Production Technician

Lancesoft; Carlsbad (CA); On-site; USD 25,000 - 36,000; Full time

Job summary

Lancesoft is seeking a reagent pack production associate to join the manufacturing team in California. You will formulate, fill, test and package chemical and biological reagents in a regulated environment, following SOPs and daily production plans.

Ideal candidates have at least 2 years of relevant experience in a regulated industry (FDA/ISO) and are proficient with Microsoft applications. You will work on setup, testing and quality control to ensure on-time completion and adherence to quality

Qualifications

• Must have 2+ years relevant experience in a regulated industry (FDA/ISO)
• Follows established SOPs and quality guidelines
• Proficiency with Microsoft applications (MS Office) and basic analytical methods

Responsibilities

• Read, comprehend and follow work instructions with emphasis on quality
• Execute the daily production plan to meet due dates and quality standards
• Train to Standard Operating Procedures (SOPs)
• Follow drawings, work orders and SOPs while maintaining FDA requirements
• Independently perform formulating, filling, testing and packaging of reagents
• Conduct basic analytical tests (pH, conductivity, density) on solutions
• Ensure compliance with GMP, QSR and ISO requirements
• Collaborate with cross-functional team to troubleshoot and improve quality

Skills

Quality focus

Teamwork

SOP compliance

Documentation

English proficiency

Microsoft Office

Tools

Microsoft Applications

Job description

Duration: 0-6+ Months Shift: 5: 30 am to 2: 00 pm, (Mon–Fri)

Job Description: Our manufacturing company is seeking a team member to join our Reagent Pack Value Stream team. In this role you will formulate, fill, test, and package chemical and biological reagent products of varied complexity according to operational plans and customer demand. We are looking for associates whom thrive in a team-oriented, goal focused environment. We operate using Daily Management principles, providing immediate guidance and feedback to our associates and focusing on daily, monthly, and quarterly objectives. You will be responsible for following established operation procedures, maintaining appropriate training records for your role, sustaining a smooth flow of material and the execution of work orders to on-time completion.

Key Responsibilities

• Read, comprehend and follow established work instructions and procedures with emphasis on quality,
• Execute the daily production plan to due date conformance and quality standards,
• Train to Standard Operating Procedures (SOPs).
• Follow engineering drawings, work order information, SOPs, and other written and verbal specifications in the manufacturing process while maintaining FDA requirements,
• Independently execute work regarding formulating, filling, testing and packaging,
• Apply basic analytical skills or scientific methods to perform daily tasks,
• Perform the set-up, calibration, testing and troubleshooting of reagent components and instruments,
• Conduct testing on solutions which include pH, conductivity, and density, to ensure adherence to production/process specifications,
• Assure compliance with FDA Quality System Regulations (QSR), Good Manufacturing Practices (GMP), and ISO regulatory requirements,
• Work directly and cooperatively with cross-functional team members to troubleshoot issues and ensure emphasis on quality,
• Identify, recommend and implement quality improvements including but not limited to production methods, equipment performance, product quality and efficiencies,
• Learn and participate in the company's lean manufacturing principles,
• Maintain a safe and clean working environment by complying with procedures, rules, and regulations,
• Perform other duties and cross training as assigned,
• Train new team members on equipment operations and work procedures as needed,
• Ability to complete appropriate paperwork, maintain accurate records of production and report status of work.
• Must read, write and speak fluent English.
• Proficiency with Microsoft applications.

Our Leadership Competencies

We value associates with solid decision making and priority setting skills, and who are going to thrive in a diverse environment where individual contribution and team effort are equally important.

Physical Demands

While performing the duties of this job, the associate is regularly required to stand for prolonged period of time. The employee is frequently required to talk and hear;use hands to handle or feel;and reach with hands and arms above shoulder height and below the waist. The associate must be able to read and speak English. Using proper lifting techniques, the employee must be able to lift up to 30 lbs. Associate must have good hand dexterity. Ability to maneuvers assembly components by hand in a repetitive manner conducive to efficiency, job specifications, safety, and quality goals. Ability to frequently stand (80%), bend, kneel, lift and sit to accomplish assembly production goals.

Education/Experience

Must have 2+ years relevant experience. Experience in a regulated industry preferred (e.G. FDA, ISO).