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Day Shift Upstream Manufacturing Associate Jobs in Riverside, CA

Avid Bioservices

Trainer, Manufacturing

Tustin, CA · On-site

$25.48 - $33.99/hr

The Manufacturing Trainer supports Avid's GMP manufacturing operations across Upstream, Downstream ... Associate's or Bachelor's degree in a scientific or technical discipline. * 1-3 years of GMP ...

Avid Bioservices

Trainer, Manufacturing

Tustin, CA

$25.48 - $33.99/hr

The Manufacturing Trainer supports Avid's GMP manufacturing operations across Upstream, Downstream ... Associate's or Bachelor's degree in a scientific or technical discipline. * 1-3 years of GMP ...

McCrometer

Maintenance - Janitor - Day Shift

Hemet, CA · On-site

$14.25 - $18.25/hr

We design, develop, and manufacture world-class flow measurement equipment, for far-reaching impact ... An associate's position within the salary range will be based on several factors, including, but ...

Marquee Staffing - OC

Be Seen First

1st Shift - Medical Device Assembler

Irvine, CA · On-site

$21 - $25/hr

Monday - Friday : 5:00 am - 2:30 pm + OT (May have occasional Saturday shifts) Overview Join our team as a Manufacturing Associate III and play a direct role in assembling high-quality medical ...

AC Pro

Warehouse Manufacturing (2nd Shift)

Fontana, CA · On-site

$19 - $22/hr

We want every one of our associates to look forward to coming to work each and every day ... Morning shift, plus overtime and Saturdays as needed. Pay Range: $19.00- $22.00 per hour (DOE) ($2 ...

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All JobsDay Shift Upstream Manufacturing Associate JobsDay Shift Upstream Manufacturing Associate Jobs in Riverside, CA

Day Shift Upstream Manufacturing Associate information

See Riverside, CA salary details

$12

$21

$34

How much do day shift upstream manufacturing associate jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for day shift upstream manufacturing associate in Riverside, CA is $21.74, according to ZipRecruiter salary data. Most workers in this role earn between $17.07 and $24.33 per hour, depending on experience, location, and employer.

What is a Day Shift Upstream Manufacturing Associate?

A Day Shift Upstream Manufacturing Associate is responsible for preparing and operating equipment to support the initial stages of biopharmaceutical production, typically involving cell culture, fermentation, and media preparation. Working during the day shift, they monitor processes, maintain sterile environments, and ensure production runs smoothly and efficiently. Their work is crucial in ensuring quality and consistency in the early phases of manufacturing biological products such as vaccines or therapeutic proteins.

What is the difference between Day Shift Upstream Manufacturing Associate vs Night Shift Upstream Manufacturing Associate?

AspectDay Shift Upstream Manufacturing AssociateNight Shift Upstream Manufacturing Associate
Work HoursTypically 8 AM - 4 PMTypically 8 PM - 4 AM
Work EnvironmentManufacturing floor during daytime operationsManufacturing floor during nighttime operations
Required SkillsSimilar technical skills, safety protocols, and certificationsSame technical skills, safety protocols, and certifications
Employer UsageCommonly used in biopharma and biotech manufacturingSame industry usage, different shift timing

The main difference between a Day Shift Upstream Manufacturing Associate and a Night Shift Upstream Manufacturing Associate lies in their working hours. Both roles require similar skills, certifications, and work environments, but they operate during different shifts. Employers in biopharma and biotech industries often employ both to ensure continuous production, with shift timing being the primary distinction.

What are the typical collaboration points between a Day Shift Upstream Manufacturing Associate and other teams in a biomanufacturing facility?

Day Shift Upstream Manufacturing Associates frequently collaborate with downstream processing teams, quality control, and process engineering staff. Daily responsibilities often involve communicating batch progress, troubleshooting issues, and ensuring compliance with safety and GMP standards. Clear documentation and timely reporting to supervisors and quality teams are crucial for maintaining production flow. This cross-functional teamwork ensures efficient handoffs and rapid response to any process deviations, making collaboration a key part of the role.

What are the key skills and qualifications needed to thrive as a Day Shift Upstream Manufacturing Associate, and why are they important?

To excel as a Day Shift Upstream Manufacturing Associate, you typically need a background in biotechnology or life sciences, experience with aseptic techniques, and an understanding of Good Manufacturing Practices (GMP). Familiarity with bioreactors, cell culture systems, and process control software is commonly required, along with relevant safety or GMP certifications. Attention to detail, teamwork, and strong problem-solving abilities are valuable soft skills in this role. These competencies ensure the efficient and compliant production of high-quality biopharmaceuticals in a regulated manufacturing environment.
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What cities near Riverside, CA are hiring for Day Shift Upstream Manufacturing Associate jobs? Cities near Riverside, CA with the most Day Shift Upstream Manufacturing Associate job openings:
Day Shift Upstream Manufacturing Associate jobs near you
Infographic showing various Day Shift Upstream Manufacturing Associate job openings in Riverside, CA as of June 2026, with employment types broken down into 4% Locum Tenens, 4% Full Time, 88% Part Time, and 4% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $45,217 per year, or $21.7 per hour.
Trainer, Manufacturing

Trainer, Manufacturing

Avid Bioservices

Tustin, CA • On-site

$25.48 - $33.99/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago

Job description

Description
Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
The Manufacturing Trainer supports Avid's GMP manufacturing operations across Upstream, Downstream, and Formulation by delivering high quality training, executing hands on qualification, and reinforcing documentation and compliance standards. This role ensures employees are trained, qualified, and supported in developing the technical, procedural, and documentation capabilities required for success.
Key Responsibilities:
Training Delivery & Facilitation
  • Deliver classroom, virtual, and on-the-floor training for Upstream, Downstream, and Formulation operations.
  • Facilitate OJT qualification sessions and ensure proper documentation.
  • Support new hire onboarding and early competency development.
  • Conduct refresher and capability-based training as needed.

Training Material Development
  • Assist in developing SOP-based modules, technical process training, e-learning content, and qualification materials.
  • Create and update training checklists, assessments, and job aids.
  • Ensure training materials reflect current processes and regulatory expectations.

Training Compliance & Documentation
  • Maintain accurate training records.
  • Support curriculum updates, retraining triggers, and assignment accuracy.
  • Reinforce GDP and ALCOA+ principles.
  • Conduct and document Training Impact Assessments.

Operational Support & Floor Presence
  • Provide routine floor support to ensure correct technique and documentation.
  • Coach employees on new processes, proper execution, and safety.
  • Identify training gaps and escalate to L&D Manager.

Metrics, Reporting & Continuous Improvement
  • Track training status, qualification progress, and compliance KPIs.
  • Support analysis of RFT documentation performance and correction trends.
  • Recommend improvements to training methods and onboarding workflows.

Cross-Functional Collaboration
  • Partner with SMEs to maintain accurate technical content.
  • Collaborate with QA to ensure compliance alignment.

Support HR during onboarding cycles.
Minimum Qualifications:
  • Associate's or Bachelor's degree in a scientific or technical discipline.
  • 1-3 years of GMP manufacturing or technical training experience.
  • Strong understanding of GMP, GDP, and ALCOA+ principles.
  • Experience delivering training or coaching.
  • Strong attention to detail and documentation accuracy.
  • Clear communication and coaching skills.
  • Ability to work in a fast-paced GMP environment.
  • Collaborative and cross-functional mindset.

Preferred Qualifications:
  • Experience in Upstream, Downstream, or Formulation operations.
  • Understanding of adult learning principles.

Position Type/Expected Hours of Work:
This role is a full-time onsite position. Days and hours of work are Monday through Friday, 8:00 a.m. to 5:00 p.m. unless otherwise stated by Supervisor. The employee must also, if instructed, have the ability to work overtime when necessary.
Compensation:
We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
The compensation range for this role is $25.48 to $33.99 hourly depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
Who you are:
  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.

Physical Demands & Work Environment:
In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 25 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

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