Top 53247 Quality Process Analyst Jobs

Quality Control Analyst I
Polysciences, Inc. —Warrington, PA
- $59,200 - $69,800 a year
- Full-time
- Microsoft Excel
- Computer literacy
- Bachelor's degree
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Quality Control Analyst I
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Quality Control Analyst I

Polysciences, Inc. -
Warrington, PA

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Job Details

Full-time
$59,200 - $69,800 a year

Qualifications

Microsoft Excel
Computer literacy
Bachelor's degree
Materials analysis (analytical chemistry specialty)
Productivity software
Chemical testing
Data analysis software

Full Job Description

Polysciences technical operations and scientific laboratories offer custom synthesis, contract manufacturing and packaging, and laboratory products. We are proud to offer a broad range of products and tailored solutions for the life sciences, bioprocessing, microparticles, medical device, specialty chemical and eChem industries. We adhere to ISO13485:2016, FDA cGMP 21 CFR 820 regulations, and SOCMA’s ChemStewards® Management System. We believe the best scientific innovations are built through collaborations.

The QC Analyst I is responsible for performing incoming raw materials, in-process samples, intermediate products, and final products analytical analysis per approved internal and customer specifications following associated procedures to support both product manufacturing and commercial product release. Will work under the supervision of more experienced analysts and follow established procedures and protocols.

Essential Functions:

Performs routine analytical analysis using the following equipment: volumetric glassware, balances, pH Meter, Conductometer, Karl Fisher (KF), TOC, Turbidimeter, GC (FID/MS), Atomic Absorption (AA), and others as required.

Responsible for QC data analysis and data entry, using both electronic systems and hard copy documentation following GDP.

Ability to effectively communicate with cross-functional teams, including production, quality assurance, and planning.
Reports OOS results to QC Manager or designee and assists with compiling required information to complete the investigation report.

Performs daily and monthly analytical equipment verification and maintenance.
Flexibility to handle unexpected situations and make adjustments to ensure compliance with 820 GMP and ISO 13485 standards.

Assists on the review and revision of procedures and test methods.
Assists on laboratory inventory maintenance.
Maintains a safe, clean, and organized environment (5S) for all QC areas.
Supports process improvements within the QC laboratory.

Qualifications:

Bachelor’s degree in chemistry or related science field required.
At least one (1) year of experience working in an ISO 13485 or FDA GMP regulated environment preferred.
At least one (1) year of experience working in an ISO 13485 or FDA GMP regulated environment preferred.
Experience with quality control GMP documentation of analytical testing results and assurance of laboratory data integrity and compliance preferred.
Knowledge of analytical equipment, analytical methods, and data analysis required.

Knowledge of compendial methods (ie. USP, EP, ISO, ASTM) preferred.

Experience with Open Lab, Chem Station and/or Empower analytical software preferred.
Proficiency with Adobe, Microsoft Word and Excel required.

Qualifications

Education Required: Bachelor's Degree Preferred: Bachelor's Degree

Certification(s): Specify preferred or required.

Computer Skills Required: Specify preferred or required.

Experience with Open Lab, Chem Station and/or Empower analytical software preferred.

Proficiency with Adobe, Microsoft Word and Excel required.

Other qualifications:

Bachelor’s degree in chemistry or related science field required.
At least one (1) year of experience working in an ISO 13485 or FDA GMP regulated environment preferred.
Bachelor’s degree in chemistry or related science field required. At least one (1) year of experience working in an ISO 13485 or FDA GMP regulated environment preferred.
Experience with quality control GMP documentation of analytical testing results and assurance of laboratory data integrity and compliance preferred.
Knowledge of analytical equipment, analytical methods, and data analysis required.
Knowledge of compendial methods (ie. USP, EP, ISO, ASTM) preferred.

Immediate Work Environment:

X-Chemicals Unprotected Height X-Fumes/Gases Persistent Noise

X-PPE used: Lab Coat, Safety Shoes, and Safety Glasses

Work Activity: [must equal number of hours worked per day]

Stand: 4 Frequency: Intermittently Walk: 1 Frequency: Intermittently

Sit: 3 Frequency: Intermittently Drive: 0 Frequency: Choose an item.

Lift/Carry Demands

Frequency: Lift/Carry Equipment Provided:

0-10 lbs. 1-3 hours a day Reagents Bottles Carriers

11-25 lbs. Not Daily Rolling Cart

26-50 lbs. Rarely Gas Tank Hand Cart/Drum Lift Cart

51-75 lbs. Never Click or tap here to enter text.

76-100 lbs. Never Click or tap here to enter text.

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Refine Your Search

Quality Process Analyst jobs

Quality Control Analyst I

Public Health Analyst II

Financial Crime Analyst

Data Analyst

Data Migration Analyst

Healthcare Claims Quality Analyst

Operations Analyst

Customer Success Operations Analyst

Workforce Analyst

Quality Analyst

Quality Control Analyst (Multiple Openings)

Sustainability Analyst

Claims Analyst

Quality Control Analyst

Financial Crimes Quality Control Analyst II

Psychometric Analyst

Quality Assurance Analyst (Remote)

Quality Assurance Analyst

Quality Control Analyst I

Quality Assurance Analyst

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