Quality Specialist I

ThermoFisher Scientific; Florence (SC); On-site; USD 65,000 - 80,000; Full time

Benefits offered by this job

Healthcare

Annual bonus

Career development

Job summary

Thermo Fisher Scientific is seeking a Quality Specialist I to ensure GMP compliance and quality oversight across manufacturing operations at the Florence, SC site. You will review documentation, monitor processes, and collaborate with cross-functional teams to drive continuous improvement in product quality and regulatory readiness.

The role supports API manufacturing, testing, and distribution, requiring a strong foundation in quality systems, CAPA, and regulatory familiarity.

Qualifications

• BS degree preferred in a scientific field; high school diploma also acceptable with experience.
• Experience in pharma/biotech regulated manufacturing and quality investigations.

Responsibilities

• Apply technical knowledge to ensure compliance with GMP and company policies across manufacturing areas.
• Review batch records and support investigations of quality events.
• Provide QA support for material disposition and quality systems.

Skills

FDA/GMP knowledge

GMP documentation review

CAPA & Change control

Technical writing

Microsoft Office

Analytical problem solving

English fluency

Cross-functional collaboration

Education

BS degree in Chemistry/Biology/Engineering/Life Sciences or related field

High School diploma or equivalent

Certifications (ISO auditor, Six Sigma) advantageous

Job description

Work Schedule

First Shift (Days)

Environmental Conditions

Office

Job Description

Title: Quality Specialist I

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.

Division/Site Specific Information

Position will sit onsite at the Florence, SC site and will support the Drug Substance Division (DSD) at Thermo Fisher Scientific. This role, reporting to the Production Planning Manager, ensures the flawless import of materials and goods at our Florence, South Carolina locations.

Discover Impactful Work:

Join our high-performing team at Thermo Fisher Scientific, where you'll ensure quality compliance across manufacturing operations while advancing our mission to make the world healthier, cleaner, and safer. As a Quality Specialist I, you'll provide essential quality oversight through detailed documentation review, process monitoring, and collaboration with cross-functional teams. You'll help maintain GMP compliance, investigate quality events, and drive continuous improvement initiatives while working in a collaborative environment focused on delivering life-changing products to our customers.

Under general supervision, provide comprehensive manufacturing technical support and quality assurance oversight to meet good business practices and the requirements of applicable regulatory agencies, supporting one of the following areas: API manufacturing, testing, disposition, quality systems and distribution of bulk drug substance.

A Day in the Life:

• Apply technical knowledge to address a broad range of issues to ensure adherence to and compliance with established company policies and procedures, as well as requirements of applicable Regulatory Agencies by working collaboratively with one or more of the following areas: manufacturing, testing, batch disposition, quality systems (Discrepancy/Investigation, change control, CAPA), qualification-validation, and distribution of bulk drug substance. Maintains quality management system associated documentation and all records required to manage the development, production and distribution of the products manufactured at this facility.

• Provide direct support to archival and retrieval of documentation and/or drawings to and from approved storage areas.

• Provide support in the monitoring and analyzing of business process performance measures and notify management of potential quality or regulatory issues that may affect product quality or regulatory compliance.

• Ensure that the products are manufactured in compliance with the regulatory and in a GMP compliant manner by reviewing batch records and performing appropriate investigations.

• Provide Quality Assurance support to resolving raw material, in-process material, bulk and final product, environmental, and system issues.

• Assist in writing and revising site SOPs or other procedures as required. Administer, document and maintain the company Quality Systems conformance to regulatory requirements and company policies where appropriate through effective utilization of the company’s Quality Systems and tools, as well as direct actions.

• Troubleshoot and direct the resolution of Quality issues by fostering effective interdepartmental and cross functional partnerships.

• Support Site Training in development, delivery and maintenance of Quality training programs (e.g., CAPA process, GMP, etc.).

• Participate in audits and inspections performed by clients and regulatory agencies, as required.

• Participate in the execution and/or administration of corporate Quality System tools such as TrackWise, Documentum, EDMS, etc.

• Provide input to the development of personal performance goals and departmental objectives; collaborate with Management to establish and meet targets and timelines.

• Participate in the design and implementation of department and cross-functional initiatives. Maintain a state of inspection readiness.

• Perform other duties as required.

Keys to Success:

Education

• BS Degree Preferred. Preferred Fields of Study: Chemistry, Biology, Engineering, Life Sciences, or related scientific field

• High School diploma, or equivalent required.

• Additional relevant certifications (e.g. ISO auditor, Six Sigma) are advantageous.

Experience

• High school diploma with 3–5 years of experience in pharmaceutical or biological manufacturing, or another regulated industry; or a bachelor’s degree in a technical science or engineering field with 0–3 years of Quality Assurance experience.

• Experience conducting quality investigations and root cause analysis.

Knowledge, Skills, Abilities

• Thorough knowledge of FDA, EMA, and international GMP regulations

• Proven ability to review and approve GMP documentation, batch records, and quality records

• Strong understanding of quality management systems and tools (e.g. CAPA, change control)

• Excellent documentation and technical writing skills

• Proficiency with quality systems software and Microsoft Office applications

• Strong analytical and problem-solving abilities with keen attention to detail

• Outstanding verbal and written communication skills

• Ability to work independently and collaborate effectively across functions

• Knowledge of environmental monitoring and contamination control principles

• Flexibility to work various shifts as needed to support manufacturing operations

• Ability to gown and work in controlled manufacturing environments when required

• Physical capability to stand, walk, and lift up to 25 pounds occasionally

• Sound judgment and decision-making skills

• Commitment to maintaining a quality-focused culture and driving continuous improvement

• Fluency in English required, additional language skills beneficial

Benefits

We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.