ZipRecruiter

Log In

1

Contract Pharma Jobs in Raleigh, NC (NOW HIRING)

Euromed Pharma Us Inc

Director of Quality US

Raleigh, NC · On-site

$110K - $130K/yr

Euromed Pharma US Inc is looking for a driven and experienced Director of Quality US to lead and ... Approve contracts and SOPs related to distribution and outsourced activities * Ensure records for ...

Aerogen Ltd

Procurement Manager

Morrisville, NC · On-site

... pharma, device, and contract manufacturing partners. • Partner with Technical and Quality teams to integrate specifications, validation, and lifecycle requirements into sourcing decisions. • ...

Intellectt INC

CQV Engineer

Holly Springs, NC · On-site

My name is Vyshu, and I'm reaching out from Intellectt Inc. regarding an exciting contract ... Required Skills * 5+ years of CQV/startup/validation experience in pharma, biotech, or life ...

previous pagenext page

Showing results 21-40

All JobsContract Pharma JobsContract Pharma Jobs in Raleigh, NC

Contract Pharma information

See Raleigh, NC salary details

$39.9K

$103.1K

$135.1K

How much do contract pharma jobs pay per year?

As of Aug 7, 2026, the average yearly pay for contract pharma in Raleigh, NC is $103,074.00, according to ZipRecruiter salary data. Most workers in this role earn between $86,500.00 and $115,700.00 per year, depending on experience, location, and employer.

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 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 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 most commonly searched types of Pharma jobs in Raleigh, NC? The most popular types of Pharma jobs in Raleigh, NC are:
What are popular job titles related to Contract Pharma jobs in Raleigh, NC? For Contract Pharma jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Contract Pharma jobs in Raleigh, NC look for? The top searched job categories for Contract Pharma jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Contract Pharma jobs? Cities near Raleigh, NC with the most Contract Pharma job openings:
Contract Pharma jobs near you
Infographic showing various Contract Pharma job openings in Raleigh, NC as of July 2026, with employment types broken down into 65% Full Time, and 35% Contract. Highlights an 81% In-person, and 19% Remote job distribution, with an average salary of $103,074 per year, or $49.6 per hour.

Senior Auditor, Vendor Audit (contract)

11 Premier Research International LLC

Raleigh, NC

$70/hr

Part-time

Posted 24 days ago

Job description

Senior Auditor, Vendor Audit (contract) Premier Research is looking for a Senior Auditor, Vendor Audit (contract) to join our Functional Services Provider (FSP) team. This role focuses on supporting global operations in biotech, medtech, and specialty pharma companies. Responsibilities Organizes and hosts Vendor audits, including preparation of audit plans, checklists, reports, and certificates. Manages complex audit activities per the Premier Research Vendor audit schedule, ensuring the approved vendor list is current and only approved vendors are used at a study level. Collaborates with operational teams to review and trend documented Vendor issues or gaps at a study level for potential systemic issues. Documents any systemic issues and implements corrective actions at a global level, including contracts as appropriate. Acts as the point of contact (POC) for vendor audit activities. Ensures compliance with internal control procedures by examining records, reports, operating practices, and documentation. Communicates audit findings by preparing a final report and discussing findings with auditees. Qualifications Bachelor's degree, or international equivalent from an accredited institution, in Health or Life Sciences, or equivalent experience. 5‐8 years of specialized GxP auditing experience (vendor, GCP, GMP audits), or 8+ years of relevant experience with 5+ years of vendor audit experience. Ability to interpret controlled documentation such as protocols, validation documents, and manufacturing records. Ability to independently review databases, trial master files, investigator sites, statistical/clinical study reports, vendors, manufacturers, master batch records, device history files, laboratories, and system validation documentation. Knowledge of ICH Guidelines, FDA Code of Federal Regulations, and other applicable regulatory authority laws and regulations. Preferred location: East Coast. Contract Details – Part‐time 6‐month 1099 contractor opportunity. Compensation – Starting hourly rate of $70/hr USD, with actual hourly rate influenced by qualifications, skills, competencies, and proficiency for the role. Equal Opportunity Statement – Premier Research is proud to be an equal opportunity employer that is compliant with all federal guidelines. All qualified applicants will receive equitable consideration without regard to race, color, religion, sexual orientation, gender identity, national origin, disability, or veteran status. #J-18808-Ljbffr

Apply