Thorough understanding of the pharmaceutical/biotech testing. * Proven ability to understand and ... Quality Control Company (Portal Searching) FUJIFILM Biotechnologies
Thorough understanding of the pharmaceutical/biotech testing. * Proven ability to understand and ... Quality Control Company (Portal Searching) FUJIFILM Biotechnologies
Position Overview The QC Specialist, Instrumentation works under the direction of senior team ... Thorough understanding of the pharmaceutical/biotech testing. * Proven ability to understand and ...
Position Overview The QC Specialist, Instrumentation works under the direction of senior team ... Thorough understanding of the pharmaceutical/biotech testing. * Proven ability to understand and ...
Associate II, Quality Control
Durham, NC · On-site
... of the world's best pharmaceutical, biotechnology and medical companies. As specialists in ... The QC Associate I/II is responsible for supporting key functional, tactical, and operational ...
Associate II, Quality Control
Durham, NC · On-site
... of the world's best pharmaceutical, biotechnology and medical companies. As specialists in ... The QC Associate I/II is responsible for supporting key functional, tactical, and operational ...
The Senior Associate, Quality Control Microbiology will report directly to the Senior Manager of ... Related experience in the pharmaceutical industry, preferrable working in a GxP Microbiology lab ...
The Senior Associate, Quality Control Microbiology will report directly to the Senior Manager of ... Related experience in the pharmaceutical industry, preferrable working in a GxP Microbiology lab ...
QC Tech II
Raleigh, NC · On-site
$18.25 - $23.25/hr
Aids in performing any non-routine quality control related tasks such as resampling, raw material ... Experience: 1 - 3 years laboratory experience in a pharmaceutical manufacturing operation preferred.
QC Tech II
Raleigh, NC · On-site
$18.25 - $23.25/hr
Aids in performing any non-routine quality control related tasks such as resampling, raw material ... Experience: 1 - 3 years laboratory experience in a pharmaceutical manufacturing operation preferred.
... Pharmaceutical, Industrial/Manufacturing, and EV/Battery/Renewables market segment groups (MSG ... Manage, supervise, and administer the implementation of the project-specific QA/QC Plan and QA/QC ...
... Pharmaceutical, Industrial/Manufacturing, and EV/Battery/Renewables market segment groups (MSG ... Manage, supervise, and administer the implementation of the project-specific QA/QC Plan and QA/QC ...
QC Tech II
Raleigh, NC · On-site
$18.25 - $23.25/hr
Aids in performing any non-routine quality control related tasks such as resampling, raw material ... Experience: 1 - 3 years laboratory experience in a pharmaceutical manufacturing operation preferred.
QC Tech II
Raleigh, NC · On-site
$18.25 - $23.25/hr
Aids in performing any non-routine quality control related tasks such as resampling, raw material ... Experience: 1 - 3 years laboratory experience in a pharmaceutical manufacturing operation preferred.
QC Analyst / Laboratory Technician
Durham, NC · On-site
$24/hr
Job Title: QC Analyst / Laboratory Technician Location: Durham, NC (100% Onsite) Duration: 12 ... pharmaceutical manufacturing environment. The ideal candidate will have experience in ...
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QC Analyst / Laboratory Technician
Durham, NC · On-site
$24/hr
Job Title: QC Analyst / Laboratory Technician Location: Durham, NC (100% Onsite) Duration: 12 ... pharmaceutical manufacturing environment. The ideal candidate will have experience in ...
Quality Control Senior Analyst (Micro)
Durham, NC · On-site
$23.25 - $31.25/hr
We're currently recruiting for a Quality Control Senior Analyst, Microbiology to join our Quality ... OXB collaborates with some of the world's most innovative pharmaceutical and biotechnology ...
Quality Control Senior Analyst (Micro)
Durham, NC · On-site
$23.25 - $31.25/hr
We're currently recruiting for a Quality Control Senior Analyst, Microbiology to join our Quality ... OXB collaborates with some of the world's most innovative pharmaceutical and biotechnology ...
Quality Control Senior Analyst (Micro)
Durham, NC · On-site
$23.25 - $31.25/hr
We're currently recruiting for a Quality Control Senior Analyst, Microbiology to join our Quality ... OXB collaborates with some of the world's most innovative pharmaceutical and biotechnology ...
Quality Control Senior Analyst (Micro)
Durham, NC · On-site
$23.25 - $31.25/hr
We're currently recruiting for a Quality Control Senior Analyst, Microbiology to join our Quality ... OXB collaborates with some of the world's most innovative pharmaceutical and biotechnology ...
Support organization and implementation of new bio- assays for QC testing of raw materials, drug ... pharmaceutical or biotech firm (minimum 2 years). Solid experience with a minimum of four of the ...
Support organization and implementation of new bio- assays for QC testing of raw materials, drug ... pharmaceutical or biotech firm (minimum 2 years). Solid experience with a minimum of four of the ...
Expert knowledge of pharmaceutical regulatory requirements and cGMP required. * Knowledge of quality systems and processes, change control, CAPA and data integrity required. * Knowledge of aseptic ...
Expert knowledge of pharmaceutical regulatory requirements and cGMP required. * Knowledge of quality systems and processes, change control, CAPA and data integrity required. * Knowledge of aseptic ...
QA/QC Technician/Inspector - Weldin/Piping Inspector (Pharmaceutical)About FST Technical ServicesFST Technical Services partners with clients in semiconductor, pharmaceutical, data center, and ...
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QA/QC Technician/Inspector - Weldin/Piping Inspector (Pharmaceutical)About FST Technical ServicesFST Technical Services partners with clients in semiconductor, pharmaceutical, data center, and ...
QA/QC Technician/Inspector - Weldin/Piping Inspector (Pharmaceutical) About FST Technical Services FST Technical Services partners with clients in semiconductor, pharmaceutical, data center, and ...
QA/QC Technician/Inspector - Weldin/Piping Inspector (Pharmaceutical) About FST Technical Services FST Technical Services partners with clients in semiconductor, pharmaceutical, data center, and ...
Representing QC Raw Materials in Tech Transfer projects, including customer interactions. * Focus ... the pharmaceutical industry, preferably within the field of starting materials and primary ...
Representing QC Raw Materials in Tech Transfer projects, including customer interactions. * Focus ... the pharmaceutical industry, preferably within the field of starting materials and primary ...
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Review & approves change control documentation, SOPs & other current good manufacturing practice ...
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Review & approves change control documentation, SOPs & other current good manufacturing practice ...
Representing QC Raw Materials in Tech Transfer projects, including customer interactions. * Focus ... the pharmaceutical industry, preferably within the field of starting materials and primary ...
Representing QC Raw Materials in Tech Transfer projects, including customer interactions. * Focus ... the pharmaceutical industry, preferably within the field of starting materials and primary ...
Representing QC Raw Materials in Tech Transfer projects, including customer interactions. * Focus ... the pharmaceutical industry, preferably within the field of starting materials and primary ...
Representing QC Raw Materials in Tech Transfer projects, including customer interactions. * Focus ... the pharmaceutical industry, preferably within the field of starting materials and primary ...
Director of Quality US
Raleigh, NC · On-site
$110K - $130K/yr
Own and manage key QMS processes, including CAPA, Change Control, Deviations, Complaints, Document ... pharmaceutical industry.
Quick apply
Director of Quality US
Raleigh, NC · On-site
$110K - $130K/yr
Own and manage key QMS processes, including CAPA, Change Control, Deviations, Complaints, Document ... pharmaceutical industry.
Director of Quality US
Raleigh, NC · On-site
$110K - $130K/yr
Own and manage key QMS processes, including CAPA, Change Control, Deviations, Complaints, Document ... pharmaceutical industry.
Quick apply
Director of Quality US
Raleigh, NC · On-site
$110K - $130K/yr
Own and manage key QMS processes, including CAPA, Change Control, Deviations, Complaints, Document ... pharmaceutical industry.
Pharmaceutical Quality Control information
What are some typical daily tasks for someone working in pharmaceutical quality control?
A typical day in Pharmaceutical Quality Control involves performing laboratory tests and analyses on raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with safety and regulatory standards. You may prepare and calibrate lab equipment, document test results, review batch records, and assist in investigations of deviations or out-of-specification findings. Additionally, collaboration with production, research, and quality assurance teams is common to maintain continuous improvement and address any quality issues quickly. This role is detail-oriented and often includes both routine testing and problem-solving activities, making each day varied and impactful.
Is pharmaceutical quality control a good career?
What are the key skills and qualifications needed to thrive in pharmaceutical quality control, and why are they important?
Pharmaceutical Quality Control professionals need a solid background in chemistry, biology, or pharmacy, often supported by a relevant degree and industry knowledge. Familiarity with laboratory instrumentation, Good Manufacturing Practices (GMP), and quality management systems, along with certifications like ASQ or GxP training, is highly beneficial. Attention to detail, strong analytical thinking, and clear communication are key soft skills that drive accuracy and collaboration. These competencies are crucial for ensuring that pharmaceutical products meet strict safety, efficacy, and regulatory standards.
What is a pharmaceutical quality control?
A Pharmaceutical Quality Control (QC) job involves ensuring that medications meet required safety, efficacy, and quality standards before distribution. Professionals in this field conduct tests, analyze raw materials and finished products, and ensure compliance with regulatory guidelines like Good Manufacturing Practices (GMP). They use analytical techniques such as HPLC, spectroscopy, and microbiological testing. QC specialists also document findings, investigate deviations, and collaborate with other departments to resolve quality issues. Their work helps maintain product integrity and patient safety.
What is the role of pharmaceutical quality control in pharmaceuticals?
- Pharmaceutical Market Access
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- Per Diem Qc Data Reviewer
- Contract Qa Batch Record Review
- Entry Level Pharmaceutical Data Scientist
- Work From Home Pharmaceutical Qa Auditor
- Per Diem Quality Assurance Pharmacist

Full-time
This job post has expired today. Applications are no longer accepted.
Fujifilm rating
8.4
Based on 67 frontline employees who took The Breakroom Quiz
50th of 536 rated manufacturers
Job description
Position Overview
The QC Specialist, Instrumentation works under the direction of senior team members to support routine operations, continuous improvement, and life-cycle management of the QC analytical instrumentation program. This role helps ensure compliance with Data Integrity standards, following regulatory guidelines and company procedures. The Specialist assists with routine maintenance, conducts periodic reviews of QC analytical instruments, and helps identify and address deviations or issues. The position also involves providing support for on-call and weekend coverage when needed.
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
Major Accountabilities:
- Supports the qualification, routine operation, maintenance, and decommissioning of QC analytical instruments.
- Ensures QC equipment and instruments adhere to regulatory guidelines and site policies.
- Assists in drafting and reviewing SOPs, technical reports, user requirements, and maintenance documentation.
- Participates in data integrity initiatives related to analytical instruments.
- Helps recommend appropriate user roles and privileges for data integrity and assists in writing operation instructions and preventative maintenance plans.
- Coordinates with vendors for maintenance activities on QC instruments.
- Completes routine periodic reviews of QC instruments and their control software.
- Identifies, reports, and follows up on excursions and deviations and assists in corrective and preventative actions (CAPAs).
- Provides support and guidance to stakeholders, including end users, on QC analytical instrumentation.
- Works cross-functionally with all end users as needed.
Knowledge, Skills and Abilities:
- Working knowledge and experience in Microsoft Office products (Outlook, Word, Excel, and Power Point).
- Demonstrated ability to work cross-functionally and to develop and maintain strong business partner relationships.
- Excellent verbal and written communication skills and attention to detail.
- Thorough understanding of the pharmaceutical/biotech testing.
- Proven ability to understand and implement data integrity standard and regulations.
- Proven ability to conduct investigations, writing deviations and CAPA's.
- Superior technical writing and problem-solving skills required.
- The ability to effectively communicate and function in a fast-paced, highly technical environment is essential to success.
Education and Experience Requirements:
- Bachelor's in relevant scientific discipline, preferably Chemistry, Biochemistry, Microbiology, Biology or Life Sciences
- 0-3 years laboratory experience
- Prior hands-on experience with analytical instrumentation associated with the following technologies: UPLC/HPLC, capillary electrophoresis/imaged capillary isoelectric focusing, gel electrophoresis/Western blot, plate readers, qPCR, spectrophotometry, and mass spectrometry.
Preferred Education and Experience:
- GMP laboratory experience
- Experience with Kneat software.
- Experience qualifying analytical instruments
Physical Requirements:
- Ability to discern audible cues.
- Ability to inspect or perform a task with 20/20 corrected vision, including distinguishing color.
- Ability to stand for up to 60 minutes.
- Ability to sit for up to 60 minutes.
- Ability to conduct activities using repetitive motions that includes wrists, hands and/or fingers.
- Ability to conduct work that includes moving objects up to 10 pounds.
- Ability to bend, push or pull, reach to retrieve materials from 18" to 60" in height, and use twisting motions.
- Will work in small and/or enclosed spaces.
- Will work in heights greater than four feet.
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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Job Locations US-NC-Holly Springs
Posted Date 4 months ago (3/20/2026 12:45 PM)
Requisition ID 2026-37345
Category Quality Control
Company (Portal Searching) FUJIFILM Biotechnologies
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