Bachelor's degree in Biology, chemistry or related field with 11+ years of relevant experience OR ... with QC Methods Preferred Requirements: 8+ years of experience working in a regulated GMP ...
Bachelor's degree in Biology, chemistry or related field with 11+ years of relevant experience OR ... with QC Methods Preferred Requirements: 8+ years of experience working in a regulated GMP ...
... degree in Biology, chemistry or related field with 11+ years of relevant experience OR • MS ... QC Microbiology methods, Raw Material testing and contamination controlPhysical and Work ...
... degree in Biology, chemistry or related field with 11+ years of relevant experience OR • MS ... QC Microbiology methods, Raw Material testing and contamination controlPhysical and Work ...
... degree in Biology, chemistry or related field with 11+ years of relevant experience OR • MS ... QC Methods Preferred Requirements: • 8+ years of experience working in a regulated GMP ...
... degree in Biology, chemistry or related field with 11+ years of relevant experience OR • MS ... QC Methods Preferred Requirements: • 8+ years of experience working in a regulated GMP ...
... degree in Biology, chemistry or related field with 11+ years of relevant experience OR • MS ... QC Methods Preferred Requirements: • 8+ years of experience working in a regulated GMP ...
... degree in Biology, chemistry or related field with 11+ years of relevant experience OR • MS ... QC Methods Preferred Requirements: • 8+ years of experience working in a regulated GMP ...
Quality Control Senior Associate
Boston, MA · On-site
$30 - $33/hr
This is an excellent opportunity for candidates with biologics testing experience, aseptic ... The Quality Control Senior Associate will perform in-process, release, and stability testing while ...
Quality Control Senior Associate
Boston, MA · On-site
$30 - $33/hr
This is an excellent opportunity for candidates with biologics testing experience, aseptic ... The Quality Control Senior Associate will perform in-process, release, and stability testing while ...
QC Manager
Exton, PA · On-site
Biomarker & Biologics Location: Exton, PA ( Onsite) Position Summary The QC Manager is responsible for oversight of the Quality Control function supporting compliant biologics and biomarker testing ...
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QC Manager
Exton, PA · On-site
Biomarker & Biologics Location: Exton, PA ( Onsite) Position Summary The QC Manager is responsible for oversight of the Quality Control function supporting compliant biologics and biomarker testing ...
Quality Control Scientist
Madison, WI · On-site
$26 - $32/hr
Quality Control Scientist The Quality Control Scientist supports an in‑house Quality Control ... Perform molecular biology assays involving DNA and RNA, including pipetting, PCR, qPCR, gel ...
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Quality Control Scientist
Madison, WI · On-site
$26 - $32/hr
Quality Control Scientist The Quality Control Scientist supports an in‑house Quality Control ... Perform molecular biology assays involving DNA and RNA, including pipetting, PCR, qPCR, gel ...
Quality Control Scientist
Madison, WI · On-site
$26 - $32/hr
Quality Control Scientist The Quality Control Scientist supports an in‑house Quality Control ... Perform molecular biology assays involving DNA and RNA, including pipetting, PCR, qPCR, gel ...
Quick apply
Quality Control Scientist
Madison, WI · On-site
$26 - $32/hr
Quality Control Scientist The Quality Control Scientist supports an in‑house Quality Control ... Perform molecular biology assays involving DNA and RNA, including pipetting, PCR, qPCR, gel ...
Collaborate with QC Biology and Manufacturing teams to ensure raw material controls are appropriate for ATMP applications * Author, review, and approve GMP documentation including SOPs, test methods ...
Collaborate with QC Biology and Manufacturing teams to ensure raw material controls are appropriate for ATMP applications * Author, review, and approve GMP documentation including SOPs, test methods ...
Collaborate with QC Biology and Manufacturing teams to ensure raw material controls are appropriate for ATMP applications * Author, review, and approve GMP documentation including SOPs, test methods ...
Collaborate with QC Biology and Manufacturing teams to ensure raw material controls are appropriate for ATMP applications * Author, review, and approve GMP documentation including SOPs, test methods ...
... quality control assays of biological products used for the development of new cell based ... in Chemistry, Biochemistry, Biology, or Biotechnology. * Academic or industrial laboratory ...
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... quality control assays of biological products used for the development of new cell based ... in Chemistry, Biochemistry, Biology, or Biotechnology. * Academic or industrial laboratory ...
Collaborate with QC Biology and Manufacturing teams to ensure raw material controls are appropriate for ATMP applications * Author, review, and approve GMP documentation including SOPs, test methods ...
Quick apply
Collaborate with QC Biology and Manufacturing teams to ensure raw material controls are appropriate for ATMP applications * Author, review, and approve GMP documentation including SOPs, test methods ...
Manage quality control activities involved with biologic drug manufacturing and facility quality control operations. * In general, oversee and review facility operation practices, complete and review ...
Manage quality control activities involved with biologic drug manufacturing and facility quality control operations. * In general, oversee and review facility operation practices, complete and review ...
Quality Control Manager, PCT
Cranbury, NJ · On-site
$73K - $155K/yr
Strong working knowledge of QC operations for biologics, including method execution, data review, and laboratory compliance. * In-depth understanding of global regulatory requirements and guidance ...
Quality Control Manager, PCT
Cranbury, NJ · On-site
$73K - $155K/yr
Strong working knowledge of QC operations for biologics, including method execution, data review, and laboratory compliance. * In-depth understanding of global regulatory requirements and guidance ...
cGMP Quality Control (QC) Specialist
$87.58K - $92K/yr
... biologics and drugs for cell and gene therapy of internal/external users in the university ... The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and ...
cGMP Quality Control (QC) Specialist
$87.58K - $92K/yr
... biologics and drugs for cell and gene therapy of internal/external users in the university ... The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and ...
cGMP Quality Control (QC) Specialist
Los Angeles, CA · On-site
$87.58K - $92K/yr
... biologics and drugs for cell and gene therapy of internal/external users in the university ... The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and ...
cGMP Quality Control (QC) Specialist
Los Angeles, CA · On-site
$87.58K - $92K/yr
... biologics and drugs for cell and gene therapy of internal/external users in the university ... The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and ...
cGMP Quality Control (QC) Specialist
$87.58K - $92K/yr
... biologics and drugs for cell and gene therapy of internal/external users in the university ... The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and ...
cGMP Quality Control (QC) Specialist
$87.58K - $92K/yr
... biologics and drugs for cell and gene therapy of internal/external users in the university ... The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and ...
Qualifications: * BS in Biology or Chemistry (or related) with 7+ years of GMP QC (biologics ... preferred) * 5+ years managing teams * Method validation/transfer expertise * Strong hands-on ...
Qualifications: * BS in Biology or Chemistry (or related) with 7+ years of GMP QC (biologics ... preferred) * 5+ years managing teams * Method validation/transfer expertise * Strong hands-on ...
Qualifications: * BS in Biology or Chemistry (or related) with 7+ years of GMP QC (biologics ... preferred) * 5+ years managing teams * Method validation/transfer expertise * Strong hands-on ...
Qualifications: * BS in Biology or Chemistry (or related) with 7+ years of GMP QC (biologics ... preferred) * 5+ years managing teams * Method validation/transfer expertise * Strong hands-on ...
Quality Control Technician
Elgin, IL · On-site
$18.75 - $23.75/hr
Science degree (Chemistry, Biology) 1(+) year of QC experience in an industrial chemical industry. New Graduate in scientific field (Chemistry, biology) with Zero years of relevant experience.
Quality Control Technician
Elgin, IL · On-site
$18.75 - $23.75/hr
Science degree (Chemistry, Biology) 1(+) year of QC experience in an industrial chemical industry. New Graduate in scientific field (Chemistry, biology) with Zero years of relevant experience.
Quality Control Biology information
See salary details
$12.98 - $14.51
1% of jobs
$14.51 - $16.04
6% of jobs
$16.04 - $17.57
12% of jobs
$18.06 is the 25th percentile. Wages below this are outliers.
$17.57 - $19.10
18% of jobs
The median wage is $20.12 / hr.
$19.10 - $20.63
19% of jobs
$20.63 - $22.16
15% of jobs
$22.75 is the 75th percentile. Wages above this are outliers.
$22.16 - $23.69
10% of jobs
$23.69 - $25.22
9% of jobs
$25.22 - $26.75
4% of jobs
$26.75 - $28.28
3% of jobs
$28.28 - $29.81
3% of jobs
$12
$20
$29
How much do quality control biology jobs pay per hour?
What are the key skills and qualifications needed to thrive as a Quality Control Biology professional, and why are they important?
What are some common challenges faced by professionals in Quality Control Biology, and how can they be managed?
What is Quality Control Biology?
What is the difference between Quality Control Biology vs Quality Assurance Biology?
| Aspect | Quality Control Biology | Quality Assurance Biology |
|---|---|---|
| Certifications | Typically requires a Bachelor's degree in Biology or related field | Requires similar degrees; certifications like ASQ may be beneficial |
| Work Environment | Laboratories, manufacturing plants, testing facilities | Quality management departments, compliance offices |
| Industry Usage | Used in biotech, pharmaceutical, food industries for testing products | Used in developing and maintaining quality systems and standards |
| Search & Comparison Intent | Focuses on testing and product quality checks | Focuses on system processes and compliance standards |
While both roles involve ensuring product quality, Quality Control Biology primarily focuses on testing and inspecting biological products, whereas Quality Assurance Biology emphasizes developing and maintaining quality systems and standards within the industry.
Other
Posted 18 hours ago
Fujifilm rating
8.3
Based on 66 frontline employees who took The Breakroom Quiz
47th of 511 rated manufacturers
Job description
The Associate Director, QC Biological is responsible for management of multiple labs within the Quality Control department including QC Microbiology. The individuals will act as a representative of QC in cross functional meeting focusing on both startup activities and routine operations. The leader will be responsible for hiring plans, budget development, strategic planning, and driving results. This role plans, schedules, and oversees multiple QC laboratories in order to drive compliance goals, schedule adherence, profit plans, and strategy objectives of the company and the department. The Associate Director, QC Biological identifies operational needs for special projects (new product sub-team, capital projects, etc.)- ensuring site/divisional linkage is achieved. This role identifies and addresses short term, intermediate, and long-term issues in a satisfactory manner, and appropriately resolves conflict and prioritizes work as necessary. The Associate Director, QC Biological will be required to manage through levels including managers, supervisors, individual contributors, etc.
Company OverviewFUJIFILM 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 DescriptionWhat You'll Do
Translates company goals into relevant department objectives, focused on assuring the compliance, supply, profit plan, strategy and people/culture objectives are appropriately implemented Provides logistical and strategic support for achieving department objectives Represents department for manufacturing, customer, and COE related activities as they relate to resource management Assures laboratory is capable of delivering to proposed or scoped customer requirements Assures adherence to headcount and budget plans Initiates and drives implementation of technology and projects aimed at cost reduction, efficiency improvements, minimization of downtime and quality/safety enhancement. Fosters an environment for continuous improvement Maintains state of inspectional readiness for department Assures appropriate training requirements are established and that the staff maintains currency to the curricula Assures team delivers on-time results with right first-time quality Makes decisions on equipment selection, qualification, maintenance Assures transferred methods align with department analytical platforms Provides training and assurance that the transferred methods are fit for purpose and QC personnel are trained to perform the methods consistently Assures Quality System requirements are delivered according to determined schedules Fosters a safe working environment through appropriate training and engagement of QC staff Assures policies, practices, standard work are consistent across the department Conducts group communication meetings to facilitate project efficiency and/or distribute information Develops and manages group against KPI's to assure alignment with objectives and manage to target Participates in the development and management of capital and expense budget Participates in and develops employee development plans to assure continuity to mid- and long-term succession plans Manages and develops direct and indirect reports Administers company policies such as time off, shift work, and inclement weather that directly impact employees Completes required administrative tasks (e.g., timecard approvals, time off approvals, expense reports etc.) Coaches and guides direct reports to foster professional development Participates in the recruitment process and retention strategies to attract and retain talent, as needed Addresses performance gaps, employee questions and concerns, and partners with HR as needed for resolution Performs other duties, as assigned
Minimum Requirements:
Bachelor's degree in Biology, chemistry or related field with 11+ years of relevant experience OR MS degree with 9+ years of relevant experience OR Ph.D. with 7+ years of relevant experience 4+ years of people management and leadership experience Experience working in a regulated GMP environment Experience managing and developing direct reports and teams Experience with QC Methods
Preferred Requirements:
8+ years of experience working in a regulated GMP environment Extensive experience with Drug Product production Experience working in a contract manufacturing or testing organization Experience with statistical experimental design and data analysis with JMP software Experience with QC Microbiology methods, Raw Material testing and contamination control
Physical and Work Environment Requirements:
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 conduct activities using repetitive motions that include writs, hands and/or fingers.
Ability to sit for prolonged periods of time up to 240 minutes.
Ability to bend, push or pull, reach to retrieve materials from 18" to 60" in height, and use twisting motions.
Will work in warm/cold environments
Will work in heights greater than 4 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.
EEO InformationFujifilm 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 InformationIf 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: OTHERAbout 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