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Pharmaceutical Manufacturing Associate Jobs in California

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ob description Upstream, Formulation & Downstream Manufacturing Associate Location: Tustin, CA ... Manufacturing, laboratory, pharmaceutical, biotechnology, or biopharmaceutical experience preferred.

Be Seen First

ob description Upstream, Formulation & Downstream Manufacturing Associate Location: Tustin, CA ... Manufacturing, laboratory, pharmaceutical, biotechnology, or biopharmaceutical experience preferred.

Manufacturing Associate

Vacaville, CA · On-site

$25 - $28/hr

Our client specializes in pharmaceutical ingredients, bioscience, biopharmaceuticals, custom ... Manufacturing Associate Location: Vacaville, CA 95688 Duration: 6 Months Job Type: Temporary ...

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Pharmaceutical Manufacturing Associate information

What does a pharmaceutical manufacturing associate do?

A Pharmaceutical Manufacturing Associate is responsible for producing medications and related products in a controlled, regulated environment. They operate and monitor manufacturing equipment, follow strict safety and quality protocols, document production processes, and ensure compliance with Good Manufacturing Practices (GMP). Their work helps guarantee that pharmaceutical products are safe, effective, and consistently meet quality standards. They may also assist in cleaning and maintaining equipment, preparing raw materials, and supporting process improvements.

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

Pharmaceutical Manufacturing Associates require knowledge of GMP regulations, attention to detail, and at least a high school diploma—though an associate's or bachelor's degree in a science field is often preferred. Familiarity with manufacturing equipment, batch record documentation systems, and safety compliance tools such as LIMS (Laboratory Information Management Systems) is typical. Strong teamwork, communication, and problem-solving skills help individuals excel in this role. These abilities ensure product quality, regulatory compliance, and efficient production in a highly regulated environment.

What are some common challenges faced by pharmaceutical manufacturing associates during production runs?

Pharmaceutical Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and ensuring consistent batch quality. Working in a regulated environment means that associates must be detail-oriented and ready to document every step to comply with regulatory standards. Additionally, they may need to adapt quickly to schedule changes or production demands, while collaborating closely with quality assurance and engineering teams to resolve any issues that arise.

What is the difference between Pharmaceutical Manufacturing Associate vs Quality Control Technician?

AspectPharmaceutical Manufacturing AssociateQuality Control Technician
CredentialsHigh school diploma or equivalent; GMP trainingHigh school diploma or equivalent; GMP and lab safety training
Work EnvironmentManufacturing floors, production linesLaboratories, testing facilities
Job FocusAssembling, packaging, and operating manufacturing equipmentTesting raw materials, in-process samples, and finished products
Industry UsageUsed across pharmaceutical manufacturing plantsCommon in quality assurance labs within pharma companies

The Pharmaceutical Manufacturing Associate primarily works on production lines, ensuring the manufacturing process runs smoothly, while the Quality Control Technician focuses on testing and verifying product quality. Both roles require GMP knowledge and are essential in pharmaceutical production, but they differ in daily tasks and work environments.

How do you get into a pharmaceutical manufacturing associate career?

To become a pharmaceutical manufacturing associate, candidates typically need a high school diploma or equivalent, with some roles preferring post-secondary education or technical training in fields like biology or chemistry. Relevant skills include attention to detail, knowledge of Good Manufacturing Practices (GMP), and familiarity with manufacturing equipment. Gaining experience through internships or entry-level positions can also improve job prospects.

Is a pharmaceutical manufacturing associate a good job?

A pharmaceutical manufacturing associate is a vital role in the production of medications, involving tasks such as operating equipment, following safety protocols, and maintaining quality standards. It often offers stable employment, opportunities for skill development, and may require certifications like GMP training; the job environment is typically clean and regulated. Whether it is a good job depends on individual career goals and interest in the pharmaceutical industry.

What are the most commonly searched types of Pharmaceutical Manufacturing jobs in California?

The most popular types of Pharmaceutical Manufacturing jobs in California are:

What cities in California are hiring for Pharmaceutical Manufacturing Associate jobs?

Cities in California with the most Pharmaceutical Manufacturing Associate job openings:

Manufacturing Associate I 2nd/3rd

Fremont, CA • On-site

Astrix Inc
Recruiting and Staffing Services • 1 - 5K employees

Contractor, Other

Medical, Dental, Vision, Retirement, PTO

Posted 26 days ago


Job description

Pay Rate Low: 24.00 | Pay Rate High: 25.00
Great opportunity to work as a Manufacturing Associate at a Global, research-driven pharmaceutical manufacturer focusing on treatment options for diseases and conditions for which there is no satisfactory treatment option to date. This is an amazing opportunity to work on cutting edge treatments and make a difference!
Manufacturing Associate
Contract: 6 month contract with conversion potential
Benefits: Medical, Dental, Holiday, PTO 401K matching
Location: Fremont, CA
2nd Shift: Mon-Fri, 2:00PM-10:30PM
or
3rd Shift: Mon-Fri, 10:00PM-6:30AM
Performs routine assembly and packaging operations in a pharmaceutical manufacturing facility while following GMP, SOPs, safety, and documentation requirements.
Key Responsibilities
  • Perform assembly, packaging, visual inspection/filling, material movement, and production area organization.
  • Assist with equipment setup, changeovers, troubleshooting, minor repairs/adjustments, and real-time problem resolution.
  • Gather and stock components, tools, equipment, and supplies needed for production.
  • Complete batch records, logbooks, and other required documentation accurately.
  • Maintain clean, safe, organized production areas and follow 5S and safety standards.
  • Communicate effectively with team members and escalate production, equipment, or safety issues.
Qualifications
  • High School diploma plus 1 year of GMP-regulated industry experience; Associate/Bachelor's degree or biotechnology training preferred.
  • Pharmaceutical/biotechnology manufacturing experience strongly preferred.
  • Detail-oriented with strong communication, teamwork, basic math, and computer skills.
  • Ability to follow written procedures and cGMP requirements and stand/walk for extended periods.
This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
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