QUALITY CONTROL TECHNICIAN I – QC LAB SUPPORT

Planet Pharma; Frederick (MD); On-site; USD 24,000 - 34,000; Part time

Job summary

Planet Pharma is seeking a Quality Control Technician I for QC Lab Support in Frederick, MD. This on-site role involves handling samples, logging in LIMS, and coordinating with QA, MM, and other QC teams.

The position emphasizes adherence to GMP, meticulous record-keeping, and active participation in Lean Lab initiatives. The role requires a relevant degree with experience in QC laboratories or biopharma settings, and offers a contract arrangement with an emphasis on process discipline and

Qualifications

• Knowledge of GMP in QC labs and FDA-regulated environments preferred.
• Demonstrated attention to detail and ability to manage multiple projects.
• Proficient with MS Office and related tools; strong documentation skills.

Responsibilities

• Receive, verify, and log samples in LIMS; ensure proper documentation.
• Process samples for receipt, processing, or aliquoting for testing and retains.
• Label, store, and organize samples per procedures and storage requirements.
• Coordinate transfers to internal and external labs for testing.
• Perform routine storage area cleaning, maintenance, and restocking.

Skills

GMP knowledge

Attention to detail

Microsoft Office

Communication skills

Education

Bachelor's Degree

AA Degree

High School Degree

Tools

LIMS

Job description

Quality Control Technician I – QC Lab Support

Location: Frederick, MD

Category: Scientific

Salary: Apply for details

Country: United States

Employment: Contract

Worksite: On-Site

Job Description

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

Reports to: Manager, Quality Control Lab Support

The team will operate 7 days a week, with an extended, overlapping shift structure.

The max pay rate is 21/hr for this position

Equal Opportunity Employer

We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.