Analyst Quality Control

Johnson & Johnson

Athens (GA)

On-site

USD 55,000 - 85,000

Full time

13 days ago
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Job summary

Johnson & Johnson in Athens, Georgia seeks an Analyst Quality Control to support environmental monitoring and microbiology testing. The role involves operating lab equipment, maintaining records, ensuring cGMP compliance, and contributing to continuous improvement within the QC unit.

The successful candidate will have a 4-year degree in microbiology or 0–2 years of related experience, strong technical writing, and the ability to work with cross-functional teams to uphold product quality and

Qualifications

  • Requires 0–2 years of experience or commensurate 4 year degree in microbiology or closely related field of study.
  • Familiarity with cGMPs, FDA regulations, and quality systems is preferred.
  • Strong analytical and documentation skills in a controlled environment.

Responsibilities

  • Designs, executes, and documents environmental and water system monitoring programs.
  • Operates and maintains laboratory equipment with calibrated precision.
  • Prepares microbiological media, reagents, and maintains lab records.
  • Ensures compliance with cGMP and safety policies; supports investigations and CAPA actions.
  • Interprets test results and communicates findings to manufacturing and QA teams.
  • Assists in training microbiology personnel and performs data reviews.
  • Oversees inventory of lab supplies and proper handling of controlled substances.
  • Prepares environmental monitoring reports and risk assessments.

Skills

Quality control
Aseptic techniques
cGMP compliance

Education

B.S. in Microbiology

Tools

Microsoft Office

Job description

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:

Athens, Georgia, United States of America

Job Description:
About Innovative Medicine

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

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 https://www.jnj.com/.

We are searching for the best talent for Analyst Quality Control
ESSENTIAL DUTIES AND RESPONSIBILITIES
  • Designs and implements environmental and water system monitoring programs using advanced knowledge.
  • Conducts preliminary data interpretation, maintains accurate documentation, and provides scientific input for abstracts and manuscripts.
  • Operates and maintains laboratory equipment, ensuring reliable and accurate test data through qualifications, maintenance, and calibrations.
  • Assists in training microbiology personnel and performs peer reviews of laboratory data for accuracy.
  • Maintains test methods, SOPs, and procedures essential for microbiology laboratory operations.
  • Prepares and analyzes samples according to USP, FDA guidelines, and test methods; performs various microbiological analyses.
  • Interprets test results and assesses their impact on manufacturing and shipping processes.
  • Conducts or assists with non-conformance investigations, documenting findings and recommending corrective actions.
  • Prepares microbiological media, standards, reagents, and maintains clear laboratory records.
  • Ensures laboratory practices comply with cGMP guidelines and maintains a clean, safe, and auditready environment.
  • Orders necessary laboratory supplies to keep stock updated, and handles controlled substances in compliance with legal requirements.
  • Prepares timely reports for environmental monitoring and other needs, while identifying risks based on data analysis.
  • Completes other duties as assigned by the Quality Control Manager or QC Supervisor.
ADDITIONAL POSITION REQUIREMENTS
  • Adheres to established test methods, procedures, and corporate guidelines.
  • Works independently while knowing when to seek assistance.
  • Collaborates with personnel from receiving, manufacturing, technical, and waste treatment operations for material testing.
  • Partners with corporate staff regarding the Microbiological Laboratory's functioning.
  • Complies with state and federal regulations, including FDA, EPA, OSHA, and DEA, ensuring data integrity and environmental responsibility.
  • Performstasks with a focus on quality, safety, and environmental matters, including proper use of personal protective equipment and hazard reporting.
  • Completes regulatory and job training requirements on time.
  • Stays updated on professional and industry trends.
  • Contributes positively by enhancing laboratory practices and quality systems.
  • Takes on additional projects or assignments as directed by management.
  • Available for scheduled or emergency overtime work.
QUALIFICATIONS EDUCATION and/or EXPERIENCE

Requires 0-2 years of experience or commensurate 4 year degree in microbiology or closely related field of study.

LANGUAGE SKILLS
  • Proficient in reading, writing, and understanding Basic English.
  • Analyzes and interprets complex documents, including scientific journals, technical procedures, governmental regulations, business periodicals, financial reports, and legal documents.
  • Writes technical reports, business correspondence, and procedure manuals.
  • Effectively presents information and responds to questions of top managers, clients, customers, regulatory agencies and the general public.
  • Demonstrates strong technical writing skills.
MATHEMATICAL SKILLS
  • Engages with mathematical concepts, including probability, statistical inference, process control, and the basics of geometry and trigonometry.
  • Utilizes concepts like fractions, percentages, ratios, and proportions for practical problem-solving.
  • Performs mathematical operations for tasks such as frequency distribution, test reliability and validity assessment, variance analysis, correlation techniques, sampling theory, dimensional analysis, linear regression,
REASONING ABILITY
  • Identifies problems and gathers data to form valid conclusions.
  • Analyzes and interprets diverse technical instructions in mathematical or diagrammatic forms while managing both abstract and tangible variables.
  • Utilizes logical and scientific reasoning to address a variety of intellectual and practical challenges.
  • Navigates and interprets complex nonverbal symbols, such as formulas and graphs, even in their most difficult stages.
OTHER SKILLS ABILITIES OR QUALIFICATIONS
  • Experienced in using aseptic techniques for sampling and testing materials.
  • Knowledgeable about cGMPs and FDA recommended procedures (e.g., Bacteriological Analytical Methods).
  • Proven ability to perform tasks accurately with minimal supervision.
  • Proficient in Microsoft Office, capable of data entry, analysis, word processing, presentations, and calculations.
  • Able to operate effectively under stress in emergency or hazardous situations.
  • Strong team player with excellent collaboration skills.
  • Knowledge of cGMPs and safety/environmental regulations relevant to pharmaceutical or chemical manufacturing.
  • Demonstrates strong technical and troubleshooting skills through past achievements.
  • Capable of managing multiple priorities and adapting to changing demands.
PHYSICAL DEMANDS
  • The employee frequently is required to stand; walk; sit; use hands to finger, handle, or feel; reach with hands and arms, and talk or hear.
  • The employee is occasionally required to climb or balance; stoop, kneel, crouch, or crawl; and smell.
  • The employee must frequently lift and/or move up to 10 pounds, and may occasionally lift and/or move up to 25 pounds.
  • Specific vision abilities required by this job include close vision, distance vision, color vision, and ability to adjust focus.
  • The employee must frequently use fine motor skills of the hands to perform detail tasks such as weighing micrograms.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected under federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers. Internal employees contact AskGS to be directed to your accommodation resource.

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
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