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Pharmaceutical Biologist Jobs in Raleigh, NC (NOW HIRING)

OR Experience leading, and developing people Experience in GMP warehouse operations Equivalent military experience Preferred Requirements Experience in pharmaceutical / biological manufacturing ...

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ORExperience leading, and developing peopleExperience in GMP warehouse operationsEquivalent military experience Preferred Requirements Experience in pharmaceutical / biological manufacturing ...

New

OR Experience leading, and developing people Experience in GMP warehouse operations Equivalent military experience Preferred Requirements Experience in pharmaceutical / biological manufacturing ...

New

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Visium Resources has been asked to identify qualified candidates for this Pharmaceutical Senior CQV ... Experience in biologics, sterile manufacturing, fill-finish, or aseptic processing environments.

The offices are delivering cutting-edge projects for the Pharmaceutical, Biologics, and Cell & Gene Therapy manufacturing facilities, supporting clients from feasibility and conceptual design through ...

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Pharmaceutical Biologist information

See Raleigh, NC salary details

$36K

$86.9K

$134.1K

How much do pharmaceutical biologist jobs pay per year?

As of Aug 17, 2026, the average yearly pay for pharmaceutical biologist in Raleigh, NC is $86,907.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,800.00 and $117,600.00 per year, depending on experience, location, and employer.

What is a pharmaceutical biologist?

A Pharmaceutical Biologist studies biological systems to develop and improve pharmaceutical drugs. They analyze the effects of compounds on living organisms, conduct laboratory experiments, and collaborate with chemists and pharmacologists. Their work helps in drug discovery, safety testing, and regulatory approval. This role is crucial in creating effective and safe medications for medical use.

What does a pharmaceutical biologist do?

A typical day for a Pharmaceutical Biologist involves designing and conducting laboratory experiments to test drug compounds, analyzing biological data, and documenting results for regulatory purposes. You’ll often collaborate with chemists, pharmacologists, and other scientists to exchange insights and refine experimental approaches. Depending on your organization, you might split your time between hands-on lab work, data interpretation, and meetings to discuss project progress. The role can also require staying current with scientific literature and contributing to regulatory submissions or technical reports. If you enjoy a balance of research, analysis, and team collaboration, this position offers a dynamic and intellectually rewarding work environment.

What are the key skills and qualifications needed to thrive as a pharmaceutical biologist?

To succeed as a Pharmaceutical Biologist, you need a strong background in biology, chemistry, and pharmacology, often supported by an advanced degree in biological sciences or a related field. Experience with laboratory technologies such as high-performance liquid chromatography (HPLC), mass spectrometry, and familiarity with Good Laboratory Practices (GLP) or regulatory certifications is highly valued. Critical thinking, keen attention to detail, and effective teamwork and communication skills help professionals excel in collaborative research environments. These skills are vital for conducting accurate research, ensuring compliance with industry standards, and contributing to the development of safe and effective pharmaceuticals.

How do you become a pharmaceutical biologist?

To become a pharmaceutical biologist, you typically need a bachelor's degree in biology, biochemistry, or a related field, followed by a master's or Ph.D. for advanced research roles. Gaining laboratory experience and developing skills in molecular biology, microbiology, and pharmacology are important, and some positions may require certification or specialized training.

How much do pharmaceutical biologists make?

Pharmaceutical biologists typically earn a median annual salary of around $70,000 to $90,000, depending on experience, education, and location. Entry-level positions may start lower, while those with advanced degrees or specialized skills can earn over $100,000 annually.

What job categories do people searching Pharmaceutical Biologist jobs in Raleigh, NC look for?

The top searched job categories for Pharmaceutical Biologist jobs in Raleigh, NC are:

Infographic showing various Pharmaceutical Biologist job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $86,907 per year, or $41.8 per hour.

Pharmaceutical Engineer

Visium Resources, Inc.

Raleigh, NC • On-site

$120K - $145K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago


Job description

Introduction
Visium Resources has been asked to identify qualified candidates for this Pharmaceutical Senior CQV Engineer position. This position is a direct hire which is expected to be on-site in Raleigh, NC.


Summary

We are seeking a highly motivated Senior CQV Engineer to support commissioning, qualification, and validation activities for pharmaceutical and biotechnology manufacturing facilities. The successful candidate will lead and execute CQV deliverables associated with upstream and downstream GMP-regulated process equipment, utilities, automation systems, cleanrooms, and manufacturing operations.

This role requires hands-on technical expertise, strong project coordination skills, and a thorough understanding of FDA and cGMP compliance requirements. The Senior CQV Engineer will work cross-functionally with Engineering, Quality, Manufacturing, Automation, and external vendors to ensure successful project execution and operational readiness within fast-paced life sciences environments.


Key Responsibilities

  • Lead and execute CQV activities for pharmaceutical and biotech capital projects. 
  • Develop and execute: 
    • Commissioning plans 
    • IQ/OQ/PQ protocols 
    • Validation test scripts 
    • Traceability matrices 
    • Summary reports 
  • Support startup and qualification of: 
    • Process equipment 
    • Clean utilities 
    • HVAC systems 
    • Manufacturing suites 
    • Automation and control systems 
  • Coordinate field execution activities with engineering, construction, vendors, and operations teams. 
  • Perform system walkdowns and turnover package reviews. 
  • Support deviation investigations, CAPAs, and change control activities. 
  • Ensure all validation documentation complies with cGMP, FDA, ISPE, and GAMP guidelines. 
  • Participate in FAT/SAT execution and acceptance activities. 
  • Support project schedule development and milestone tracking. 
  • Collaborate with Quality Assurance and Manufacturing teams to support inspection readiness and successful system release. 
  • Mentor junior CQV engineers and validation specialists as needed.


Required Qualifications

  • Bachelor's degree in Engineering, Life Sciences, Biotechnology, or related technical discipline. 
  • 5-10+ years of CQV, validation, or pharmaceutical engineering experience within GMP-regulated environments. 
  • Strong knowledge of: 
    • cGMP regulations 
    • FDA validation requirements 
    • ISPE Baseline Guides 
    • GAMP 5 principles 
  • Experience executing commissioning and qualification for: 
    • Process equipment 
    • Utilities 
    • HVAC systems 
    • Cleanrooms 
    • Automation systems 
  • Experience authoring and reviewing validation lifecycle documentation. 
  • Strong technical writing and documentation skills. 
  • Ability to work independently within fast-paced project environments. 


Preferred Qualifications

  • Experience in biologics, sterile manufacturing, fill-finish, or aseptic processing environments. 
  • Previous consulting experience within life sciences industries preferred. 
  • Familiarity with: 
    • DeltaV 
    • MES systems 
    • SCADA platforms 
    • Kneat or electronic validation systems 
  • PMP certification or equivalent project leadership experience is a plus. 
  • Strong client-facing communication and leadership skills. 

Additional Skills & Competencies

  • Excellent organizational and multitasking abilities 
  • Strong problem-solving and analytical skills 
  • Ability to manage multiple priorities and deadlines 
  • Comfortable working in both office and field environments 
  • Ability to travel to client sites as required

Company Description

Visium Resources is an award-winning employment firm with a mission to match talented individuals with highly successful organizations. At Visium, our company’s success is based on your success. When you work with us, you are never “just a number”. You are our most important asset. Here, you will know us by name through our regular visits to client sites and even occasional luncheons. We will always be there when you need assistance and will always go the extra mile to ensure that you are as successful as possible. Whether you're looking for contract, contract-to-hire or permanent opportunities, we firmly believe there is no employment agency that will work harder for you than Visium. Visium Resources is an equal opportunity employer and values diversity. All employment is decided based on qualifications, merit and business need.