Johnson & Johnson is currently seeking a Associate Manufacturing Operator to join our team in Athens, GA.

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/.

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.

• 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.
• 2/2/3 schedule with a 3-day weekend every other week.
• Tuition Reimbursement for eligible degree programs.
• $3,000 sign-on bonus and/or company paid relocation available.

• Operating and cleaning production equipment used to produce intermediate or finished products and completing all associated support activities in the production of these products to ensure products are correctly manufactured and removed from defects as required.

• Handling-controlled substance in compliance with all state and federal regulations and guidelines including FDA, EPA, OSHA and DEA while maintaining compliance with all company and site policies and procedures and the intent of our Credo.

• Following and accurately completing batch records/logs, SAP transactions and other documentation associated with all production processes to ensure efficient operations and compliance with cGMP and standard operating procedures.
• Transporting materials of varying weight in accordance with established safety guidelines using material handling equipment and additional assistance as required.
• Performing all duties with attention to quality, safety and environmental matters including wearing appropriate personal protective equipment, recognizing, reporting, and appropriately responding to hazards in the work area, maintaining proper housekeeping, and properly labeling and storing chemicals.
• Perform other duties as assigned by site leadership.

• High school diploma or GED.
• Able to read, write, and understand basic English and math and work effectively as part of a team.
• Available for overtime work on a scheduled or emergency basis.
• Available and willing to work a starting shift of 7:00am-7:00pm for training, then transition to biweekly rotating hours of 7:00am to 7:00pm and 7:00pm to 7:00am shifts, including weekends and overtime.

• High school diploma or GED.
• Able to read, write, and understand basic English and math and work effectively as part of a team.
• Available for overtime work on a scheduled or emergency basis.
• Available and willing to work a starting shift of 7:00am-7:00pm for training, then transition to biweekly rotating hours of 7:00am to 7:00pm and 7:00pm to 7:00am shifts, including weekends and overtime.

• Standing, walking, climbing, bending, stooping, reaching with hands and arms, and using hands to finger, handle or feel; frequently required to talk, hear, taste and smell; must have the ability to work from ladders or platforms up to 30 feet in the air and the ability to lift, push or pull up to 40 lbs.
• Specific vision abilities required by this job include close vision, distance vision, color vision, depth perception, and ability to adjust focus.
• Must be able to qualify for respiratory protective equipment use.

• 1+ year experience in a regulated manufacturing industry.
• 6+ months of work experience in chemical, pharmaceutical, or other industry that complies with cGMP environment.
• Knowledge of Digital Control System and SAP systems.
• Basic PC navigation such as the ability to enter data into programs/software applications.