QC Scientist - Microbiology

Employer
System One
Location
Exton, Pennsylvania, US
Salary
Competitive
Posted
Jul 14, 2021
Closes
Jul 26, 2021
Ref
2317121058
Discipline
Biology, Energy
Employment Type
Full time
Salary Type
Salary
Title: QC Scientist Microbiology
Location: Exton, PA
Duration: Contract
Schedule: M-F Full Time
Target Start Date: ASAP

Responsibilities:
The QC Scientist-Microbiology is responsible for day to day operations of the QC Microbiology laboratory in a cGMP biopharmaceutical pilot plant. The individual prioritizes, oversees, and tracks multiple microbiological projects ensuring timely completion and efficient utilization of staff and equipment. The QC Scientist is responsible for leading and/or collaborating in the routine operation of the microbiology lab. The individual provides technical expertise and trains other analysts on microbiological analyses. The QC Scientist has responsibility for maintaining analytical instruments, using knowledge and experience to appropriately respond to malfunctions, scheduling, monitoring, and interfacing with external personnel as necessary. In addition to prioritizing overall workflow, analyst training and equipment maintenance, the individual provides technical expertise, generates compliant laboratory data for release, validation of assays as appropriate and support of critical utility, environmental and process stream testing. The QC Scientist serves as a first-line resource to other analysts in assessing and resolving technical issues. The QC Scientist authors and updates SOPs for laboratory procedures, and operation of equipment, investigates and documents microbiology alert/actions, OOS/OOT events and implements the appropriate CAPA when necessary. The QC Scientist is responsible assisting with routine trending of critical utilities and environmental monitoring results. Schedules and performs (as needed) daily routine microbiological testing including sample collection and testing within the QC Microbiology Laboratory in support of all Pilot Plant needs
Leads and coordinates investigations on behalf of QC Microbiology. This includes internal investigations as well as processing investigations. Investigate and document assay failures and OOS events, and implement associated laboratory CAPA in a timely manner.
Oversees the work of junior analysts performing all laboratory tasks. Ensures laboratory data generated during testing is captured accurately and timely into respective data systems (e.g. LIMS).
Performs data review and approval as necessary. Promptly communicates any non-conformances to QC Management and participates in non-conformance resolution as needed
Coordinates and prioritizes the management of raw materials, data review and data management for the Raw Material Program as well as general laboratory data.
Oversee routine calibrations and preventive maintenance of laboratory equipment and instruments; and performs instrument qualifications as necessary
Maintains the laboratory maintenance in a compliant manner by overseeing, coordinating, and assisting with cleaning, inventory, calibration, training, SOP and test method revision
Leads microbiological projects as necessary

Requirements: BS in Microbiology, or other relevant scientific discipline.
A minimum of 5+ years working experience in a cGMP Quality Control department in an FDA-regulated industry
Experience in Biopharmaceutical industry required
Proficiency gained through wide exposure / experience in technical field; broad grasp and application of scientific theory and principles
Expert working experience with microbiological testing such as membrane filtration and direct plating bioburden, endotoxin testing using kinetic chromogenic systems, microbial identifications and environmental monitoring experience using viable and non-viable methods.
Experience with aseptic technique, TOC and conductivity is required
Experience with LIMS required
Expected to conduct projects, evaluate experimental results, provide solutions to problems require choosing from multiple alternatives
Strong working knowledge of cGMP/ICH/FDA/EMEA regulations and guidelines
Proficient in MS Office applications; particularly Excel graphing.
Experience with statistical software such as MinitabĀ© or JMP

Joule, a System One division is a leader in specialized workforce solutions and integrated services. With more than 6,000 employees and roughly 50 offices throughout the U.S. we provide scientific, clinical, engineering, energy, IT, legal and administrative staffing services. For more than 40 years, we have delivered workforce solutions and integrated services to clients nationally.

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