Production Operator

Lancesoft

Union City (CA)

On-site

USD 36,000 - 60,000

Full time

5 days ago
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Job summary

Lancesoft is seeking a Manufacturing Associate to support routine production activities across multiple manufacturing areas and shifts. The role requires adherence to approved procedures, quality requirements, and safety practices, with training provided for assigned tasks.

You will perform routine operations, follow detailed SOPs and batch records, and maintain accurate logs and records while working with a team to meet productivity and quality goals.

Qualifications

  • Ability to read, understand, and follow detailed procedures and controlled documents.
  • Strong attention to detail, organization, and commitment to quality.
  • Clear communication and dependable attendance for team work.

Responsibilities

  • Perform routine manufacturing operations across multiple areas, including assembly, inspection, packaging, cleaning, preparation, sampling, and other standard steps.
  • Follow SOPs, work instructions, batch records, and controlled documents; complete records accurately and on time.
  • Perform visual inspection using standard tools and magnification after training.
  • Use basic lab techniques such as measuring, pipetting, sampling, and labware cleaning.
  • Operate basic or semi-automated equipment and conduct routine checks after training.
  • Maintain a clean, organized work area in line with GLP, cGMP, ISO, and site requirements.
  • Follow safety practices and PPE requirements; report deviations or safety concerns to supervisor.
  • Maintain logs and electronic records; use basic computer applications as needed.
  • Collaborate with team members and leadership to meet productivity and quality goals; participate in cross-training and improvement initiatives.
  • Flex across manufacturing areas and shifts based on business needs.

Skills

Attention to detail
Reading procedures
Teamwork
Good communication
Documentation accuracy

Education

High school diploma or GED

Job description

Actual Job Title: Manufacturing Associates

The Manufacturing Associate supports routine production activities across multiple manufacturing areas. Associates may be assigned to different manufacturing areas and shifts based on business needs and will perform work in accordance with approved procedures, quality requirements, and safety practices.

Job Responsibilities
  • Perform routine manufacturing operations as assigned, which may include assembly, inspection, packaging, cleaning, preparation, sampling, and other standardized process steps.
  • Follow detailed standard operating procedures, work instructions, batch records, and other controlled documentation;complete required records accurately and on time.
  • Perform visual inspection of products or components using standard inspection tools, including magnification, after completing required training.
  • Use basic laboratory techniques as trained, such as measuring, pipetting or aliquoting, sample or solution preparation, labware cleaning, and other routine techniques relevant to the assigned area.
  • Operate basic or semi-automated equipment and perform routine process checks after qualification and training.
  • Maintain a clean, organized work area in accordance with applicable GLP, cGMP, ISO, cleanroom, or other site requirements.
  • Follow company safety practices and required personal protective equipment (PPE) requirements;promptly report deviations, safety concerns, or other issues to the appropriate lead or supervisor.
  • Maintain required logs, operational records, and electronic records;use basic computer applications as needed.
  • Work cooperatively with team members and leadership, support productivity and quality goals, and participate in cross-training or continuous improvement activities as assigned.
  • Flex across manufacturing areas and responsibilities based on business needs and schedule demands.
Technical Skill Requirements
  • Ability to learn and consistently perform a variety of routine manufacturing tasks in a fast-paced environment;no specialized expertise is required at hire.
  • Ability to read, understand, and follow detailed written procedures and controlled documents.
  • Strong attention to detail, organization, and commitment to quality.
  • Ability to perform repetitive work and maintain accuracy and productivity throughout the workday.
  • Basic computer skills and ability to complete paper or electronic records.
  • Clear communication skills, dependable attendance, positive attitude, and ability to work effectively as part of a team.
  • Ability and willingness to work in a different manufacturing area or on a different shift with at least one week's notice, based on business needs.
  • Availability to work assigned shifts and occasional weekend or overtime hours may be required.
Education and Experience Requirements
  • High school diploma or GED required.
  • 6+months of manufacturing experience (laboratory, medical device, pharmaceutical, or other regulated-environment experience preferred).
  • Successful completion of required site, safety, quality, and task-specific training is required.
  • Training will be provided for assigned work.
Physical Requirements
  • Must be available to work all 3 shifts.
  • Ability to stand, walk, and perform repetitive tasks for extended periods; perform fine motor tasks and work with small components or products.
  • Ability to perform visual inspection of products or components, including small details or features, using magnification or other standard inspection tools as required.
  • Ability to frequently lift to 20 pounds and occasionally lift to 50 pounds.
  • Ability to safely handle or transfer liquid nitrogen when required for assigned work, using required PPE and following site procedures and training; prior liquid nitrogen experience is not required.
  • Ability to work in controlled environments as required, including areas requiring PPE or gowning, temperature-controlled areas, and areas with moving equipment or moderate noise.
  • Ability to access and work in applicable areas of the facility.
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