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HomeCompaniesCareers Noven Icims ComQC Analyst

QC Analyst

Careers Noven Icims Com · Miami, FL, US · Active · iCIMS

Job facts

FieldValue
CompanyCareers Noven Icims Com
TitleQC Analyst
Normalized title-
Department / teamQuality
LocationMiami, FL, United States
Work model-
Employment typeOTHER
Salary-
Statusactive
ATS provideriCIMS
Posted / first seen2024-06-06 / 2026-06-02
Changed / last seen2026-06-06 / 2026-06-06

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Linked records

CompanyCareers Noven Icims Com
Sourcebb5477b2-4611-4c36-b640-2c131f65ffb3
ATS provideriCIMS

Description

Overview Performs professional, technical laboratory functions. Responsibilities The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. Performs physical and chemical analysis of raw materials, components, in-process and finished pharmaceutical products, including products on stability, according to written methods or compendial methods as applicable, material specifications, using analytical techniques such as IR spectroscopy, UV-Vis spectroscopy, and chromatographic techniques adhering to company policies as identified in standard operating procedures (SOPs). Prepares samples for analysis involving thorough cleanliness and complex steps for analysis using chromatographic techniques and other analytical techniques as applicable in compliance with cGMP and current safety regulations. Creates and maintains laboratory record documentation in compliance with regulatory requirements. Actively participates in investigation of laboratory results, when required. Prepares volumetric test solutions following USP or in-house methods for wet chemical tests, standardizes such solutions as required, standardizes API for use as in-house reference standard as assigned. Qualifications Competencies: Education / Experience: Bachelor’s Degree (BA/BS) in Chemistry or related field – Required. Less than one year testing of chemicals/pharmaceutical products – Required. Must be able to read and understand analytical procedures – Required. Must be able to effectively communicate results, problems, or issues, in English verbally as well as in writing – Required. Must be computer literate. Must be precise and consistent in day-to-day analysis, easily trainable, and ready to learn. Must be able to work in a team environment and be flexible to easily adapt to changes in assignments. Must follow safe practices as identified in appropriate SDS while working with chemicals and must follow applicable state and federal regulations. Must possess a working knowledge of analytical chemistry techniques, such as analytical weighing, quantitative transfer, preparation of quantitative solutions, analytical dilutions, spectrophotometric analytical techniques, dissolution and drug release, disintegration, moisture determination (Karl Fischer, Coulometric, LOD), thin-layer chromatographic technique, gas chromatographic techniques, HPLC, and measuring physical parameters (bulk and tapped densities, and particle size by sieve analysis). Must be able to follow compendial (USP/EP/BP/JP) procedures for wet chemical tests. Must understand and apply cGMP requirements applicable to quality control laboratory. Judgment / Decision Making: Duties are performed within framework of departmental or functional guidelines, requiring interpretation and original thinking. Work Environment: A laboratory environment with exposure to chemicals, caustics, fumes, heat and electrical current. Physical Demands: Visual acuity and manual dexterity required to operate computer, analytical instrumentation, sample preparation. Majority of time spent standing. Often required to lift objects weighing up to 20 pounds.

Full job record

Job ID2fb4d6c7312564cf7436123d100acaf29b8a41df
Org ID1d27a48f-189b-4e01-a214-42e0a7ef2dab
Source IDbb5477b2-4611-4c36-b640-2c131f65ffb3
Board IDbb5477b2-4611-4c36-b640-2c131f65ffb3
Providericims
Provider Job Key2587
TitleQC Analyst
Normalized Title
Statusactive
Activeyes
Location TextMiami, FL, US
DepartmentQuality
Team
Employment TypeOTHER
Workplace Type
Remote Policy
CountryUnited States
RegionFL
CityMiami
Salary RawOverview Performs professional, technical laboratory functions. Responsibilities The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. Performs physical and chemical analysis of raw materials, components, in-process and finished pharmaceutical products, including products on stability, according to written methods or compendial methods as applicable, material specifications, using analytical techniques such as IR spectroscopy, UV-Vis spectroscopy, and chromatographic techniques adhering to company policies as identified in standard operating procedures (SOPs). Prepares samples for analysis involving thorough cleanliness and complex steps for analysis using chromatographic techniques and other analytical techniques as applicable in compliance with cGMP and current safety regulations. Creates and maintains laboratory record documentation in compliance with regulatory requirements. Actively participates in investigation of laboratory results, when required. Prepares volumetric test solutions following USP or in-house methods for wet chemical tests, standardizes such solutions as required, standardizes API for use as in-house reference standard as assigned. Qualifications Competencies: Education / Experience: Bachelor’s Degree (BA/BS) in Chemistry or related field – Required. Less than one year testing of chemicals/pharmaceutical products – Required. Must be able to read and understand analytical procedures – Required. Must be able to effectively communicate results, problems, or issues, in English verbally as well as in writing – Required. Must be computer literate. Must be precise and consistent in day-to-day analysis, easily trainable, and ready to learn. Must be able to work in a team environment and be flexible to easily adapt to changes in assignments. Must follow safe practices as identified in appropriate SDS while working with chemicals and must follow applicable state and federal regulations. Must possess a working knowledge of analytical chemistry techniques, such as analytical weighing, quantitative transfer, preparation of quantitative solutions, analytical dilutions, spectrophotometric analytical techniques, dissolution and drug release, disintegration, moisture determination (Karl Fischer, Coulometric, LOD), thin-layer chromatographic technique, gas chromatographic techniques, HPLC, and measuring physical parameters (bulk and tapped densities, and particle size by sieve analysis). Must be able to follow compendial (USP/EP/BP/JP) procedures for wet chemical tests. Must understand and apply cGMP requirements applicable to quality control laboratory. Judgment / Decision Making: Duties are performed within framework of departmental or functional guidelines, requiring interpretation and original thinking. Work Environment: A laboratory environment with exposure to chemicals, caustics, fumes, heat and electrical current. Physical Demands: Visual acuity and manual dexterity required to operate computer, analytical instrumentation, sample preparation. Majority of time spent standing. Often required to lift objects weighing up to 20 pounds.
Salary Min
Salary Max
Salary Currency
Salary Periodday
Source URLhttps://careers-noven.icims.com/jobs/2587/qc-analyst/job
Apply URLhttps://careers-noven.icims.com/jobs/2587/qc-analyst/job
First Seen At2026-06-02 13:50:27Z
Last Seen At2026-06-06 08:33:58Z
Last Checked At2026-06-06 08:33:58Z
Last Changed At2026-06-06 08:33:58Z
Inactive At
Source Posted At2024-06-06 08:33:57Z
Source Updated At2026-06-01 17:02:56Z
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=icims/board=careers-noven.icims.com/date=2026-06-06/2026-06-06T08-33-57-660Z-1688ee6039b36d78b697965d87e5bb06fc28ad91012ab1d346228083a5bc07ff.json
Event Fields
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Parsed Structured
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