Top 3 Quality assurance specialist Jobs in Florence Sc

Quality Specialist II
Thermo Fisher Scientific —Florence, SC
- Full-time
- No experience needed
- Mid-level
- Office
- Paid parental leave
- Paid holidays
Admission and Quality Nurse Specialist
Lake City Scranton Health Care Cener —Scranton, SC
- $38 - $42 an hour
- Full-time
- Nursing
- LVN
- RN License
- Loan repayment program
- Disability insurance
6d
Quality Improvement Specialist - (Radiology Degree Required) - Breast Imaging
McLeod Health —Florence, SC
- Online Application
- Hospital
- BLS Certification
- HIPAA
Quick Apply
1d

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Quality Improvement Specialist - (Radiology Degree Required) - Breast Imaging
McLeod Health —Florence, SC
Registry-eligible candidates must obtain ARRT-M certification within one (1) year of hire. South Carolina Radiation Quality Standards Association certification…
Quick Apply
1d

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Quality Assurance Specialist
Accel Inc —New Albany, OH
Assist with non-conformance assessments, findings, reports, CAPAs, and root cause analysis. Accel is hiring a *Quality Assurance Specialist* to perform routine…
$19 an hour
Quick Apply
Senior Specialist, Quality Assurance
Cardinal Health —Columbus, OH
Bachelor's degree in related field, or equivalent work experience, preferred. Applies working knowledge in the application of concepts, principles and technical…
$66,500 - $95,000 a year

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Quality Specialist II

Thermo Fisher Scientific -
Florence, SC

Apply Now

Job Details

Full-time

Benefits

Paid parental leave
Paid holidays
Health insurance
Dental insurance
Tuition reimbursement
Paid time off
Parental leave
Vision insurance
401(k) matching
Employee discount
Benefits from day one
Opportunities for advancement
Referral program

Qualifications

Quality control corrective actions
Biology
Regulatory inspections
Foreign language proficiency
Biotechnology
Content creation for technical audiences
Defect resolution root cause analysis
Technical documentation
ISO standards
Preventive action implementation
Continuous improvement standards implementation
Internal compliance auditing
Technical writing experience within manufacturing
Production deviation management
TrackWise
Corrective and preventive actions (CAPA)
No experience needed
GMP
Cleanroom protocols
Mid-level
Internal investigations
Project management experience in manufacturing
Bachelor's degree in biology
Manufacturing facility experience
Bachelor's degree in engineering
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
Compliance documentation
Internal compliance assessments
Sterile attire donning

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Excellent Benefits Package

Review our company’s Total Rewards

Medical, Dental, & Vision benefits-effective Day 1

Paid Time Off & Holidays

401K Company Match up to 5%

Tuition Reimbursement – eligible after 90 days!

Employee Referral Bonus

Employee Discount Program

Recognition Program

Charitable Gift Matching

Company Paid Parental Leave

Career Advancement Opportunities

Discover Impactful Work:

Join Thermo Fisher Scientific as a Quality Specialist II and contribute to global healthcare and scientific advancement. In this role, you'll ensure compliance with GMP standards, FDA regulations, and international quality requirements while supporting manufacturing operations across multiple product lines. Working with cross-functional teams, you'll implement continuous improvement initiatives, conduct investigations, and maintain quality management systems that enable our mission of making the world healthier, cleaner, and safer.

A Day in the Life:

Support manufacturing operations through quality oversight, deviation investigations, CAPA management, change control activities, audit support, documentation review, and continuous improvement initiatives. Partner with cross-functional teams to ensure compliance with GMP, FDA, ISO, and internal quality requirements.

Keys to Success:

Education

Advanced degree with no prior experience, or Bachelor's degree with 2 years of experience in pharmaceutical/biotech manufacturing, quality assurance, or related GMP environment
Preferred fields of study: Biology, Chemistry, Engineering, Life Sciences, or related scientific field

Knowledge, Skills, Abilities

Knowledge of cGMP regulations, ISO standards (9001/13485), and international regulatory requirements
Experience with quality management systems and documentation (TrackWise, MasterControl, or equivalent)
Experience in deviation investigations, CAPA, change control, and root cause analysis
Proficient in Microsoft Office suite and quality management software systems
Technical writing and documentation skills
Analytical and problem-solving abilities
Clear verbal and written communication skills
Ability to work independently and collaboratively in cross-functional teams
Experience conducting internal audits and supporting external regulatory inspections
Project management and organizational skills
Ability to work in cleanroom environments and follow gowning procedures where required
Additional language skills may be beneficial

Additional Requirements

Must be able to work various shifts to support manufacturing operations
Physical requirements include standing/walking for extended periods and occasional lifting up to 25 lbs

Apply Now

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quality assurance specialist jobs in florence sc

Quality Specialist II

Admission and Quality Nurse Specialist

Quality Improvement Specialist - (Radiology Degree Required) - Breast Imaging

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