Specimen Management Associate

Shift: (Second Shift) Tuesday-Saturday, 11am-7:30pm The Specimen Management Associate processes incoming specimens, captures all relevant and accompanying data and documents deviations according to expectations, in order to enable timely, high quality specimen services per work lists. To maintain and document chain of custody from box opened until next service destination to ensure full accountability and traceability at all times. To ensure appropriate storage, destruction, and shipping of samples.,

Sample Registration Specimen Management Associate

• Fully own and process incoming shipments and make corrective actions in a proper, compliant and transparent way according to corporate SOPs.
• Receive shipments from couriers, unpacking shipments, and maintain appropriate temperature of specimens during the registration process.
• Enter and control the subject demographics and visit details into the LIMS system.
• Ensure the specimen quality meets expectations and document any deviations (LIMS system or paper log).
• Transfer the specimens to their next service destination and document handshake.
• Resolve deviations from processing work lists or elevate to management.
• Drive completion of investigations captured in QS Tickets and actions captured within HDL Tickets.

• Prepare, control and complete specimen shipments including paper work and manifests.
• Adhere to timeline commitments for shipping and destruction of samples.
• Create and execute specimen work lists to meet planned completion service timelines.
• Dispose of residual specimens according to company policy and applicable local regulations.
• Ensure proper storage of samples utilizing a LIMS system.
• Resolve deviations from processing work lists or elevate to management.
• Drive completion of investigations captured in QS Tickets and actions captured within HDL Tickets.

• High School Diploma or equivalent, required. Professional or Technical degree (minimum 2-year apprenticeship or equivalent), preferred.
• Drivers license and proof of insurance.
• Minimum 2 years in a production environment, preferably in healthcare, life sciences or pharmaceutical settings, preferred
• Minimum 2 years of experience working with enterprise-grade application (LIMS preferred), preferred.
• Proven (testimonial and/or references) track record as a successful team player
• Authorization to work in the United States indefinitely without restriction or sponsorship., Basic knowledge of English, both written and oral.
• May experience prolonged exposure to low temperatures.
• Standing may exceed 50% of the time.
• Prolonged usage of computer systems (75%).
• Ability to lift 25lbs. repeatedly.
• Ability to bend and lift required.
• Ability to follow priorities, pay attention to detail, follow SOPs and work accurately under deadlines.
• Capable of identifying problems and notifying superiors.
• Ability to work weekend shifts every other weekend, required.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the…