Biopharmaceutical Validation Engineer I

1 month ago

Frederick, United States Frederick National Laboratory for Cancer Research Full time

Biopharmaceutical Validation Engineer I / II

Job ID: req3934
Employee Type: exempt full-time
Division: Clinical Research Program
Facility: ATRF: Other
Location: 8560 Progress Drive, Frederick, MD 21701 USA

The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc.  The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.

Accountability, Compassion, Collaboration, Dedication, Integrity and Versatility; it's the FNL way.

PROGRAM DESCRIPTION        

The Biopharmaceutical Development Program (BDP) of Leidos Biomedical Research, Inc. supports the Frederick National Laboratory Cancer Research (FNLCR) and other government agencies through the development of novel agents for first-in-man clinical studies.

KEY ROLES/RESPONSIBILITIES

Responsible for the setup, operation, and maintenance of equipment and instrumentation used in the validation and quality oversight of facilities, utility systems, process equipment, software, and manufacturing processes used in the CGMP production of biopharmaceutical products Generate, review, and process calibration records, engineering events (failures and change control), environmental and utility monitoring data & excursions, and similar engineering related data, SOPs, and records Identify utility and equipment trends or problems and participate in the diagnosis and implementation of appropriate solutions

 BASIC QUALIFICATIONS

To be considered for this position, you must minimally meet the knowledge, skills, and abilities listed below:

Possession of Bachelor’s degree in a science, technical, or engineering discipline from an accredited college/university according to the Council for Higher Education Accreditation (CHEA) or four (4) years relevant experience in lieu of degree. Foreign degrees must be evaluated for U.S. equivalency  
Validation Engineer I: No work experience required with a Bachelors degree Validation Engineer II: In addition to the education requirement, a minimum of two (2) years' related experience in the pharmaceutical, biopharmaceutical, &/or biologic industries Ability to obtain and maintain a security clearance

PREFERRED QUALIFICATIONS

Candidates with these desired skills will be given preferential consideration:

Two (2) years of job related experience in a GMP or related position in the pharmaceutical, biopharmaceutical, &/or biologic industriesGMP calibration, validation, environmental & utility monitoring, and related experienceExperience with drafting, executing, data analysis, or reviewing of validation protocolsExperience writing or revising SOPs and technical reportsExperience with use of validation tools and equipment such as temperature mapping devices i.e. Kaye or Ellab, multi-meters, temperature standards, temperature baths/heat blocks, and biological indicatorsExperience with operation, maintenance, and troubleshooting of equipment, software, and utilities to support biopharmaceutical operations including fermentors, bioreactors, autoclaves, ovens, washers, chromatography skids, HVAC, WFI, and clean/pure steamKnowledge of aseptic operations, aseptic filling, or airflow visualization principlesAbility to read and understand engineering P&ID and layout drawingsProficiency with basic hand tools and a foundational knowledge of mechanical principlesKnowledgeable and skilled at compliance, training, auditing, and investigation of non-conformancesQA compliance experience including GMP documentation, change control, non-conformance investigation, and corrective and preventative action administrationProficiency with software application including Microsoft Office, Microsoft Project, Blue Mountain Regulatory Assets Manager (BMRAM), Kaye Validator, Master Control, and Microsoft AccessStrong written and verbal communicationWell organized, with the ability to work both independently and as part of a group  

JOB HAZARDS

This position is subject to working with or have potential for exposure to infectious material, requiring medical clearance and immunizations

Commitment to Diversity
All qualified applicants will receive consideration for employment without regard to sex, race, ethnicity, age, national origin, citizenship, religion, physical or mental disability, medical condition, genetic information, pregnancy, family structure, marital status, ancestry, domestic partner status, sexual orientation, gender identity or expression, veteran or military status, or any other basis prohibited by law. Leidos will also consider for employment qualified applicants with criminal histories consistent with relevant laws.

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