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Associate Quality Control Analyst Jobs in New York

PDI (NY)

QC Investigator

Orangeburg, NY · On-site

$24.25 - $32.75/hr

We have several locations across the US and are looking for new Associates to join our team ... This position utilizes knowledge of chemistry, cGMP, and analytical techniques to guide the ...

PDI

QC Investigator

Orangeburg, NY · On-site

$24.25 - $32.75/hr

We have several locations across the US and are looking for new Associates to join our team ... This position utilizes knowledge of chemistry, cGMP, and analytical techniques to guide the ...

Blue Nile

QC Associate

Manhattan, NY · On-site

$17 - $24/hr

Quality Control Associate R2Net Inc. is an innovative technology company that provides e-commerce ... Strong analytical and problem-solving skills to propose improvement processes and strategies.

Blue Nile

QC Associate

Manhattan, NY · On-site

$17 - $24/hr

Quality Control Associate R2Net Inc. is an innovative technology company that provides e-commerce ... Strong analytical and problem-solving skills to propose improvement processes and strategies.

Careers at RK Pharma Inc.

QC Chemist

Pearl River, NY · On-site

$55K - $95K/yr

Perform calibrations of all the QC analytical instruments/equipment 's as per the calibration calendar schedule or when required. * Perform Instrument/ equipment performance qualification as and when ...

Cellares

Quality Control Raw Material Analyst

Bridgewater, NJ · On-site

$24.50 - $33/hr

We are seeking a detail-oriented and operationally rigorous Quality Control Raw Material Analyst to ... associates in sampling and testing procedures * Support internal audits and external regulatory ...

CookUnity

Quality Control Associate

New York, NY

The Role As a Quality Control (QC) Associate at CookUnity, you play a key role in ensuring the quality, accuracy, and presentation of meals throughout the production process. You'll support the QC ...

SDC Designs

Quality Control Associate

Manhattan, NY · On-site

$21.63 - $26.44/hr

We are seeking a diligent and detail-oriented Quality Control Associate to join our Quality Control team at our leading diamond jewelry company. The successful candidate will be responsible for ...

SDC Designs

Quality Control Associate

New York, NY

$21.63 - $26.44/hr

We are seeking a diligent and detail-oriented Quality Control Associate to join our Quality Control team at our leading diamond jewelry company. The successful candidate will be responsible for ...

SDC Designs

Quality Control Associate

Manhattan, NY · On-site

$21.63 - $26.44/hr

We are seeking a diligent and detail-oriented Quality Control Associate to join our Quality Control team at our leading diamond jewelry company. The successful candidate will be responsible for ...

Artius Solutions

QC Chemist

Central Islip, NY · On-site

$65K - $90K/wk

We are looking for a dedicated Quality Control Chemist to join our team and perform analytical testing in a GMP-regulated laboratory environment. The ideal candidate will have experience in ...

Cellares

Manager, Quality Control

Bridgewater, NJ

$90K - $210K/yr

This individual will lead a group of QC analysts performing analytical testing of in-process and final product from cell therapy products. They will interface across different parts of the company to ...

Cellares

Manager, Quality Control

Bridgewater, NJ · On-site

$90K - $210K/yr

This individual will lead a group of QC analysts performing analytical testing of in-process and final product from cell therapy products. They will interface across different parts of the company to ...

Cellares

Manager, Quality Control

Bridgewater, NJ · On-site

$90K - $210K/yr

This individual will lead a group of QC analysts performing analytical testing of in-process and final product from cell therapy products. They will interface across different parts of the company to ...

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All JobsAssociate Quality Control Analyst JobsAssociate Quality Control Analyst Jobs in New York

Associate Quality Control Analyst information

What are some common challenges faced by associate quality control analysts during routine testing, and how can they be addressed?

Associate Quality Control Analysts often encounter challenges such as tight deadlines, managing multiple sample types, and handling complex analytical instruments. Staying organized and maintaining clear documentation helps manage workflow efficiently. Regular calibration and maintenance of laboratory equipment, along with ongoing training, are essential to minimize errors and ensure accurate results. Collaborating closely with senior analysts and cross-functional teams can also help troubleshoot unexpected issues and streamline processes.

What is the difference between Associate Quality Control Analyst vs Quality Control Technician?

AspectAssociate Quality Control AnalystQuality Control Technician
CredentialsBachelor's degree in life sciences or related field; certifications like CQE are commonHigh school diploma or associate degree; technical certifications may be preferred
Work EnvironmentLaboratories, manufacturing facilities, quality assurance departmentsManufacturing sites, laboratories, production lines
Job ResponsibilitiesData analysis, documentation, reviewing quality processes, supporting auditsPerforming tests, inspecting products, recording test results

While both roles support quality assurance, the Associate Quality Control Analyst typically focuses on data analysis and documentation, whereas the Quality Control Technician primarily conducts tests and inspections. The analyst role often requires a higher level of education and analytical skills, making it suitable for those interested in quality systems and compliance.

What does an associate quality control analyst do?

An Associate Quality Control Analyst is responsible for testing and inspecting products, materials, or processes to ensure they meet established quality standards. They perform routine laboratory tests, document results, and identify any deviations from specifications. These analysts often work in industries like pharmaceuticals, manufacturing, or food production, supporting senior analysts and quality managers. Their role is crucial in maintaining product safety, consistency, and regulatory compliance.

What are the key skills and qualifications needed to thrive as an associate quality control analyst?

To thrive as an Associate Quality Control Analyst, you need a solid background in biology, chemistry, or a related scientific field, often with a relevant bachelor's degree. Familiarity with laboratory equipment, quality management systems (such as LIMS), and regulatory guidelines like GMP is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for identifying and resolving quality issues. These skills and qualifications ensure accuracy, compliance, and consistent product quality in laboratory and manufacturing environments.
What are the most commonly searched types of Quality Control Analyst jobs in New York? The most popular types of Quality Control Analyst jobs in New York are:
What cities in New York are hiring for Associate Quality Control Analyst jobs? Cities in New York with the most Associate Quality Control Analyst job openings:
Associate Quality Control Analyst jobs near you

Quality Control Analytical Scientist

Lynkx Staffing LLC

Saddle Brook, NJ • On-site

Full-time

Re-posted 7 days ago

Job description

Quality Control Analytical ScientistAllendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Devices industries in New Jersey. The QC Analytical Scientist will be a member of the Quality Control Department. As a Senior Member of the team the QC Analytical Scientist will be involved in various QC projects and should have a deep understanding of general QC flow and the Product Cycle.
  • Support internal and external customers to ensure that proper and timely execution of all aspects of the clinical analytical method life cycle across clients.
  • Support routine GMP testing as assigned. Mentor and train team members
  • Evaluate corporate and regulatory requirements along with coordination of activities for implementation of these requirements.
  • Write the contents of Analytical Method Transfer and Validation life cycle documentation including master plans, protocols, test methods, and reports.
  • Create validation project plan i.e., timelines and resources and provides status updates to management. Utilize statistical tools for evaluation of method validation and trending data.
  • Identify, evaluate, and implement continuous business process improvements.
  • Perform troubleshooting activities with respect to methods/assays, equipment malfunctions and investigations (Deviations and OOS).
  • Provide support during laboratory investigations.
  • Train QC personnel during method transfer and validation. Provide support during equipment qualification.
  • Consistently produce elevated level of documentation accuracy and clarity according to cGMP documentation practices.
  • Ability to set deadlines and prioritize work for self, group members, and support groups involved. Ability to review/approve work performed by coworkers for accuracy and alignment with procedures.
  • Indirectly may supervise cross functional teams including product development, QA, PMP, and Manufacturing.
REQUIREMENT
  • B.S Analytical Chemistry or other scientific field or MS/Ph.D. in Analytical Chemistry or other scientific field with demonstrated experience in Quality Control laboratories for biotechnology products.
  • 8-10 years of experience in the areas of method development, validation, and transfer.
  • Direct GMP Experience.
  • Proficiency in project management skills and tools.
  • Strong background and in-depth knowledge in analytical chemistry e.g. Flow Cytometry, ELISA, HPLC, CE, PCR, etc.
  • Extensive knowledge and experience of QC assay development, transfer and validation, along with cGMPs.
  • Strong Quality orientation with attention to detail required. Analytical and problem-solving skills required.
  • Excellent communication skills, both written and verbal, with all levels of the organization, including the ability to state opinions clearly, ask questions, seek clarification, communicate facts objectively, challenge when appropriate, and pursue issues to resolution.
  • Excellent presentation skills. Ability to communicate to upper management, across departments and within the immediate QC team.
  • Ability to create and manage work plans and timelines and independently manage competing priorities with limited instruction.
  • Highly motivated individual with good interpersonal skills that have proven effective in managing relationships and negotiating solutions while maintaining a level of approachability with colleagues both internal and external.
  • Must be familiar with GMP lab environment and Aseptic techniques.
Working EnvironmentMust have the ability to work in a team-oriented environment and with clientsMust be able to work during the weekend, holidays, or overtime and as required by the companyMay be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluidsMust utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogenMust have the ability to work with specialized equipmentMust be able to handle the standard/moderate noise of the manufacturing facilityMay work with hazardous materials and chemicals Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.