Demo

Qualtiy Control Compliance Investigator

Lynkx Staffing LLC
Saddle Brook, NJ Full Time
POSTED ON 2/3/2025
AVAILABLE BEFORE 5/2/2025

Job Description

Job Description

QC Microbiology Compliance Investigator Allendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Device, IT & Human Resources disciplines in New Jersey. Leads life-cycle investigations, including but not limited to deviations, environmental excursions, non-conformances, discrepancies, etc. to improve the processes by implementing corrective and preventative actions to ensure compliance.

  • Determine the causes and preventative actions of Deviations, Non-Conformances, OOS, OOT, environmental excursion investigations.
  • Drive investigations to true root cause using appropriate investigation tools.
  • Benchmark industry standards to develop, advocate, and implement investigative and impact assessment tool sets.
  • Define and implement effective preventative actions to prevent recurrence.
  • Manage multiple investigations in different stages of the process to efficiently meet compliance deadlines and product release dates.
  • Collaborate with cross-functional teams to develop and track CAPA plans.
  • Identify and create appropriate trending rules that trigger corrective actions.
  • Analyze process data and evaluate trends to identify major improvement opportunities.
  • Effectively utilize change management approach.
  • Develop materials to train and educate personnel on writing problem statements and use of root cause analysis tools, discrepancy and deviation process.
  • Manage CAPA plans and implementation.
  • Provide communication plan for on-going deviations & CAPA’s.
  • Effectively create and communicate CAPA plan to responsible parties.
  • Oversee timely completion of deviations, CAPAs, and Change Controls as necessary.
  • Ability to abide by quality standards.

REQUIREMENTS

  • BS in a Quality / Process related field or equivalent experience.
  • 3-5 years of experience in quality control or quality assurance within the bio-pharma, biologics, or pharmaceutical industry or equivalent experience.
  • Experience successfully leading event investigations, Root Cause Analysis (RCA), and CAPA
  • Must have technical experience writing and assessing deviations, investigations, and Out of Specifications
  • Must be able to analyze data / information and to assess and resolve complex problems
  • Strong knowledge and understanding of U.S. and international cGMPs, ICH, and other regulations applicable to clinical and commercial manufacturing
  • Knowledge of operational processes and controls in non-sterile and sterile operations
  • Experience using e-Quality Management Systems preferred.
  • Relevant IT skills (able to work with Visio, Microsoft Project and Excel)
  • Ability to think strategically and tactically (detail-oriented)
  • Strong collaborative and influencing skills and ability to work well in a cross-functional, matrixed environment
  • Analytical and problem-solving skills
  • Strong written and oral communication skills
  • Flexible and able to adapt to company growth and evolving responsibilities
  • Integrity, accountability and strong dedication to regulatory compliance
  • Continuous improvement mindset
  • Ability to work effectively as a team and independently.
  • Training; GMP Training, Quality Systems Training (Deviation / CAPA), Safety Training, Working Environment
  • While performing the duties of this job, the employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens. 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.

    If your compensation planning software is too rigid to deploy winning incentive strategies, it’s time to find an adaptable solution. Compensation Planning
    Enhance your organization's compensation strategy with salary data sets that HR and team managers can use to pay your staff right. Surveys & Data Sets

    What is the career path for a Qualtiy Control Compliance Investigator?

    Sign up to receive alerts about other jobs on the Qualtiy Control Compliance Investigator career path by checking the boxes next to the positions that interest you.
    Income Estimation: 
    $106,113 - $127,991
    Income Estimation: 
    $127,094 - $153,876
    Income Estimation: 
    $47,729 - $61,141
    Income Estimation: 
    $103,208 - $149,238
    Income Estimation: 
    $55,058 - $69,785
    Income Estimation: 
    $53,971 - $69,835
    Income Estimation: 
    $57,415 - $77,967
    Income Estimation: 
    $91,665 - $118,322
    Income Estimation: 
    $103,208 - $149,238
    Income Estimation: 
    $72,210 - $96,012
    Income Estimation: 
    $72,210 - $96,012
    Income Estimation: 
    $91,665 - $118,322
    Income Estimation: 
    $103,208 - $149,238
    Income Estimation: 
    $90,652 - $121,490
    Income Estimation: 
    $90,652 - $121,490
    Income Estimation: 
    $91,665 - $118,322
    Income Estimation: 
    $103,208 - $149,238
    Income Estimation: 
    $116,025 - $158,364
    View Core, Job Family, and Industry Job Skills and Competency Data for more than 15,000 Job Titles Skills Library

    Not the job you're looking for? Here are some other Qualtiy Control Compliance Investigator jobs in the Saddle Brook, NJ area that may be a better fit.

    Quality Control Analytical Compliance Investigator

    Lynkx Staffing LLC, Saddle Brook, NJ

    Compliance Investigator, Clinical Manufacturing

    Lynkx Staffing LLC, Saddle Brook, NJ

    AI Assistant is available now!

    Feel free to start your new journey!