Manufacturing Operator (2nd Shift)

Nesco Resource; Fall River (MA); On-site; USD 35,000 - 50,000; Full time

Job summary

A leading company in the pharmaceutical industry seeks a Manufacturing Operator I for the 2nd shift in Fall River, Massachusetts. The role involves dispensing materials, monitoring production, and ensuring compliance with cGMP standards. Candidates should have a high school diploma, relevant manufacturing experience, and strong safety adherence. Competitive benefits are offered, emphasizing a commitment to employee well-being and development.

Benefits

Medical insurance

Vision insurance

Dental insurance

401K

Employee Assistance Program (EAP)

Qualifications

• 1 year of manufacturing experience in pharmaceutical industry.
• Proficient in English (Speaking/Reading/Writing).
• Ability to follow verbal and written instructions.

Responsibilities

• Dispensing raw materials and ensuring batch quality.
• Daily monitoring of production performance.
• Performing cleaning and sanitation of production area.

Skills

Health & Safety procedures

Mathematical skills

Organizational skills

Education

High school diploma or equivalent

Accredited college certificate or university degree

Job description

Manufacturing Operator I – 2nd Shift

Responsibilities

• Dispensing raw material and primary packing materials as per work order and checking of raw material and primary packing materials.
• Ensure the proper planning and execution of batches.
• Performing cleaning and sanitation of production area and machinery as per respective procedures.
• Daily monitoring of production performance.
• Perform manufacturing processes and document activities in batch records and logbooks.
• Machine operation with minimum rejections and maximum outputs while maintaining quality standards within the standard norms.
• Operating equipment and performing necessary maintenance on machinery.
• Ensure equipment upkeep in co-ordination with engineering for preventive maintenance and calibration.
• Maintaining inventory of machine parts, tools and accessories.
• Working individually and in collaboration with others as part of a team.
• Collaborate with packaging, maintenance, quality teams for cross functional activities.
• Ensure status labelling at all stages of manufacturing, filling and cleaning.
• Identifying and assisting in any corrective actions.
• Perform, check and ensure calibration/verification of instruments, equipment and weighing balances as per schedule.
• Perform line clearance checks.
• Wearing appropriate PPE as stated in the SOP before entering any processing areas.
• Following procedures to complete tasks in a safe and efficient manner.
• Performing duties through the proper safe use of equipment, according to Health & Safety procedures and Equipment Manuals.
• Be able to operate computer systems with ease.
• Knowledge of pharmaceutical manufacturing and related documents.
• Basic understanding of deviation, CAPA, change control, FMECA , OOS,OOT and OOAC.
• Maintaining and followed 100% cGMP, GDP and SOP Compliance during complete operation hours.
• Complying with all company policies and procedures.
• Reporting all issues that arises to the department head or reporting manager.
• Performing daily maintenance on equipment and machinery.
• Completing all documentation in a timely manner, ensuring their integrity, accuracy and completeness.
• Maintaining discipline in department.
• May be required to assist in the training of other employees in the department.
• Flexible to work extended hours, to achieve manufacturing schedule when needed.
• All employees must undergo various training activities at the start of their employment. New trainings and re-trainings will occur periodically. Operators may be required cross-train in all areas of the manufacturing operations. Employees must strictly adhere to all safety, health, and environmental guidelines at all times and ensure that all safety precaution are being taken during handling of machines

Requirements

• 1 year of manufacturing experience in pharmaceutical industry. MDI experience is highly preferred.
• High school diploma or equivalent is required.
• Accredited college certificate or university degree is preferred.
• Proficient in the English language (Speaking/Reading/Writing) to understand work instructions and document results.
• Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment highly preferred.
• Basic understanding of mechanical machinery and the operating principles of control systems.
• Ability to follow both verbal and written instructions.
• Demonstrated ability to work in both independent and team environments.
• Good knowledge of Health & Safety procedures, including, OSHA.
• Strong mathematical and organizational skills.
• This position requires the ability to do heavy lifting / bending frequently.
• Ability to wear appropriate PPE is required.
• Individual may be required to wear respiratory devices that include but are not limited to: Air Purifying Respirators (APR) which include half-face and full-face negative pressure respirators, hooded powered air purifying respirators, or Supplied Air Respirators (SAR), which include hooded or full face supplied air respirators.

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.