Current jobs related to Quality Control Laboratory Analyst - Brown Summit - PGBPGNGLOBAL


  • Summit, United States SSi People Full time

    Must Haves:2+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.2+ years of experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, ELISA, Tissue Culture).2+ years of experience in writing technical documents.3+ years...


  • Summit, United States Aequor Full time

    Job ID: 59497-1Position: Quality Control TechnicianLocation: Summit, NJ 07901Duration: 12 months 100% on-siteThe QC Analyst is responsible for supporting Quality Control bioanalytical testing for the release of clinical and commercial products. This includes the ability to interface with multiple groups, the ability to independently perform tasks, interpret...


  • Summit, United States Futran Solutions Inc Full time

    Job Description: 100% onsiteThe QC Analyst is responsible for supporting Quality Control bioanalytical testing for release of clinical and commercial productsThis includes the ability to interface with multiple groups, the ability to independently perform tasks, interpret results, and troubleshootAdditionally, when needed, this position will be able to...


  • Summit, United States Sunrise Systems Inc Full time

    Job Title: Quality Control Technician Job ID: 24-03880 Location: Summit, NJ, 07901 Duration: 12 Months contract on W2 100% onsite The QC Analyst is responsible for supporting Quality Control bioanalytical testing for release of clinical and commercial products. This includes the ability to interface with multiple groups, the ability to...


  • Summit, United States Sunrise Systems Inc Full time

    Job Title: Quality Control Technician Job ID: 24-03880 Location: Summit, NJ, 07901 Duration: 12 Months contract on W2 100% onsite The QC Analyst is responsible for supporting Quality Control bioanalytical testing for release of clinical and commercial products. This includes the ability to interface with multiple groups, the ability to...


  • Summit, New Jersey, United States Sunrise System Inc Full time

    Job Title: Quality Assurance Analyst Company: Sunrise System Inc Location: Summit, NJ Duration: 12 Months contract on W2 POSITION SUMMARY: The Quality Assurance Analyst is integral to upholding the cGMP quality standards for Vector External Manufacturing. Key responsibilities encompass the examination of cGMP Controlled Documents, including SOPs,...

  • Laboratory Specialist

    3 weeks ago


    Summit, New Jersey, United States Sunrise System Inc Full time

    Position Title: Laboratory SpecialistCompany: Sunrise System IncJob Overview:This role is a 100% onsite position focused on supporting laboratory operations.Work Schedule: Monday to Friday during standard business hours.Role Summary:The Laboratory Specialist is tasked with the management of test specimens throughout their lifecycle, from initial receipt to...


  • Lee's Summit, Missouri, United States MLee Healthcare Staffing and Recruiting, Inc Full time

    Medical Technologist / Medical Laboratory Technician (MT/MLT)Shift: NightCompetitive Pay | Excellent BenefitsJob Summary:We are seeking a skilled Medical Laboratory Technician or Medical Technologist (MLT/MT) to join our team on the night shift. This role involves performing diagnostic testing under the Clinical Director's supervision, maintaining lab...


  • Summit, New Jersey, United States Omni Inclusive Full time

    Job SummaryWe are seeking a highly skilled Quality Assurance Document Control Specialist to join our team at Omni Inclusive. The successful candidate will be responsible for supporting the cGMP Document Control operations for our Cell Therapy Above-site organization.Key ResponsibilitiesManage an electronic document system, reviewing and approving document...


  • Summit, New Jersey, United States Omni Inclusive Full time

    Job SummaryWe are seeking a highly skilled Quality Assurance Document Control Specialist to join our team at Omni Inclusive. The successful candidate will be responsible for supporting the cGMP Document Control operations for our Cell Therapy Above-site organization.Key ResponsibilitiesManage an electronic document system, reviewing and approving document...


  • Lee's Summit, Missouri, United States MLee Healthcare Staffing and Recruiting, Inc Full time

    Job SummaryWe are seeking a skilled Medical Laboratory Technician or Medical Technologist (MLT/MT) to join our team on the night shift at MLee Healthcare Staffing and Recruiting, Inc. This role involves performing diagnostic testing under the Clinical Director's supervision, maintaining lab equipment, conducting quality assessments, and managing workloads...

  • Data Quality Analyst

    16 hours ago


    Lee's Summit, United States TEKsystems Full time

    This company is a nonprofit member association that provides medical and dental benefits to more than two million federal employees and retirees, military retirees and their families. We celebrate diversity and are committed to creating an inclusive environment for all employees. This company has one mission: To empower federal workers to be healthy and...


  • Summit, New Jersey, United States Bristol-Myers Squibb Full time

    Job Title: Senior Specialist, Quality Assurance Label ControlBristol-Myers Squibb is seeking a highly skilled Senior Specialist, Quality Assurance Label Control to join our team. As a key member of our Quality Assurance team, you will be responsible for supporting site Label Control activities at our S-12 Cell Therapy manufacturing facility.Key...


  • Summit, New Jersey, United States SSi People Full time

    Job SummaryWe are seeking a highly skilled Quality Control Analyst to join our team at SSi People. As a Quality Control Analyst, you will play a critical role in ensuring the quality and integrity of our products.Key ResponsibilitiesTesting and Quality AssurancePerform testing of in-process, final product, and stability samples to ensure compliance with...


  • Summit, New Jersey, United States Bristol-Myers Squibb Full time

    Transforming Patients' Lives through ScienceBristol Myers Squibb is a leading biopharmaceutical company dedicated to transforming patients' lives through science. We are seeking a highly skilled Senior Specialist, Quality Assurance Label Control to join our team.About the RoleThe Senior Specialist, Quality Assurance Label Control will be responsible for...


  • Lee's Summit, Missouri, United States Lee's Summit Medical Center Full time

    IntroductionAre you seeking a rewarding career as a Clinical Laboratory Technologist ASCP? At Lee's Summit Medical Center, part of HCA Healthcare, we offer a fulfilling opportunity to contribute to patient care.BenefitsLee's Summit Medical Center provides a comprehensive rewards package designed to support the health, life, career, and retirement of our...


  • Summit, New Jersey, United States Bristol-Myers Squibb Full time

    Transforming Patients' Lives through ScienceBristol-Myers Squibb is a leading biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that help patients with serious diseases. We are seeking a highly skilled Senior Specialist, Quality Assurance Label Control to join our team.About the RoleThe Senior Specialist,...


  • Summit, New Jersey, United States Bristol-Myers Squibb Full time

    Job SummaryBristol-Myers Squibb is seeking a highly skilled Senior Specialist, Quality Assurance Label Control to join our team. As a key member of our Quality Assurance team, you will be responsible for supporting site Label Control activities at our S-12 Cell Therapy manufacturing facility.Key ResponsibilitiesPerform in-process and drug product label...


  • Brown City, Michigan, United States Schneider Full time

    Position Summary: Schneider is looking for a Lead Financial Analyst to join our team in the Green Bay region. This role involves engaging in financial close activities, which include generating internal reports and conducting comprehensive variance analysis. The Lead Financial Analyst will be responsible for compiling period-end journal entries, executing...

  • Quality Engineer

    4 weeks ago


    Summit, United States SSi People Full time

    Job Title: Commissioning/Qualification Specialist / Specific Commissioning and Validation support Location: Summit, NJ (Hybrid)Duration: 12+ monthsPay Rate: 40-45/hr on W2Essential Functions:Maintains all qualified and validated equipment and systems in compliance with policies, guidelines and procedures.Support Lifecycle Document Management SystemDevelops...

Quality Control Laboratory Analyst

4 months ago


Brown Summit, United States PGBPGNGLOBAL Full time

Job Location

Brown Summit

Job Description

Do you have a passion for working in a laboratory? Do you thrive in a dynamic environment? We're looking for great teammates that have these qualities and want to make a difference by cultivating good manufacturing practices (GMP's) and company quality principles to deliver the product performance and quality for the consumers P&G serves. We have several types of Quality Control roles available at our Brown Summit Plant.

As a QC Laboratory Analyst, you could work in a manufacturing laboratory environment that stays in sync with Good Laboratory Practice (GLP) and current Good Manufacturing Practice (cGMP). The work will require collection, labeling, analysis, and results recording related to raw materials, intermediate products, finished goods, packaging materials and other samples. Tracking, trend analysis, and other Quality Control (QC) related responsibilities will be performed as directed by laboratory systems.

We also have roles for a QC Analyst require writing control documents like Standards Operating Procedures (SOPs), deliver training, perform system health assessments, on the floor coaching, products disposition, facilitate or participate on quality system failures investigations. Maintain cGMP principles and Good Documentation practices.

Where do you fit in?


Meaningful work on Day 1

We do various types of work including performing raw material, finished goods, intermediate, and development sample analysis according to standard analytical procedures. We perform routine instrument maintenance and calibration as needed during analytical work. We conduct limited instrument troubleshooting and problem diagnosis. We use discernment based on knowledge and experience as to the accuracy and reliability of analytical results. You will observe and identify problems with results and report to your supervisor. You will conduct analytical method development work with direct supervision and mentorship from the Lab Coordinator or other staff members. You may sample and label materials as needed according to written procedures or specific instructions, inspect empty bulk trucks prior to loading and appearance of raw materials during unloading as needed. Another responsibility will include coordinating the work with the Production Lead on night and weekend shifts to ensure appropriate prioritization of work.

Job Qualifications

Education:

  • Have a 2 year degree or more in a Science Field.
  • Commensurate experience of 5 years in a QC lab or GMP manufacturing operations will be considered.

We believe you will be an excellent fit here if, you:

  • Have Computer literacy sufficient to use standard software (MS Office) as well as the ability to learn specific software and instrumentation.
  • Possess experience and knowledge of basic laboratory operations such as weighing, titrating, and preparing volumetric solutions.
  • Interpret analytical method procedures and safety instructions using standard chemistry terms and measures.
  • Perform routine calculations pertaining to analytical chemistry (e.g. dilution, concentration, test results).
  • Have Experience resolving operational or processes failures to understand root cause and able to develop an improvement plan
  • Have effective verbal and written communication skills with supervisor, other employees, and departments.
  • Are willing to wear appropriate safety equipment, such as safety shoes, hearing protection, and eye protection, wherever these things are necessary
  • Will work on a rotating shift schedule, including weekends.
  • Are able to work 24/7 rotating shifts and are available for overtime and call-in as needed.

We want you to know:

  • Starting Pay / Salary Range: $ $23.42 per hour
  • Compensation for roles at P&G varies depending on a wide array of non-discriminatory factors including but not limited to the specific office location, role, degree/credentials, relevant skill set, and level of relevant experience. At P&G compensation decisions are dependent on the facts and circumstances of each case. Total rewards at P&G include salary + bonus (if applicable) + benefits. Your recruiter may be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the hiring process.
  • You will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, disability status, age, sexual orientation, gender identity and expression, marital status, citizenship, HIV/AIDS status or any other legally protected factor.
  • Immigration sponsorship is not available for this position. Applicants for U.S. based positions are generally required to be eligible to work in the U.S. without the need for current or future sponsorship. Except in rare situations based on Procter & Gamble's sole discretion. Procter & Gamble does not sponsor applicants for permanent residency. Any exceptions would be based on the Company's specific business needs at the time and place of recruitment as well as the qualifications of the individual.
  • Procter & Gamble participates in e-verify as required by law.

Qualified individuals will not be disadvantaged based on being unemployed

Job Schedule

Full time

Job Number

R

Job Segmentation

Plant Technicians (Job Segmentation)

Starting Pay / Salary Range

$ $23.42 / hour