Top 427 Quality Control Iii Jobs

Scientist III (Quality Control Specialist)
Thermo Fisher Scientific —High Point, NC
- Full-time
- Background check
- Pass drug screening
- Master's degree
- Paid holidays
- Health insurance
Quality Control Scientist III
Velocity Bioworks Inc —San Antonio, TX
- Weekends as needed
- Customer service
- 3 years
- Bachelor's degree
Quick Apply
Quality Technician 2nd Shift (3:30PM-2:00AM)
Exential —Colchester, VT
- $20 - $24 an hour
- Full-time
- Mid-level
- Office
- High school diploma or GED
- Health savings account
- Health insurance
Quick Apply
Multi-Certified QC Inspector – Baxley, GA – Tentative Start Aug. 3 - Tentative End April 15, 2027
International Quality Consultants, Inc —Baxley, GA
- From $50 an hour
- Email
- 3 years
- Quality control
- In-person
Quick Apply
2d
Quality Inspector Level 3 / CMM Programmer
Modus Advanced, Inc. —Livermore, CA
- $55 - $65 an hour
- Full-time
- English
- High school diploma or GED
- Analysis skills
- Paid holidays
- Health insurance
Quick Apply
Aggregate QA/QC Technician III
Michels Corporation —Fond du Lac, WI
- Full-time
- Construction site
- Mid-level
- Driver's License
- Health savings account
- Disability insurance
Quick Apply
Quality Technician 2nd Shift (3:30pm-2:00am)
Exential —Tolleson, AZ
- $20 - $24 an hour
- Full-time
- Mid-level
- Office
- High school diploma or GED
- Health savings account
- Health insurance
Quick Apply
Quality Assurance Technician - 2nd Shift 3:00 - 11:00 PM|M-F
Vonco Products LLC —Trevor, WI
- $19 an hour
- Overtime
- Microsoft Word
- Computer literacy
- Bachelor of Science
Quick Apply
14d
Quality Control Analytical Color Matcher - 2nd Shift (3:00pm - 11:00pm) & 3rd Shift (11:00pm - 7:00a
DMI Personal Care —Wharton, NJ
- $24 an hour
- Full-time
- Ability to walk for extended periods
- Computer literacy
- Bachelor of Science
- Health insurance
- Dental insurance
Quick Apply
QA Inspector 2nd Shift (3:45pm-12:15am)
Ambrit Engineering Corp. —Santa Ana, CA
- $18 - $23 an hour
- 12 hour shift
- English
- High school diploma or GED
- Math
- Health insurance
- Dental insurance
Quick Apply
Quality Technician - 2 - 3 years experience in Manufacturing Quality 2nd & 3rd Shift
Diversified Engineering & Plastics LLC —Jackson, MI
- From $16 an hour
- Overtime
- Background check
- Computer literacy
- Basic math
- Health insurance
- Dental insurance
Quick Apply
Quality Technician III
Johnson Health Tech Retail Inc —Bloomington, MN
- $22.47 - $30.00 an hour
- Full-time
- Research
- Mid-level
- High school diploma or GED
- Health insurance
- Dental insurance
Quick Apply
Quality Inspector III (B,C & D Shifts)
SRG —Acton, MA
- $35 - $40 an hour
- Night shift
- 5 years
- In-person
- Senior level
Quick Apply
8d
Quality Assurance Technician (2nd shift / 3:00pm - 11:00pm)
Jetson Specialty Marketing —Hamburg, PA
- Full-time
- Mid-level
- High school diploma or GED
- Continuous improvement
- Health insurance
- Dental insurance
Quick Apply
Quality Technician III
Exegistics —Indianapolis, IN
- Temporary
- Microsoft Excel
- Microsoft Access
- 5 years
Quick Apply
5d
Quality Technician III
Edmund Optics, Inc. —Tucson, AZ
- $23 - $30 an hour
- Overtime
- Microsoft Word
- Microsoft Excel
- 5 years
- Health savings account
- Relocation assistance
8d
WAX INSPECTOR - Plant 3
Howmet Aerospace —Whitehall, MI
- Full-time
- Mid-level
- High school diploma or GED
- US work authorization
Quick Apply
Inspector 2 / 3
Northrop Grumman —Ridgecrest, CA
- $44,600 - $88,300 a year
- Overtime
- Computer literacy
- Mid-level
- High school diploma or GED
- Paid holidays
- Disability insurance
Quality Inspector III
Watts —Franklin, NH
- Full-time
- 6 years
- Office
- Residential
- Paid parental leave
- Paid holidays
C-Shift Quality Inspector III
Howmet Aerospace —Torrance, CA
- $21 - $30 an hour
- Full-time
- Mid-level
- US work authorization
- Manufacturing
- Paid holidays
- Health insurance
Quick Apply

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Scientist III (Quality Control Specialist)

Thermo Fisher Scientific -
High Point, NC

Apply Now

Job Details

Full-time

Benefits

Paid holidays
Health insurance
Dental insurance
Tuition reimbursement
Paid time off
Vision insurance
Benefits from day one
Retirement plan

Qualifications

Raw material quality management
Customer communication
Bachelor's degree
Pharmaceutical analysis
Chemical testing
Pharmaceutical manufacturing facility experience

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Division/Site Specific Information

Position is based High Point, North Carolina. Position will support our Drug Product Division (DPD) at Thermo Fisher Scientific.

Discover Impactful Work:

The Quality Control Specialist acts as a senior technical leader within the chemistry or microbiological quality control environment. Independently evaluates complex analytical, compendial, technical transfer, specification, change control, and quality system activities in support of pharmaceutical development, manufacturing, and commercial operations. Authors and manage test method lifecycle activities, risk assessments, reduced testing programs, quality system documentation, electronic document management activities, SAP quality data updates, and client-driven quality changes.

Day in the Life:

Interprets, verifies, and approves analytical data; leads quality initiatives through participation on group and department project teams; mentors junior team members; and advises on best practices, technical challenges, and industry trends.
Leads method lifecycle activities, including analytical gap assessments, method transfer, qualification, validation, and implementation of new or revised test procedures and specifications.
Assesses compendial updates for potential impact, authors compendial revision assessment protocols and reports, and initiates associated changes to test procedures, specifications, quality documents, or quality system records.
Owns or supports change controls for test procedures, specifications, reduced testing programs, client-requested changes, raw material changes, and associated quality system updates from initiation through approval and publication.
Partners with technical, quality, and client-facing teams to evaluate raw material manufacturer changes, alternate or new manufacturers, and related risk assessments, including necessary updates to specifications and test procedures.
Authors, revises, routes, and maintains quality documents, including analytical protocols, reports, work instructions, standard operating procedures, specifications, test procedures, and policy or instructional documents.
Maintains quality system and electronic document management activities, including document approval routing, periodic reviews, document publication, and subject matter expert support for controlled documentation systems.
Supports SAP quality activities, including new or revised material master quality data, certificate of analysis configuration, reduced testing profiles, inspection lot activities, and updates related to revised specifications or procedures.
Authors and revises elemental impurity and residual solvent assessments for new materials, additional manufacturers, manufacturer changes, and other quality or regulatory-driven updates.
Communicates technical conclusions clearly and accurately through documented analysis, reports, client interactions, cross-functional communications, and presentations to internal stakeholders or external partners.

Keys to Success:

Education:

Bachelor’s degree in a physical science, preferably Chemistry, Biology, Microbiology, or a related scientific discipline. Master’s degree in Chemistry, Biology, Microbiology, or a related scientific discipline preferred.

Experience and Qualifications:

Requires a minimum of 8 years of experience performing tests, analyses, technical documentation, method lifecycle activities, quality systems work, or related quality control support for pharmaceutical raw materials, finished products, microbiological samples, stability samples, or commercial manufacturing operations.

Competencies:

Strong knowledge of GMP, GLP, data integrity, controlled documentation, and pharmaceutical quality systems.
Proficient with analytical techniques including HPLC, GC, LC/MS, dissolution, spectroscopy, wet chemistry, and method validation.
Experienced in change control, technical transfer, specification management, risk assessment, reduced testing, and SAP quality processes.
Advanced problem-solving skills with the ability to resolve complex scientific, quality, and documentation challenges.
Excellent written, verbal, presentation, and client-facing communication skills.
Proven leadership, mentoring, prioritization, and cross-functional collaboration abilities.
Skilled in interpreting technical procedures, regulatory guidance, and quality system requirements.
Experienced in authoring and revising SOPs, specifications, protocols, reports, and quality documents.
Capable of managing complex customer, stakeholder, and regulatory inquiries.

Physical Requirements:

Capable of standing, walking, stooping, kneeling, and crouching for extended periods.
Able to lift, carry, and move materials weighing 10–35 lbs.
Strong hand and finger dexterity for equipment operation, typing, and laboratory tasks.
Visual acuity to operate instruments, use computers, and review technical documents.
Ability to sit, reach, communicate, and hear effectively for prolonged periods.
Wear required PPE, including safety glasses, safety shoes, lab coat, gloves, apron, and respirator as needed.

Excellent Benefits

Benefits & Total Rewards | Thermo Fisher Scientific
Medical, Dental, & Vision benefits-effective Day 1
Paid Time Off & Designated Paid Holidays
Retirement Savings Plan
Tuition Reimbursement

OTHER

Relocation assistance is NOT provided
Must be legally authorized to work in the United States now or in the future, without sponsorship.
Must be able to pass a comprehensive background check, which includes a drug screening.

Apply Now

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