Quality Control Technician , MD, Frederick

Position: Quality Control Technician Jobs in USA, MD, Frederick | Rose International Job
Education:

High School

Required Skills:

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

Skills:

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

Summary:

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:

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.

• ** Only those lawfully authorized to work in the designated country associated with the position will be considered.**

• ** Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client's business needs and requirements.**

Benefits:

For information and details on employment benefits offered with this position, please visit

here
. Should you have any questions/concerns, please contact our HR Department via our secure
website

California Pay Equity:

For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website

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Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise,

please contact our HR Department

Rose International has an official agreement (), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).