Position : General Assembler

Location : El Paso, TX

Duration : 12 Months

Total Hours/week : 40.00
pay range -$16-20/hr

1^st &2^nd Shifts

Client: Medical Device Company

Job Category: Industrial

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)

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.