Analyst 1, Lab Quality Control (Multiple Openings)

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at

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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 are searching for the best talent for an Analyst 1 Lab 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.

Purpose: The Associate Analyst is responsible for testing and analyzing raw materials in-process samples and products such as chemicals and Active Pharmaceutical Ingredients (API) to determine stability purity chemical content and other characteristics. They follow standardized test-methods procedures and work instructions document test results and communicate status of test results.

What you will be responsible for:

• Set up operate and clean laboratory equipment used to support production of intermediate raw material and finished products for API medical device raw material components and other products as directed; complete all associated support activities in the laboratory.
• Assure that QC laboratories run in a safe clean and environmentally sound manner.
• Review peer laboratory data to ensure accuracy and completeness.
• Demonstrate and develop experience on HPLC UPLC Karl Fischer UV analysis NIR and other analytical techniques and train other laboratory personnel on these techniques.
• Develop skills to troubleshoot and perform minor maintenance calibration and repair of laboratory instrumentation.
• Provide input on investigations (OOS OOT invalid assays and other lab-related non-conformances including investigations of audit observations) as needed.
• Support the implementation of relevant CAPAs and monitor effectiveness of CAPAs.
• Carry out duties in compliance with all state and federal regulations and guidelines including FDA ISO EPA OSHA and DEA and adheres to all company and site policies and procedures.

Qualifications / Requirements:

Required:

• Requiresability and flexibility to work weekends and overtime (on a scheduled or emergency basis) to support shift operations.
• High school diploma or two-year technical degree in a science or laboratory related field with four (4) years of Experience in a Quality Control (GMP regulated) Laboratory

OR

• Bachelors or Masters degree in Chemistry or related science degree.

Preferred:

• Experience applying mathematical operations to such tasks as frequency distribution determination of test reliability and validity analysis of variance correlational techniques sampling theory and/or factor analysis.
• Experience identifying and defining problems collecting data establishing facts and making scientific-based conclusions.
• Knowledgeable of FDA/EMEA regulatory requirements applicable to pharmaceuticals and medical device.
• Experience in Lab Operations and/or Quality processes/systems in a GMP Lab setting
• Experience working with Lab Systems or processes such as eLIMs TrackWise Non-conformances and/or Change Control.
• Familiarity with a variety of laboratory equipment such as: GC HPLC UPLC and/or Karl Fisher.

Are you interested in joining a team that is positively impacting patients lives by ensuring high quality in our pharmaceutical products Apply today for this exciting role!

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 () or contact AskGS to be directed to your accommodation resource.

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