Quality Control Analyst Jobs in Readington, NJ

- 229 Jobs
  • Associate Chemist

    * Iselin, NJ: Reliably commute or planning to relocate before starting work (Required) We are looking to hire an Associate Chemist to work in the X-ray Diffraction Section of the Analytics and Materials Characterization Group in Iselin, New Jersey.
    $27 hourly60d+ ago
  • Research & Development Quality Technician - Food Industry

    Backup The Research and Development Manager is the Backup when the Research and Development Technician is absent.
    $70k-104k yearly est.10h ago
  • QC Analyst (Media Prep Technician)

    Preparation, production and storage of media to adhere to the production schedule. Documents all steps in the assigned Batch record in line with GMP requirements. Responsible for successful on time completion of required training curriculum comprising of the necessary Global Operating Procedures (GOPs), Standard Operating Procedures (SOPs) and Aseptic Techniques, Gowning Qualifications and other relevant training including HSE for the specific role. Requires handling of chemicals such as corrosives, solvents and bio-hazardous materials Maintains an “audit ready” module. Perform other duties as assigned; ie. batch record review, process streamline improvements, safety walk-thrus. Media preparation adheres to the production schedule to ensure adequate approved media inventories. ISO 8 Activities: Ensure accurate SAP inventories are maintained for all components. Proper status segregation and storage of media lots. Support the maintenance of an “audit ready” state of the ISO 8 Area. Timely response to all module requests. Batch Records are properly kitted and staged based on production schedule. All gowning materials in the ISO 8 area are maintained to adequate levels. ISO 8 area has ample supply of non-inventory items. Qualifications: Associate degree in in Biology or scientific discipline; OR In lieu of degree, a minimum of 1-3 years experience in cGMP/FDA regulated industry Experience in aseptic manufacturing preferred Knowledge of cGMP regulations and FDA guidance preferred Strong interpersonal, written and communication skills along with problem solving and follow-up skills are required Must be well organized, flexible and work with minimal supervision Ability to lift up to 35 lbs. Ability to gown aseptically and work in a clean room environment (ISO 8, 7 and ISO 5) areas for extended periods of time Knowledgeable in the use of production related IT systems such as SAP and MES Ability to adapt and learn new systems Ability to collaborate with other groups, teams and departments in addressing inventory related issues Speak Up Mentality Demonstrate a high level of discipline and self-motivation Maintains composure during stressful situations Provides innovative solutions to complex or process improvement issues FULL TIME/EOE position
    $46k-62k yearly est.15d ago
  • Chem Tech

    Our client, a leader in contract laboratory services, regulatory guidance and supply chain assurance within the pharmaceutical and biopharma industry is hiring for a Chem Tech.
    $36k-47k yearly est.14d ago
  • Pharmaceutical QA Associate

    This exciting Pharmaceutical QA Associate opportunity offers a competitive salary plus an excellent benefits package including medical insurance, dental insurance, vision insurance, stock options, paid PTO, tuition reimbursement, tuition assistance etc. Then this Pharmaceutical QA Associate could be the right fit for you.
    $23 hourly18d ago
  • GC Lab Analyst

    2 or more years of GC Laboratory Analyst experience. Experience: * GC Lab Analyst: 2 years (Required) Seeking an experienced GC Laboratory Analyst for a career opportunity with a thriving organization.
    $36k-56k yearly est.60d+ ago
  • QC Analyst

    In this individual contributor role, the Quality Control Raw Materials Scientist will support patient throughput and compliance activities within the Quality department. Onsite role. Pay rate range ***-*** Major Accountabilities: • Perform raw material testing following United States Pharmacopoeia (USP), European Pharmacopoeia (EP) and in-house methods • Perform testing on raw materials per using HPLC, GC, UV, FTIR, NIR, wet chemistry and other techniques. • Perform all testing and activities compliantly following appropriate SOPs and procedures. • Review data generated by other team members. • Review QC documents to ensure completeness, accuracy, consistency, and clarity. • Perform quality impacting assessments and make decisions. • Participate special projects and facilitate any issues that arise. • Initiate change controls. • Author validation documentation. • Independently leads investigations of the highest complexity • Drive complex investigations to understand root cause. • Participate in OOS/OOE investigation • Participate in deviation investigation/CAPA implementation in a timely manner • Responsible for evaluating compendial updates against internal methods • Serve as Quality Control representative on cross-functional teams. • Knowledge of LabWare LIMS and/or other QC data systems. • Knowledge of appropriate GMP/GLP quality systems (eSOPs, TEDI, etc.). • Plan and schedule activities. • Ability to lift 35lbs. In addition to these primary duties, provide coverage for all appropriate areas. Perform other job duties as assigned. BA, or MS in biology, chemistry, biochemistry, microbiology, or other related science. Experience in Analytical Quality Control, method development, or a technical support function. At least 3 years of experience. Thorough knowledge of raw material test methods. Analytical chemistry knowledge to facilitate investigations.
    $48k-66k yearly est.15d ago
  • INT16520 Quality Control Inspector

    Role: Quality Control Inspector II Location: Plainsboro, NJ - 8536
    $30k-49k yearly est.6d ago
  • QC Lead Inspector

    Piper Companies is looking for a QC Lead Inspector in Warminster, PA to join a leading manufacturer in the medical and aerospace industry.
    $25-27 hourly10d ago
  • QC Lab Tehnician

    Assist QC Lab in monitoring, logging and ordering essential items
    $36k-52k yearly est.17d ago
  • Entry Level Chemist

    Students should have a bachelors in chemistry/chemical engineering or any scientific field Perform lab raw material release testing and other analyses as needed for cosmetic/ drug products and provide critical analysis of results. Provide detailed reports of analytical results to project leadership. The candidate should have experience in lab scale batching and formulation , Proficient with laboratory Standard Operating Procedures, Good Manufacturing Practices (GMP), and Good Laboratory Practices (GLP). • Proficient with the use of basic lab instrumentation skills like Viscometer, pH Meter. • Skilled in technical documentation including writing scientific reports. • Proficient in Microsoft Office and excellent verbal and written skills • Preferably exposure or an internship in a personal care products company formulating Emulsions and Cleansers and at minimum, the candidate should have a Bachelor's degree in Science/Engineering. • Ability to work cross-functionally in a team environment while being an individual contributor is required and experience managing multiple projects is required. Chemistry background
    $59k-82k yearly est.2d ago
  • Quality Control Technician I

    Quality Control Technician Max Payrate: $21 HR ON W2 2nd shift Hours: 2pm-10pm Location: NJ34 116 The American Rd. Morris Plains, NJ Job Summary Responsible for the daily QC Lab functions, including testing of product, calibration of lab equipment, testing for raw materials and paperwork and process audits. Essential Duties And Responsibilities To perform this job successfully, a qualified individual must be able to perform each essential duty satisfactorily either with or without reasonable accommodation. The requirements listed in this job description document are representative of the knowledge, skill, and/or ability required. Follows priorities utilizing the Daily Priorities form. Responsible for timely achievement of assigned tasks and efficient time management, typically works under close supervision. Learns to perform and report daily testing of product according to established methods and requirements related to raw materials test/inspection/approval/release, final release processes. Supports the in-process testing. Actively participates in the Quality Control Daily Targets related to safety, quality, delivery and cost. Under detailed instruction evaluates test data to support production and engineering. Monitor and report test status of various production runs to QC Manager, Manufacturing Manager, QC Supervisor, Technology, or Process Engineer. Identifies out-of-specification materials, including placing product on hold, proper identification, and segregation of nonconforming materials, initiating non-conforming material report (NCR) and participating in investigations. Provides support to Engineering, IT and R&D including participation in product/process development trials, carrying out new types of raw material and product characterization/performance testing and use of experimental materials. Maintains and performs necessary calibration of densitometers. Supports data collection activities by entering information into various databases and spreadsheets. Supports calibration program activities to ensure overall Quality Management Process (QMP) compliance. Verifies completeness of quality related documentation. Maintains and adheres to all company safety policies and procedures. Maintains work area organization and documentation to satisfy ISO and GMP standards. Maintains good communication and working relationships with all departments and effectively functions within a team environment. Exhibits professional etiquette that exemplifies the values of the organization. Note: The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, abilities, and skills required of personnel so classified. Job Requirements Minimum Education Must have High School Diploma or GED Minimum Work Experience (years) 0+ years of relevant work experience Key Skills And Competencies Licenses/Certifications, special qualifications: Equivalencies No certification necessary. Experience in an ISO or GMP environment is highly desirable. Qualifications & Competencies: Excellent organizational skills. Ability to work independently with little supervision. Good communication skills, written and oral. Ability to read and interpret data, including graphs, as they relate to test results. Ability to collect pertinent data, establishes facts, draw conclusions, and identify problems. Computer Skills: Word processing, spreadsheet (Corel & Excel), and e-mail software in a Windows environment;
    $21 hourly20d ago
  • Global Product Quality Complaints Associate

    Pay Range: $23hr- $26.50hr Support the Global Product Quality Complaint (PQC) process for the biosterile, pharmaceuticals and combination drug/device products with respect to product quality complaints. Analyze, identify and execute continuous improvement initiatives within the process while collaborating within the PQC headquarters team as well as with key stakeholders, including internal and external sites and in-market supply chain quality. This individual will be a valued team member of one of several cross-functional, multi-divisional teams which are responsible for developing and executing Global Quality Systems (GQS) initiatives and strategies for clients, with focus on the global PQC process. Roles and Responsibilities: Provide ongoing management for PQCs ensuring compliance to global framework of GMP policies and client procedures. Support the Global Product Quality Complaint (PQC) processing activities at PQC Headquarters. Participate in PQC HQ team meetings for the processing of, and improvements to, global client PQC processes, including but not limited to: PQC case intake, triage, due diligence activities, product replacements and patient reimbursements/refunds; metrics generation and slide presentation; PQC training delivery and management; new product launches; PQC related Quality Management System (QMS). Support tracking, trending and other ancillary activities for controlled documents (SOPs/Job Aids/Templates); record archivals; quality deviations and CAPA involving PQC HQ and provide quality and compliance support for these processes. Assist in implementation of Quality Risk Management principles in evaluation and investigation of PQCs. Support PQC related audits and inspections as necessary. Participate in QMS business process requirements development and validation activities as necessary. This opportunity is cross functional and will involve the management of mid-size projects between PQC HQ and other areas of the organization. Qualification Requirements: BS/BA in Sciences (i.e Chemistry, Biology, Biochemistry, Microbiology, Pharmacy), engineering, business. Enrolled in a Bachelor's, Masters or MBA degree program. Preferred Completion of Bachelors and enrolled in graduate studies. Skills/Competencies: Microsoft Office (Power point, Excel, Word, Outlook). Project Management expertise with advanced PowerPoint preferred. Basic statistics/analytics; clear communications. Ability to manage deliverables within target timelines. Must have strong analytical, interpersonal, communication, organization, and project management skills and passion to learn and grow within the biopharmaceutical industry.
    $23 hourly22d ago
  • Research And Development Technician

    Day-to-Day A CPG client in Florham Park is looking for an R&D technician to help start their production team.
    $84k-125k yearly est.2d ago
  • Quality Control Chemist - HPLC

    , melting point apparatus, pH meter, pycnometer, viscometer, FTIR and wet chemistry to do the analysis. Testing raw materials as per the USP/NF monographs Relevant experience in the pharmaceutical/cosmetic industry Communicate with the Analytical lab Manager of any issues during testing is essential.
    $67k-79k yearly est.18d ago
  • QC Analytical Chemist I

    Location: On-site in Cranbury, NJ
    $64k-79k yearly est.23d ago
  • Quality Control Chemist II (QC)

    Sun Pharmaceutical Industries Inc. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world. Sunology is a combination of Sun Values and Ideology and is the way of life at Sun Pharma.
    $64k-80k yearly est.23d ago
  • Chemist

    Responsibilities: • Complete routine sample analysis using a diverse set of methods (e.g., HPLC, GC, Karl Fisher, IR, Specific Rotation, Titration, Nephelometer, etc.) • Wet chemistry (e.g., preparation of mobile phases and standard solutions, sample dilutions, etc.) • Data interpretation (e.g., integration and reporting of chromatography data using Empower) • Data reporting (e.g., through documentation in electronic NB in compliance with all ALCOA principles) • Team will provide training and opportunities to practice/refamiliarize with methods during onboarding. Qualifications : • Minimum: BS in Chemistry. • Preferred: 1-2 years' experience in a Pharmaceutical Analytical Research or a GMP environment.
    $60k-84k yearly est.22d ago
  • QC Analyst (Analytical Chemistry)

    Source One Technical Solutions - A WBENC Certified Company Experience in Analytical Chemistry Quality Control, method development, and to facilitate investigations (CAPA, Deviation, OOS/OOE) In this individual contributor role, the Quality Control Raw Materials Scientist will support patient throughput and compliance activities within the Quality department. Serve as Quality Control representative on cross-functional teams Source One is a consulting services company and we're currently looking for the following individual to work as a consultant to our direct client, a global pharmaceutical company in Morris Plains, NJ.
    $43k-67k yearly est.5d ago
  • Quality Control Analyst

    - Design and execute lab experiments with input from Technical chemist and Quality Control Supervisor/Manager
    $43k-72k yearly est.19d ago

Learn More About Quality Control Analyst Jobs

How much does a Quality Control Analyst earn in Readington, NJ?

The average quality control analyst in Readington, NJ earns between $31,000 and $82,000 annually. This compares to the national average quality control analyst range of $40,000 to $86,000.


What is the job market like for quality control analysts in Readington, NJ?

You can compare the number of available jobs in Readington to the number of quality control analyst jobs in surrounding cities.

Active Quality Control Analyst Jobs In Nearby Cities

Nearby CityJobs In Nearby CityJobs in ReadingtonDifference
Bridgewater, NJ1,8700-1,870
East Brunswick, NJ2,4280-2,428
Easton, PA6120-612
Edison, NJ2,5850-2,585
Ewing, NJ1,4570-1,457

What are the biggest employers of Quality Control Analysts in Readington, NJ?

The biggest employers of Quality Control Analysts in Readington, NJ are:
  1. Mattson
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