2,339 Qc Professionals jobs in the United States

Job Description

Job Description

Position Summary:
Valbin Corporation is seeking a Quality Control (QC) Manager for a potential contract supporting the Federal Law Enforcement Training Center. The QC Technician conducts inspections, audits, and reports to ensure contract performance meets or exceeds government standards.
Valbin Corporation’s mission is to provide linguistic support, cultural sensitivity training, project management, and exercise support services to the US Government and private sector. Based in the Washington, D.C. Metropolitan Area, Valbin has an established and on-going partnership with the US Government through its GSA Schedule and the Valbin Mission Readiness Support Center.
As the cornerstone of Valbin's strength, Mission Readiness Support provides government agencies and service members with role players, battlefield immersions, and cultural awareness training. Valbin’s efforts ensure that the U.S. agencies receive the best possible training support.

**Position contingent upon contract award**

Requirements:

• Minimum of 3 years of experience in quality control, compliance, or contract monitoring, preferably in a government or training environment, within the last 10 years.
• Experience implementing and managing Quality Control Plans (QCPs).
• Strong knowledge of federal contract compliance standards.
• Proficiency in Microsoft Office Suite (Excel, Word, Outlook, Teams).
• Excellent attention to detail, analytical, and problem-solving skills.
• Strong written and verbal communication skills.
• Ability to conduct inspections and compile detailed reports.
• Experience in training, auditing, and process improvement.
• Ability to work independently and as part of a team.
• Prior experience in government contracting, training support, or logistics is a plus.
• Ability to coordinate and adjust schedule to fulfill the requirements of the contract; will include observation of night exercises.

Main Responsibilities:

• Implement and maintain the Quality Control Plan (QCP) in compliance with contract requirements.
• Conduct regular inspections and audits of training support, role player services, educational aides, supply management, and project management activities.
• Monitor contract performance metrics, ensuring all work meets the established quality standards.
• Investigate non-conformances and deficiencies, identifying root causes and recommending corrective actions.
• Document and report findings and trends, ensuring compliance with contractual obligations.
• Conduct employee training to reinforce quality and compliance expectations.
• Review and analyze data, logs, and reports to identify potential risks and improvement areas.
• Maintain detailed records of inspections, audits, and corrective actions.
• Collaborate with the Project Manager and government officials to ensure contract compliance.
• Assist in preparing for government audits and evaluations.
• Ensure safety and operational compliance across all contract activities.
• Provide quarterly reports on quality control performance and participate in performance review meetings.
• Perform other duties as assigned to support the overall success of contract operations.

Hours of Operation: Monday-Friday
Job Type: Contract
 

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The HT Group is hiring for an experienced Construction Quality Control (QC) Manager  to support a Data Center project in TX.  Responsible for the overall daily operations of quality related policies, procedures, techniques, initiatives on the project from start to completion.
 
Primary Duties:

• Works with project manager, superintendents, and subcontractors in developing processes and procedures that effectively accomplish the goal of 100% compliant work that exceeds expectations.
• Collaboration among project team and subcontractors
• Maintains active relationships with engineers, consultants, and industry association
• Assists teams with developing a project specific quality management plan
• Supports and follows up to ensure that project teams are following their project specific quality management plan
• Verify and document that all matters received for the project are in conformance with the approved submittal, are handled and stored appropriately, and are acceptable for use
• Oversee daily and weekly QC/QA reports that reinforce activities that are being constructed in conformance with established standards

Qualifications

• An associate or undergraduate university degree or higher (preferably in Quality Management, Construction Management, Engineering, or a closely related field) is preferred
• Other relevant education, training or work experience may substitute for bachelor’s degree
• Minimum of three (3) years of construction experience as a part of a quality control supervision
• Minimum of five (5) years industrial and/or commercial construction experience
• Experience with large/complex quality plan implementation

Regeneron is currently looking to for a Quality Control (QC) Analyst with a 1st shift, Monday-Friday, 8am-4:30pm schedule to join our Gels Team. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. The QC Analyst will be part of the lot release for market use of our products. They will perform a variety of biochemical analyses on products, in-process materials or stability samples in support of the company's quality programs.
As a QC Analyst, a typical day might include the following:
+ Develops and maintains efficient processes to support commercial testing in laboratory functions. Examples include management of materials, reagents, equipment, electronic systems, documents, laboratory safety and inspection readiness.
+ Conduct testing on in-process, product, stability and/or research samples.
+ Executes and/or coordinates the completion of lab operations activities.
+ Ensures timely completion of activities impacting the QC commercial operations.
+ Review test results to ensure compliance with standards; report any quality anomalies.
+ Perform laboratory OOT, atypical and OOS investigations.
+ Writes and revises control test procedures and SOPs.
+ Conduct efforts to continuously improve processes while maintaining GxP compliance and keeping tasks on track.
+ May be responsible for maintain a specific project.
+ May devise and develop new analytical methods and techniques.
+ May assist in validation of methods.
+ May be involved in establishing the transfer of methodology from R&D.
This role might be for you if you:
+ Are able to maintain integrity and honesty at all time.
+ Enjoy working independently or as part of a team.
+ Thrive in a fast-paced setting where your priorities can quickly change based on the needs of the business and our patients.
+ Have effective time management skills to work on multiple projects.
+ Have strong interpersonal skills.
+ Have excellent written and verbal communication skills
To be considered for the QC Analyst position you must be willing and able to work 1st shift, Monday-Friday, 8am-4:30pm. You must have the following; BS/BA in Life Sciences or related field or AS/AAS Degree/Certificate in Biotechnology/Biological Science, or an equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
**Salary Range (hourly)**
$24.38 - $43.80

The HT Group is hiring for an experiencedConstructionQuality Control (QC) Manager to support a Data Center project in TX. Responsible for the overall daily operations of quality related policies, procedures, techniques, initiatives on the project from start to completion.

Primary Duties:

• Works with project manager, superintendents, and subcontractors in developing processes and procedures that effectively accomplish the goal of 100% compliant work that exceeds expectations.
• Collaboration among project team and subcontractors
• Maintains active relationships with engineers, consultants, and industry association
• Assists teams with developing a project specific quality management plan
• Supports and follows up to ensure that project teams are following their project specific quality management plan
• Verify and document that all matters received for the project are in conformance with the approved submittal, are handled and stored appropriately, and are acceptable for use
• Oversee daily and weekly QC/QA reports that reinforce activities that are being constructed in conformance with established standards

Qualifications

• An associate or undergraduate university degree or higher (preferably in Quality Management, Construction Management, Engineering, or a closely related field) is preferred
• Other relevant education, training or work experience may substitute for bachelors degree
• Minimum of three (3) years of construction experience as a part of a quality control supervision
• Minimum of five (5) years industrial and/or commercial construction experience
• Experience with large/complex quality plan implementation

JOB SUMMARY:
Responsible for park wide quality control inspections and audits in one or more of the following areas: Dimensional conformity, fiberglass laminate construction (FRP)/carbon fiber composites, material specification conformity, mechanical and structural non-destructive testing (NDT), process specification conformity, receiving, and welding. Provides neat, timely, and accurate inspection reports; facilitates problem resolution; provides input to Engineering and/or Management in areas of expertise during problem resolution or project planning stage(s). Performs all duties in accordance with Universal Orlando and Technical Services Engineering /Quality Control Departments policies and procedures.
MAJOR RESPONSIBILITIES:
+ Inspection of Ride and Show related elements including ride tracks, ride vehicles and all ride related components to assure product quality, accuracy, quality of workmanship, conformity to material specifications and welding procedure specifications (WPS) in accordance with the applicable codes and UO QC NDT procedures.
This includes both final products and in-process items. Also includes inspection of welding setups, excavations of defects, preparation and final welding using visual, magnetic particle, and liquid penetrant methods; inspection of received parts and components for dimensional accuracy; material conformity to specifications; and inspection of fiberglass/carbon fiber composite assemblies, both in-process and for final acceptance. Perform Non-Destructive Testing (NDT MT/ PT/ VT NDT methods) of structural and mechanical ride and facility equipment.
+ Provides detailed/ accurate written reports of all inspections performed in a timely manner.
+ Communicates clear and accurate information as needed to UOR Engineering Team.
+ Research at Document Control, with Vendors, and Internet Sites for information and data relevant to inspection of goods under scrutiny.
+ Understands and actively participates in Environmental, Health & Safety responsibilities by following established UO policy, procedures, training and team member involvement activities.
+ Performs other duties as assigned.
EDUCATION:
+ Technical school is preferred.
+ Associate degree (AA) or (AS) in quality or related field is preferred.
EXPERIENCE:
+ Required - 1+ Year: experience in a technical field.
+ Preferred - 1 Year: Experience with major Ride and Show attractions and performing inspections of structural (including bolting), mechanical, hydraulic and pneumatic equipment elements essential to those attractions.
+ Preferred 1 Year: Experience or can show experience in or provide documented proof in performing NDT Inspection of equipment using Visual Inspection (VT), Magnetic Particle Inspection (MT) and Liquid Penetrant Inspections (PT).
+ Preferred -1 Year: Experience working with machine and weld shop fabrication and Q/C inspection for compliance with mechanical drawings;
+ or equivalent combination of education and experience.
Your talent, skills and experience will be rewarded with a competitive compensation package.
Universal is not accepting unsolicited assistance from search firms for this employment opportunity. All resumes submitted by search firms to any employee at Universal Orlando via-email, the Internet or in any form and/or method without a valid written Statement of Work in place for this position from Universal Orlando HR/Recruitment will be deemed the sole property of Universal Orlando. No fee will be paid in the event the candidate is hired by Universal Orlando as a result of the referral or through other means.
Universal Orlando Resort. Here you can.
Universal Orlando is an equal opportunity employer. Universal elements and all related indicia TM & © 2025 Universal Studios. All rights reserved. EOE

We're here for one reason and one reason only - to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.
Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows.
**Job Description**
We are seeking a highly motivated individual to join us as a **QC Technician I, Quality Control Lab Support** , reporting to the Manager, Quality Control Lab Support in Frederick, MD. In this role, you will execute tasks associated with sample management, shipment of samples, and other lab support QC functions, while interacting cross-functionally with personnel from other QC groups, Quality Assurance, Analytical Development, Manufacturing, Material Management (MM), and corporate teams.
Shift: **Wednesday through Saturday from 3pm to 2am**
**Key Responsibilities**
+ Receive incoming samples, verify documentation, and log sample information into LIMS.
+ Execute processes to support sample receipt and processing or aliquoting for release/stability testing and retains.
+ Label, store, and organize samples according to established procedures and storage requirements.
+ Coordinate sample transfers to internal and external testing labs.
+ Perform routine cleaning, maintenance, and restocking of sample storage areas.
+ Collaborate with MM, QA, and other QC functions-including Corporate QC-to support requirements around sampling, testing, and disposition.
+ Manage and complete all shipping activities
+ within QC functions.
+ Complete routine review of records, such as sample chain of custody forms, processing logs, logbooks, and other documentation generated within QC Lab Support.
+ Assist with deviation and investigation activities as needed.
+ Provide updates during daily and weekly meetings.
+ Participate in Lean Lab and other Operational Excellence initiatives.
+ Comply with all safety, quality, and regulatory guidelines.
+ Perform other duties as assigned.
**Basic Qualifications**
+ AA Degree and 1+ years of relevant experience: OR
+ High School diploma and 2+ years' experience
+ Experience working in Quality Control or biopharma laboratories (preferably in an FDA regulated laboratory)
**Preferred Qualifications**
+ Strong knowledge in applying GMP in QC lab.
+ Exceptional attention to detail and ability to keep track of multiple ongoing projects
+ Proficient in Microsoft Office, Excel, Visio, and other related applications
+ Excellent interpersonal, verbal and written communications skills which are essential in this collaborative work environment
+ Comfortable in a fast-paces small company environment and able to adjust workload based on changing priorities.
+ Ability to be flexible with schedule, and work overtime as needed ( **s** **hift** : **Wednesday thru Saturday 3pm to 2am)**
The salary range for this position is: $55,930.00 - $72,380.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.
For additional benefits information, visit:
Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit . Sign up to follow @KitePharma on Twitter at .
**For jobs in the United States:**
Kite Pharma is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact for assistance.
For more information about equal employment opportunity protections, please view the 'Know Your Rights' ( poster.
NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT ( RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT
Kite Pharma will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law.
Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.
Kite Pharma provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.
**For Current Kite Pharma Employees and Contractors:**
Please apply via the Internal Career Opportunities portal in Workday.
**Change The World With Us**
Everyone at Kite is grounded by one common goal - curing cancer. Every day, we aim to establish a direct line between that purpose and our day-to-day work.
We are creating Kite together, with the recognition that the best teams are built by the best people. We maintain an attitude of curiosity, and creativity with each challenge as we develop a new market for cancer therapies. We appreciate and respect one another, and most importantly, we don't take success for granted.
While we've come a long way to make what others viewed as impossible, possible, we know one thing is certain. Today is just the beginning.