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Qc Associate Pharma Jobs (NOW HIRING)

Fladger Associates

QC Associate

Fremont, CA · On-site

Excellent employment opportunity for a QC Associate III in the Fremont, CA area. * Performs sampling/testing/inspection of raw materials, conducts lab investigations, and reports aberrant results to ...

Blue Nile

QC Associate

New York, NY · On-site

$17 - $24/hr

We are seeking a detail-oriented and highly organized QC Associate (Quality Control Associate) to join our manufacturing team. In this role, they will be responsible for ensuring that all jewelry ...

Signetjewelers

QC Associate

New York, NY · On-site

$17 - $24/hr

We are seeking a detail-oriented and highly organized QC Associate (Quality Control Associate) to join our manufacturing team. In this role, they will be responsible for ensuring that all jewelry ...

System One

Quality Control Associate

Oro Valley, AZ · On-site

$25.75/hr

Quality Control Associate Location: Oro Valley, AZ Type: Contract Compensation: $25.75/hr Work Model: Onsite Hours: M-F normal business hours Security Clearance: Not specified Overview Leave ...

Tree Brand Packaging, Inc

Be Seen First

Quality Control Associate

Decatur, AL · On-site

$18 - $19/hr

The Quality Associate is an entry-level position responsible for supporting basic quality control activities within a pallet manufacturing environment. This role assists QC Technicians and the QC ...

The Rizzo Companies

QA/QC Associate

Danbury, CT · On-site

Quality Assurance/Quality Control Associate Position Summary Rizzo Corporation is seeking a full-time Quality Assurance/Quality Control (QA/QC) Associate. This individual is responsible for ...

The Rizzo Companies

QA/QC Associate

Danbury, CT

Quality Assurance/Quality Control Associate Position Summary Rizzo Corporation is seeking a full-time Quality Assurance/Quality Control (QA/QC) Associate. This individual is responsible for ...

Fanatics Collectibles

QC Associate

Allen, TX · On-site

Role Summary The QC Associate ensures the highest standards of quality in the production of trading cards. This role inspects cards for defects, verifies that products and counts meet established ...

Onin Staffing

Quality Control Associate

Meridian, MS · On-site

$15 - $16/hr

We are seeking a detail-oriented and dependable Quality Control Associate to inspect products and materials to ensure they meet established quality standards. The ideal candidate will have strong ...

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Qc Associate Pharma information

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How much do qc associate pharma jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for qc associate pharma in the United States is $25.46, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $31.01 per hour, depending on experience, location, and employer.

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For Qc Associate Pharma jobs, the most frequently searched job titles are:

Infographic showing various Qc Associate Pharma job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $52,962 per year, or $25.5 per hour.

QC Associate

Fremont, CA • On-site

Fladger Associates
See more jobs at Fladger Associatesexternal

Contractor

Re-posted 4 days ago

Job description

Fremont, CA
Contract Duration: 12-24 months
Rate: Negotiable

Responsibilities:

  • Excellent employment opportunity for a QC Associate III in the Fremont, CA area.
  • Performs sampling/testing/inspection of raw materials, conducts lab investigations, and reports aberrant results to management.
  • Includes, not limited to: Pulling and aliquoting raw material samples and distributing to the appropriate laboratories.
  • Prepares paperwork, ships samples, and follows-up with appropriate testing laboratories.
  • AQL inspection (e.g., visual, dimension, etc.)
  • On call/weekend/swing shift coverage for urgent samples.
  • Data entry and reviews QC documentation (e.g., test results, data packets, etc.)
  • Generates, reviews and/or maintains records or documents in a detailed and consistent manner (e.g., sample summary form, test records, etc.).
  • Reconciles samples.
  • Perform required reviews of appropriate forms (e.g., test records) and logbooks.
  • Performs an Owner role for Change Controls and Deviations
  • Prepares and reviews-trend reports, generate metrics and other reports as needed.
  • Maintains raw material data. Revises SOPs, training doc, etc.
  • Ensures equipment calibration and preventive maintenance are up to date.
  • Performs an Owner role for Change Controls and Deviations.

Experience:

  • Bachelors' Degree in a Scientific Discipline. In depth experience in a laboratory environment Five (5) years cGMP or appropriate experience required.
  • Knowledge of ANSI/ASQ Z1.4, DIN ISO 2859 or other sampling standards desired.
  • Strong technical writing required.
  • Knowledge of CFR, USP, and ICH required.
  • Knowledge of SAP Track wise and LIMS desired.
  • Working knowledge of Microsoft Office systems, LIMS, lab instrumentation and other relevant systems.
  • Demonstrated problem-detection and problem-resolution skills required
  • Lifting, carrying, pushing or pulling up to 50 pounds occasionally Frequent periods of sitting, walking, and standing
  • Occasionally must climb stairs or ladders, balance, bend or stoop, crouch or squat
  • Occasional low-level work, fine finger dexterity/ including grasping or pinching required
  • Occasional use of personal protective equipment
  • Required Skills: GMP, USP, EUROPEAN PHARMACOPIA, MS OFFICE, LIMS,
  • Additional Skills: GMP ISO, ICH,