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Quality Control Technician I
9021 Bennett Creek Boulevard Frederick, MD 21704 US
Job Description
*Depending on experience
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:
· 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
The team will operate 7 days a week, with an extended, overlapping shift structure.
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.
Fraud Alert: Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.
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