Planet Pharma
Quality Control Technician I - QC Lab Support
Skills
9 days ago
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Important information
Contract type:
Freelance / Contract
Location:
Frederick, MD, USA
Work mode:
Onsite
Published on:
16 October 2026
What they need
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
- Bachelors 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
The team will operate 7 days a week, with an extended, overlapping shift structure.
The max pay rats is 20.40/hr for this position
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