Analyst Quality Control

Johnson & JohnsonMalvern, PA
Onsite

About The Position

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine We are searching for the best talent for R-066286 Analyst Quality Control Purpose: Assists staff in various processes in the Quality Control function. Supports day-to-day laboratory activities such as sample management, supply ordering and receipt, and general housekeeping. Assists with analysis, qualification/validation activities, and lab investigations. Supports data review and metrics reporting. Executes continuous improvement projects with supervision. May execute testing under supervision. Assists laboratory staff with sample receipt, management of reagents and supplies, and general housekeeping. Tests samples of finished goods under general supervision. Applies developing knowledge of Quality Control standards to review results of quality analysis and report issues as required. Supports data review and analysis, and leads implementation of risk mitigations and continuous improvement initiatives under supervision. Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.

Requirements

  • Bachelor's Degree or equivalent
  • Requires 0-2 Years Work Experience of Related Work Experience
  • Skilled in performing basic testing within the QC laboratory
  • Experience, knowledge and understanding using Good Laboratory Practices (GLP) and basic knowledge of current Good Manufacturing Practices (cGMP) related to the QC laboratory
  • Ability to read and interpret documents such as SOPs, work instructions, test methods and protocols
  • Proficient with using Microsoft Office applications (Outlook, Excel, Word, and Powerpoint)
  • Makes GMP laboratory decisions both independently and with guidance from QC supervision

Nice To Haves

  • Analytical Reasoning
  • Business Behavior
  • Compliance Management
  • Continuous Improvement
  • Controls Compliance
  • Data Analysis
  • Execution Focus
  • ISO 9001
  • Persistence and Tenacity
  • Quality Control (QC)
  • Quality Standards
  • Quality Systems Documentation
  • Report Writing
  • Sample Testing
  • Technologically Savvy

Responsibilities

  • Responsible for in-process and final product quality analyses/inspection in compliance with standards and regulatory requirements, interpreting and evaluating the analyses in terms of accuracy and precision against established specifications.
  • Identifies ongoing quality issues, prevents potential production issues and makes suggestions for improvement.
  • Uses various measuring devices, testing equipment, predetermined methods, operations, setups and prescribed specifications to accept or reject products.
  • Audits, monitors and determines the quality of manufacturing processes and/or outputs against defined internal and regulatory standards.
  • Tests random samples of finished goods.
  • Reports manufacturing process deviations and defects in finished goods.
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