Top 6 Quality control manager Jobs in Sanford, Nc

Supervisor, QC Chemistry
FUJIFILM —Holly Springs, NC
- Call employer
- Master's degree
- Bachelor's degree
- Mentoring
8d
Construction Quality Control Manager- USACE
Thalle Construction Company —United States
- Full-time
- Construction site
- Senior level
- Leadership
- Paid holidays
- Disability insurance
Quick Apply
Quality Control Manager- Dam Project
Thalle Construction Company —United States
- Full-time
- Construction site
- Senior level
- Professional Engineer
- Paid holidays
- Disability insurance
Quick Apply

Related jobs to explore

Based on your search for quality control manager

Technician Supervisor
National Seating & Mobility, Inc. —Raleigh, NC
Experience in assembly and/or repair of mechanical or electronic devices. Ability to manage and educate Technicians on advanced testing, diagnostics and repair…
Quick Apply
Service Manager
Concentric LLC —Greensboro, NC
Certification from a technical school focused on electrical, mechanical repair or battery maintenance preferred. Growth of existing customer services utilized.
$75,000 - $110,000 a year
Quick Apply

Show more related jobs

Explore jobs in cities nearby

Check out jobs in cities near your current location, Columbus

QC Supervisor
WESTERMAN INC —Hebron, OH
Assists teams (including maintenance and engineering) with continuous improvement initiatives (driving safety, quality and process efficiencies).
$85,000 - $95,000 a year
Quick Apply
Quality Control Supervisor
Hims & Hers —New Albany, OH
A Pharmacy Technician license or willingness to obtain one within the first six months of employment (we cover costs and will help you obtain your trainee hours…
2d

Show more jobs in cities nearby

I want to receive the latest job alert for quality control manager in sanford, nc

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

quality control manager jobs near sanford, nc

Quality Control Manager jobs in Framingham, MA

Finance Manager jobs in New York, NY

Quality Control Manager jobs in Temple, TX

Quality Control Manager jobs in Mount Olive, NC

Traffic Control jobs in Nashville, TN

Quality Control Manager jobs in Liverpool, NY

Mosquito Control jobs in Florida

Food Quality Assurance jobs in Hayward, CA

Chicago Animal Control jobs in Chicago, IL

Quality Control Manager jobs in New Kensington, PA

Control Document jobs in San Diego, CA

Quality Control Manager jobs in Ohio

Quality Control Manager jobs in Boise, ID

Animal Control jobs in Maine

Quality Control Manager jobs in Guam

Quality Assurance Manager jobs in Saint Cloud, MN

Janitorial Manager jobs in Baltimore, MD

Quality Assurance Manager jobs in Portland, OR

Quality Coordinator jobs in Houston, TX

Quality Assurance Manager jobs in Mountainhome, PA

Supervisor, QC Chemistry

FUJIFILM -
Holly Springs, NC

Apply Now

Job Details

8 days ago

Qualifications

Staff supervision
Chemist team management
Managing laboratory teams
Biochemical laboratory techniques
Pharmaceutical company experience
Pharmaceutical analysis
Materials analysis (analytical chemistry specialty)
Leading team collaboration initiatives
Physical analysis
Regulatory compliance analysis
Chemical testing
Pharmaceutical manufacturing facility experience

Full 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 ([email protected]).

Apply Now

Refine Your Search

quality control manager jobs in sanford, nc

Supervisor, QC Chemistry

Construction Quality Control Manager- USACE

Quality Control Manager- Dam Project

Related jobs to explore

Explore jobs in cities nearby

I want to receive the latest job alert for quality control manager in sanford, nc

Explore jobs in more locations

Position Overview

Company Overview

Job Description

EEO Information

ADA Information

Job Seeker Tools

Employer Tools

Browse

Stay Connected