Lab Tech - I*

Mindlance

Frederick, MD

Apply

JOB DETAILS

SKILLS

Chain of Custody, Detail Oriented, Documentation, FDA (Food and Drug Administration), GMP (Good Manufacturing Practices), Housekeeping/Cleaning, Interpersonal Skills, Laboratory, Laboratory Information Management System (LIMS), Laboratory Management, Laboratory Operations, Microsoft Excel, Microsoft Office, Microsoft Visio, Multitasking, Presentation/Verbal Skills, Quality Assurance, Quality Control, Regulations, Safety Compliance, Secondary School, Small Company, Team Player, Test Lab, Testing, Writing Skills

LOCATION

Frederick, MD

POSTED

8 days ago

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.

EEO:

“Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”

About the Company

Mindlance

Resume Resources

Free Resume Templates Free Resume Builder