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 an Analyst Quality Control to be in Athens, GA.
Benefits you will enjoy starting your first day:
Competitive pay based on experience, night shift differential, plus an annual performance bonus.
Full medical, dental and vision coverage, competitive 401k, HSA/FSA, and company paid Pension plan.
120 hours paid vacation, plus 40 hours paid sick leave and an additional 40 hours paid personal leave.
Tuition Reimbursement for eligible degree programs.
GENERAL PURPOSE OF JOB
Responsible under general supervision or working independently, for sampling and/or testing of raw materials, in-process materials, final products, water, and other samples (e.g., equipment sanitization rinses) in adherence to appropriate test procedures and specifications for microorganisms and endotoxins. Designs, conducts, and interprets microbiological experiments to support ongoing operations, process improvement initiatives, and new product development activities.
Provides microbiological scientific support to technology and product development. Authors and reviews scientific and technical summaries and provides recommendations for potential business applications.
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.
Performs tasks 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
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 by 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 and 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, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.
#LI-Onsite
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 Standards, Quality Systems Documentation, Report Writing, Sample Testing, Technologically Savvy
