Job Description
Title: Quality Engineer
Location: Frederick, MD (Oniste 5 days a week)
Contract Duration: 12 Months
Pay Range: $30.00 - $35.75 USD hourly on W2
Responsibilities:
Provide Quality oversight and guidance for all cGMP Work Orders performed on critical equipment, facility and utilities necessary for commercial and clinical production.
Provide Quality oversight and resolution guidance for all alarms generated by our Equipment Monitoring System (EMS) which actively monitors our critical equipment, facility, and utilities necessary for commercial and clinical production.
Demonstrate intimate working knowledge of pharmaceutical relevant standards, principles and best practices.
Collaborate with project teams and necessary departments (e.G. Manufacturing, engineering, product development, quality control, supplier quality, supply chain) in the execution of CQV and CSV, as needed.
Track, review and report metric information as necessary.
Support Quality Engineering functions as necessary, including oversight of validation activities and quality risk management.
Additional duties as assigned.
These duties can be delegated to designated deputies of a satisfactory qualification level as needed.
Basic Qualifications:
Master s Degree OR
Bachelor s Degree and 2+ years experience in a pharmaceutical or FDA regulated environment OR
AA Degree and 4+ years experience in a pharmaceutical or FDA regulated environment OR
High School Degree and 5+ years experience in a pharmaceutical or FDA regulated environment.
Preferred Qualifications:
Familiarity with cGMP maintenance planning, execution and closure thru a Computerized Maintenance Management System.
Familiarity with cGMP calibration planning, execution, and closure thru CMMS
Experience in building management systems (e.G. Siemens Desigo) is a plus.
Experience in CMMS (e.G. BMRAM and/or Maximo) is a plus.
Must be able to prioritize, manage and follow-up on numerous projects and activities
Must exhibit effective written and verbal communication skills
Must be detail oriented and exhibit a high degree of flexibility and initiative
Ability to function efficiently in a diverse, fast paced, changing environment.
Must be able to work independently as well as part of a team.
Ability to think critically, and utilize troubleshooting and problem solving skills
Cell and Gene Therapy experience is a plus
Location: Frederick, MD (Oniste 5 days a week)
Contract Duration: 12 Months
Pay Range: $30.00 - $35.75 USD hourly on W2
Responsibilities:
Provide Quality oversight and guidance for all cGMP Work Orders performed on critical equipment, facility and utilities necessary for commercial and clinical production.
Provide Quality oversight and resolution guidance for all alarms generated by our Equipment Monitoring System (EMS) which actively monitors our critical equipment, facility, and utilities necessary for commercial and clinical production.
Demonstrate intimate working knowledge of pharmaceutical relevant standards, principles and best practices.
Collaborate with project teams and necessary departments (e.G. Manufacturing, engineering, product development, quality control, supplier quality, supply chain) in the execution of CQV and CSV, as needed.
Track, review and report metric information as necessary.
Support Quality Engineering functions as necessary, including oversight of validation activities and quality risk management.
Additional duties as assigned.
These duties can be delegated to designated deputies of a satisfactory qualification level as needed.
Basic Qualifications:
Master s Degree OR
Bachelor s Degree and 2+ years experience in a pharmaceutical or FDA regulated environment OR
AA Degree and 4+ years experience in a pharmaceutical or FDA regulated environment OR
High School Degree and 5+ years experience in a pharmaceutical or FDA regulated environment.
Preferred Qualifications:
Familiarity with cGMP maintenance planning, execution and closure thru a Computerized Maintenance Management System.
Familiarity with cGMP calibration planning, execution, and closure thru CMMS
Experience in building management systems (e.G. Siemens Desigo) is a plus.
Experience in CMMS (e.G. BMRAM and/or Maximo) is a plus.
Must be able to prioritize, manage and follow-up on numerous projects and activities
Must exhibit effective written and verbal communication skills
Must be detail oriented and exhibit a high degree of flexibility and initiative
Ability to function efficiently in a diverse, fast paced, changing environment.
Must be able to work independently as well as part of a team.
Ability to think critically, and utilize troubleshooting and problem solving skills
Cell and Gene Therapy experience is a plus
Numbers & Facts
| Location | Frederick, MD |
| Industry | Staffing/Employment Agencies |
| Salary | $30–$35.75 Per Hour |
| Company Size | 2,000 to 2,499 employees |
| Year Founded | 2000 |
| Website | http://www.lancesoft.com/ |
About Company
We are a $125 Million, NMSDC-certified Minority & Woman owned Workforce Solutions Company headquartered in the DC metro area with presence across US with global presence - Canada, Mexico, India, UK, Malaysia, Indonasia, Hongkong, Singapore, UAE. We are specialized in providing Workforce Solutions, SOW project delivery, Engineering Solutions, Creative Services. We currently support 100+ Fortune companies globally and across multiple industry segments. We are currently supporting several massive programs across industry segment nationally/globally (Intel, Ally, AMD, QUALCOMM, Morgan Stanley, Kraft/ Mondelez, MNP, Amdocs, Dell, SanDisk, Medtronic, Becton Dickinson, GE, Lockheed Martin, UTC, L-3 Communications, Caterpillar, BMW, Mercedes Benz, National Grid, Dominion, Energy Future Holdings, PSEG, 3M, Fidelity, Aetna, Humana, Johnson & Johnson, Pfizer, Merck etc).
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, identity, national origin, disability, or protected veteran status.
Skills
- Best Practicesunmatched
- Biotech and Pharmaceuticalunmatched
- Calibrationunmatched
- Communication Skillsunmatched
- Computerized Maintenance Management System (CMMS)unmatched
- Current Good Manufacturing Practice (cGMP)unmatched
- Detail Orientedunmatched
- Establish Prioritiesunmatched
- FDA (Food and Drug Administration)unmatched
- Gene Therapyunmatched
- IBM Maximo Asset Managementunmatched
- Manufacturingunmatched
- Metricsunmatched
- Presentation/Verbal Skillsunmatched
- Product Developmentunmatched
- Property Managementunmatched
- Quality Controlunmatched
- Quality Engineeringunmatched
- Quality Managementunmatched
- Risk Managementunmatched
- Secondary Schoolunmatched
- Supply Chainunmatched
- Team Playerunmatched
- Writing Skillsunmatched
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