Analyst Quality Control

Johnson & Johnson•Athens, GA

1d•Onsite

About The Position

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/. An internal pre-identified candidate for consideration has been identified. However, all applications will be considered. We are searching for the best talent for an Analyst Quality Control to be in Athens, GA.

Requirements

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

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 audit-ready 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.
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.