How will you make an impact?

TheSr. Technician – QC Sample Managementwill beperforming a variety of duties to support Quality Control- Sample Management. Responsibilities of Sample Managementincludechain of custody,dispensing to laboratories, preventative maintenanceof equipment,managing reference standards and critical reagents,shipping samples to sites as applicable, and aliquoting from bulk material.This personis responsible fordrafting procedures,participatingin special projects, and performing more elaboratefunctions asrequired 

What will youdo?

• Documentation of all activities to meet cGMPcGDPrequirements.  Maintaincomplianceinassigned work and follow all safety procedures,to includethe use of Person Protective Equipment.

• Perform and complete area assignedequipment preventative maintenanceas requested

• Performs routine Sample Management tasks:sample pick-up, aliquoting, LIMS, kitting, critical reagent management,sample shipment, sample disposal

• Clearly and accurately communicates status of samples(picked up, for testing, for send-out)to cross-functional area teams

• Participate in cross-functional activities

• Maintainup to date training records

• Participate in 1-1’s, meetings, attend meetings as necessary tofacilitatearea needs based on changes, etc. (lean activities)

• Performs all duties in strict compliancewith Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines.Maintainsthe necessary compliance status required by company and facility standards.

• AuthorSample Management documents in the site electronic document management system

• Investigate and complete investigation of minor sample management deviations

How will you get here?

Education

• Minimumtwo(2) yearsof college in a Science or Engineering related field (Biology, Biochemistry or Chemistry preferred)

Experience

• At least2years of related experience in biopharmaceutical or pharmaceutical industry preferred

• At least 2years of experience in a cGMP laboratory preferred

Knowledge, Skills, Abilities

Knowledge

• Working knowledge of GMP regulations in a GMP environment

• Knowledge of cGMPpractices andaseptic techniques

Skills

• Analytical Skills

• MS Office

• Strong math skills

• Strong prioritization skills

• Detail oriented

• Results driven

• Safety Mindset

• Electronic document system

• Trackwiseor equivalentdeviation system

• Electronic Sample Management System (LIMS)

• SAP

• Electronic Laboratory Monitoring(LabWatchor BAS)

Abilities

• Ableto read, write, and communicate in English

• Able to understand and carry out instructions

• Reliable

• Strong communication(written and verbal)

• Effectively multi-task

• Able to work in an environment of change

• Able to work independently and as part of a team

• Able to recognize problems developing, not just occurring

• Occasional heavy lifting or moving required

At Thermo Fisher Scientific, each one of our65,000extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier,cleanerand safer.