Manufacturing Associate

Aequor; Union City (CA); On-site; USD 38,000 - 52,000; Full time

Job summary

Aequor in Union City, CA is seeking Manufacturing Associates to support routine production across multiple areas. You will follow approved procedures, maintain logs, and work in a cleanroom or GMP environment.

The role requires a high school diploma or GED, 6+ months of manufacturing experience preferred, and flexibility to work all shifts, including weekends or overtime. Training will be provided to cover site-specific procedures and safety practices.

Qualifications

• Must be able to read, understand, and follow detailed written procedures
• Strong attention to detail and quality
• Able to work in a team and communicate effectively
• Able to perform repetitive tasks with accuracy and reliability

Responsibilities

• Perform routine manufacturing operations such as assembly, inspection, packaging, cleaning, and sampling
• Follow SOPs, work instructions, batch records, and ensure accurate records
• Conduct visual inspections using standard tools and magnification
• Operate basic or semi-automated equipment and perform process checks
• Maintain clean, organized work area per GLP, cGMP, ISO and site requirements
• Report safety concerns and follow PPE requirements
• Maintain logs and electronic records; use basic computer applications
• Cross-train and support productivity and quality goals across shifts

Skills

Detail-oriented

Team player

Reading SOPs

Basic computer skills

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.

Flexibility in all shift schedules is required.