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Job Requirements of QC Analyst:
-
Employment Type:
Contractor
-
Location:
Clayton, NC (Onsite)
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QC Analyst
Careers Integrated Resources Inc
Clayton, NC (Onsite)
Contractor
TRUE JOB TITLE: QC Technician I
Pay $30.99/hr on w2
LOCATION: Clayton, NC 27527
DURATION: 1 year (possibility to extend)
REPORTING EXPECTATIONS: On-Site - 5 day/wk
TOP SKILLS PER MGR:
Preparation of Microbiological media
Washing and sterilization with autoclaves of equipment and media
Reading and interpretation of Environmental monitoring samples
Bioburden testing of utilities samples via membrane filtration
PURPOSE: Perform & review analysis of in-process, release & stability samples of API &/or filled product in accordance with cGMP, site & corporate procedures & policies. Transfer of technology & processes in accordance with relevant project plans & timelines.
ESSENTIAL FUNCTIONS:
Ensure accuracy & scientific soundness of lab data
Ensure environmental compliance
Support & ensure GMP Laboratory Compliance
Maintain testing proficiency for methods
Ensure timeliness of lab results & investigations
Perform analysis of samples ? Support deviations
Follow all safety & environmental requirements in the performance of duties
Other accountabilities, as assigned
PHYSICAL REQUIREMENTS:
Moves equipment &/or supplies weighing up to 33 pounds within the facility using various body positions.
Ability to do close precision work with their hands.
Must be able to remain in a stationary position (sitting and standing) 50% of the time.
Occasionally ascends/descends a ladder.
May be required to work at elevated heights.
Occasionally works around odorous &/or hazardous materials.
Vision screening NOT REQUIRED.
Color Vision NOT REQUIRED
QUALIFICATIONS:
Associate's degree in science or a relevant field of study from an accredited university required
Bachelor's Degree in science or a relevant field of study from an accredited university preferred One (1) year of work experience in a clinical or industrial/pharmaceutical laboratory preferred
Ability to author scientific & technical reports is a plus
Able to perform routine testing per SOP & GMP standards preferred
Basic level of troubleshooting for laboratory equipment is a plus
Knowledgeable in GMP & laboratory techniques is a plus
Demonstrate attention to detail required
Strong communication skills (verbal & written) preferred
Skills or knowledge in one of the following disciplines: Chemistry Analysis (HPLC, UPLC, GC, TOC, AA, UV, PH, KF), Microbiology Analysis (Isolator, Sterility, Bacterial Endotoxin testing, Growth Promotion and Microbial Identification, ELISA, BIOBURDEN) or Raw Materials Analysis (Compendial Testing, FTIR, NIR, Titration and UVVis) is a plus
Pay $30.99/hr on w2
LOCATION: Clayton, NC 27527
DURATION: 1 year (possibility to extend)
REPORTING EXPECTATIONS: On-Site - 5 day/wk
TOP SKILLS PER MGR:
Preparation of Microbiological media
Washing and sterilization with autoclaves of equipment and media
Reading and interpretation of Environmental monitoring samples
Bioburden testing of utilities samples via membrane filtration
PURPOSE: Perform & review analysis of in-process, release & stability samples of API &/or filled product in accordance with cGMP, site & corporate procedures & policies. Transfer of technology & processes in accordance with relevant project plans & timelines.
ESSENTIAL FUNCTIONS:
Ensure accuracy & scientific soundness of lab data
Ensure environmental compliance
Support & ensure GMP Laboratory Compliance
Maintain testing proficiency for methods
Ensure timeliness of lab results & investigations
Perform analysis of samples ? Support deviations
Follow all safety & environmental requirements in the performance of duties
Other accountabilities, as assigned
PHYSICAL REQUIREMENTS:
Moves equipment &/or supplies weighing up to 33 pounds within the facility using various body positions.
Ability to do close precision work with their hands.
Must be able to remain in a stationary position (sitting and standing) 50% of the time.
Occasionally ascends/descends a ladder.
May be required to work at elevated heights.
Occasionally works around odorous &/or hazardous materials.
Vision screening NOT REQUIRED.
Color Vision NOT REQUIRED
QUALIFICATIONS:
Associate's degree in science or a relevant field of study from an accredited university required
Bachelor's Degree in science or a relevant field of study from an accredited university preferred One (1) year of work experience in a clinical or industrial/pharmaceutical laboratory preferred
Ability to author scientific & technical reports is a plus
Able to perform routine testing per SOP & GMP standards preferred
Basic level of troubleshooting for laboratory equipment is a plus
Knowledgeable in GMP & laboratory techniques is a plus
Demonstrate attention to detail required
Strong communication skills (verbal & written) preferred
Skills or knowledge in one of the following disciplines: Chemistry Analysis (HPLC, UPLC, GC, TOC, AA, UV, PH, KF), Microbiology Analysis (Isolator, Sterility, Bacterial Endotoxin testing, Growth Promotion and Microbial Identification, ELISA, BIOBURDEN) or Raw Materials Analysis (Compendial Testing, FTIR, NIR, Titration and UVVis) is a plus
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