QC Scientist
Memphis, TN · On-site
This position is responsible for carrying out T-SPOT assays and other processes during validation of procedures, QC of finished product and raw materials, and to support the Quality Manager in the ...
Memphis, TN · On-site
This position is responsible for carrying out T-SPOT assays and other processes during validation of procedures, QC of finished product and raw materials, and to support the Quality Manager in the ...
Memphis, TN · On-site
This position is responsible for carrying out T-SPOT assays and other processes during validation of procedures, QC of finished product and raw materials, and to support the Quality Manager in the ...
Florence, KY · On-site
Join us at Thermo Fisher Scientific as a QC Scientist I to contribute to global health through quality control testing that ensures the safety and efficacy of pharmaceutical products. You will ...
Florence, KY · On-site
Join us at Thermo Fisher Scientific as a QC Scientist I to contribute to global health through quality control testing that ensures the safety and efficacy of pharmaceutical products. You will ...
Qualifications Minimum 5 - 8 years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry. BS/BA Degree in Science/related field or other appropriate education ...
Qualifications Minimum 5 - 8 years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry. BS/BA Degree in Science/related field or other appropriate education ...
Quality Control Scientist I Reports To: Quality Control Supervisor Group/Division: MBD Career Band: Band IV Job Track: Quality Control Position Location: Lenexa, Kansas Number of Direct Reports none ...
Quality Control Scientist I Reports To: Quality Control Supervisor Group/Division: MBD Career Band: Band IV Job Track: Quality Control Position Location: Lenexa, Kansas Number of Direct Reports none ...
Florence, KY · On-site
As a QC Scientist II, you'll conduct complex analytical testing to support GMP manufacturing of biopharmaceutical products, from early-stage clinical development through commercial release. You'll ...
Florence, KY · On-site
As a QC Scientist II, you'll conduct complex analytical testing to support GMP manufacturing of biopharmaceutical products, from early-stage clinical development through commercial release. You'll ...
Florence, SC · On-site
As a QC Scientist II, you'll conduct complex analytical testing to support GMP manufacturing of biopharmaceutical products, from early-stage clinical development through commercial release. You'll ...
Florence, SC · On-site
As a QC Scientist II, you'll conduct complex analytical testing to support GMP manufacturing of biopharmaceutical products, from early-stage clinical development through commercial release. You'll ...
San Diego, CA · On-site
$95K - $115K/yr
The Quality Control Scientist, Controls will lead the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
San Diego, CA · On-site
$95K - $115K/yr
The Quality Control Scientist, Controls will lead the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
$95K - $115K/yr
The Quality Control Scientist, Controls will lead the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
$95K - $115K/yr
The Quality Control Scientist, Controls will lead the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
The Quality Control Scientist, Controls will lead the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
Quick apply
The Quality Control Scientist, Controls will lead the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for ...
Fishers, IN · On-site
Description Weekend QC Scientist Summary The Weekend QC Scientist supports GMP manufacturing and laboratory operations by performing routine microbiology and chemistry testing, sample handling, and ...
Fishers, IN · On-site
Description Weekend QC Scientist Summary The Weekend QC Scientist supports GMP manufacturing and laboratory operations by performing routine microbiology and chemistry testing, sample handling, and ...
Weekend QC Scientist Summary The Weekend QC Scientist supports GMP manufacturing and laboratory operations by performing routine microbiology and chemistry testing, sample handling, and laboratory ...
Weekend QC Scientist Summary The Weekend QC Scientist supports GMP manufacturing and laboratory operations by performing routine microbiology and chemistry testing, sample handling, and laboratory ...
Fishers, IN · On-site
Weekend QC Scientist Summary The Weekend QC Scientist supports GMP manufacturing and laboratory operations by performing routine microbiology and chemistry testing, sample handling, and laboratory ...
Fishers, IN · On-site
Weekend QC Scientist Summary The Weekend QC Scientist supports GMP manufacturing and laboratory operations by performing routine microbiology and chemistry testing, sample handling, and laboratory ...
Los Angeles, CA · On-site
$86K - $184K/yr
The Lead QC Scientist will oversee compendial and non-compendial methods for test of products manufactured/prepared at the HGCTF. The Lead QC Scientist will lead and perform analytical testing of ...
Los Angeles, CA · On-site
$86K - $184K/yr
The Lead QC Scientist will oversee compendial and non-compendial methods for test of products manufactured/prepared at the HGCTF. The Lead QC Scientist will lead and perform analytical testing of ...
Weekend QC Scientist Summary The Weekend QC Scientist supports GMP manufacturing and laboratory operations by performing routine microbiology and chemistry testing, sample handling, and laboratory ...
New
Weekend QC Scientist Summary The Weekend QC Scientist supports GMP manufacturing and laboratory operations by performing routine microbiology and chemistry testing, sample handling, and laboratory ...
New
Fishers, IN · On-site
Weekend QC Scientist Summary The Weekend QC Scientist supports GMP manufacturing and laboratory operations by performing routine microbiology and chemistry testing, sample handling, and laboratory ...
New
Quick apply
Fishers, IN · On-site
Weekend QC Scientist Summary The Weekend QC Scientist supports GMP manufacturing and laboratory operations by performing routine microbiology and chemistry testing, sample handling, and laboratory ...
New
The QC Scientist I works in a fast-paced environment supporting the quality control department cell therapy analytical method qualifications and validations. The QC Scientist I will be responsible ...
The QC Scientist I works in a fast-paced environment supporting the quality control department cell therapy analytical method qualifications and validations. The QC Scientist I will be responsible ...
The QC Scientist I works in a fast-paced environment supporting the quality control department cell therapy analytical method qualifications and validations. The QC Scientist I will be responsible ...
Quick apply
The QC Scientist I works in a fast-paced environment supporting the quality control department cell therapy analytical method qualifications and validations. The QC Scientist I will be responsible ...
The QC Scientist I works in a fast-paced environment supporting the quality control department cell therapy analytical method qualifications and validations. The QC Scientist I will be responsible ...
The QC Scientist I works in a fast-paced environment supporting the quality control department cell therapy analytical method qualifications and validations. The QC Scientist I will be responsible ...
$31 - $40/hr
Eurofins PSS is seeking a QC Scientist to help launch and support a new raw materials testing facility. This role will perform testing in compliance with cGMP guidelines and support team leadership ...
$31 - $40/hr
Eurofins PSS is seeking a QC Scientist to help launch and support a new raw materials testing facility. This role will perform testing in compliance with cGMP guidelines and support team leadership ...
Monday - Friday 8:00am - 5:00pm Purpose and Scope The Quality Control Scientist I - NMR is a technical leader within the QC functional area with a primary role in scientific development, testing and ...
Monday - Friday 8:00am - 5:00pm Purpose and Scope The Quality Control Scientist I - NMR is a technical leader within the QC functional area with a primary role in scientific development, testing and ...
$17.31 - $21.31
4% of jobs
$24.70 is the 25th percentile. Wages below this are outliers.
$21.31 - $25.31
24% of jobs
$25.31 - $29.31
19% of jobs
The median wage is $29.88 / hr.
$29.31 - $33.30
15% of jobs
$37.14 is the 75th percentile. Wages above this are outliers.
$33.30 - $37.30
13% of jobs
$37.30 - $41.30
7% of jobs
$41.30 - $45.30
4% of jobs
$45.30 - $49.30
1% of jobs
$49.30 - $53.30
5% of jobs
$53.30 - $57.30
2% of jobs
$57.30 - $61.30
4% of jobs
$17
$34
$61
A Quality Control Scientist ensures that products meet required safety, quality, and regulatory standards. They perform laboratory tests, analyze data, and identify deviations in manufacturing processes. Their role is crucial in industries like pharmaceuticals, biotechnology, and food production to maintain compliance and product consistency. They also collaborate with production teams to implement corrective actions and improve quality control procedures.
A Quality Control Scientist typically needs a solid background in chemistry, biology, or related sciences, backed by a relevant degree and experience with laboratory testing protocols. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practice (GMP) standards, and analytical instruments such as HPLC or GC is crucial, and certifications like ASQ or Six Sigma can be advantageous. Strong attention to detail, analytical thinking, and effective communication skills help individuals excel in this role. These competencies ensure precise, compliant testing processes and facilitate reliable product quality in regulated industries.
Quality Control Scientists often face challenges such as meeting tight production deadlines while maintaining strict adherence to regulatory and quality standards. They must also troubleshoot unexpected test results or equipment issues, which requires patience and analytical problem-solving skills. In addition, collaborating with cross-functional teams, such as manufacturing or R&D, to resolve quality concerns can present communication and coordination challenges. Overcoming these obstacles is essential to ensure that products consistently meet required specifications and industrial regulations.

A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Our client is a public and rapidly growing diagnostics company that is looking to expand their Quality team in Memphis TN. They are willing to assist with relocation. This position will have no direct reports.
This position is responsible for carrying out T-SPOT assays and other processes during validation of procedures, QC of finished product and raw materials, and to support the Quality Manager in the running of the Quality Management System and general administration of documentation for the QMS. This will include the following:
Overall responsibilities:
1. Maintenance of reference material, including cell culture and stock validation
2. QC of raw materials, incoming goods and any product manufactured by Oxford Immunotec
3. QC of manufactured products and assembled kits
4. Validation of procedures, equipment and software
5. Planning and conducting of stability testing procedures
6. Performing other laboratory testing as required
7. Maintaining the equipment databases to ensure all equipment is calibrated, maintained and serviced as required
8. Assisting with the control of Quality Management system documentation
9. Assisting with the preparation of further documentation for the Quality Management system
10. Assisting with the monitoring of compliance with the QMS and with tracking systems associated with CLIA, CAP, State requirements, ISO 13485:2012, ISO 9001:2008 and ISO 17025:2005 and the QSR
11. Assist the Quality Manager to ensure the continuing effectiveness of the QMS
12. Assist during internal and external audits
13. Conduct laboratory spot check audits
14. Assist with the QA review of documentation including non-conformances, CAPAs and complaints
15. Perform miscellaneous duties as necessary and requested by the Quality Manager
Specific deliverables for the role are:
1. Contributing towards the maintenance of the quality of the Company's products in fulfillment of the Company goals
2. Control and conduct of product stability testing to support expiry dates and shipping claims
3. Monitoring of product conformity through archive kit testing
4. Assisting with ensuring compliance in the manufacturing process and documentation
5. Ensure that areas of responsibility do not contribute to any major non-conformance during external audits for GMP, ISO 13485:2003, ISO 17025:2005 and ISO 9001:2008
6. Regular communication with QA/QC team members and other functional groups to provide QC and validation support for both Process and Design controls
7. Working to Oxford Immunotec's Company Values at all times.
8. Follows all company safety policies & other safety precautions within work area
9. Regular attendance and timeliness is essential
QUALIFICATIONS:
Bachelor's degree, or college education and equivalent experience
5+ years Quality experience, preferably in laboratory or medical device environmen
***Must have cell culture experience***
Good working knowledge of MS Office
Experienced in working to GLP and Quality Management principles
Strong attention to detail and Quality commitment
High standards of mathematics and writing ability
Conscientious, thrives in high pressure work, and demonstrates strong initiative
PHYSICAL DEMANDS:
The physical demands described within the Position Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Minimal travel required including international travel. Job requires employee to walk considerable distances in the facility during the course of his or her work.
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Recruiting and staffing services
51 - 200 Employees
Edison, NJ, US
1996