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Granulation Jobs in California (NOW HIRING)

Aerotek

Manufacturing Operator

Hayward, CA

$20 - $24/hr

Experience working in compression or wet granulation processes, such as using large mixers similar to industrial kitchen equipment. * Exoperience in compounding, production, or machine operator roles ...

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Granulation information

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$11

$19

$36

How much do granulation jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for granulation in California is $19.47, according to ZipRecruiter salary data. Most workers in this role earn between $14.59 and $21.42 per hour, depending on experience, location, and employer.

What is a granulation job?

A Granulation job involves the process of breaking down or combining materials into granules, typically in pharmaceutical or manufacturing industries. This process helps improve the flowability, compressibility, and consistency of powders before further processing, such as tablet compression. Granulation technicians operate machinery, monitor production parameters, and ensure adherence to quality and safety standards. Their role is crucial in producing uniform and high-quality products.

What are the typical day-to-day responsibilities in a granulation job?

In a Granulation job, your daily tasks typically include setting up, operating, and cleaning granulation equipment, monitoring material feeds and process parameters, and performing quality checks to ensure product consistency. You may also be responsible for documenting production batches, troubleshooting equipment issues, and following strict safety and hygiene protocols. Most granulators work as part of a team, collaborating closely with line supervisors, quality assurance staff, and maintenance technicians to maintain smooth operation and meet production goals. These responsibilities are especially important in industries like pharmaceuticals or food production, where precision and regulatory compliance are critical.

What are the key skills and qualifications needed to thrive in a granulation position, and why are they important?

To thrive in a Granulation role, you need a solid understanding of manufacturing processes, equipment operation, and safety regulations, typically supported by a background in industrial manufacturing or pharmaceutical production. Familiarity with granulation machinery, process control systems, and potentially GMP (Good Manufacturing Practice) certification is often required. Strong attention to detail, problem-solving skills, and effective teamwork help operators excel in this position. These abilities are essential for ensuring consistent product quality, safe operations, and efficiency within the manufacturing environment.

What are popular job titles related to Granulation jobs in California?

For Granulation jobs in California, the most frequently searched job titles are:

What job categories do people searching Granulation jobs in California look for?

The top searched job categories for Granulation jobs in California are:

Granulation jobs near you
Infographic showing various Granulation job openings in California as of August 2026, with employment types broken down into 87% Full Time, 6% Part Time, 3% Contract, and 4% Nights. Highlights an 97% Physical, and 3% Remote job distribution, with an average salary of $40,500 per year, or $19.5 per hour.

Director/Senior Director Drug Product Development and Manufacturing

Corvus Pharmaceuticals, Inc.

San Francisco, CA • On-site

$150 - $200/hr

Other

Re-posted 22 days ago

Job description

Director/Senior Director Drug Product Development and Manufacturing

Department/Group: CMC
Location: South San Francisco, CA
Position Type: Full time

Job Description Role and Responsibilities
  • Define and lead drug product development strategy for Corvus’ programs.
  • Develop robust, scalable formulations and drug product manufacturing processes that ensure product quality.
  • Establish specifications and control strategies aligned with global regulatory and quality expectations.
  • Serve as a scientific and technical expert in formulation challenges for investigational drugs
  • Oversee technical activities at drug product CMOs, including technology transfer, clinical trial material (CTM) production, process troubleshooting, QbD and PAR studies, risk assessments, registration batch production, and process validation
  • Coordinate with Quality and Supply Chain teams to ensure timely manufacture and release of drug product lots by leading technical reviews of batch records, deviations, change controls, and nonconformance investigations; proactively identify and mitigate risks related to clinical supply
  • Partner with Chemical Development and Analytical Development functions to define optimal drug substance properties and control strategies
  • Ensure adherence to applicable regulations and guidelines, including FDA, EMA, ICH, GCP, and GMP
  • Provide person-in-plant support for drug product manufacturing
  • Serve as the drug product subject matter expert for internal program teams, due diligence activities, and CMO selection, management, and audits
  • Author and review CMC sections of regulatory filings, including INDs, IMPD/IND amendments, and NDA/MAA submissions
  • Coordinate with Analytical teams to ensure expiry and retest dating are current and aligned with drug product supply and commercialization plans
  • Contribute to internal and external presentations and publications
  • Manage, mentor, and develop scientists and engineers
  • Writes and reviews manuscripts for publication.
  • Develops strategies to ensure effective achievement of scientific objectives.
  • Monitors and evaluates completion of tasks and projects.
  • May develop budgets for capital expenditures and labor.
  • Collaborates with other top managers to establish company policies.
  • Leads the selection, development and evaluation of personnel to ensure the efficient operation of the function.
  • Makes final decisions on administrative or operational matters and ensures operations effective achievement of objectives.
  • Works on complex issues where analysis of situations or data requires an in-depth knowledge of the company and its objectives.
  • Ensures that budgets and schedules meet corporate timelines.
  • Must have strong negotiation skills with vendors and management to influence senior leaders regarding matters of significance to the organization.
  • Directs and controls the activities of a broad functional area through partnership with cross-functional department managers within the company.
Qualifications and Education Requirements
  • Ph.D. in Chemistry, Pharmaceutical Sciences, Engineering, or a related discipline with at least 10 years of late-phase, including NDA/MAA filing, small-molecule drug product development experience (M.S. with 15+ years considered)
  • Extensive experience in GMP oral solid dose manufacturing, including spray drying, granulation, hot melt extrusion, tableting, and encapsulation
  • Demonstrated expertise in formulation development and manufacturing of enabled formulations
  • Significant experience managing third-party drug product CMOs, including tech transfer, QbD studies, clinical supply production, registration batches, and commercial launch activities
  • Strong understanding of product/packaging interactions, barrier properties, stability, global packaging regulations, and package testing
  • In-depth knowledge of cGMP, ICH, FDA, and EMA requirements
  • Proven ability to collaborate effectively across internal and external stakeholders
  • Excellent written and verbal communication skills with strong problem-solving capabilities
  • Ability to manage multiple priorities in a fast-paced environment and navigate complex technical challenges
  • Willingness to travel domestically and internationally up to 25%
  • Excellent teamwork and collaboration skills
  • Able to build effective working relationships throughout the organization internally and externally to achieve goals.
  • Flexibility and willingness to solve problems that fall outside of immediate area of expertise
  • Clear and concise verbal and written communication skills and strong organizational skills, with an exceptional attention to detail.
  • Work independently in an interdisciplinary, fast-paced, often changing environment.
  • Committed to the values of integrity, accountability, transparency, and drive.
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