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Manufacturing Process Associate Jobs in California

Job Title: Manufacturing Associate Location: Novato, CA Type: Contract Compensation: $28.00 ... Monitor process performance and identify issues, escalating concerns and supporting resolution to ...

Manufacturing Associate Location: Novato, CA Type: Contract Compensation: $28.00 + shift ... Monitor process performance and identify issues, escalating concerns and supporting resolution to ...

Manufacturing Associate

Brea, CA ยท On-site

$20 - $24/hr

Summary: The role of the manufacturing associate is to support rework and related manufacturing processes utilizing a variety of production equipment. Individuals in the role of manufacturing ...

$93K - $127K/yr

Senior Associate, Additive Manufacturing Engineer Job ID: 40294 Job Location: Canoga Park, CA Job ... This role is responsible for developing and improving process flows, work instructions, process ...

Showing results 41-60

Manufacturing Process Associate information

What is a manufacturing process associate?

Manufacturing Process Associates are professionals who support production activities in manufacturing facilities. They are responsible for operating equipment, monitoring production processes, ensuring quality standards, and maintaining a safe work environment. Typically, they assist in assembling products, conducting inspections, and troubleshooting minor equipment issues. This role often requires attention to detail, adherence to safety protocols, and the ability to work as part of a team. Manufacturing Process Associates play a vital role in ensuring that products are made efficiently and meet company standards.

What are the key skills and qualifications needed to thrive as a manufacturing process associate?

To thrive as a Manufacturing Process Associate, you need a solid understanding of production processes, quality control, and safety protocols, often supported by a high school diploma or associate degree in a related field. Familiarity with manufacturing equipment, ERP systems, and basic troubleshooting tools is commonly required. Attention to detail, teamwork, and effective communication are important soft skills that help ensure efficient workflow and collaboration. These skills and qualities are crucial for maintaining product quality, meeting production targets, and supporting a safe and productive work environment.

What are some common challenges faced by manufacturing process associates, and how can they be addressed?

Manufacturing Process Associates often face challenges such as adapting to rapidly changing production schedules, troubleshooting equipment malfunctions, and maintaining strict quality control standards. To address these issues, it's important to stay organized, communicate effectively with team members and supervisors, and proactively seek training on new machinery or procedures. Collaborative problem-solving and a willingness to learn can help associates thrive in a dynamic manufacturing environment.

What is the difference between Manufacturing Process Associate vs Manufacturing Technician?

AspectManufacturing Process AssociateManufacturing Technician
CredentialsHigh school diploma or equivalent; some roles may require technical certificationsHigh school diploma; technical certifications or associate degree often preferred
Work EnvironmentAssembly lines, production floors, manufacturing plantsManufacturing floors, equipment maintenance areas, quality control stations
Job FocusAssisting in production processes, monitoring equipment, ensuring workflowMaintaining, troubleshooting, and repairing manufacturing equipment
Common UsageEntry-level roles supporting manufacturing operationsTechnical roles focused on equipment and process optimization

The Manufacturing Process Associate primarily supports production workflows and monitors manufacturing processes, while the Manufacturing Technician focuses on maintaining and repairing equipment to ensure smooth operations. Both roles are essential in manufacturing environments and often require similar certifications, but they differ in technical responsibilities and focus areas.

Manufacturing Associate

Novato, CA โ€ข On-site

System One
Business Consulting Servicesย โ€ขย 5 - 10K employees

$28/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Re-posted 24 days ago


Job description

Job Title: Manufacturing Associate Location: Novato, CA Type: Contract Compensation: $28.00 Contractor Work Model: Onsite – onsite Hours: Thursday - Saturday with Alternating Wednesdays (6am to 7pm) / Rotating 12hour shift

Overview Leading biotechnology company looking for an experienced Manufacturing Associate. Ideal candidates should have a Bachelor’s degree in science or engineering, or Associates degree in science or Biotech certificate with 2+ years of biotech manufacturing or regulated industry experience.

Responsibilities

  • Operate and support biopharmaceutical manufacturing processes including mammalian cell culture, filtration, chromatography, centrifugation, purification, and bulk drug formulation.
  • Monitor process performance and identify issues, escalating concerns and supporting resolution to maintain production continuity.
  • Execute manufacturing steps according to standard operating procedures and batch records in a cGMP-regulated environment.
  • Provide feedback on operational procedures and support updates to incorporate new technologies, standards, and best practices.
  • Write and review technical and process documentation as required.
  • Utilize quality systems to document and address deviations, CAPAs, change controls, and related compliance activities.
  • Support process optimization initiatives and departmental performance metrics.
  • Gain working knowledge of manufacturing automation and data systems such as LIMS, MES, and PI.
  • Participate in cross-functional projects and support implementation of business systems such as TrackWise and ERP platforms.
Requirements
  • Bachelor’s degree in a science or engineering discipline or Associate’s degree in a science-related field or biotech certificate with 2+ years of experience in biotech manufacturing or another regulated industry.
  • Experience working in cGMP-regulated manufacturing environments.
  • Understanding of biopharmaceutical manufacturing processes such as cell culture, filtration, chromatography, or protein purification.
  • Ability to write and review technical documentation and operational procedures.
  • Experience working with quality systems such as deviations, CAPAs, and change controls.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

Ref: #558-Scientific


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About System One

Sourced by ZipRecruiter

System One helps employers get work done more efficiently and economically without compromising quality. Over our 35+ year history, we've helped connect thousands of talented people with innovative companies. The excitement of a perfect fit motivates us every single day.

Industry

Business consulting services and recruiting and staffing services

Company size

5,001 - 10,000 Employees

Headquarters location

Pittsburgh, PA, US