262 Quality Control Specialists jobs in North Carolina

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
**Primary Responsibilities:**
+ **Participate in the development and review of the Clinical SOPs, Regulatory documents and Study Plans**
+ Participate in the Clinical SOPs periodic reviews as well as in the creation of new procedures
+ Participate in the study plans reviews
+ Participate in the review of Regulatory Documents (Clinical Study Protocol, Investigators Brochure, Informed Consent Form, Clinica Study Report)
+ **Provide quality oversight on the conduct of the clinical studies**
+ Perform periodic quality reviews of the critical clinical procedures on the different clinical studies
+ Interact with Drug Development department to provide guidance and consultancy to resolve compliance issues
+ Coordinate the management of study, internal and vendor deviations
+ Participate in the review of critical protocol deviations and Serious Breaches
+ Participate in project team internal meetings providing information about quality metrics of studies
+ **Collaborate in the development of the Quality Risk Management Assessment of the different clinical studies**
+ Initiate the Quality Risk Assessment for every clinical study
+ **Qualification and periodic assessment of clinical and pharmacovigilance vendors participating in the clinical studies**
+ Perform a quality assessment (including a risk assessment) of all the vendors selected as candidates to participate in the clinical studies
+ Qualify the clinical vendors before their participation in the clinical studies and re-qualify them when applicable
+ Perform an annual assessment of the performance and compliance of the vendors participating in the clinical studies
**Requirements:**
+ Life Sciences Degree.
+ A minimum of 5 years in a similar role or provide experience in Quality and Clinical Trials.
+ Ability and willingness to travel.
+ Ability to work both in a team and independently.
+ Ability to meet deadlines, multitasks, and prioritize based on study needs.
+ Ability to works on assignments with a diverse scope.
+ Ability to work with a very limited direct supervision.
+ Advanced knowledge of ICH/GCP Guideline.
+ Advanced knowledge of electronic data capture (EDC) systems.
+ Advanced knowledge of medical terminology.
+ Advanced knowledge of the therapeutic areas assigned.
+ Routinely demonstrates mastery of technical skills
**Occupational Demands Form:**
Work is performed in an office environment with exposure to electrical office equipment. Frequently sits for 6-8 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Occasionally walks and stands. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 25lbs. Frequently drives to site locations with occasional travel within the United States. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken and written words and sentences. Interacts with others, relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues.
Third Party Agency and Recruiter Notice:
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
**Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.**
Learn more about Grifols ( ID:**
**Type:** Regular Full-Time
**Job Category:** Quality

Hourly Wage: **$21.1 - $4.6 per/hour**
*The actual hourly rate will equal or exceed the required minimum wage applicable to the job location.
Additional compensation includes annual or quarterly performance incentives.
Additional compensation in the form of premiums may be paid in amounts ranging from 0.35 per hour to 3.00 per hour in specific circumstances. Premiums may be based on schedule, facility, season, or specific work performed. Multiple premiums may apply if applicable criteria are met.
Employment Type: **Full-Time**
Available shifts: **Weekend - 4th**
Location
**Supply Chain Grocery #6858**
2837 SENATOR RALPH SCOTT PARKWAY, MEBANE, NC, 27302, US
Job Overview
Career opportunities in Administration and Clerical roles include Service Shop and Maintenance Clerk, Quality Assurance, System Operator. Administration roles such as Human Resource Clerk and Office Assistant.
Benefits & perks
At Walmart, we offer competitive pay as well as performance-based incentive awards and other great benefits for a happier mind, body, and wallet. Health benefits include medical, vision and dental coverage. Financial benefits include 401(k), stock purchase and company-paid life insurance. Paid time off benefits include parental leave, family care leave, bereavement, jury duty, and voting. Other benefits include short-term and long-term disability, company discounts, Military Leave Pay, adoption and surrogacy expense reimbursement, and more.
You will also receive PTO and/or PPTO that can be used for vacation, sick leave, holidays, or other purposes. The amount you receive depends on your job classification and length of employment. It will meet or exceed the requirements of paid sick leave laws, where applicable. For information about PTO, see Smart Guide page ( Better U is a Walmart-paid education benefit program for full-time and part-time associates in Walmart and Sam's Club facilities. Programs range from high school completion to bachelor's degrees, including English Language Learning and short-form certificates. Tuition, books, and fees are completely paid for by Walmart.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to a specific plan or program terms. For information about benefits and eligibility, see One.Walmart.com.
Walmart is committed to maintaining a drug-free workplace and has a no tolerance policy regarding the use of illegal drugs and alcohol on the job. This policy applies to all employees and aims to create a safe and productive work environment.
Walmart, Inc. is an Equal Opportunity Employer- By Choice. We believe we are best equipped to help our associates, customers, and the communities we serve live better when we really know them. That means understanding, respecting, and valuing diversity- unique styles, experiences, identities, abilities, ideas and opinions- while being inclusive of all people.

Title: QC Investigations, Senior Specialist Location: A regulated manufacturing site is seeking a Senior Quality Control professional to lead laboratory investigations and support continuous improvement within the quality system. Lead investigations into laboratory incidents, data trends, and unexpected results.

Develop and document CAPAs and formal investigation reports.

Collaborate with QC and cross-functional teams to resolve quality issues.

Analyze data and present findings to site and corporate leadership.

Support regulatory submissions and documentation for post-approval changes.

Conduct training on investigation procedures, GMP compliance, and lab systems.

Participate in project teams and continuous improvement initiatives.

Bachelor's degree with 4+ years of experience in QC and GMP environments (or equivalent).

Strong understanding of pharmaceutical quality systems, analytical chemistry, and GMP standards.

Effective communication and data analysis skills;

Job Summary:

We are seeking a highly motivated QC Technical Specialist with expertise in vaccine manufacturing and quality control processes. This role provides technical support for QC operations, business systems, and equipment, ensuring compliance with quality objectives and driving process improvements. The ideal candidate will have strong attention to detail, excellent communication skills, and the ability to collaborate across cross-functional teams.

Key Responsibilities:

• Lead deviation (DR) investigations, identify root causes, and implement corrective and preventative actions (CAPAs) to prevent recurrence.
• Initiate and perform EDMS workflows, including change control, self-inspections, and CAPA actions.
• Support business process systems related to QC, including SAP, LIMS, EDMS, LMS, and Work Order Tracking.
• Track work orders, metrics (KPIs), and project statuses, and deliver presentations to team and cross-functional groups.
• Perform GMP documentation activities and adhere to defined schedules.
• Work within standard operating procedures and scientific methods, ensuring compliance with quality guidelines.
• Demonstrate exceptional teamwork and a willingness to support colleagues beyond assigned responsibilities.

Minimum Qualifications:

• 2+ years of experience in vaccine manufacturing.
• Bachelor’s or Associate degree in a scientific discipline.
• Ability to interpret and follow detailed instructions.
• Strong attention to detail.
• Excellent written and verbal communication skills.
• Experience with technical writing, particularly investigations, preferred.

Preferred Qualifications:

• Knowledge of GMPs and safety regulations.
• Familiarity with data integrity principles.

Job Title: Quality Control Chemist
Job Description
We are seeking a dedicated Quality Control Chemist to perform routine analytical testing of raw materials, in-process samples, and finished products, along with wastewater sampling and adjustments. The role requires strict adherence to standard operating procedures and conducting triplicate assessments on testing procedures to ensure accuracy and compliance.
Responsibilities
+ Ensure compliance with safety, health, and environmental protocols by wearing proper personal protective equipment.
+ Adhere to the company's Code of Conduct while conducting all business activities.
+ Perform in-process and finished product testing on various products.
+ Complete laboratory records and other documentation accurately following good documentation practices.
+ Communicate with the Shift Production Supervisor regarding in-process batch adjustments based on analytical test results.
+ Maintain cleanliness of the work area and notify colleagues when consumables need to be ordered.
+ Keep the workplace organized and orderly.
+ Facilitate effective communication within the Quality Control department and with other business units and customers.
Essential Skills
+ Understanding and adherence to safety, health, and environmental standards in the laboratory and facility.
+ Ability to communicate effectively and relate to employees at all levels within the company.
+ Ability to work independently while adjusting to the priorities of production.
+ Capability to walk and stand for extended periods.
Additional Skills & Qualifications
+ Bachelor's degree in a science discipline, with a preference for Chemistry.
+ Familiarity with basic laboratory equipment such as GC/LC/FTIR and techniques like titration and liquid-liquid partition.
+ Previous laboratory experience is preferred.
+ Basic computer skills, including familiarity with spreadsheet programs.
+ Strong math and analytical problem-solving skills.
+ At least 5 years of previous work experience.
+ Self-motivated and well-organized individual.
+ Proficient in speaking, reading, and writing English.
Pay and Benefits
The pay range for this position is $26.00 - $28.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in SALISBURY,NC.
Application Deadline
This position is anticipated to close on Oct 17, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

Job Title: Quality Control Chemist
Job Description
We are seeking a dedicated Quality Control Chemist to perform routine analytical testing of raw materials, in-process samples, and finished products, along with wastewater sampling and adjustments. The role requires strict adherence to standard operating procedures and conducting triplicate assessments on testing procedures to ensure accuracy and compliance.
Responsibilities
+ Ensure compliance with safety, health, and environmental protocols by wearing proper personal protective equipment.
+ Adhere to the company's Code of Conduct while conducting all business activities.
+ Perform in-process and finished product testing on various products.
+ Complete laboratory records and other documentation accurately following good documentation practices.
+ Communicate with the Shift Production Supervisor regarding in-process batch adjustments based on analytical test results.
+ Maintain cleanliness of the work area and notify colleagues when consumables need to be ordered.
+ Keep the workplace organized and orderly.
+ Facilitate effective communication within the Quality Control department and with other business units and customers.
Essential Skills
+ Understanding and adherence to safety, health, and environmental standards in the laboratory and facility.
+ Ability to communicate effectively and relate to employees at all levels within the company.
+ Ability to work independently while adjusting to the priorities of production.
+ Capability to walk and stand for extended periods.
Additional Skills & Qualifications
+ Bachelor's degree in a science discipline, with a preference for Chemistry.
+ Familiarity with basic laboratory equipment such as GC/LC/FTIR and techniques like titration and liquid-liquid partition.
+ Previous laboratory experience is preferred.
+ Basic computer skills, including familiarity with spreadsheet programs.
+ Strong math and analytical problem-solving skills.
+ At least 5 years of previous work experience.
+ Self-motivated and well-organized individual.
+ Proficient in speaking, reading, and writing English.
Pay and Benefits
The pay range for this position is $26.00 - $28.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in SALISBURY,NC.
Application Deadline
This position is anticipated to close on Oct 14, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

Job Title: Quality Control Chemist
Job Description
We are seeking a dedicated Quality Control Chemist to perform routine analytical testing of raw materials, in-process samples, and finished products, along with wastewater sampling and adjustments. The role requires strict adherence to standard operating procedures and conducting triplicate assessments on testing procedures to ensure accuracy and compliance.
Responsibilities
+ Ensure compliance with safety, health, and environmental protocols by wearing proper personal protective equipment.
+ Adhere to the company's Code of Conduct while conducting all business activities.
+ Perform in-process and finished product testing on various products.
+ Complete laboratory records and other documentation accurately following good documentation practices.
+ Communicate with the Shift Production Supervisor regarding in-process batch adjustments based on analytical test results.
+ Maintain cleanliness of the work area and notify colleagues when consumables need to be ordered.
+ Keep the workplace organized and orderly.
+ Facilitate effective communication within the Quality Control department and with other business units and customers.
Essential Skills
+ Understanding and adherence to safety, health, and environmental standards in the laboratory and facility.
+ Ability to communicate effectively and relate to employees at all levels within the company.
+ Ability to work independently while adjusting to the priorities of production.
+ Capability to walk and stand for extended periods.
Additional Skills & Qualifications
+ Bachelor's degree in a science discipline, with a preference for Chemistry.
+ Familiarity with basic laboratory equipment such as GC/LC/FTIR and techniques like titration and liquid-liquid partition.
+ Previous laboratory experience is preferred.
+ Basic computer skills, including familiarity with spreadsheet programs.
+ Strong math and analytical problem-solving skills.
+ At least 5 years of previous work experience.
+ Self-motivated and well-organized individual.
+ Proficient in speaking, reading, and writing English.
Pay and Benefits
The pay range for this position is $26.00 - $28.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in SALISBURY,NC.
Application Deadline
This position is anticipated to close on Oct 15, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

**Quality Control Inspector**
PeopleReady of Hickory, NC is now hiring Quality Control Inspectors in Morganton, NC!
Apply today and you could start as soon as tomorrow.
**As a PeopleReady associate you'll benefit from:**
+ Next-day pay for many of our open positions
+ The choice of long-term positions for steady work or short-term positions for extra cash
+ The convenience of applying for and accepting jobs right from our mobile app, JobStack! Text "READY" to 81555 to download JobStack and get started today
**Pay Rate:**
_The pay rate for this job is $14.50 - $15 / hour*_
**What you'll be doing as a Quality Control Inspector:**
+ Inspect raw materials to ensure consistency and integrity
+ Maintain, test, and troubleshoot all QA devices
+ Test a certain percentage of all products based on industry standards
+ Report problems or concerns to management
+ Assist with various production tasks as needed
**Available shifts:**
Shift Timings: 1st Shift (Day)
**Job requirements:**
+ Previous QA/QC experience helpful
+ Ability to stand, lift and bend frequently
+ Meticulous attention to detail
+ Basic math skills
+ Strong communication skills
+ Background check and drug screening required
**Ready to take control of the way you work?**
Complete our application to join the PeopleReady team today.
**Please contact our Hickory, NC branch for more information:**
**Branch # 3307**
**Address: 509 2nd Ave SW, Hickory, NC **
**Email Address: **
*Hourly pay rates are a good-faith estimate based on factors such as relevant skills, experience, education, training, geographic location and other considerations permitted by law. An employee's pay history will not be a contributing factor where prohibited by local law. Applications are accepted on an ongoing basis unless a deadline is otherwise stated.
Employees and their eligible dependents are offered Medical/Dental/Vision insurance and short term disability, in addition to other programs ,as well as number of paid days off and/or more generous paid sick leave days). More details about our benefits can be found by copying and pasting this URL into your browser: Associate Benefits Guide ( considers all applicants for employment regardless of background, in compliance with applicable laws regarding fair hiring practices. PeopleReady is an equal opportunity employer, all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, sexual orientation, gender identity, or any other characteristics protected by law. We consider qualified applicants with arrest and conviction records in accordance with applicable law.
TrueBlue, Inc. and its brands welcome and encourage applications from candidates with disabilities. Accommodations are available on request for candidates taking part in the selection process. If you require disability-related accommodation during the recruitment process, please contact your Recruiter or Employee Relations at or . TrueBlue, Inc. and its brands will consult with all applicants who request disability-related accommodation during the recruitment process to ensure that the accommodation provided takes into account the applicant's individual accessibility needs.
#PriL
PeopleReady is an equal opportunity employer, and we value diversity. We do not discriminate based on race, religious affiliation, color, national origin, gender, age, marital status, sexual orientation, gender identity, veteran status, disability, or any other basis protected by law. We will get to know you and connect you with jobs that match your skills, experience and preferences. We work hard every single day to find jobs so each employee has opportunity and variety in their work.