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Quality Control Analyst I

Polysciences, Inc.
Posted 2 months ago, valid for 23 days
Location

Warrington, PA, US

Salary

$59,200 - $69,800 per year

Contract type

Full Time

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Sonic Summary

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  • The position is for a QC Analyst I at Polysciences in Warrington, PA, requiring a bachelor's degree in chemistry or a related field.
  • The role is entry-level and offers a salary range of $59,200.00 to $69,800.00, with no travel required.
  • Candidates should have at least one year of experience in an ISO 13485 or FDA GMP regulated environment, preferably with quality control documentation experience.
  • The analyst will perform various analytical analyses and assist with data entry, equipment verification, and maintaining laboratory compliance.
  • Proficiency in Microsoft Word, Excel, and familiarity with analytical software is required for this position.

Job DetailsLevel: EntryJob Location: Warrington, PA 18976Position Type: Full TimeEducation Level: 4 Year DegreeSalary Range: $59,200.00 - $69,800.00 SalaryTravel Percentage: NoneJob Shift: M-F / 1st shiftJob Category: QA - Quality ControlPolysciences 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.   QualificationsQualifications   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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