https://amzn.to/44P6GXZ
Benefits you will enjoy starting your first day:
Competitive pay based on experience, night shift differential, and annual performance bonus.
Full medical, dental, and vision coverage, competitive 401k, HSA/FSA, and company-paid Pension plan.
120 hours of paid vacation, 40 hours of paid sick leave, and an additional 40 hours of 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.
Are you interested in joining a team that positively impacts patients’ lives by ensuring high quality in our pharmaceutical products? Apply today for this exciting role!
As an Associate Manufacturing Operator, you will:
Performs duties related to the preparation and manufacture of active pharmaceutical ingredients, intermediates, and/or medical devices.
In this role, you will be responsible for:
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 substances 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.
Independently and optimally demonstrate the operation of dryers, centrifuges, mills, reactors, water systems, DCS, and PLC control systems and appropriately respond to alarms and interlocks.
Complete process sampling requirements following applicable schedules and techniques
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.
Basic Qualifications:
Required:
High school diploma or GED.
Able to read, write, understand basic English and math, and work effectively as a team.
Available for overtime work on a scheduled or emergency basis.
Available and willing to work a starting shift of 7:00 am-7:00 pm for training, then transition to biweekly rotating hours of 7:00 am to 7:00 pm and 7:00 pm to 7:00 am shifts, including weekends and overtime.
Physical Requirements:
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 the ability to adjust focus.
Must be able to qualify for respiratory protective equipment use.
Preferred Qualification:
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 Systems and SAP systems.
Basic PC navigation, such as the ability to enter data into programs/software applications.
Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.
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