New!
Clinical Lab Scientist, Level 2, Second or Third Shift, Hoxworth Immunohematology Reference Lab University of Cincinnati
Cincinnati, OH2 days ago
- $31–$38 Per Hour
Highlights
Key Responsibilities Perform routine chemical and physical testing of pharmaceutical finished products and stability samples using chromatographic, spectroscopic, dissolution, and other analytical techniques. Qualifications Bachelor's degree in Chemistry, Biochemistry, or another technical/scientific field or equivalent with 2 3 years of GMP and regulatory experience.
Numbers & Facts
| Location | Cincinnati, OH |
| Industry | Staffing/Employment Agencies |
| Company Size | 2,000 to 2,499 employees |
| Year Founded | 2000 |
| Website | http://www.lancesoft.com/ |
Description
Title: R&D/Mfg Scientist II
Location: Cincinnati, OH 45237
Duration: 0-12+ months
Shift: M-F 6: 00 AM and 9: 00 AM
Pay Rate: $35/HR on w2
Job Description:
Support pharmaceutical development and manufacturing through analytical testing, method development and validation, data review, and laboratory troubleshooting. The role contributes to high-quality, compliant analytical work and effective delivery of project objectives.
Key Responsibilities
Qualifications
Technical Skills
Core Competencies
Physical & Work Environment Requirements
Comments for Suppliers
Location: Cincinnati, OH 45237
Duration: 0-12+ months
Shift: M-F 6: 00 AM and 9: 00 AM
Pay Rate: $35/HR on w2
Job Description:
Support pharmaceutical development and manufacturing through analytical testing, method development and validation, data review, and laboratory troubleshooting. The role contributes to high-quality, compliant analytical work and effective delivery of project objectives.
Key Responsibilities
- Perform routine chemical and physical testing of pharmaceutical finished products and stability samples using chromatographic, spectroscopic, dissolution, and other analytical techniques.
- Develop analytical methods and participate in validation of methods for pharmaceutical raw materials and finished products.
- Write and execute validation protocols in accordance with regulatory requirements and approved laboratory procedures.
- Process, review, interpret, document, and report analytical data;communicate results clearly to internal teams and external clients and make data-based recommendations.
- Maintain and troubleshoot analytical instrumentation and support implementation of new methods and processes.
- Manage assigned project tasks with minimal supervision, ensuring deliverables are completed and next steps are clearly identified.
- Perform all work in compliance with SOPs, GMPs, GLPs, and applicable safety requirements.
Qualifications
- Bachelor's degree in Chemistry, Biochemistry, or another technical/scientific field or equivalent with 2 3 years of GMP and regulatory experience.
- Experience performing chemical testing using chromatographic, spectroscopic, or other analytical techniques.
- Pharmaceutical industry experience required.
Technical Skills
- HPLC/UPLC, including assay and related substances required.
- Empower experience preferred.
- GC and GCHS;chromatographic troubleshooting.
- Dissolution testing;oral solid dosage (OSD) and ARS experience required.
- Method validation, including repeatability, intermediate precision, filter studies, linearity, accuracy, and solution stability.
- Working knowledge of chemistry, analytical instrumentation, and pharmaceutical quality/regulatory requirements.
Core Competencies
- Strong written and verbal communication and interpersonal skills.
- Organized, diligent, and effective at problem-solving.
- Customer-focused with a commitment to quality, timely delivery, and continuous improvement.
- Proactively identifies ideas and solutions that strengthen team and site performance.
Physical & Work Environment Requirements
- Ability to stand, walk, stoop, and kneel as needed.
- Lift up to 40 lbs. Without assistance.
- Work may involve hazardous/toxic materials and requires adherence to GMP safety standards and use of appropriate PPE, including safety glasses, gowning, gloves, lab coat, and hearing protection as applicable.
- Adequate vision is required for computer and laboratory equipment use.
Comments for Suppliers
- Start time can be flexible after training, between 6: 00 AM and 9: 00 AM.
- Conversion based on business needs.
- Hard no on candidates with no Pharmaceutical GMP lab experience.
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.
Similar Job Searches
Research Manager Jobs in Cincinnati, OHScience Manager Jobs in Cincinnati, OHEnvironmental Manager Jobs in Cincinnati, OHClinical Research Manager Jobs in Cincinnati, OHEnvironmental Technician Jobs in Cincinnati, OHResearch Specialist Jobs in Cincinnati, OHData Scientist Jobs in Cincinnati, OHLaboratory Assistant Jobs in Cincinnati, OHResearch Assistant Jobs in Cincinnati, OHLaboratory Technician Jobs in Cincinnati, OH