Analyst Quality Control (Contract)

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.

Job Function:

Quality

Job Sub Function:

Quality Control

Job Category:

Professional

All Job Posting Locations:

Incheon, Korea, Republic of

Job Description:

1.Company: Janssen Vaccines

2. Location: Incheon, Songdo

3. Job type: Fixed-term

Johnson & Johnson has announced preliminary plans to close the manufacturing facility in Incheon as part of a global supply chain reorganization. The plan remains under review and may evolve as discussions progress. Any potential closure would follow applicable legal requirements, regulatory approvals, and other customary conditions.

If you accept this role, you would be employed by Janssen Vaccines on a fixed-term basis throughout the transition period, and your employment would be governed by Janssen Vaccines’ processes, programs, policies, and benefit plans. Additional details will be shared by Janssen Vaccines at the appropriate stage.

Essential Job Duties & Responsibilities:

General Laboratory Activity

Complies with laboratory safety requirements

Complies with laboratory related regulation and requirements

Preparation/Revision and review of GMP/GLP documents (Test method documents, Lab notes (Worksheet), Procedures)

Usage and Management of GMP document / Assure that GMP/GLP documents are properly maintained and/or archived

Internal and external audit/inspection Preparation and Response

Other laboratory Support activity (e.g., housekeeping)

( The responsibilities listed below may be assigned based on business needs, organizational priorities, and the individual's qualifications and competencies. )

QC Laboratory Test Activity

Perform QC testing in compliance with GMP and corporate requirements/procedures.

Review analytical data and test results.

Conduct and/or support laboratory investigations when issues occur.

Perform data integrity activities in accordance with applicable regulations and J&J requirements.

Utilize electronic systems (e.g., LIMS, MES, LES, Empower) for execution, review, and documentation of laboratory activities.

QC Laboratory Management

Laboratory system administration (LIMS. Empower, etc.)

Lab equipment management (Qualification (Instrument Decommissioning included), Calibration, Maintenance, etc.)

Coordinate/Document/Handling non-conformances, corrective actions (CAPAs) and changes (change control management)

Lab activities for creating a Safe Lab Environment

Accompany visitors and provide training to visitors

Manage and Review of GMP data in compliance with GMP and corporate requirements/Procedures

Keep supervisor informed of task status and issues

Complete corrective and preventative actions (CAPA) as assigned

Minimum Qualification

Minimum Bachelor's degree (in Chemistry, Chemical Engineering, Life Science, Pharmaceutical Engineering, or related fields

Knowledge and understanding of current Good Manufacturing Practices (cGMP) or GLP related to the QC laboratory is preferred.  Basic knowledge of compendial (USP, EP, JP, etc.) requirements pertaining to their functional area of QC is helpful

Fluency in written English and conversational spoken English is preferred.

Interpersonal communication skills, persuasiveness and an active desire to work together with colleagues and external parties

Demonstrated ability to organize and prioritize workload

Good knowledge in the application of Microsoft Office programs. (Outlook, Excel, Word, and PowerPoint)

Preferred Qualification

At least 3 years of experience

Experience in pharmaceutical industry

Experience in QC department is preferred.

Skilled in performing basic and some advanced testing within the functional laboratory is preferred

Experience in performing independent troubleshooting & basic root cause analysis skills are preferred

Required Skills:

Preferred Skills:

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