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Contract Pharma Jobs in Delaware (NOW HIRING)

Datavant

Client Partner, Pharma

Dover, DE · On-site

$160K - $180K/yr

... contracts. * Leverage deep knowledge of your client's organizational structure and initiatives to discover new business opportunities for Datavant solutions. * Gather valuable feedback from customers ...

Katalyst CRO

Quality Assurance Engineer

Newark, DE · On-site

Required : • 10+ years of experience in QA / Testing • Experience in Life Sciences / Pharma ... Contract Research and Knowledge Process Outsourcing Organization (CRO) dedicated to driving ...

Fusion Life Sciences

System Engineers

Newark, DE · On-site

Newark, DE Long Term Contract Job Overview: We are seeking highly skilled and experienced System ... Sincerely, Subash Kondala Medical/Pharma Recruiter www.fusionlifesolutions.com Subash ...

Datwyler

4th Shift Maintenance Technician

Middletown, DE · On-site

$23.50 - $30/hr

... our clean pharma manufacturing facility. Primary responsibilities will focus on thorough ... Effective management and execution of contract work. Responsibilities * Follows up on equipment ...

Datwyler

4th Shift Maintenance Technician

Middletown, DE

$23.50 - $30/hr

... our clean pharma manufacturing facility. Primary responsibilities will focus on thorough ... Effective management and execution of contract work. Responsibilities * Follows up on equipment ...

All JobsContract Pharma JobsContract Pharma Jobs in Delaware

Contract Pharma information

See Delaware salary details

$41K

$106.1K

$139.1K

How much do contract pharma jobs pay per year?

As of Aug 22, 2026, the average yearly pay for contract pharma in Delaware is $106,125.00, according to ZipRecruiter salary data. Most workers in this role earn between $89,100.00 and $119,100.00 per year, depending on experience, location, and employer.

What is a contract pharma?

A Contract Pharma job typically involves working for a contract development and manufacturing organization (CDMO) that provides outsourced services to pharmaceutical companies. These roles can include research and development, manufacturing, quality control, regulatory compliance, and packaging. Employees in this field help pharmaceutical companies bring drugs to market efficiently while ensuring compliance with industry regulations. Contract Pharma professionals work with multiple clients, offering expertise in drug formulation, scale-up, and commercialization.

What are the typical day-to-day responsibilities for someone working in a contract pharma role?

In a Contract Pharma position, your day-to-day tasks often involve coordinating with internal teams and external clients to manage project timelines, ensure compliance with industry regulations, and oversee the progress of drug development or manufacturing contracts. You may also be responsible for preparing documentation, monitoring the quality of outputs, and troubleshooting issues that arise during production or delivery. Collaboration is a significant aspect of the role, as you will work closely with R&D, quality assurance, and regulatory affairs departments to meet project milestones. The environment is dynamic, with shifting priorities based on client needs and industry developments, making adaptability and strong organizational skills essential.

What are the key skills and qualifications needed to thrive in the contract pharma position, and why are they important?

To excel in Contract Pharma roles, candidates need a strong background in pharmaceutical sciences, regulatory compliance, and project management, often supported by a degree in pharmacy, chemistry, or related fields. Familiarity with Good Manufacturing Practices (GMP), quality management systems, and industry-standard software such as LIMS or ERP platforms is typically required. Excellent communication, organizational abilities, and problem-solving skills help professionals manage client relationships and coordinate complex projects. These skills are critical for ensuring high-quality service delivery, compliance with regulations, and successful collaboration in a fast-paced, client-driven environment.

What are the most commonly searched types of Pharma jobs in Delaware?

The most popular types of Pharma jobs in Delaware are:

What are popular job titles related to Contract Pharma jobs in Delaware?

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

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

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

What cities in Delaware are hiring for Contract Pharma jobs?

Cities in Delaware with the most Contract Pharma job openings:

Contract Pharma jobs near you
Infographic showing various Contract Pharma job openings in Delaware as of August 2026, with employment types broken down into 2% As Needed, 85% Full Time, 6% Part Time, 6% Contract, and 1% Nights. Highlights an 82% Physical, 4% Hybrid, and 14% Remote job distribution, with an average salary of $106,125 per year, or $51 per hour.

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