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Pharma Qc Jobs in Delaware (NOW HIRING)

Roquette

Head of Quality North America

Wilmington, DE · On-site

$172K - $234K/yr

We are looking for our next Head of Quality - North America (HPS) within our Health & Pharma ... Ensure strong QA and QC performance, including product release and lab efficiency * Drive ...

Roquette

Head of Quality North America

Wilmington, DE · On-site

$172.94 - $234.11/hr

We are looking for our next Head of Quality - North America (HPS) within our Health & Pharma ... Ensure strong QA and QC performance, including product release and lab efficiency. Drive ...

Datwyler

Laboratory Technician 3rd Shift

Middletown, DE · On-site

$18 - $23.75/hr

Summary The Laboratory Technician is a critical member of the Quality Control team, ensuring the ... Pharma, Biotech, or Medical Device). • Technical Skills: o Proficiency in MS Office and SAP. o ...

Datwyler

Laboratory Technician 3rd Shift

Middletown, DE · On-site

$18 - $23.75/hr

Summary The Laboratory Technician is a critical member of the Quality Control team, ensuring the ... Experience: 1-3 years in a regulated laboratory environment (Pharma, Biotech, or Medical Device)

Roquette

EHS Specialist

Wilmington, DE · On-site

$82K - $110K/yr

Evaluate, improve, implement and ensure compliance with regulatory requirements, EHS best-practices, procedures and policies for pharma process, analytical, QC, and biology labs and production ...

Roquette Laisa España SA

EHS Specialist

Newark, DE · On-site

$82 - $110/hr

Evaluate, improve, implement and ensure compliance with regulatory requirements, EHS best‑practices, procedures and policies for pharma process, analytical, QC, and biology labs and production ...

MDAEdge

LabWare LIMS-LES Developer

Port Penn, DE · On-site

... users, QA, and IT teams to gather requirements and deliver effective solutions. • Ensure data ... Preferred : • Experience with LabWare Pharma Template. • Knowledge of SQL and relational ...

Fusion Life Sciences

System Engineers

Newark, DE · On-site

Lead efforts to develop and implement robust design control processes for new and existing products ... Work closely with other engineering disciplines, such as hardware, software, and quality teams, to ...

Roquette Laisa España SA

Plant Manager

Newark, DE · On-site

$173 - $234/hr

Ensures follow up and consistency of pharma compliance protocols and continuous improvement plans ... Oversee Cost of Goods Sold and product quality and modifies production and inventory control ...

Roquette

Head of Finance, NORAM

Wilmington, DE · On-site

$122K - $198K/yr

This position is responsible for leading core financial operations across assigned Health & Pharma ... Maintain and enhance internal control frameworks to ensure financial integrity * Identify, assess ...

All JobsPharma Qc JobsPharma Qc Jobs in Delaware

Pharma Qc information

What is the difference between Pharma Qc vs Pharma Quality Assurance (QA)?

AspectPharma QcPharma QA
CertificationsGMP, GMP-related trainingGMP, GMP-related training
Work EnvironmentLaboratory testing, sample analysisProcess audits, documentation review
ResponsibilitiesTesting raw materials, in-process, finished productsDeveloping, implementing quality systems, audits
Industry UsageQuality control testing in manufacturingEnsuring compliance, process quality assurance

Pharma Qc and Pharma QA roles both focus on quality in pharmaceutical manufacturing but differ in scope. Pharma Qc primarily involves laboratory testing and sample analysis to ensure product quality, while Pharma QA emphasizes process oversight, audits, and compliance systems. Both roles require GMP knowledge and are essential for maintaining industry standards.

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

What job categories do people searching Pharma Qc jobs in Delaware look for?

The top searched job categories for Pharma Qc jobs in Delaware are:

Pharma Qc jobs near you
Infographic showing various Pharma Qc job openings in Delaware as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 85% Full Time, 9% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 4% Hybrid, and 4% Remote job distribution.

GMP QC Systems Consultant

Stark Pharma Solutions Inc

Frankford, DE • On-site

Contractor

Re-posted 2 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on GMP QC Systems Consultant position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Position: GMP QC Systems Consultant

Location: Frankford, DE (100% Onsite)
Duration: 12+ Month Contract

Job Overview

We are seeking an experienced GMP QC Systems Consultant to support the implementation, integration, and validation of Quality Control laboratory systems in a regulated pharmaceutical environment. The ideal candidate will have strong expertise in GMP laboratory systems, Computer System Validation (CSV/CSA), and cross-functional project execution.

Key Responsibilities

  • Lead implementation and integration of GMP QC laboratory systems.
  • Coordinate system configuration, data migration, deployment, and go-live activities.
  • Manage project timelines, risks, budgets, and stakeholder communications.
  • Support Computer System Validation (CSV/CSA), including IQ/OQ/PQ execution and documentation.
  • Perform risk assessments, testing, and validation activities in compliance with GAMP5 and GxP requirements.
  • Collaborate with QA, IT, laboratory teams, vendors, and business stakeholders to ensure successful project delivery.
  • Ensure compliance with GxP, Data Integrity, and internal quality standards.
  • Prepare project status reports and support release readiness activities.

Required Qualifications

  • 8+ years of experience in Pharmaceutical, Biotechnology, or other GMP-regulated environments.
  • Strong experience implementing and validating QC/Laboratory systems.
  • Hands-on knowledge of CSV, CSA, GAMP5, GxP, IQ/OQ/PQ, and risk-based validation.
  • Experience with system integration, data migration, and cross-functional project coordination.
  • Familiarity with laboratory platforms such as LIMS, SDMS, Empower, LabX, QuantStudio, SoftMax Pro, or similar systems.
  • Excellent communication, documentation, and stakeholder management skills.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com