriate biochemical methods as assigned by supervisor. Perform routine QC responsibilities as needed.
Apply acceptable cGMP practices during execution of all work tasks. Work independently with moderate supervisory guidance.
Manage for Results /Strategic Planning:
1. Perform routine QC responsibilities as assigned by supervisor such as (as applicable): o
a. Conduct routine and non-routine analyses of test articles as assigned by o supervisor by appropriate biochemical methods such as: SDS-PAGE, HPLC,CESDS, ELISA, Cell Based Bioassay, etc.
b. Demonstrate initiative to perform routine QC responsibilities such as sample coordination, lab equipment maintenance, QC document management, QC inventory control and reconciliation of sample requests/documents as needed.
c. Monitor laboratory equipment for temperature and conformance to specifications.
d. Apply acceptable cGMP practices during execution of all work tasks.
e. Work independently with minimal supervisory guidance. Exhibit strong teamwork skills.
f. Update supervisor of progress at scheduled intervals. Seek additional guidance as needed.
g. Use scientific expertise to provide assistance for troubleshooting, laboratory investigations and problem resolution. Suggest process improvements to QC management.
h. Perform assay data review.
2. Perform independent assignments such as:
a. Compile data and prepare graphs for documentation of test procedures and preparation of reports.
b. Conduct document reviews, author standard operating procedures (SOPs), and assay review.
c. Lead special projects such as method validation, troubleshooting, optimization, and investigations.
Manage Relationships with Key Stakeholders and Customers:
Requirements: BS or MS in a related science such as a Biology or Biochemistry
BS requires 3-5 years and MS requires 1-3 years of previous related experience.
Good working knowledge of cGMP regulations
Ability to work independently with moderate supervisory guidance.
Excellent teamwork and communication skills.
#M3
Location: Branchburg, NJ
Schedule: M-F 8-5, 1 hour lunch
Type: Contract
Responsibilities:
Conduct routine and non-routine analyses of in-process materials, raw materials, environmental/water samples, finished goods and stability samples by appropriate biochemical methods as assigned by supervisor. Perform routine QC responsibilities as needed.
Apply acceptable cGMP practices during execution of all work tasks. Work independently with moderate supervisory guidance.
Manage for Results /Strategic Planning:
1. Perform routine QC responsibilities as assigned by supervisor such as (as applicable): o
a. Conduct routine and non-routine analyses of test articles as assigned by o supervisor by appropriate biochemical methods such as: SDS-PAGE, HPLC,CESDS, ELISA, Cell Based Bioassay, etc.
b. Demonstrate initiative to perform routine QC responsibilities such as sample coordination, lab equipment maintenance, QC document management, QC inventory control and reconciliation of sample requests/documents as needed.
c. Monitor laboratory equipment for temperature and conformance to specifications.
d. Apply acceptable cGMP practices during execution of all work tasks.
e. Work independently with minimal supervisory guidance. Exhibit strong teamwork skills.
f. Update supervisor of progress at scheduled intervals. Seek additional guidance as needed.
g. Use scientific expertise to provide assistance for troubleshooting, laboratory investigations and problem resolution. Suggest process improvements to QC management.
h. Perform assay data review.
2. Perform independent assignments such as:
a. Compile data and prepare graphs for documentation of test procedures and preparation of reports.
b. Conduct document reviews, author standard operating procedures (SOPs), and assay review.
c. Lead special projects such as method validation, troubleshooting, optimization, and investigations.
Manage Relationships with Key Stakeholders and Customers:
Requirements: BS or MS in a related science such as a Biology or Biochemistry
BS requires 3-5 years and MS requires 1-3 years of previous related experience.
Good working knowledge of cGMP regulations
Ability to work independently with moderate supervisory guidance.
Excellent teamwork and communication skills.
#M3
You need to sign in or create an account to save a job.
Get job alerts
Create a job alert and receive personalized job recommendations straight to your inbox.
Create alert