Manufacturing Operator

Adecco US, Inc.; Fremont (CA); On-site; USD 54,002,000 - 72,186,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401K plan

Paid leave

Job summary

Adecco Healthcare and Life Sciences is hiring a Manufacturing Operator in Fremont, CA. The role supports manufacturing by operating production equipment, preparing materials, and ensuring products are manufactured safely and accurately under cGMP and quality system requirements.

The ideal candidate has at least 1 year of experience in manufacturing or a lab setting and is comfortable in a regulated, team-oriented environment.

Qualifications

• High School Diploma or equivalent required.
• Minimum 1 year of experience in manufacturing, production, operations, or a laboratory setting.
• cGMP, GDP, or Good Warehouse Practices experience preferred.
• Direct machine operation experience preferred.
• Proficient in Microsoft Word and Excel.
• Experience with electronic management systems such as QAD or Oracle preferred.
• Able to read, write, and communicate effectively in English.

Responsibilities

• Manufacture and test products following cGMP requirements and quality procedures.
• Review and complete SOPs, batch records, and other documentation accurately.
• Set up and operate production equipment and perform basic troubleshooting under supervision.
• Read work orders and prepare materials for production.
• Inspect materials and products throughout the production process.
• Close and seal containers and package finished products as required.
• Enter material usage and production data into electronic systems.
• Perform line clearance activities including reconciliation and disposal of materials.

Skills

Teamwork

Attention to detail

Regulatory compliance

Written and verbal English

Reading and following SOPs

Education

High School Diploma or equivalent

Tools

Microsoft Word

Microsoft Excel

QAD

Oracle

Job description

Adecco Healthcare and Life Sciences is hiring an Manufacturing Operator for a leading life sciences organization in Fremont, CA. This position supports manufacturing operations by operating production equipment, preparing and inspecting materials, completing required documentation, and ensuring products are manufactured safely and accurately in accordance with cGMP and quality system requirements .

The ideal candidate has at least one year of experience in manufacturing, production, operations, or a laboratory environment and is comfortable working in a highly regulated, team-oriented setting.

Job Type: Minimum 1-year temporary/contract role

Pay Rate: $ 22.00/hour

Schedule: Monday-Friday, 6:00 AM-2:45 PM

Location: Fremont, CA

KEY RESPONSIBILITIES

• Manufacture and/or test products while following cGMP requirements and established quality procedures.

• Review and complete SOPs, work instructions, batch records, and other required documentation accurately.

• Set up and operate production equipment and perform basic troubleshooting and adjustments under the direction of production leadership.

• Read work orders and prepare, verify, and count materials required for production.

• Inspect materials and products throughout the production process.

• Close and seal containers and sort, label, tag, and package finished products as required.

• Enter material usage and production information into electronic systems.

• Complete line clearance activities, including reconciliation and disposal of materials.

• Clean and sanitize work areas, equipment, machines, and printers.

• Work closely with Production Leads and other Operators to resolve production, equipment, scheduling, and logistics issues.

• Support engineering teams with process improvement and equipment validation activities.

• Follow ISO/cGMP quality standards with a strong focus on documentation accuracy, product quality, safety, and housekeeping.

• Report discrepancies in SOPs, batch records, or other procedures to appropriate leadership.

• Participate in Lean, 5S, and Practical Process Improvement initiatives.

• Perform additional production duties as assigned.

QUALIFICATIONS

• High School Diploma or equivalent required.

• Minimum 1 year of experience in manufacturing, production, operations, or a laboratory setting.

• Previous cGMP, Good Documentation Practices (GDP), or Good Warehouse Practices experience preferred.

• Direct machine operation experience preferred.

• Working knowledge of Microsoft Word and Excel .

• Experience using electronic management systems such as QAD or Oracle is preferred.

• Ability to read, write, and communicate effectively in English.

• Ability to understand and follow written, verbal, and diagram-based instructions.

• Basic math skills, including addition, subtraction, multiplication, and division.

• Strong attention to detail and documentation accuracy.

• Ability to manage multiple tasks and changing priorities.

• Strong teamwork and communication skills.

• Ability to stand for extended periods.

PHYSICAL REQUIREMENTS & WORK ENVIRONMENT

• Ability to lift up to 50 lbs. without assistance .

• Position may involve working in cold environments, potentially as low as -20°C , and around loud equipment.

• Must wear required PPE, including steel-toe shoes, lab coats, gloves, safety glasses, and hearing protection.

• This position involves handling controlled substances and requires strict adherence to applicable safety and regulatory procedures.

• Successful completion of a background check, including required controlled-substance screening, is required.

SCHEDULE FLEXIBILITY

The standard schedule is Monday-Friday, 6:00 AM-2:45 PM . Candidates must be flexible to support:

• Overtime and weekend overtime as needed

• Staggered shifts, approximately 9:00 AM-5:45 PM

• Swing shifts, approximately 4:00 PM-4:00 AM , based on production needs and supervisory assignment

WHY CONSIDER THIS OPPORTUNITY?

• Gain experience in a regulated life sciences manufacturing environment.

• Work with established manufacturing and quality systems.

• Opportunity to develop experience with production equipment, cGMP, documentation, and process improvement.

• Day-shift schedule with potential overtime opportunities.

Pay Details: $22.00 per hour

Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.

Equal Opportunity Employer/Veterans/Disabled

Military connected talent encouraged to apply

To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.adecco.com/en-us/candidate-privacy

The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:

• The California Fair Chance Act

• Los Angeles City Fair Chance Ordinance

• Los Angeles County Fair Chance Ordinance for Employers

• San Francisco Fair Chance Ordinance

Massachusetts Candidates Only:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.