Quality Control Laboratory Technician

Unicon Pharma Inc; Maryland; Presencial; USD 51.950 - 64.943; Jornada completa

Descripción de la vacante

A leading pharmaceutical company in Maryland is seeking a Quality Control Laboratory Technician for monitoring and managing sample processes. Responsibilities include verifying incoming samples, supporting lab processes, and coordinating with other functions to ensure compliance with GMP standards. Candidates should possess a Bachelor’s Degree or relevant experience in Quality Control within an FDA regulated setting. This contract role is ideal for entry-level candidates looking to gain experience in a fast-paced lab environment.

Formación

• Bachelor’s Degree in relevant field or equivalent experience in Quality Control.
• GMP experience in FDA regulated laboratory is preferred.
• Strong communication skills for team collaboration.

Responsabilidades

• Receive, verify, and log incoming samples into LIMS.
• Coordinate sample transfers to testing labs.
• Perform routine cleaning and maintenance in QC labs.

Conocimientos

GMP knowledge in QC lab

Attention to detail

Microsoft Office proficiency

Interpersonal skills

Ability to adapt to changing priorities

Flexibility with schedule

Educación

Bachelor’s Degree

AA Degree with 2+ years experience

High School Degree with 3+ years experience

Descripción del empleo

• 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.

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.

Required 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-paced small company environment and able to adjust workload based on changing priorities.
• Ability to be flexible with schedule, and work overtime as needed.

Seniority level

• Entry level

Employment type

• Contract

Job function

• Production

Industries

• Environmental Quality Programs and Pharmaceutical Manufacturing

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