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Cro Chemistry Jobs in Raleigh, NC (NOW HIRING)

... CRO), or Contract Laboratory Organization (CLO). * 3+ years of experience working in a regulated ... chemistry, glycan analysis, peptide mapping, and physical appearance. * Proven ability to lead ...

... CRO), or Contract Laboratory Organization (CLO). * 3+ years of experience working in a regulated ... chemistry, glycan analysis, peptide mapping, and physical appearance. * Proven ability to lead ...

... CRO), or Contract Laboratory Organization (CLO). * 3+ years of experience working in a regulated ... chemistry, glycan analysis, peptide mapping, and physical appearance. * Proven ability to lead ...

As a Sr. Director, CMC at Allucent, you are responsible for assisting clients with Chemistry ... Prior CRO experience preferred. Skills: * Critical thinking and analytical skills, financial acumen ...

As a Sr. Director, CMC at Allucent, you are responsible for assisting clients with Chemistry ... Prior CRO experience preferred. Skills: * Critical thinking and analytical skills, financial acumen ...

As a Sr. Director, CMC at Allucent, you are responsible for assisting clients with Chemistry ... Prior CRO experience preferred. Skills: * Critical thinking and analytical skills, financial acumen ...

Principal Scientist- NMR Spectroscopy

Morrisville, NC · On-site

$110K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Minimum of 8-10 years of analytical chemistry experience in a CRO, pharmaceutical, or regulated laboratory environment. * Expert-level proficiency in NMR spectroscopy is required , including ...

Principal Scientist- NMR Spectroscopy

Morrisville, NC · On-site

$110K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Minimum of 8-10 years of analytical chemistry experience in a CRO, pharmaceutical, or regulated laboratory environment. * Expertlevel proficiency in NMR spectroscopy is required , including ...

MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... biology or chemistry, or related field, with industry experience within regulatory writing ...

Cro Chemistry information

See Raleigh, NC salary details

$13

$21

$31

How much do cro chemistry jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for cro chemistry in Raleigh, NC is $21.63, according to ZipRecruiter salary data. Most workers in this role earn between $17.74 and $23.85 per hour, depending on experience, location, and employer.

What is the difference between Cro Chemistry vs Clinical Research Associate?

AspectCro ChemistryClinical Research Associate
Required CredentialsBachelor's degree in chemistry, pharmacy, or related field; often requires industry certificationsBachelor's degree in life sciences, health sciences, or related; often requires clinical research certifications
Work EnvironmentLaboratories, pharmaceutical companies, research institutionsClinical trial sites, hospitals, research organizations
Industry UsagePharmaceutical, biotech, chemical industriesHealthcare, pharmaceutical, clinical trial management

Cro Chemistry professionals focus on chemical analysis, formulation, and laboratory research within the pharmaceutical and chemical industries. Clinical Research Associates (CRAs) oversee clinical trials, ensuring compliance and data integrity. While both roles support drug development, Cro Chemistry is lab-based, whereas CRAs work in clinical settings. Understanding these differences helps job seekers identify the right career path in the industry.

What are common challenges faced by professionals in CRO chemistry and how can they be addressed?

Professionals in CRO (Contract Research Organization) Chemistry often encounter challenges such as tight project timelines, shifting client requirements, and the need to quickly adapt to new scientific techniques or technologies. Effective communication with both clients and internal teams is essential to manage expectations and ensure project goals are met. Additionally, strong organizational skills and a proactive approach to problem-solving can help overcome unexpected technical hurdles. Continuous learning and collaboration within multidisciplinary teams also contribute to smoother project execution and personal growth within the field.

What is a CRO chemist?

CRO chemists are professionals who work at Contract Research Organizations (CROs), providing specialized chemical research and development services to pharmaceutical, biotechnology, and other industries. They are involved in tasks such as synthesis, analysis, and characterization of chemical compounds. CRO chemists support drug discovery, process development, and sometimes regulatory submissions, helping clients advance their projects efficiently without expanding in-house capabilities. Their expertise allows companies to access advanced chemistry services on a contract basis, saving both time and resources.

What skills and qualifications are needed to thrive as a CRO chemist?

To thrive as a CRO Chemist, a solid background in organic and analytical chemistry, supported by a degree in chemistry or related fields, is essential. Familiarity with laboratory instrumentation such as HPLC, GC-MS, NMR, and proficiency in using LIMS or ELN systems are typically required, along with any relevant safety or GLP certifications. Strong attention to detail, problem-solving skills, and effective teamwork enable chemists to deliver accurate results on client-driven projects. These competencies ensure high-quality research, regulatory compliance, and successful collaboration within contract research organizations.

What cities near Raleigh, NC are hiring for Cro Chemistry jobs?

Cities near Raleigh, NC with the most Cro Chemistry job openings:

Supervisor, QC Chemistry

Fujifilm

Holly Springs, NC • On-site

Full-time

Posted 20 days ago


Fujifilm rating

8.4

Company rating: 8.4 out of 10

Based on 67 frontline employees who took The Breakroom Quiz

50th of 539 rated manufacturers


Job description

The Supervisor, QC Chemistry, first shift is responsible for day-to-day supervision, audit readiness, and planning activities for the Chemistry laboratory. This Supervisor will lead a team responsible for performing routine testing of QC analytical chemistry methods used in biological product manufacturing, including chromatography, spectroscopy, electrophoresis, wet chemistry, glycan analysis, peptide mapping, and physical appearance.


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


What You’ll Do

  • Provide supervision and manage scheduling of the QC Chemistry team to ensure testing timelines are achieved.
  • Ensure analytical testing of in-process, drug substance (DS), drug product (DP), and stability samples is performed according to appropriate GMP regulations.
  • Perform, review, and provide expertise in physical and chemical analytical testing methods, including chromatography (HPLC, UPLC, SEC), spectroscopy (UV, UV-Vis, ELSD), electrophoresis (GE, non-reducing and reducing CE-SDS, imaged capillary isoelectric focusing (icIEF)), wet chemistry, glycan analysis, peptide mapping, and physical appearance per Standard Operating Procedures (SOPs) and test methods.
  • Act as primary point of contact for the team and first-line escalation.
  • Lead the team to meet project deliverables.
  • Set up and maintain operations of a QC testing laboratory.
  • Review and approve SOPs, protocols, reports, change controls, TrackWise deviations, out-of-specification (OOS) and out-of-trend (OOT) investigations, and CAPAs for the QC Chemistry team, as needed.
  • Assist senior management with resource planning and budget-related tasks.
  • Gather recommendations for enhancements and gaps; collaborate with leadership to prioritize and implement solutions.
  • Liaise with Contract Laboratory Organizations (CLOs) to monitor method execution and the timely delivery of results, as needed.
  • Participate in cross-functional collaborations with other QC Departments, Manufacturing, Process Science, and Quality Assurance stakeholders to achieve customer and FUJIFILM Biotechnologies objectives.
  • Allocate and plan adequate resources for laboratory testing activities and QA support; provide technical guidance to the team.
  • Lead cross-functional teams to achieve operational readiness objectives and new product introduction goals using a risk-based, right-sized approach.
  • Lead or guide laboratory staff in investigating deviations/excursions and implementing CAPAs as needed.
  • Serve as SME in audits and inspections; prepare and guide the laboratory team to ensure audit readiness.
  • Collaborate with the LIMS team and IT department to build new method functionality that meets end-user and customer requirements.
  • Establish and maintain internal and external training goals for self and team to ensure compliance with cGMPs and regulatory requirements.
  • Provide training, coaching, and mentorship; identify areas for improvement, reduce blind spots, and create growth opportunities aligned to career objectives.
  • Perform other duties, as assigned.

Minimum Qualifications

  • Bachelor’s in Chemistry, Biochemistry, Biological Sciences, or related science field with 5+ years of experience; OR,
  • Master’s in Chemistry, Biochemistry, Biological Sciences, or related science field with 3+ years of experience.
  • 2+ years of team management experience.
  • Analytical laboratory experience preferably in biotechnology, Pharma, Contract Research Organization (CRO), or Contract Laboratory Organization (CLO).
  • 3+ years of experience working in a regulated GMP environment.
  • Ability to guide and influence teams in a laboratory setting.
  • Excellent oral and written communication skills.
  • Experience in large pharma/biotech operations or projects.
  • Knowledge and experience of physical and chemical analytical testing methods for biological products, including chromatography (GC, HPLC, UPLC, SEC), spectroscopy (MS, GC/MS, LCMS/MS, UV, UV-Vis, FTIR), electrophoresis (GE, non-reducing and reducing CE-SDS, imaged capillary isoelectric focusing (icIEF)), wet chemistry, glycan analysis, peptide mapping, and physical appearance.
  • Proven ability to lead teams.

Preferred Qualifications

  • Experience managing complex projects.
  • Experience with customer relationship management.
  • Prior drug substance or manufacturing experience, including process validation, transfer, commercialization, and manufacturing support and troubleshooting.
  • Experience using quality systems (e.g., deviation management system, change control, corrective and preventive action (CAPA), document management system).
  • Working knowledge of LIMS, Smartsheet, TrackWise, and/or Kneat validation software.
  • Experience and high-level familiarity/understanding of laboratory equipment, utilities qualification, environmental monitoring qualification, quality systems, automation, IT systems, and/or method validation.
  • Experience in and thorough understanding of Data Integrity and application of regulatory requirements for QC assays.

Physical Requirements:

The physical demands described here are representative of those that must be met by an employee to

successfully perform the essential functions of this job. Reasonable accommodations may be made to

enable individuals with disabilities to perform essential functions. While performing the duties of this job,

the employee is required on a regular basis to:

  • Ability to discern audible cues.
  • Ability to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color.
  • Ability to stand for prolonged periods of time up to 240 minutes.
  • Ability to sit for prolonged periods of time up to 240 minutes.
  • Ability to conduct activities using repetitive motions that include wrist, hands and/or fingers.
  • Ability to conduct work that includes moving objects up to 10 pounds.
  • Ability to bend, push or pull, and reach to retrieve materials from 18” to 60” in height, and use twisting motions.
  • Will work in warm/cold environments.
  • Will work in small and/or enclosed spaces.

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.


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.


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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