Quality Control Technician I - QC Lab Support

TekWissen LLC

Frederick, MD

JOB DETAILS
SALARY
$19–$21
SKILLS
Analytical Development, Biotech and Pharmaceutical, Chain of Custody, Cross-Functional, Detail Oriented, Diversity, Documentation, Drug Development, FDA (Food and Drug Administration), GMP (Good Manufacturing Practices), HIV/AIDS (Acquired Immune Deficiency Syndrome), Hepatitis B, Hepatitis C, Housekeeping/Cleaning, Interpersonal Skills, Laboratory, Laboratory Information Management System (LIMS), Laboratory Management, Laboratory Operations, Manufacturing Management, Materials Management, Microsoft Excel, Microsoft Office, Microsoft Visio, Multitasking, Presentation/Verbal Skills, Quality Assurance, Quality Control, Regulations, Research & Development (R&D), Safety Compliance, Secondary School, Small Company, Specimens/Samples, Team Player, Test Lab, Testing, Workforce Management, Writing Skills
LOCATION
Frederick, MD
POSTED
1 day ago
Overview:

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The company focuses primarily on antiviral drugs used in the treatment of HIV, hepatitis B, hepatitis C, and influenza, including Harvoni and Sovaldi.

Position: Quality Control Technician I - QC Lab Support
Location: Frederick, MD 21704
Duration: 12 Months
Job Type: Temporary Assignment
Work Type: Onsite
Sun - Wed. 7:00 am-6:00 pm
DAY Shifts: 4/10 (4 days x 10 hours/day)
Role: Execute tasks associated with sample management, shipment of samples, and other lab support QC functions, while interacting cross-functionally with personnel from other QC groups, Quality Assurance, Analytical Development, Manufacturing, Material Management (MM), and Corporate teams.
Responsibilities (include but are not limited to):
  • Receive incoming samples, verify documentation, and log sample information into LIMS.
  • Execute processes to support sample receipt and processing or aliquoting for release/stability testing and retains.
  • Label, store, and organize samples according to established procedures and storage requirements.
  • Coordinate sample transfers to internal and external testing labs.
  • Perform routine cleaning, maintenance, and restocking of sample storage areas.
  • Collaborate with MM, QA, and other QC functions-including Corporate QC-to support requirements around sampling, testing, and disposition.
  • Manage and complete all shipping activities within QC functions.
  • Complete routine review of records, such as sample chain of custody forms, processing logs, logbooks, and other documentation generated within QC Lab Support.
  • Assist with deviation and investigation activities as needed.
  • Provide updates during daily and weekly meetings.
  • Participate in Lean Lab and other Operational Excellence initiatives.
  • Comply with all safety, quality, and regulatory guidelines.
  • Perform other duties as assigned.
Basic Qualifications:
  • Bachelor's Degree OR
  • AA Degree and 2+ years' experience working in Quality Control or biopharma laboratories preferably in an FDA regulated laboratory OR
  • High School Degree and 3+ years' experience working in Quality Control or biopharma laboratories preferably in an FDA regulated laboratory.
Preferred Qualifications:
  • Strong knowledge in applying GMP in QC lab.
  • Exceptional attention to detail and ability to keep track of multiple ongoing projects
  • Proficient in Microsoft Office, Excel, Visio, and other related applications
  • Excellent interpersonal, verbal and written communications skills which are essential in this collaborative work environment
  • Comfortable in a fast-paces small company environment and able to adjust workload based on changing priorities.
  • Ability to be flexible with schedule, and work overtime as needed
Reports to: Manager, Quality Control Lab Support
The team will operate 7 days a week, with an extended, overlapping shift structure.
TekWissen Group is an equal opportunity employer supporting workforce diversity.

About the Company

T

TekWissen LLC

WE THE TEKWISSEN PEOPLE

TekWissen offers you a broader portfolio of services, industry-leading solutions, and the meaningful innovations that give you greater flexibility and speed to respond to market dynamics, reduced costs and risk to improve enterprise performance, and increased productivity to enable growth.

To keep pace with global market demands, TekWissen keeps its finger on the pulse of change. Our organized approach to guiding a project from its inception to closure. Managing projects is becoming more and more important as we enter the digital era. To cope with the pace that this transition demands, a method is required to manage projects so they can yield quality work, while incorporating efficient use of time and resources.

Project involves identifying which quality standards are relevant to the project and determining how to satisfy them.

It is important to perform quality planning during the Planning Process and should be done alongside the other project planning processes because changes in the quality will likely require changes in the other planning processes, or the desired product quality may require a detailed risk analysis of an identified problem. It is important to remember that quality should be planned, designed, then built in, not added on after the fact.

Capabilities and accomplishments in one TekWissen business enhance the opportunity for success in the others. Put simply, TekWissen's unique combination of attributes promotes success.



COMPANY SIZE
100 to 499 employees
INDUSTRY
Computer/IT Services
FOUNDED
2009
WEBSITE
http://www.tekwissen.com/