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Drug Safety Associate Jobs in Raleigh, NC (NOW HIRING)

CaptiveAire

Safety Coordinator

Raleigh, NC · On-site

Position Summary The School Safety Coordinator is responsible for developing, implementing, and ... Employees in this position are subject to drug and alcohol testing in accordance with Thales' Drug ...

CaptiveAire

Safety Coordinator

Raleigh, NC · On-site

Position Summary The School Safety Coordinator is responsible for developing, implementing, and ... Employees in this position are subject to drug and alcohol testing in accordance with Thales' Drug ...

Cooper Equipment Rentals

Safety Manager

Raleigh, NC · On-site

As a Safety Manager , you will be responsible for leading and fostering a strong safety culture ... Pre-employment background and drug screening required. Disclaimer: The above statements are ...

Liberty Waste Solutions

Safety Manager

Raleigh, NC

$90K - $105K/yr

... drug and alcohol testing programs in compliance with FMCSA regulations • Maintain OSHA logs, reporting requirements, and safety documentation • Develop and conduct safety trainings, toolbox talks ...

Unitek Global Services

Safety Specialist

Cary, NC · On-site

$60K - $70K/yr

Associate degree in Safety Management or a related field, or equivalent experience preferred. * Bachelor's degree in occupational safety & health preferred. * At least 2 years of telecommunications ...

Conti Civil

Safety Engineer

Raleigh, NC · On-site

Conti Civil is on the lookout for a motivated and safety-minded individual to join our team. This ... All applicants who receive a conditional offer of employment must take a pre-employment drug test ...

North Carolina Jobs

Safety Assistant

Raleigh, NC · On-site

$38K - $50K/yr

Safety Assistant REPORTS TO : Transportation Director BEGINNING DATE : Open Until Filled NATURE OF ... Candidate must submit to random and post accident drug testing and background checks * Candidate ...

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Drug Safety Associate information

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How much do drug safety associate jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for drug safety associate in Raleigh, NC is $47.77, according to ZipRecruiter salary data. Most workers in this role earn between $37.40 and $53.99 per hour, depending on experience, location, and employer.

How does a Drug Safety Associate typically collaborate with other teams during the drug development process?

Drug Safety Associates regularly work in close coordination with clinical research, regulatory affairs, and medical affairs teams. They are responsible for collecting, evaluating, and reporting adverse event data, which often requires clear communication with clinical trial staff and investigators. Additionally, they may participate in cross-functional safety review meetings to discuss safety findings and ensure compliance with regulatory requirements. This collaborative environment helps ensure comprehensive safety monitoring throughout the drug's lifecycle.

What Does a Drug Safety Associate Do?

A drug safety associate works in the medical industry to monitor the safety of pharmaceutical drugs and to evaluate and prevent adverse reactions in patients. A career in drug safety, also called pharmacovigilance, can include work with clinical research organizations that conduct trials, biotechnology firms, pharmaceutical companies, or government agencies like the National Institutes of Health (NIH). Drug safety associates need excellent research skills, a strong background in medical or biological science, and in-depth knowledge of the Food and Drug Administration (FDA) regulations. Your responsibilities include analyzing clinical trial data, writing reports, and determining whether specific pharmaceutical drugs are safe.

What are Drug Safety Associates?

Drug Safety Associates are professionals responsible for monitoring and evaluating the safety of pharmaceutical products. They collect, analyze, and report data on adverse drug reactions to ensure compliance with regulatory requirements and to protect patient safety. Their work involves reviewing case reports, maintaining safety databases, and communicating safety information to regulatory agencies and healthcare professionals. Drug Safety Associates play a vital role in the pharmacovigilance process throughout the lifecycle of a drug.

What is the difference between Drug Safety Associate vs Pharmacovigilance Specialist?

AspectDrug Safety AssociatePharmacovigilance Specialist
CredentialsTypically requires a degree in life sciences or healthcare, with certifications like PV or drug safety trainingSimilar credentials, often with additional certifications or experience in pharmacovigilance
Work EnvironmentPharmaceutical companies, CROs, or healthcare settings focusing on safety data managementSame as Drug Safety Associate, often with more specialized pharmacovigilance tasks
Employer & IndustryPharmaceutical, biotech, and healthcare industriesSame industries, with a focus on drug safety monitoring and compliance

Both roles involve monitoring drug safety data, reporting adverse events, and ensuring regulatory compliance. The main difference lies in the scope and specialization, with Pharmacovigilance Specialists often handling more complex safety data analysis and regulatory submissions. However, the roles overlap significantly, and job titles are sometimes used interchangeably depending on the organization.

What are the key skills and qualifications needed to thrive as a Drug Safety Associate, and why are they important?

To thrive as a Drug Safety Associate, you need a solid background in life sciences or pharmacy, knowledge of pharmacovigilance principles, and attention to detail. Familiarity with drug safety databases (such as Argus or ARISg), MedDRA coding, and regulatory reporting systems is typically required. Strong organizational skills, effective communication, and the ability to work under deadlines help you excel in collaborating with cross-functional teams. These skills ensure accurate adverse event reporting, regulatory compliance, and protection of patient safety throughout the drug development lifecycle.
More about Drug Safety Associate jobs
What are the most commonly searched types of Drug Safety jobs in Raleigh, NC? The most popular types of Drug Safety jobs in Raleigh, NC are:
What are popular job titles related to Drug Safety Associate jobs in Raleigh, NC? For Drug Safety Associate jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Drug Safety Associate jobs in Raleigh, NC look for? The top searched job categories for Drug Safety Associate jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Drug Safety Associate jobs? Cities near Raleigh, NC with the most Drug Safety Associate job openings:
Drug Safety Associate jobs near you
Infographic showing various Drug Safety Associate job openings in Raleigh, NC as of June 2026, with employment types broken down into 1% As Needed, 53% Full Time, 41% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $99,363 per year, or $47.8 per hour.
Manufacturing Associate 4, Drug Product Filling (1st Shift)

Manufacturing Associate 4, Drug Product Filling (1st Shift)

Fujifilm

Holly Springs, NC • On-site

Other

Posted 7 days ago

Fujifilm rating

8.3

Company rating: 8.3 out of 10

Based on 66 frontline employees who took The Breakroom Quiz

46th of 518 rated manufacturers

Job description

Position Overview
The manufacturing associate in Drug Product Manufacturing will have a primary task for operation of filling line including all tasks related. This role will also support projects which influence manufacturing processes for DPM including training of others. This position will also support and assist in scheduling daily manufacturing activities for the team. This manufacturing facility will be 24/7 operational and the role may require to be flexible with working hours or shift rotation.
Company Overview
FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.
We're looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we're proud to cultivate a culture that will fuel your purpose, energy, and drive-what we call Genki. Ready to shape the future of medicine? Let's transform healthcare together!
Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh's thriving tech scene, making it the perfect blend of community and opportunity.
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: https://www.fujifilm.com/us/en/about/region/careers
Job Description
What You'll Do
During the project phase
  • Participate and support testing activities, such as FAT, PQ etc. as well as other related activities
  • Support and contribute to the preparation of the documentation package as e.g., Standard Operating Procedures, Work Instructions
  • Contribute to the preparation for operational readiness related to bulk drug product manufacturing
  • Possible assignments include: Supporting projects related to procedure review and/or creation, development or transfer of manufacturing business processes as well as testing and commissioning support
  • Travel up to 0-25% (international or domestic) may be required during the project phase

In operations
  • Lead, execute and document manufacturing processing steps and/or manufacturing support activities as well as process monitoring and control
  • Perform operations of the Drug product filling line
  • Execute validation protocols according to cGMP Standard Operating Procedures (SOPs)
  • Own the establishment of processes and trainings to become a trainer for coworkers
  • Maintain compliance of GMP documents and ensure own training level is complaint and maintained
  • Support and/or assist senior level associates or supervisor with scheduling daily activities on drug product manufacturing floor, as needed
  • This role requires shift work (weekend and potential for nights)
  • Perform other duties as assigned

Basic Requirements
  • High School Diploma or GED
  • 6+ years of direct experience in a manufacturing environment
  • Preferred Requirements
  • Associate's Degree + 4 years of direct experience in a cGMP manufacturing environment OR
  • BA/BS + 2 years of direct experience in a cGMP manufacturing environment
  • Equivalent Military training or experience
  • Experience on specific unit operations (ex: Viral Filtration and Bulk Dispensing)
  • Understanding of manufacturing run cadence and order of shift activities
  • Knowledge of cGMP, safety and operational procedures
  • A high degree of knowledge and expertise of the operation of specific production equipment

Working Conditions & Physical Requirements
  • Be exposed to an environment that may necessitate respiratory protection
  • Be exposed to noisy environments
  • Have a normal range of vision
  • Climb ladders and stairs of various heights
  • Experience prolonged sitting, standing, walking, bending, stooping and stretching throughout the shift, up to 12 hours
  • Use hand-eye coordination and manual dexterity sufficient to operate a computer keyboard, telephone, calculator, and other office equipment is required
  • May be required to lift up to 50 pounds on occasion

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.
*#LI-Onsite
EEO Information
Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.
ADA Information
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_PNC@fujifilm.com).

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About Fujifilm

Sourced by ZipRecruiter

With each Industry we enter, We’ve learned to Leverage and Adapt our knowledge, Expertise and rRsources to make the World a better place. When it comes to Innovating for a Healthier World and a more sustainable society, we’ll NEVER STOP. Fujifilm will contribute to the social challenges by creating new value in a wide range of business domains through innovation in Products, Services, and Technological Development. We launched our Healthcare Business with X-ray film in 1936. And now, We are developing our business in areas of prevention, diagnosis, and treatment as a Comprehensive Healthcare Company. We will never stop Innovating for a Healthier World.

Industry

Chemical manufacturing

Company size

10,000+ Employees

Headquarters location

Minato-ku, Tokyo, JP

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