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Quality Control Analyst I
Polysciences, Inc Warrington, PA
$63k-84k (estimate)
Other Just Posted
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Polysciences, Inc is Hiring a Quality Control Analyst I Near Warrington, PA

Job Details

Level: Experienced
Job Location: Warrington, PA
Position Type: Full Time
Education Level: 4 Year Degree
Salary Range: $65,000.00 - $75,000.00 Salary/year
Travel Percentage: None
Job Shift: M-F / 1st shift
Job Category: QA - Quality Control

Description

Who We Are

Ott Scientific

The Ott Scientific family of companies comprises Polysciences, Bangs Laboratories, and Ethos Biosciences. Together, we bring the whole of our experience with best-in-class facilities and scientific, technical, analytical, and manufacturing capabilities to serve customers around the globe. We deliver highly specialized products and services that support scientific discovery and innovations.

Polysciences

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.

Summary of Position:

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

Education Required: Bachelor's Degree in chemistry or related science field required.

Computer Skills Required:

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

Proficiency with Adobe, Microsoft Word and Excel required.

Other qualifications:  

• 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.

What We Offer

Culture

Great people

Peer to Peer Recognition

Broader, hands-on work experience

Clean and Modern Equipment & Labs

Fun company events

Competitive Wages & Generous Year-end Bonus

Comprehensive Benefits

4 Medical PPO Medical Plans with Telemedicine, Rx, & Vision

2 Dental Plans

Healthcare, Dependent care, & Commuter Flexible Spending Accounts

401(k) with company match

Financial Health & Wellness w/1:1 Coaching

Basic & Supplemental Life Insurance

Accident, Hospital Indemnity, & Critical Illness

Paid Time Off

Short & Long-term Disability

9 Paid Holidays

Must have legal authorization to work in the US and will not require sponsorship.

Polysciences is an equal opportunity employer. Drug-free workplace. Tobacco-free work site.

Polysciences does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status, or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit and business need.

Equal access to programs, services, and employment is available to all persons. Those applicants requiring reasonable accommodation to the application process and/or interview process should notify a representative of the Human Resources Department.

Find us here Poly 424

Qualifications


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.

Job Summary

JOB TYPE

Other

SALARY

$63k-84k (estimate)

POST DATE

05/30/2024

EXPIRATION DATE

07/29/2024

WEBSITE

cis.co.za

HEADQUARTERS

Warrington, PA

SIZE

<25

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The following is the career advancement route for Quality Control Analyst I positions, which can be used as a reference in future career path planning. As a Quality Control Analyst I, it can be promoted into senior positions as a Building Inspector, Sr. that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Quality Control Analyst I. You can explore the career advancement for a Quality Control Analyst I below and select your interested title to get hiring information.