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Quality Control Supervisor - Manassas, VA

Lucas Group
Manassas, VA
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* This company is specifically seeking candidates with U.S. military experience *

What You Will Do :

Responsibilities include providing quality guidance, product resolution decisions, and statistical problem-solving techniques to manufacturing operations and project teams for new product introduction, process improvements, continuous improvements, and validation activities. Responsible for the quality of the product and process for the assigned product line(s). Will directly supervise quality control associates across all production crews.

  • Coordinates product team support for receiving inspection, manufacturing operations and the release of product (including, customer complaints, help desk responses, statistical analysis, validation support, inspection plans, quality metrics and reporting functions.)
  • Support the investigation of Corrective & Preventive Actions (CAPA), product non-conformances, and of customer complaints, providing solutions where possible; support Continuous Improvement activities.
  • Develop and implement incoming inspection plans for raw materials.
  • Develop/Revise Quality Plans including incoming, in-process, and final inspection; provide training to those affected by the plans.
  • Implement proven inspection and metrology improvements and associated training.
  • Create / Revise technical process documents that fit the business needs and maintain compliance to the regulatory requirements of the FDA and ISO standards.
  • Serve as a resource for performing internal audits to ensure quality system compliance.
  • Process incoming customer complaints assist with complaint investigations and provide documented feedback of corrective actions to the customers; provide customer support through help desk ticket responses, including completion of requested technical questionnaires, and providing evidence of quality/ regulatory certification for the plant.

Education and Skill Requirements:

  • Bachelor's Degree in technical field (Engineering or Statistics preferred.)
  • 3+ years of Quality Control experience with corresponding leadership or supervisory responsibilities.
  • Familiar with regulatory industry requirements such as ISO13485, ISO 15378, Quality Systems Regulation CFR 21 part 820, GDP / GMP-Good Doc / Good Manufacturing Practices.

Title : Quality Control Supervisor

Location : Manassas VA

Client Job ID : 1586620

#LucasHMG

60d+ ago
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Supervisor, QC Environmental Monitoring

Emergent Biosolutions
Rockville, MD
Those who join Emergent BioSolutions feel a sense of ownership about their future. You will excel in an environment characterized by respect, innovation and growth opportunities. Here, you will join passionate professionals who advance their scientific, technical and professional skills to develop products designed-to protect life.

The QC Supervisor, position supports the Quality Control group at Emergent BioSolutions Rockville Campus. The QC Supervisor is responsible for reviewing and scheduling activities in support of the Microbiology, Environmental Monitoring, Analytical (including testing and method transfer), Critical Utility testing programs, Manufacturing Support Testing, and supporting quality initiatives. Individuals will manage teams of 4-7 analysts. An individual in this role will serve as a QC trainer and a coach for their team. Analyst's performance review, goal planning and compensation planning will be the responsibility of an individual in this role.
II: ESSENTIAL FUNCTIONS

Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions.

* Assist the QC Manager with feasibility assessment of client projects
* Reviews/Approves microbiological / analytical work per SOPs, and applicable protocols
* Informs supervisor/manager upon observing OOS, OOL, or generation of deviations
* Leads/Assists with complex investigations by obtaining root cause and implementing changes
* Writes, reviews, revises, and approves SOP's and Testing Standards as necessary
* Trains QC analyst
* Reviews, analyzes, interprets, reports, and approves data
* Applies Environmental/Analytical knowledge to support change and risk management
* Support department compliance and productivity goals
* Track time Individual and Team time worked per project and holiday
* Identify and implement continuous improvement opportunities to reduce non-value-added work or complexity.
* May require work on weekends and nights, travel, or work with 3rd party vendor
* Detailed oriented - Able to complete required tasks and associated documentation with minimal error.
* Adaptability - Maintain positive attitude in a changing work environment
* Communication - Effectively communicates with all levels of manufacturing and support staff.
* Requires vaccination against different viruses including Vaccinia virus.

The above statements are intended to describe the general nature of work performed by those in this job. It is not an exhaustive list of all duties, and other duties may be assigned.

III: MINIMUM EDUCATION, EXPERIENCE, SKILLS

Education:

* BS in Microbiology/Biology/Chemistry or related field

Experience:

* 5+ years (MS with 3+ years) in the Pharmaceutical or Biotechnology with emphasis in aseptic processing, QC microbiology, environmental monitoring, water system, quality control, validation, and manufacturing processes.
* Proven track record of achievement and sustained performance in a cGMP/GLP environment.
* Strong technical and communication skills: oral/written and listening. Personal Competencies: Self - awareness, Integrity, Team Player, Creative and Flexible

Skills:

* Knowledge of MS Word, Excel, LIMS and PowerPoint.

There are physical/mental demands and work environment characteristics that must be met by an individual to successfully perform the essential functions of the job. This information is available upon request from the candidate.

Reasonable accommodations may be made to enable individuals with disabilities to perform all essential functions.

Emergent BioSolutions is an Equal Opportunity/Affirmative Action Employer and values the diversity of our workforce. Emergent does not discriminate on the basis of race, color, creed, religion, sex or gender (including pregnancy, childbirth, and related medical conditions), gender identity or gender expression (including transgender status), sexual orientation, age, national origin, ancestry, citizenship status, marital status, physical or mental disability, military service or veteran status, genetic information or any other characteristics protected by applicable federal, state or local law.

Information submitted will be used by Emergent BioSolutions for activities related to your prospective employment. Emergent BioSolutions respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy .

Emergent BioSolutions does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on Emergent BioSolutions' approved agency list. Unsolicited resumes or candidate information submitted to Emergent BioSolutions by search/recruiting agencies not already on Emergent BioSolutions' approved agency list shall become the property of Emergent BioSolutions and if the candidate is subsequently hired by Emergent BioSolutions, Emergent BioSolutions shall not owe any fee to the submitting agency.

ABOUT EMERGENT

Protecting and Enhancing 1 billion lives by 2030 focuses our energy to improve the quality of life for individuals around the world, giving them the opportunity to experience the fullness of life.

Our drive towards this vision informs all of our actions-whether it is our approach to product development, manufacturing, encouraging employee health and wellness or giving back to the community-we strive every day to achieve this shared goal.

WE BELIEVE IN OUR VALUES

* Stand shoulder to shoulder no matter what
* We combine our best thinking and communicate openly to support each other.

* Break through thinking
* We take smart risks, pursue innovation and challenge ourselves to constantly improve.

* Own it always
* Every person at Emergent is engaged and accountable for delivering on our commitments.

* Compete where it counts
* We set the right goals and respect each other as we conquer them together.
60d+ ago

Superintendent/QC

J&J Worldwide Services
Bethesda, MD
Throughout our 50+ year history in the Government services industry, J&J Worldwide Services has demonstrated an unwavering commitment to our people, our customers, and our industry. When coming to work at J&J, you will be joining more than just a company, you will be joining a family that takes great pride in serving the men and women of the U.S. Military and other Government agencies. We believe a healthy work-life balance is an essential component of our employees' success and we work hard to support our employees' participation in important events that occur in their personal lives.
Knowledge, Experience and Skill Requirements

* Five (5) years of relevant work experience, or an equivalent combination of education and experience sufficient to successfully perform the essential duties of the job
* Four (4) years supervisory experience preferred
* Experience with US Corps of Engineers, government contracting, general construction
* Experience in healthcare facilities is preferred
* Knowledge of U.S. Government procurement regulations and labor laws desirable
* Must pass Corps of Engineers CQM class for contractors
* Must pass ASHE HCC certification class.
* Excellent management and employee, and customer relations skills.
* Excellent verbal and written communication skills.
* Knowledge of Microsoft Office suite of products, including Word, Excel, Access, PowerPoint and Project.
* Experience with P6 (Oracle) is preferred.
* Experience with ProCore is preferred
* Superior attention to detail.
* Ability to work in a fast-paced environment while attending to multiple tasks and demands.

Essential Duties and Responsibilities

* The ability to perform remedial task using basic computer software like, scheduling, update reports, and email.
* Must have the ability to read, and interpret construction drawings to properly direct subcontractors to execution of work.
* Perform difficult and challenging construction and project management functions including planning, directing and budgeting for assigned projects.
* Perform construction and project management administration functions, handling a variety of actions and problems relating to assigned projects. Report project fund status reports, reviews billing procedures and contractual requirement submittals.
* Assist with project design plan review to accomplish contractual objectives and provide direction and support to subcontractors, support staff, trades and crafts.
* Monitor requirements necessary to obtain progress payments, quantity options, government-furnished property, etc. and/or administers specific phases of complex contracts.
* May be responsible for assisting on the development of agendas for both pre-and post-job conferences.
* Perform desktop publishing. Creates and assists in the development of visual presentations for the section.
* Prepare worksheets for cost accounting by analyzing blueprints, plans, and related customer documents. This position may also consult with engineering staff and other technical personnel as required.
* Responsible for assisting Project Manager with budgets for assigned projects.
* Responsible for keeping current on government regulations and commercial trends. Monitors project compliance requirements to ensure compliance with Service Contract Act, Davis Bacon Act and other Federal regulations as required.
* Maintain customer relations through communication both face to face, and digital. Professional appearance is desirable.
* Responsible for scheduling of work to be performed and overall project completion time based on IAW project plan. Communicate with customer regarding any deviations from the schedule.
* Perform other duties as assigned.

Physical, Environmental and Sensory Requirements

* Position works in office areas as well as through construction jobsites.
* Physical demands include intermittent sitting, standing, and walking, and occasional bending, reaching, and lifting.
* Moderate exposure to elements such as heat, cold, noise, dust, dirt, chemicals, moving machinery, etc., typical of a construction site.
* Ability to travel 10-20% of the time.

This job description is subject to change by the employer as the needs of the employer and requirements of the job change.

We maintain a drug-free workplace and perform pre-employment substance abuse testing.
60d+ ago

Superintendent/QC

J&J Worldwide Service
Bethesda, MD
Throughout our 50+ year history in the Government services industry, J&J Worldwide Services has demonstrated an unwavering commitment to our people, our customers, and our industry. When coming to work at J&J, you will be joining more than just a company, you will be joining a family that takes great pride in serving the men and women of the U.S. Military and other Government agencies. We believe a healthy work-life balance is an essential component of our employees' success and we work hard to support our employees' participation in important events that occur in their personal lives.
Knowledge, Experience and Skill Requirements

+ Five (5) years of relevant work experience, or an equivalent combination of education and experience sufficient to successfully perform the essential duties of the job

+ Four (4) years supervisory experience preferred

+ Experience with US Corps of Engineers, government contracting, general construction

+ Experience in healthcare facilities is preferred

+ Knowledge of U.S. Government procurement regulations and labor laws desirable

+ Must pass Corps of Engineers CQM class for contractors

+ Must pass ASHE HCC certification class.

+ Excellent management and employee, and customer relations skills.

+ Excellent verbal and written communication skills.

+ Knowledge of Microsoft Office suite of products, including Word, Excel, Access, PowerPoint and Project.

+ Experience with P6 (Oracle) is preferred.

+ Experience with ProCore is preferred

+ Superior attention to detail.

+ Ability to work in a fast-paced environment while attending to multiple tasks and demands.

Essential Duties and Responsibilities

+ The ability to perform remedial task using basic computer software like, scheduling, update reports, and email.

+ Must have the ability to read, and interpret construction drawings to properly direct subcontractors to execution of work.

+ Perform difficult and challenging construction and project management functions including planning, directing and budgeting for assigned projects.

+ Perform construction and project management administration functions, handling a variety of actions and problems relating to assigned projects. Report project fund status reports, reviews billing procedures and contractual requirement submittals.

+ Assist with project design plan review to accomplish contractual objectives and provide direction and support to subcontractors, support staff, trades and crafts.

+ Monitor requirements necessary to obtain progress payments, quantity options, government-furnished property, etc. and/or administers specific phases of complex contracts.

+ May be responsible for assisting on the development of agendas for both pre-and post-job conferences.

+ Perform desktop publishing. Creates and assists in the development of visual presentations for the section.

+ Prepare worksheets for cost accounting by analyzing blueprints, plans, and related customer documents. This position may also consult with engineering staff and other technical personnel as required.

+ Responsible for assisting Project Manager with budgets for assigned projects.

+ Responsible for keeping current on government regulations and commercial trends. Monitors project compliance requirements to ensure compliance with Service Contract Act, Davis Bacon Act and other Federal regulations as required.

+ Maintain customer relations through communication both face to face, and digital. Professional appearance is desirable.

+ Responsible for scheduling of work to be performed and overall project completion time based on IAW project plan. Communicate with customer regarding any deviations from the schedule.

+ Perform other duties as assigned.

Physical, Environmental and Sensory Requirements

+ Position works in office areas as well as through construction jobsites.

+ Physical demands include intermittent sitting, standing, and walking, and occasional bending, reaching, and lifting.

+ Moderate exposure to elements such as heat, cold, noise, dust, dirt, chemicals, moving machinery, etc., typical of a construction site.

+ Ability to travel 10-20% of the time.

This job description is subject to change by the employer as the needs of the employer and requirements of the job change.

We maintain a drug-free workplace and perform pre-employment substance abuse testing.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

The contractor 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, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c)
60d+ ago

Installation Quality Control Supervisor - REMOTE - With Travel

Talascend, LLC
Remote or Elk Grove Village, IL
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Talascend is currently seeking an Installation Quality Control Supervisor, due to growth of the organization, this is a new position. Location is OPEN as the role is REMOTE with travel to sites.
(MUST HAVE current or prior MATERIAL HANDLING SYSTEMS exp)

The Installation Quality Control Supervisor (IQCS) is responsible for managing the daily QC responsibilities of specific projects to ensure compliance of customer requirements by managing quality policies, standards, and procedures and driving continuous improvement.

RESPONSIBILITIES:

Establishes and maintains a quality management system by developing quality assurance policies and procedures that comply with our client's Installation Specifications.

Reviews quality assurance budgets for projects and plans resources accordingly.
Coordinates on-site quality assurance needs with project managers and schedules resources required
As needed, provides on-site oversight of quality assurance efforts; serves as on-site contact and coordinates quality control activities with the customer and with the site manager
Assists the project manager to develop quality control budgets and schedules; informs project manager of all site activities, particularly those that affect costs, schedule, and resources
Creates equipment specific quality checklists and tests to be performed by QC Team to ensure quality install.
Plans and monitors according to the master schedule; reports on progress and issues and takes corrective action as needed
Travels for 50% - 75%

EDUCATION AND EXPERIENCE:

Bachelor's degree in a technical engineering field OR “equivalent experience”
Experience in quality management
Material handling industry experience, preferably with distribution centers and warehouse automation; construction experience a plus.
Management experience

Employees are to perform in both a professional and personable manner. The way the employee relates to fellow employees, customers, vendors, competitors and visitors is considered parallel in importance to technical knowledge and ability and is a requisite for successful job performance.
New
6d ago
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Supervisor, Quality Control Analytical

Gilead Sciences, Inc.
Frederick, MD
Kite is continuing to hire for all open roles. Our interview process may be conducted virtually and some roles will be asked to temporarily work from home. Over the coming weeks and months, we will be implementing a phased approach to bringing employees back to site to ensure the health and safety of our teams.
**For Current Kite Pharma Employees and Contractors:**

Please log onto your Internal Career Site (https://www.myworkday.com/gilead/d/inst/13102!CK5mGhIKBggDEMenAhIICgYI1A0QtgI~/cacheable-task/2997$2151.htmld#backheader=true) to apply for this job.

**Job Description**

We are seeking a highly motivated individual to join us as a Supervisor, Quality Control Analytical, reporting to the Associate Director, Quality Control in Frederick, MD. In this role, you will execute tasks associated with managing a group responsible for analytical testing and release of cell therapy final product using techniques such as **qPCR/dd PCR, Flow cytometry, Cell-culture-ELISA** and will have cross-functional interaction with personnel from other QC groups, Quality Assurance, Analytical Development, Manufacturing, Material Management (MM) and Corporate teams.

As the site transitions into operations mode, you will be responsible for the day to day oversight of one of the QC Analytical teams. This group will operate 7 days a week, with an extended, overlapping shift structure. • This role will start as a 5day/8hr shift position and will move to a 4 day /10 hour shift position in 2022 **

**Position Responsibilities (include but are not limited to):**

+ Training on Analytical Assays using **qPCR/dd PCR, Flow cytometry, Cell-culture-ELISA**

+ Supervise all QC Analytical laboratory testing using **qPCR/dd PCR, Flow cytometry, Cell-culture-ELISA**

+ Responsible for the efficient operation of the QC Analytical labs including the planning, coordination and direct supervision of activities conducted by QC Analysts.

+ Manages QC Analytical training program

+ Hire, mentor and develop exceptional QC personnel

+ Works with QC raw materials team to establish testing process of raw materials

+ Generates of CoAs for product release

+ Develops, revises, and reviews SOPs, tech transfer/qualification/validation protocols and reports

+ Conduct and/or manage investigation of OOS, aberrant results and trends in invalid assay in product and raw material testing.

+ Manage and author deviations related to QC Analytical procedures to investigate root cause, impact and corrective and preventative actions.

+ Participate and/or lead daily and weekly team meetings

+ Monitors the GMP systems currently in place to ensure compliance with established SOPs, Policies, cGMPs and other relevant regulatory requirements. Conduct investigations to support deviations when required.

+ Review proposed changes to systems, procedures, methods, and submissions to regulatory agencies, as appropriate

+ Author controlled documents such as SOPs, forms, etc., as needed.

+ Participate and Support development and implementation of Operational Excellence initiatives to maximize laboratory and staff efficiencies

+ Review proposed changes to systems, procedures, methods, and submissions to regulatory agencies, as appropriate

+ Other duties as assigned

**Basic Qualifications:**

+ Master's Degree and 3+ years' experience working in QC Analytical OR

+ Bachelor's Degree and 5+ years' experience working in QC Analytical or biopharma laboratories

+ High School Degree and 9+ years' experience working in QC Analytical or biopharma laboratories

**Preferred Qualifications:**

+ Experience supervising/managing analytical labs within the biotechnology or pharmaceutical industry

+ Well versed and experienced in bioanalytical methods working under GMP conditions.

+ Strong experience in applying GMP in QC lab in conformance to US, EU and ROW standards.

+ Experience in conducting investigations, writing deviations, implementing CAPA and initiating change controls.

+ Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211), Quality Control, GMPs, GLP

+ Ability to effectively negotiate and build collaboration within teams and amongst individuals.

+ Demonstrated ability to create and maintain highly functioning teams.

+ Excellent interpersonal, verbal and written communications skills which are essential in this collaborative work environment

+ Comfortable in a fast-pace small company environment with minimal direction and able to adjust workload based on changing priorities.

Does this sound like you? If so, apply today!

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 www.kitepharma.com . Sign up to follow @KitePharma on Twitter at www.twitter.com/kitepharma .

**For jobs in the United States:**

As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, 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 careers@gilead.com for assistance.

**_Following extensive monitoring, research, consideration of business implications and advice from internal and external experts, Kite has made the decision to require all U.S. employees and contractors to receive the COVID-19 vaccines as a condition of employment. "Full vaccination" is defined as two weeks after both doses of a two-dose vaccine or two weeks since a single-dose vaccine has been administered. Anyone unable to be vaccinated, either because of a sincerely held religious belief or a medical condition or disability that prevents them from being vaccinated, can request a reasonable accommodation. _**

For more information about equal employment opportunity protections, please view the 'EEO is the Law' (http://www.eeoc.gov/employers/upload/poster\_screen\_reader\_optimized.pdf) poster.

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT (http://www.dol.gov/whd/regs/compliance/posters/eppac.pdf)

YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

PAY TRANSPARENCY NONDISCRIMINATION PROVISION (https://www.dol.gov/ofccp/pdf/pay-transp\_formattedESQA508c.pdf)

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.

Gilead 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 log onto your Internal Career Site (https://www.myworkday.com/gilead/d/inst/13102!CK5mGhIKBggDEMenAhIICgYI1A0QtgI~/cacheable-task/2997$2151.htmld#backheader=true) to apply for this job.

**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.

**_Following extensive monitoring, research, consideration of business implications and advice from internal and external experts, Kite has made the decision to require all U.S. employees and contractors to be fully vaccinated against COVID-19 as a condition of employment. The health of our employees, contractors, their loved ones, our partners and the communities and people we serve is a top priority. Vaccination is the most effective way currently available to deliver on that priority._**

**_The purpose of the vaccination requirement is to minimize the spread of COVID-19 in the workplace and support the health and safety of our communities. A person is considered fully vaccinated two weeks after the second dose of a two-dose vaccine or two weeks after a single-dose vaccine has been administered. Anyone unable to be vaccinated, either because of a sincerely held religious belief or a medical condition or disability that prevents them from being vaccinated, can request an accommodation._**
New
2d ago

Supervisor, Quality Control

Lonza Group AG
Walkersville, MD
United States, Walkersville (Maryland)

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

Lonza Walkersville, is actively seeking a Supervisor of Quality Control. This role is responsible for providing management of the QC Endotoxin Detection Laboratory. This role will be responsible for the supervision of team members including but not limited to work distribution, scheduling, training, answering of questions related to work, assistance in solving problems, etc. Includes personnel functions such as salaries, discipline, promotions, timesheets, etc. Also provides guidance and direction over individuals who proceed on their own initiative in compliance with policies, practices, and procedures prescribed by their immediate supervisor. Works on problems of diverse scope where analysis of situation or data requires evaluation of identifiable factors. Exercises judgment within generally defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining solutions. Acts as supervisor to subordinates to meet schedules and/or resolve technical problems. Develops and administers budgets, schedules and performance requirements.

Key responsibilities:

* Supervise day-to-day operation of QC Endotoxin Detection Laboratory.
* Attend meetings and preparation and monitoring of department budgets
* Participate in Customer and Regulatory Audits
* Resolve Problems.
* Delegate Projects
* Hire, train and conduct evaluations of department personnel
* Conduct Periodic Staff Meetings
* Maintain adherence to company policies and procedures
* Provide monthly department reports

Key requirements:

* A minimum of Bachelor's Degree in Life Sciences (preferably an advanced degree) or related discipline.
* Substantial professional experience in a laboratory environment, sales, management or technical services.
* Laboratory experience and knowledge of LAL methodologies.
* Personnel interview/ review administration, computer skills (spreadsheet, database, word processing), strong management skills, training skills
* Written communication, public speaking, team building skills, independent work skills, strong work ethic, time management, good organization skills, stress management, professional image, decision making skills.
* Diplomacy, negotiation skills, team building skills, independent work skills, coaching, delegating skills

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Reference: R34964

Apply
60d+ ago

Supervisor, Quality Control Analytical

Gilead Sciences, Inc.
Frederick, MD
Kite is continuing to hire for all open roles. Our interview process may be conducted virtually and some roles will be asked to temporarily work from home. Over the coming weeks and months, we will be implementing a phased approach to bringing employees back to site to ensure the health and safety of our teams.
**For Current Kite Pharma Employees and Contractors:**

Please log onto your Internal Career Site (https://www.myworkday.com/gilead/d/inst/13102!CK5mGhIKBggDEMenAhIICgYI1A0QtgI~/cacheable-task/2997$2151.htmld#backheader=true) to apply for this job.

**Job Description**

Everyone at Kite is grounded by one common goal - curing cancer. Every single day, we seek to establish a direct line between that purpose and our day-to-day work. Join us in our mission!

We are seeking a highly motivated leader to join us as a Team Lead of Quality Control to support the startup of Kite's brand new, state of the art, commercial Cell Therapy facility in Frederick, Maryland. Reporting to the Senior Manager of Quality Control, the Team Lead will be a hands-on resource for QC Analytical. Initially as part of the start-up activities, the Incumbent will be responsible for executing Assay Technical Transfers including being trained on all the Analytical Assays and implementing and Train-the-Trainer program.

As the site transitions into operations mode, you will be responsible for the day to day oversight of the QC Analytical team during a 40-hour work week. Come 2022, this group will operate 7 days a week, with an extended, overlapping shift structure (40 hours per week).

**Responsibilities for the** **Team Lead of Quality Control** **Analytics** **include** **:**

+ Training on Analytical Assays

+ Team Lead of all QC Analytical laboratory testing

+ Manages QC Analytical training program

+ Works with QC raw materials team to establish testing process of raw materials

+ Completes routine record review of test data and related documents for in-process testing, drug substance and drug product release

+ Generates of CoAs for product release

+ Develops, revises, and reviews SOPs, tech transfer/qualification/validation protocols and reports

+ Conducts investigations regarding out of specifications (OOS) results, trends in invalid assay and address and manage deviations related to QC Analytical procedures

+ Identifies and leads teams for lean improvement activities

+ Provides updates at daily and weekly meetings

+ Monitors the GMP systems currently in place to ensure compliance with documented policies

+ Reviews proposed changes to systems, procedures, methods, and submissions to regulatory agencies, as appropriate

**Basic Qualifications:**

MA / MS Degree with 3 years of analytical and/or cGMP operations and/or quality experience

OR

BA/BS Degree with 5 years of analytical and/or cGMP operations and/or quality experience

OR

High School Degree with 9 years of analytical and/or cGMP operations and/or quality experience

**Preferred Qualifications:**

+ Demonstrated leadership and management skills, including establishing direction and goals, and guiding execution while fostering a team-based environment

+ 7+ years' experience working in Quality Control or biopharma laboratories

+ 3+ years' experience supervising/managing analytical biology labs within the biotechnology or pharmaceutical industry

+ Well versed in various analytical techniques such as Flow Cytometry, ELISA, PCR, and cell bioassays and other applicable methods to the testing of biopharmaceuticals

+ Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211)

+ Quality Control, GMPs, method development and validation

Does this sound like you? If so, apply today!

\#LI-ML1

\#QUAL123MD

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 www.kitepharma.com . Sign up to follow @KitePharma on Twitter at www.twitter.com/kitepharma .

**For jobs in the United States:**

As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, 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 careers@gilead.com for assistance.

**_Following extensive monitoring, research, consideration of business implications and advice from internal and external experts, Kite has made the decision to require all U.S. employees and contractors to receive the COVID-19 vaccines as a condition of employment. "Full vaccination" is defined as two weeks after both doses of a two-dose vaccine or two weeks since a single-dose vaccine has been administered. Anyone unable to be vaccinated, either because of a sincerely held religious belief or a medical condition or disability that prevents them from being vaccinated, can request a reasonable accommodation. _**

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**For Current Kite Pharma Employees and Contractors:**

Please log onto your Internal Career Site (https://www.myworkday.com/gilead/d/inst/13102!CK5mGhIKBggDEMenAhIICgYI1A0QtgI~/cacheable-task/2997$2151.htmld#backheader=true) to apply for this job.

**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.

**_Following extensive monitoring, research, consideration of business implications and advice from internal and external experts, Kite has made the decision to require all U.S. employees and contractors to be fully vaccinated against COVID-19 as a condition of employment. The health of our employees, contractors, their loved ones, our partners and the communities and people we serve is a top priority. Vaccination is the most effective way currently available to deliver on that priority._**

**_The purpose of the vaccination requirement is to minimize the spread of COVID-19 in the workplace and support the health and safety of our communities. A person is considered fully vaccinated two weeks after the second dose of a two-dose vaccine or two weeks after a single-dose vaccine has been administered. Anyone unable to be vaccinated, either because of a sincerely held religious belief or a medical condition or disability that prevents them from being vaccinated, can request an accommodation._**
60d+ ago

Quality Control Inspector

Randstad Us
Gaithersburg, MD
**job details:**

+ location:Gaithersburg, MD

+ salary:$20 - $25 per hour

+ date posted:Tuesday, October 19, 2021

+ job type:Temp to Perm

+ industry:Professional, Scientific, and Technical Services

+ reference:878482

**job description**

Quality Control Inspector

job summary:

Client is a fast growing digital technology company that is disrupting the manufacturing industry. We are hiring a mid-shift Quality Control Inspector to support our rapid customer growth. Do you thrive on working on the edge? Do you want to transform an industry? This job is for you if your true strength is the ability to prioritize and communicate effectively to get you through even the most demanding of situations.

As a Quality Control Inspector, you will be part of a fast moving team of quality professionals who conduct visual and hands-on inspections along with solving quality assurance problems for customized parts.

location: Gaithersburg, Maryland

job type: Contract

salary: $20 - 25 per hour

work hours: 3pm to 12am

education: Bachelors

responsibilities:

As a Quality Control Inspector at client, your day-to-day might include the following:

+ Inspecting machined parts and other finished goods for conformance to customer-defined standards. Product will be inspected using the AQL sampling plan detailed in ANSI/ASQ Z1.4.

+ Accurately document the results of all testing and inspections in accordance to ISO standards.

+ Maintain controlled electronic documents and test records in a timely and accurate manner.

+ Contribute to the writing and revision procedures for the inspection functions.

+ Coordinate the calibration of all company measurement and test equipment. Assists in customer complaint and quality system investigations.

+ Performs other duties as assigned to maintain efficiency throughout the company.

+ Performs all work in compliance with client's quality and safety systems, policies and procedures.

This job is for you, if you have

+ Minimum of 3 years inspection experience in a machine shop / manufacturing environment

+ Ability to interpret engineering drawings

+ In the absence of a drawing, having the ability to generate a drawing from a CAD program is a strong plus (we use SolidWorks Inspector add-in to generate reports)

+ Ability to use Standard measuring Equipment i.e. Micrometers, Calipers, Height Gauges

+ Experience with PC-DMIS with CMM is a plus

+ Familiarity with ISO standards a plus

+ Team player, open to new ideas and teamwork, self-motivated individual, willingness to continually strive to increase personal knowledge and value

+ strong clerical and math skills

+ Extreme attention to detail

qualifications:

+ Experience level: Experienced

+ Minimum 3 years of experience

+ Education: Bachelors

skills:

+ Solidworks

+ Quality (3 years of experience is required)

+ Calipers (2 years of experience is preferred)

+ Micrometers (2 years of experience is preferred)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
New
3d ago

Quality Control Inspector

Xometry
Gaithersburg, MD
Xometry is a fast growing digital technology company that is disrupting the manufacturing industry. We are hiring a mid-shift Quality Control Inspector to support our rapid customer growth. Do you thrive on working on the edge? Do you want to transform an industry? This job is for you if your true strength is the ability to prioritize and communicate effectively to get you through even the most demanding of situations.

As a Quality Control Inspector, you will be part of a fast moving team of quality professionals who conduct visual and hands-on inspections along with solving quality assurance problems for customized parts.
As a Quality Control Inspector at Xometry, your day-to-day might include the following:

* Inspecting machined parts and other finished goods for conformance to customer-defined standards. Product will be inspected using the AQL sampling plan detailed in ANSI/ASQ Z1.4.
* Accurately document the results of all testing and inspections in accordance to ISO standards.
* Maintain controlled electronic documents and test records in a timely and accurate manner.
* Contribute to the writing and revision procedures for the inspection functions.
* Coordinate the calibration of all company measurement and test equipment. Assists in customer complaint and quality system investigations.
* Performs other duties as assigned to maintain efficiency throughout the company.
* Performs all work in compliance with Xometry's quality and safety systems, policies and procedures.

This job is for you, if you have

* Minimum of 3 years inspection experience in a machine shop / manufacturing environment
* Ability to interpret engineering drawings
* In the absence of a drawing, having the ability to generate a drawing from a CAD program is a strong plus (we use SolidWorks Inspector add-in to generate reports)
* Ability to use Standard measuring Equipment i.e. Micrometers, Calipers, Height Gauges
* Experience with PC-DMIS with CMM is
* Familiarity with ISO standards a plus
* Team player, open to new ideas and teamwork, self-motivated individual, willingness to continually strive to increase personal knowledge and value
* Strong clerical and math skills
* Extreme attention to detail

Xometry is the source for on-demand manufacturing, offering massive capacity, instant online quotes, fast lead times, and affordable pricing. Our global network of over 5,000 manufacturing facilities enables us to maintain consistently fast lead times while offering a broad array of capabilities includes CNC machining, injection molding, sheet metal fabrication, urethane casting, and a industry-leading 3D printing service. We have a diverse customer base, ranging from startups to Fortune 100 companies and can make anything from a single prototype to millions of parts.

If this job isn't for you but you have a friend who may be a perfect fit - share this job with them!

Xometry is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

Xometry participates in E-Verify and after a job offer is accepted, will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
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Average Salary For a Quality Control Supervisor

Based on recent jobs postings on Zippia, the average salary in the U.S. for a Quality Control Supervisor is $40,779 per year or $20 per hour. The highest paying Quality Control Supervisor jobs have a salary over $61,000 per year while the lowest paying Quality Control Supervisor jobs pay $27,000 per year

Average Quality Control Supervisor Salary
$40,000 yearly
$20 hourly
Updated October 23, 2021
27000
10 %
40000
Median
61000
90 %

Highest Paying Cities For Quality Control Supervisor

0 selections
CityascdescAvg. salaryascdescHourly rateascdesc
New York, NY
$72,486
$34.85
Detroit, MI
$71,579
$34.41
Lawrence, MA
$70,902
$34.09
Overland Park, KS
$69,187
$33.26
Coppell, TX
$69,131
$33.24
Kokomo, IN
$67,561
$32.48

5 Common Career Paths For a Quality Control Supervisor

Quality Control Manager

A quality control manager is responsible for checking the quality of products and materials, especially for release and delivery, ensuring that the items are free of any defects. Quality control managers coordinate with other organization heads to develop effective processes to maintain and improve the products' efficiency, following the regulatory procedures and standard protocols. They monitor production, identify areas of improvement, inspect the finished products, and adjust product development techniques based on the client's specifications. A quality control manager must have excellent communication and leadership skills to handle the production team and address concerns immediately.

Quality Assurance Manager

A Quality Assurance Manager's responsibility varies on the organization or industry where one is assigned. Most of the time, the duties will revolve around quality control, such as overseeing a company's manufacturing operations, ensuring that the process followed all of the necessary protocols, and the products met all of the standards in adherence to the company's policies and regulations. Furthermore, one must be able to detect and identify mistakes, conduct constant inspections, coordinate with various staff and supervisors, develop the workforce's quality by training employees, and come up with strategies that will help the company attain financial gains.

Project Manager

Project managers oversee a specific project related to the organization's business. They manage the whole project from inception to evaluation. They initiate planning with involved departments, follow-through on the plans, ensure smooth execution of the plans, and evaluate the project for further improvements should these be needed. In line with this, project managers also ensure that the project is cost-efficient and well within the budget. They also manage the different work teams involved in the project and ensure that things are running smoothly on this aspect as well.

Quality Manager

A quality manager is a professional who is responsible for ensuring that the level of quality of the company's product outputs is met for customers. Quality managers monitor and evaluate the internal production process so that they can produce statistical reports on the standard of quality and communicate them to upper management. To ensure health and safety standards, quality managers must create and maintain up-to-date product or process specifications. They also train employees on quality assurance standards and processes.

Manager

Managers are responsible for a specific department, function, or employee group. They oversee their assigned departments and all the employees under the department. Managers are responsible that the department they are handling is functioning well. They set the department goals and the steps they must take to achieve the goals. They are also in charge of assessing the performance of their departments and their employees. Additionally, managers are responsible for interviewing prospective candidates for department vacancies and assessing their fit to the needs of the department. Managers also set the general working environment in the department, and they are expected to ensure that their employees remain motivated.

Illustrated Career Paths For a Quality Control Supervisor