Job Description

Job SummaryMedpace Reference Laboratories (MRL) plays a pivotal role in research-based drug development within the pharmaceutical industry. Due to our recent growth, we are in need of a qualified and focus-driven Medical Technologist (Histo) / Histo-technician in Singapore. The incumbent is expected to perform complex procedures within the Histopathology Laboratory, including routine histotechnology, H&E stain, special stains, immunohistochemistry (IHC) and in-situ hybridization (ISH) stains, as well as other duties as assigned. The candidate must be capable of completing assigned tasks in a timely manner using standard operating procedures and techniques established by the laboratory.Responsibilities

• Perform clinical sample management (accessioning), tissue processing, embedding, FFPE sectioning, and staining;
• Possess knowledge of and experience with routine stains (e.g. H&E), special stains (e.g. Trichrome , PAS, reticulin, etc) as well as specific IHC/ISH stains following protocols according to global SOPs;
• Participate in assay validation activities, experimental design, instrument set-up (IQ/OQ/PQ) and audits;
• Knowledge of clinical trial processes and procedures, including federal and local regulations preferred, but not required
• Ensure accuracy and scientific validity of laboratory data reported;
• Contribute to maintaining a Quality Control/Quality Assurance and Quality Management environment;
• Maintain overview of reagent and tissue inventories; and
• Comply with Good Clinical Practices (GCP) and Good Documentation Practices (GDP).

Qualifications

• 5+ years of experience in a diagnostic histology laboratory performing tissue processing, tissue embedding, sectioning, slide preparation, H&E and special staining, IHC/ISH, and process troubleshooting required; and
• 2+ year of experience in a high throughput diagnostic laboratory production environment using LIMS, Data Management systems, automatic tissue processing systems, and automated H&E/IHC stainers preferred, but not required
• Clinical trial or central reference laboratory experience preferred, but not required

Medpace OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.The work we\xe2\x80\x99ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.Medpace Perks

• Hybrid work-from-home options (dependent upon position and level)
• Competitive PTO packages
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Flexible work schedule
• Competitive compensation and benefits package
• Structured career paths with opportunities for professional growth

Awards

• Recognized by Forbes as one of America\'s Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.EO/AA Employer M/F/Disability/Vets

Medpace