Job Listing Description

Sr. Technician - QC Sample Management

Description:
Chipton-Ross is seeking a Sr. Technician - QC Sample Management for an opening in St. Louis, MO.

SUMMARY:
The Sr. Technician QC Sample Management will be performing a variety of duties to support Quality Control- Sample Management. Responsibilities of Sample Management include chain of custody, dispensing to laboratories, preventative maintenance of equipment, managing reference standards and critical reagents, shipping samples to sites as applicable, and aliquoting from bulk material. This person is responsible for drafting procedures, participating in special projects, and performing more elaborate functions as required.

RESPONSIBILITIES:
Documentation of all activities to meet cGMP/cGDP requirements. Maintain compliance in assigned work and follow all safety procedures, to include the use of Person Protective Equipment. Perform and complete area assigned equipment preventative maintenance as 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. Maintain up to date training records. Participate in 1-1s, meetings, attend meetings as necessary to facilitate area needs based on changes, etc. (lean activities). Performs all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines. Maintains the necessary compliance status required by company and facility standards. Author Sample Management documents in the site electronic document management system. Investigate and complete investigation of minor sample management deviations.

REQUIREMENTS:
At least 2years of related experience in biopharmaceutical or pharmaceutical industry preferred. At least 2 years of experience in a cGMP laboratory preferred. Working knowledge of GMP regulations in a GMP environment. Knowledge of cGMP practices and aseptic techniques. Analytical Skills. MS Office. Strong math skills. Strong prioritization skills. Detail oriented. Results driven. Safety Mindset. Electronic document system. Trackwise or equivalent deviation system. Electronic Sample Management System (LIMS). SAP. Electronic Laboratory Monitoring (LabWatch or BAS) Able to 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

EDUCATION:
Minimum two(2) years of an accredited college in a Science or Engineering related field (Biology, Biochemistry or Chemistry preferred)

WORK HOURS:
Full-Time

 
Job Number: 194519
Job Location: St. Louis, MO
Rate: $22.5 to $24.00 DOE
Duration: 9 mos
Input Date: 11/16/2021
Firm Name: CHIPTON ROSS
Attention: Patrick Costello
Address: 420 CULVER BLVD
City, State: PLAYA DEL REY, CA 90293
Phone: 310/414-7800 X286
800 Phone: 800/927-9318
Fax Phone: 310/414-7808
Email: pcostello@chiptonross.com
Website: www.chiptonross.com

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