Manufacturing Operator II

Nesco Resource; North Great River (NY); On-site; USD 40,000 - 60,000; Full time

Job summary

A leading company in pharmaceutical manufacturing is seeking a Manufacturing Operator II responsible for operating production machinery and ensuring compliance with SOPs and BMR requirements. The role requires a strong background in pharmaceutical manufacturing, documentation skills, and the ability to adhere to safety and quality standards. This position offers a competitive salary, comprehensive benefits, and the opportunity to work in a dynamic environment that values employee contributions.

Benefits

Comprehensive benefits package

Medical, Vision, Dental

401K

Employee Assistance Program

Qualifications

• 3 years of direct work experience in pharmaceutical manufacturing.
• Understanding of granulation, compression, coating, and encapsulation machines.
• Proficiency in English required.

Responsibilities

• Operate pharmaceutical production machinery and ensure cleanliness and setup.
• Execute manufacturing procedures following SOPs and BMR.
• Complete manufacturing documents accurately and on time.

Skills

Legible handwriting

Documentation

Technical writing

Troubleshooting

Communication

Education

High School Diploma or equivalent (i.e. GED)

Job description

Manufacturing Operator II

Responsibilities

• Must be willing to work in a pharmaceutical setting.
• Must be able to know how to operate pharmaceutical production machinery independently and thoroughly complete required documentation (legible writing, accurate reporting, maintain and file, etc.)
• Execute procedures for manufacturing processes in accordance with batch manufacturing record (BMR) and Standard Operating Procedures (SOP) requirements.
• Perform machine changeovers, cleaning and set up as per SOPs. Ensure the proper area & equipment cleanliness and setup in stipulated time.
• Prepare a room and equipment for line clearance, replace room filters, Ensure verification and calibration of balance/scale and check pressure differential for the rooms.
• Ensure line clearance before initiating manufacturing activities in each area.
• Receive/transfer material from/to dispensing/manufacturing storage and check dispensed materials/final mix blend/compressed tablets and labeling as per BMR.
• Wear appropriate personal protective equipment (PPE) as stated in the SOP/BMR before initiating the process.
• Able to operate applicable equipment independently as per area of operation.
• Ensure adherence to quality standards during all stages of the manufacturing process.
• Complete manufacturing documents on time, ensuring accuracy and completeness.
• Responsible for training on all relevant SOPs and always maintain compliance with related SOPs and current Good Manufacturing Practices (cGMP) in the manufacturing process.
• Perform duties through the proper, safe use of equipment, according to Health & Safety procedures and Equipment Manuals.
• Flexible to work extended hours, to achieve manufacturing schedule when needed.
• Maintain discipline and comply with company policies and procedures.
• Perform entire duties as communicated time to time by department management/designee.
• Participate in safety related programs and or safety teams as needed.
• Enforce and follow safety regulations and ensure the working area is clean.
• Adhere to companies Safety, Health, and Environmental policies.
• Must be able to work under general supervision and able to work independently and in a team environment.
• Must be able to exercise appropriate professional judgment on matters of significance.
• Other duties assigned by Manufacturing Management.

Requirements

• 3 years of direct work experience in pharmaceutical manufacturing.
• High School Diploma (or educational equivalent (i.e. GED)
• Preference will be given to candidates with experience in generic pharmaceutical manufacturing.
• Must have legible handwriting, and the ability to perform accurate documentation.
• Understanding of granulation, compression, coating, and encapsulation machines.
• Capable of conducting troubleshooting, investigations and root cause identification and analysis.
• Able to prioritize, plan and work under tight schedules and deadlines.
• Technical writing skills and application of relevant scientific principles and practices (preferred).
• Must communicate clearly and concisely, both orally and in written.
• English proficiency required.
• Should not have any restriction to work with powder containing active pharmaceutical ingredients.
• This position requires the ability to do heavy lifting / bending frequently.
• Long periods of standing up/walking during the working hours; ability to ascend/descend ladders; and able to lift to 35 pounds.
• Must be able to move pallets/equipment weighing about 200 – 300 kgs using suitable moving equipment like pallet jacks.

Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.

Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.