General Assembler

MillenniumSoft Inc; El Paso (TX); On-site; USD 22,000 - 28,000; Part time

Job summary

MillenniumSoft Inc in El Paso, TX is seeking an entry-level General Assembler under a 12-month contract on a W2 basis. Shifts available: 1st and 2nd, with total 40 hours per week and pay range $16–$20 per hour, dependent on experience and performance.

You will follow GMP and SOPs to prepare and manufacture active pharmaceutical ingredients, intermediates, or medical devices, under supervision. Basic English, safety procedures, and teamwork are essential in this manufacturing environment.

Qualifications

• High School Diploma/GED preferred or 4 months of work experience in a manufacturing environment required.
• Experience leading manufacturing machines is preferred.
• Work experience in chemical, pharmaceutical, or industry that complies with GMP is highly preferred.
• Able to read, write, and understand Basic English preferred.
• Operating skills of manufacturing equipment, tools, and hand/pallet jack is preferred.
• Basic PC navigation such as the ability to enter data into programs/software applications preferred.
• Experience of leading small group of people is preferred.
• Problem solving skills is highly preferred.
• Ability to communicate and effectively work as part of a team is preferred.

Responsibilities

• Possess a basic understanding of production processes within area of assignment and a working knowledge of manufacturing equipment.
• Follow GMP, s and standard operating procedures.
• Follow process and utility flow diagrams.
• Transport materials of varying weight in accordance with established safety guidelines using material handling equipment and additional assistance as required.
• Perform area safety inspections to identify safety hazards and report findings in accordance with company protocols.
• Demonstrates adherence to safety procedures by monitoring personal and peer behaviours, work environment and housekeeping.
• Participate in internal audits and support additional team activities as requested.
• Participate on site investigative teams and where applicable, NCR, s and behavioural safety assessments. Correct and/or mitigate findings from assessments.
• Available for overtime as needed
• Performs all duties with attention to quality, safety, and environmental matter such as wearing appropriate personal protective equipment, identifying, reporting, and appropriately responding to hazards in the work area (spills/accidents/near misses), always maintaining proper housekeeping, and properly labelling and storing chemicals.
• Carries out duties in compliance with all state and federal regulations and guidelines including FDA, ISO, and OSHA. Complies with all company and site policies and procedures.
• Assume responsibility for the environmental effects of work performed and for the identification and recording of environmental problems as they arise.
• Follow all applicable aspects of the site Environmental Management System as it pertains to normal job duties.
• Complete all regulatory training as assigned (GPM, s, ISO14001, OSHA, etc.).
• Complete Operator Training Program according to established guidelines.
• Be available for other projects or assignments as requested by management.
• Looking for ways to simplify or improve products, services, systems, and processes to achieve
• Makes a positive contribution through demonstration of ability to seek out assistance from co-workers as needed; to suggest ways to improve upon current operations practices and systems; and to learn new skills, procedures, and processes

Skills

Basic English

Problem solving

Teamwork

Communication

Education

High School Diploma/GED

Tools

Pallet jack

Job description

Level of Experience: Entry Level

Employment Type: Contract on W2 (Need US Citizens or GC Holders Only)

1st Shift (6:00 AM - 2:00 AM)

2nd Shift (2:00 PM - 10:00 PM)

Position: General Assembler

Location: El Paso, TX

Duration: 12 Months

Total Hours/week: 40.00

pay range -$16-20/hr

Client: Medical Device Company

Job Category: Industrial

Job Description

• Under direct supervision, trains to perform duties related to the preparation and manufacture of active pharmaceutical ingredients, intermediates, and/or medical devices in accordance with standard operating procedures, as regulated by quality, environmental, and safety agencies (FDA, OSHA, etc.).

Responsibilities

• Possess a basic understanding of production processes within area of assignment and a working knowledge of manufacturing equipment.
• Follow GMP, s and standard operating procedures.
• Follow process and utility flow diagrams.
• Transport materials of varying weight in accordance with established safety guidelines using material handling equipment and additional assistance as required.
• Perform area safety inspections to identify safety hazards and report findings in accordance with company protocols.
• Demonstrates adherence to safety procedures by monitoring personal and peer behaviours, work environment and housekeeping.
• Participate in internal audits and support additional team activities as requested.
• Participate on site investigative teams and where applicable, NCR, s and behavioural safety assessments. Correct and/or mitigate findings from assessments.
• Available for overtime as needed
• Performs all duties with attention to quality, safety, and environmental matter such as wearing appropriate personal protective equipment, identifying, reporting, and appropriately responding to hazards in the work area (spills/accidents/near misses), always maintaining proper housekeeping, and properly labelling and storing chemicals.
• Carries out duties in compliance with all state and federal regulations and guidelines including FDA, ISO, and OSHA. Complies with all company and site policies and procedures.
• Assume responsibility for the environmental effects of work performed and for the identification and recording of environmental problems as they arise.
• Follow all applicable aspects of the site Environmental Management System as it pertains to normal job duties.
• Complete all regulatory training as assigned (GPM, s, ISO14001, OSHA, etc.).
• Complete Operator Training Program according to established guidelines.
• Be available for other projects or assignments as requested by management.
• Looking for ways to simplify or improve products, services, systems, and processes to achieve
• Makes a positive contribution through demonstration of ability to seek out assistance from co-workers as needed; to suggest ways to improve upon current operations practices and systems; and to learn new skills, procedures, and processes

Qualifications

• High School Diploma/GED preferred or 4 months of work experience in a manufacturing environment required.
• Experience leading manufacturing machines is preferred.
• Work experience in chemical, pharmaceutical, or industry that complies with GMP is highly preferred.
• Able to read, write, and understand Basic English preferred.
• Operating skills of manufacturing equipment, tools, and hand/pallet jack is preferred.
• Basic PC navigation such as the ability to enter data into programs/software applications preferred.
• Experience of leading small group of people is preferred.
• Problem solving skills is highly preferred.
• Ability to communicate and effectively work as part of a team is preferred.