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Associate Quality Control Analyst Jobs in New York

Quality Control Analyst

Summit, NJ ยท On-site

$25.50 - $34.25/hr

Responsible for assisting with laboratory analysis for clinical release and routine stability testing. May conduct routine release and stability analyses of developmental compounds, prototype ...

Adheres to GMPs and current Good Documentation Practices (GDPs) Requirements Associate QC Analytical Chemist - Bachelors degree in Chemistry or related science field and 0-3 years lab experience in a ...

Quality Control Associate

Manhattan, NY ยท On-site

$22.50 - $24/hr

Blue Nile is seeking a detail-oriented and highly organized QC Associate (Quality Control Associate ... Strong analytical and problem-solving skills to propose improvement processes and strategies.

Blue Nile is seeking a detail-oriented and highly organized QC Associate (Quality Control Associate ... Strong analytical and problem-solving skills to propose improvement processes and strategies.

Quality Control Associate

Manhattan, NY ยท On-site

$22.50 - $24/hr

Blue Nile is seeking a detail-oriented and highly organized QC Associate (Quality Control Associate ... Strong analytical and problem-solving skills to propose improvement processes and strategies.

Quality Control Associate

New York, NY ยท On-site

$22.50 - $24/hr

Blue Nile is seeking a detail-oriented and highly organized QC Associate (Quality Control Associate ... Strong analytical and problem-solving skills to propose improvement processes and strategies.

QC Associate

New York, NY ยท On-site

$17 - $24/hr

We are seeking a detail-oriented and highly organized QC Associate (Quality Control Associate) to ... Strong analytical and problem-solving skills to propose improvement processes and strategies.

We are seeking a detail-oriented and highly organized QC Associate (Quality Control Associate) to ... Strong analytical and problem-solving skills to propose improvement processes and strategies.

Quality Control Associate

New York, NY ยท On-site

$22.50 - $24/hr

Blue Nile is seeking a detail-oriented and highly organized QC Associate (Quality Control Associate ... Strong analytical and problem-solving skills to propose improvement processes and strategies.

Micro QC Analyst I

Ridgefield, NJ ยท On-site

$33 - $38/hr

Have previous quality control microbiology experience. * Experience in bioburden testing, membrane ... help a fellow analyst. Benefits Our Benefits Include: * Medical, Dental & Vision Insurance ...

Showing results 21-40

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:

Quality Control Analyst

PSG Global Solutions

Summit, NJ โ€ข On-site

$25.50 - $34.25/hr

Contractor

Re-posted 15 days ago


Job description

Company Description

At Real we're always looking for new and ambitious people to help deliver exceptional service levels, change the lives of the candidates we represent and partner with some of the world's best pharmaceutical, biotechnology and medical companies.

As specialists in recognising talent we pride ourselves on not just finding the best people for our client partners but on our ability to spot the best and brightest talent to work for us. We are also renowned for providing training and long-term career opportunities to help our employees be the best they can be, so they can continue to deliver the expertise Real has become famous for.

Relationships are at the heart of everything we do and ensure that our clients and candidates continue to work with us again and again. This ethos is also what shapes how we work as a business. We encourage and reward knowledge sharing and have various support networks and international forums to enable our employees to keep up-to-date with changes happening across their industries and share local insight to deliver true global perspectives.

Job Description
  • Responsible for assisting with laboratory analysis for clinical release and routine stability testing. May conduct routine release and stability analyses of developmental compounds, prototype formulations and finished products in support of clinical testing for IND and NDA submissions.
  • Perform laboratory analysis under guidance of a supervisor or designee.ย 
  • Responsibilities will include, but are not limited to, the following:ย 
  • Able to conduct testing independently and may assist other analysts in analytical testing including HPLC, dissolution, Karl Fischer, UV/Vis and other analytical laboratory testing.ย 
  • Conducts routine analytical experiments using analytical methods and procedures.ย 
  • Draws basic conclusions from data and results and communicates with other analysts and management.ย 
  • Performs instrument/method troubleshooting within analytical method parameters and management guidance.ย 
  • Performs testing for development and commercial samples, release and stability samples in accordance with established methods, specifications and protocols with limited supervision.ย 
  • Good laboratory documentation skills.ย 
  • Understands cGMP documentation requirements.ย 
  • Documents/reviews laboratory work using laboratory notebooks/worksheets that is detailed, timely and in compliance with GLP/cGMP requirements.ย 
  • Other duties as assigned by management.ย 


Qualifications
  • BS/MS Chemistry or relevant discipline with equivalent experience.ย 
  • Minimum 2 - 4 years recent cGMP/GLP pharmaceutical laboratory experience.ย 
  • Experience with HPLC, dissolution, FT-IR, UV/Vis spectrophotometry, KF.ย 
  • Good communication skills.ย 
  • Able to work well in team environment to achieve results.ย 
  • Exhibits sound scientific judgment based on reasonable assumptions and available information.
Additional Information

All your information will be kept confidential according to EEO guidelines.ย 

IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 646-618-8925 ASAP! I want to know more about your preferences.

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