Qc Analyst (analytical Instrument and Lab Systems - Empower (waters) Chromatography Data System (cds))

Johnson & Johnson Johnson & Johnson · Pharma · Wilson, NC +1

The QC Analyst will be responsible for laboratory equipment lifecycle management, CSV support, and introducing & maintaining lab systems at a Biotherapeutics Manufacturing facility. This role requires expertise in the Empower (Waters) chromatography data system (CDS) and supporting its implementation, validation, user access, troubleshooting, and continuous improvement. The analyst will also participate in the qualification of analytical equipment and author SOPs, work instructions, and protocols, ensuring compliance with cGMP regulations and FDA/EU guidance.

What you'd actually do

  1. Serve as a site SME for Empower (Waters) chromatography data system (CDS), supporting implementation, validation (CSV), user access, troubleshooting, and continuous improvement. Participate in activities to introduce and sustain laboratory technologies and computer-based applications (eLIMS/iLABS, SDMS, Empower, SoftMax Pro) to improve laboratory efficiency and promote a culture of Innovation.
  2. Participate in the qualification of analytical equipment for related testing functions, for example, IQ/OQ/PQ of HPLC, Spectrophotometry, Endotoxin, Cell Culture and Total Organic Carbon equipment.
  3. Author SOP’s, Work Instructions and protocols.
  4. Responsible for the quality control laboratory equipment lifecycle management and CSV support.
  5. Interact with the QC Global organization for the different center of excellence for equipment and information technologies.
  6. The resolution of unexpected complex compliance or lab instrument and system issues as they arise

Skills

Required

  • Bachelor’s Degree in Chemistry, Biochemistry, Micro or science related field with 2+ years related experience in biopharmaceutical or pharmaceutical industry.
  • Working knowledge of regulatory requirements, policies and guidelines.
  • Experience with Quality Control document reviews and regulatory inspection processes.
  • Working knowledge of laboratory systems.
  • Hands-on experience administering and/or using Empower (Waters) CDS in a GMP QC environment.
  • Strong technical knowledge in and experience with QC analytical equipment.
  • Knowledge of cGMP regulations and FDA/EU guidance.

Nice to have

  • An equivalent combination of education and experience.
  • Excellent communication and interpersonal skills.
  • Ability to effectively collaborate with cross-functional teams.
  • Communicate complex quality concepts to stakeholders at all levels.
  • Proven ability to manage multiple priorities and work independently with minimal supervision.
  • Detail-oriented mindset.
  • Keen eye for identifying opportunities for process improvements.
  • Proven ability to prioritize tasks and meet deadlines in a dynamic manufacturing environment.
  • Ability to work in a team environment and interact with all levels of the organization.

What the JD emphasized

  • Working knowledge of regulatory requirements, policies and guidelines.
  • Experience with Quality Control document reviews and regulatory inspection processes.
  • Hands-on experience administering and/or using Empower (Waters) CDS in a GMP QC environment (e.g., project setup, processing, reporting, user management, audit trails, and data integrity controls).
  • Knowledge of cGMP regulations and FDA/EU guidance is required.