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Chemistry Manager Jobs in Raleigh, NC (NOW HIRING)

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 ...

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 ...

Provides fundamental analysis and interpretation and counsel to staff, management, and functional leaders regarding chemistry policies, programs, and practices; involves standard operations.

Overseeing and administering standard chemistry functions. * Training others in policies and procedures related to the work. * Serving as a team member and the development and management of projects.

Assistant/Associate/Senior Chemist

Clayton, NC · On-site

$20.75 - $27.25/hr

The Chemist position requires basic time/work management skills as the incumbent is expected to complete work assignments accurately and efficiently with only infrequent review by the Lab Supervisor.

Familiarity with standard chemistry lab equipment - HPLC, ICP, GC-MS, LUMiSizer, pH Meter, etc ... Requires excellent time management and organization skills. * Excellent communication and ...

Reporting to the Product Development and Applications Manager , this position is responsible for designing and executing tasks associated with the development of innovative chemistry-based products ...

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Chemistry Manager information

What is the difference between Chemistry Manager vs Chemist?

AspectChemistry ManagerChemist
Required CredentialsBachelor's or Master's in Chemistry, often with management experienceBachelor's or Master's in Chemistry, sometimes with specialized certifications
Work EnvironmentLeads teams in laboratories or manufacturing facilities, oversees projectsConducts experiments, analyzes data, and develops chemical solutions
Employer & Industry UsageUsed in industries like pharmaceuticals, manufacturing, and R&D for leadership rolesCommon in research labs, quality control, and product development

The main difference between a Chemistry Manager and a Chemist lies in their responsibilities. Chemistry Managers oversee teams and projects, focusing on management and strategic planning, while Chemists primarily conduct experiments and analyze chemical data. Both roles require strong chemistry credentials, but the managerial position involves leadership skills and experience in supervising staff.

What is a chemistry manager?

Chemistry Managers are professionals who oversee the operations and staff within a chemistry laboratory or department. They are responsible for managing projects, ensuring compliance with safety and regulatory standards, supervising chemists and technicians, and maintaining lab equipment. Their role often involves coordinating research and development activities, budgeting, and implementing quality control procedures. Chemistry Managers play a vital role in ensuring that laboratory work is conducted efficiently and safely, often serving as a bridge between technical staff and upper management.

What are some common challenges faced by chemistry managers when leading a laboratory team?

Chemistry Managers often encounter challenges such as balancing administrative responsibilities with hands-on scientific oversight, ensuring strict compliance with safety and regulatory standards, and managing diverse teams of chemists and technicians. They also need to facilitate effective communication between team members and other departments, such as quality assurance or production. Addressing resource constraints and maintaining project timelines while fostering professional growth within their team are also typical aspects of the role.

What are the key skills and qualifications needed to thrive as a chemistry manager, and why are they important?

To thrive as a Chemistry Manager, you need an in-depth understanding of chemical processes, laboratory management, and a relevant degree in chemistry or chemical engineering, often supplemented by prior leadership experience. Familiarity with laboratory information management systems (LIMS), regulatory compliance standards (such as OSHA and EPA), and quality control protocols is typically required. Strong leadership, problem-solving, and effective communication skills help manage teams and collaborate across departments. These skills ensure safe, efficient laboratory operations and high-quality analytical results that support organizational goals.
What are the most commonly searched types of Chemistry jobs in Raleigh, NC? The most popular types of Chemistry jobs in Raleigh, NC are:
What job categories do people searching Chemistry Manager jobs in Raleigh, NC look for? The top searched job categories for Chemistry Manager jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Chemistry Manager jobs? Cities near Raleigh, NC with the most Chemistry Manager job openings:
Infographic showing various Chemistry Manager job openings in Raleigh, NC as of July 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, 1% Temporary, and 2% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution.

Supervisor, QC Chemistry

Fujifilm

Holly Springs, NC • On-site

Other

Posted 11 days ago


Fujifilm rating

8.4

Company rating: 8.4 out of 10

Based on 67 frontline employees who took The Breakroom Quiz

49th of 536 rated manufacturers


Job description

Position Overview

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.

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

  • 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.

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).

Employment Type: OTHER

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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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