Top 22 Quality specialist Jobs in Mebane, Nc

Data Review (QC Specialist) 6-Mo Contract
BioAgilytix —Durham, NC
- Contract
- Mid-level
- Master's degree
- Bachelor's degree
- Health savings account
- Paid holidays
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2d
Manufacturing Quality Assurance Specialist
Novartis —Durham, NC
- $43.08 - $80.00 an hour
- Full-time
- 5 years
- Bachelor of Science
- Analysis skills
- Health insurance
- 401(k) matching
1d
QA Specialist - Raw Materials
KBI Biopharma —Durham, NC
- Full-time
- Military encouraged
- Senior level
- Commercial
Quality Specialist III
Precision Biosciences —Durham, NC
- 5 years
- Travel
- Senior level
Quality Assurance Specialist
Science Corporation —Durham, NC
- Mid-level
- Continuous improvement
- Fair chance
Senior Specialist Quality Assurance, CSV
Definium Therapeutics —Durham, NC
- $101,147 - $122,757 a year
- Remote
- 7 years
- Psychiatry
- Bachelor's degree
- Health insurance
- Dental insurance
ELSP Supplier Quality Specialist
Industrial Connections & Solutions LLC —Mebane, NC
- Full-time
- Mid-level
- US work authorization
- 2 years
- Paid parental leave
- Health savings account
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Senior Quality Specialist
Industrial Connections & Solutions LLC —Mebane, NC
- Full-time
- Remote
- Bachelor of Science
- Analysis skills
- Supervising experience
- Health savings account
- AD&D insurance
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10d
Clinical Quality Assurance Specialist - Bone Marrow Transplant Program
UNC Health —Chapel Hill, NC
- $35.87 - $51.57 an hour
- Full-time
- Hybrid work
- Nursing
- RN License
- Mid-level
QA/QC Specialist CWI (Wendell, Charlotte, Elon & Surrounding Areas)
SPC Mechanical —Elon, NC
- Full-time
- Management
- Construction site
- Driver's License
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QA Specialist II
KBI Biopharma —Durham, NC
- Full-time
- Word processing
- Bachelor of Science
- 8 years
QA Area Specialist I - SDF (2nd shift)
Novo Nordisk —Durham, NC
- 6 years
- Computer literacy
- Mid-level
- Paid holidays
- Disability insurance
Senior QA Specialist, External Manufacturing, US
Bavarian Nordic —Durham, NC
- $120,000 - $155,000 a year
- Full-time
- Remote
- Travel
- Senior level
- Communication skills
Validation Area Specialist I/II - SDF
Novo Nordisk —Durham, NC
- Microsoft Word
- Microsoft Excel
- Computer literacy
- Paid holidays
- Disability insurance
14d
QA Specialist II (Nights 12 hour Rotating Shift)
KBI Biopharma —Durham, NC
- 12 hour shift
- Laboratory experience
- Mid-level
- High school diploma or GED
21h
Sr/Principal Computer Systems Validation Specialist
KBI Biopharma —Durham, NC
- $118,000 - $183,700 a year
- Full-time
- Bachelor of Science
- 8 years
- Bachelor's degree
- Paid holidays
- Health insurance
Experienced Advanced Practice Provider (NP/PA) - Clinical Quality Specialist I - EPIC Certified
Avance Care —Durham, NC
- Full-time
- Hybrid work
- Background check
- Private practice
- Nursing
Quick Apply

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Documentation Control Specialist
Morinaga America Foods —Mebane, NC
Bachelor’s degree in Biology, Microbiology, Food Science, Animal Science or related field preferred and/or 5-10 years in Food Quality.
$41,600 - $60,000 a year
Quick Apply
7d
Manufacturing Quality Assurance Specialist
Novartis —Durham, NC
Provide quality expertise in manufacturing batch record design, review, and continuous improvement. Support media, buffer, cell expansion, upstream, downstream,…
$43.08 - $80.00 an hour
1d

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Quality Specialist
Engineered Profiles LLC —Columbus, OH
Assist in training floor associates on procedures & quality gauges / tools. 401k Retirement Plan- Company matching. Assist in tracking trends or quality issues.
$16.97 - $22.05 an hour
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Quality Specialist
US AMR-Jones Lang LaSalle Americas, Inc. —New Albany, OH
Bachelor’s degree in a scientific, engineering, or technical field. This position is highly visible and requires strong documentation discipline, technical…
$67,000 - $97,000 a year
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Data Review (QC Specialist) 6-Mo Contract

BioAgilytix -
Durham, NC

Quick Apply

Job Details

Contract
2 days ago

Benefits

Health savings account
Paid holidays
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Paid time off
Parental leave
Vision insurance
401(k) matching
Life insurance
Referral program

Qualifications

Pharmaceutical regulatory compliance
Employee relationship building
Biological analysis

Full Job Description

At BioAgilytix, we are passionate about premier science and the impact it has on our world. Our team of highly experienced scientists and professionals deliver tailored services for supporting new medicine breakthroughs with best-in-class bioanalytical services. We are tirelessly committed to our customers by being solution-oriented and deadline-driven. . . and we are growing. Our culture is fast-paced, fun and never boring. Because we work across numerous clients and drug modalities, your career can develop rapidly. You’ll gain experience with a variety of challenges all while you enable life-changing, life-saving therapeutics to the patients who need them.

Our clients trust us to deliver excellence in data and bioanalysis and in this role and you will be a critical part of our beginning-to-end client data quality processes. Through your technical reviews of raw and processed data, you will ensure data integrity standards are met across various equipment, regulatory settings, and workflows. You are the bridge between the lab and the quality assurance team, combining observations on regulatory requirements with your knowledge of plate-based assays, cell work, gene therapy and more.

We are looking for candidates who have practical regulatory experience with bioanalytical data in a corporate GxP setting. This role is not lab-based, but our best candidates have lab experience or experience with the types of assays we do here. You are self-motivated, an independent thinker, and highly organized. If you influence others by being a trusted advisor and advocate, are energized by a deadline-driven environment, and aspire to provide the best caliber of data to our customers, then you’ll be right at home here at BioAgilytix.

Essential Responsibilities

Perform Quality Control (QC) technical, scientific, and compliance review of data and documentation generated by the Bioanalytical Operations group in support of regulated studies (e.g. GLP, GMP).
Identify deviations, OOS and OOT associated with Bioanalytical Operations data as applicable
Issue QC review observations and work closely with the scientific staff to ensure data integrity
Collect metrics data used to monitor the QC reviews, and may identify process improvements
Assist in educating, guiding and influencing the scientific staff in regard to best practices in GxP compliance

Minimum Preferred Qualifications: Education/Experience

Bachelor’s degree in biological science or related field, with between 2-10 years’ experience working in biotech, pharmaceutical, CRO/CMO or similar organization; or Master’s or PhD. with equivalent experience
Knowledge and/or extensive knowledge of GxP regulations
Two-Four (2-4) years’ experience performing data review in a GxP environment
Experience with relevant bioanalytical methods such as immunoassays, cell-based assays, or qPCR

Minimum Preferred Qualifications: Skills

Self-motivated and demonstrated ability to learn and work in a fast-paced environment where multiple concurrent projects must be completed in a timely manner
Ability to perform your role independently with attention to detail and minimal oversight
Ability to perform technical review of data following GxP regulations and scientific principles
Expertise in communicating and building relationships with others, where all feel heard and respected
The confidence to make and share observations in a considerate manner
Proficiency in LIMS and Quality Management software packages

BENEFITS AND OTHER PERKS

Medical Insurance (HDHP with HSA; PPO), Dental Insurance, Vision Insurance, Flexible Spending Account (medical; dependent care), Short Term Disability \u007C Long Term Disability Life Insurance, Paid Time Off (4 weeks per year), Parental Leave, Paid Holidays (9 scheduled; 5 floating), 401k with Employer Match, Employee Referral Program

COMMITMENT TO EQUAL OPPORTUNITY

BioAgilytix provides equal employment opportunities to all employees and applicants for employment without regard to race, color, ancestry, national origin, gender, sexual orientation, marital status, religion, age, disability, gender identity, results of genetic testing, service in the military, or any other group protected by federal, state, or local law.

To learn more about how we collect, use, and protect your information, please review our Privacy Policy and Terms of Use.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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Refine Your Search

quality specialist jobs in mebane, nc

Data Review (QC Specialist) 6-Mo Contract

Manufacturing Quality Assurance Specialist

QA Specialist - Raw Materials

Quality Specialist III

Quality Assurance Specialist

Senior Specialist Quality Assurance, CSV

ELSP Supplier Quality Specialist

Senior Quality Specialist

Clinical Quality Assurance Specialist - Bone Marrow Transplant Program

QA/QC Specialist CWI (Wendell, Charlotte, Elon & Surrounding Areas)

QA Specialist II

QA Area Specialist I - SDF (2nd shift)

Senior QA Specialist, External Manufacturing, US

Validation Area Specialist I/II - SDF

QA Specialist II (Nights 12 hour Rotating Shift)

Sr/Principal Computer Systems Validation Specialist

Experienced Advanced Practice Provider (NP/PA) - Clinical Quality Specialist I - EPIC Certified

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Essential Responsibilities

Minimum Preferred Qualifications: Education/Experience

Minimum Preferred Qualifications: Skills

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