What are the responsibilities and job description for the Technician position at Chipton-Ross?
Chipton-Ross is seeking a Quality Control Technician for a contract opportunity in St. Louis, MO.
RESPONSIBILITIES:
The QC Sample Management Technician II will be performing department inventory audits and reconciliations for various samples, reference materials, reagents, etc. Individual will utilize the site's LIMS systems, logbooks, and other inventory trackers to optimize department inventory systems. Some of this work may include data entry from older inventory items into the department's current systems and/or discarding items eligible for disposal following department SOPs.
What will you do?
REQUIREMENTS:
Knowledge
EDUCATION:
Accredited two years of college in a Science or Engineering related field (Biology, Biochemistry or Chemistry preferred)
SHIFT:
Full-Time- 1st Shift
Monday- Friday 08:00am-05:00pm
RESPONSIBILITIES:
The QC Sample Management Technician II will be performing department inventory audits and reconciliations for various samples, reference materials, reagents, etc. Individual will utilize the site's LIMS systems, logbooks, and other inventory trackers to optimize department inventory systems. Some of this work may include data entry from older inventory items into the department's current systems and/or discarding items eligible for disposal following department SOPs.
What will you do?
- Work on a small team dedicated to a project for inventory reconcilliation of frozen, refrigerated, and room temperature storage units.
- Use the site's LIMS system to audit inventory units, reconcile inventory records, and escalate gaps in physical inventory vs. inventory records.
- May be responsible for re-generation of legacy inventory items into newer LIMS systems.
- 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.
- Maintain up to date training records.
- 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.
REQUIREMENTS:
Knowledge
- Basic knowledge of GMP regulations in a GMP environment.
- Knowledge of cGMP practices and good inventory controls.
- MS Office- Proficent. MS Excel will primarily be used and no advanced skills are needed (Macros, Pivot Points, etc).
- Strong prioritization skills
- Detail oriented
- Safety Mindset
- Highly organized
- 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
- Occasional heavy lifting or moving required
EDUCATION:
Accredited two years of college in a Science or Engineering related field (Biology, Biochemistry or Chemistry preferred)
SHIFT:
Full-Time- 1st Shift
Monday- Friday 08:00am-05:00pm
Employment will be contingent on clearing a drug screen and background check. Both must clear prior to start date.
Contact
Tyler Harrell
tharrell@chiptonross.com
CHIPTON-ROSS, INC.
420 Culver Boulevard
Playa Del Rey, CA 90293
Phone: (310) 414-7800 x307 or (800) 927-9318 x307
tharrell@chiptonross.com
CHIPTON-ROSS, INC.
420 Culver Boulevard
Playa Del Rey, CA 90293
Phone: (310) 414-7800 x307 or (800) 927-9318 x307
Behavior Technician (BT)
Behavior Technician -
Oakbrook Terrace, IL
Pharmacy Intern
Certified Technician -
Annandale, MN
Departmental Analyst 9-P11 - Energy Services Unit
Library Technician -
Lansing, MI