Microbiology QC Analyst II
- Employer
- Eurofins Lancaster Laboratories
- Location
- Mantua Heights, New Jersey, US
- Salary
- Competitive
- Closing date
- Dec 8, 2021
View more
- Sector
- Consultancy/Private Sector
- Field
- Conservation science
- Discipline
- Biology
- Salary Type
- Salary
- Employment Type
- Full time
You need to sign in or create an account to save a job.
Job Description
Overview:
The Quality Control Analyst will support quality control testing operations at a client's Cell Therapy Center (iCTC). The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxin, gram stain, environmental monitoring, and/or sterility techniques.
Specific Responsibilities
Education and Qualifications:
Position is full-time with overtime as needed. Candidates currently living within a commutable distance of Philadelphia, PA are encouraged to apply.
by Jobble
Overview:
The Quality Control Analyst will support quality control testing operations at a client's Cell Therapy Center (iCTC). The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxin, gram stain, environmental monitoring, and/or sterility techniques.
Specific Responsibilities
- Perform daily cGMP quality control laboratory microbiological testing activities at the iCTC facility
- Perform data analysis and result reporting of microbiology assays to support product lot release with adherence to turnaround times
- Perform all activities with respect to cGMP compliance
- Support thorough cGMP investigations for out-of-specification test results
- Support technical problem solving
- Support product stability programs including execution of stability testing, stability data analysis, and final reporting of stability data
- Operate at a consistent and exemplary level of efficiency, producing high quality and accurate results
Education and Qualifications:
- Bachelors degree in a relevant discipline (biological sciences or equivalent)
- Minimum three (3) years of experience in the pharmaceutical industry within a Quality Control role; experience with cell therapy products is a plus
- Successfully interface with multi-disciplined teams
- Extremely detail-oriented with strong technical skills
- Ability to effectively manage multiple priorities involving aggressive timelines at a high level of productivity
- High level of ownership and accountability
- Demonstrate sense of urgency; ability to recognize time sensitivity
Position is full-time with overtime as needed. Candidates currently living within a commutable distance of Philadelphia, PA are encouraged to apply.
- Excellent full time benefits including comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
by Jobble
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