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Quality Control Pharma Jobs in Santa Rosa, CA (NOW HIRING)

Rack and Riddle

Lab Lead

Healdsburg, CA · On-site

$26 - $28/hr

... quality control experience within a regulated manufacturing environment (food, beverage, wine, consumer goods, or pharma). Prior experience in high-volume custom crush facilities or dedicated wine ...

LGC Group

Principal Chemist

Petaluma, CA · On-site

We deliver mission critical genomics to our diverse customer base in molecular diagnostics, pharma ... Deliver and control new methods, workflows, and manufacturing protocols for oligonucleotide ...

LGC Group

Principal Chemist

Petaluma, CA

We deliver mission critical genomics to our diverse customer base in molecular diagnostics, pharma ... Deliver and control new methods, workflows, and manufacturing protocols for oligonucleotide ...

LGC Group

Principal Chemist

Petaluma, CA

We deliver mission critical genomics to our diverse customer base in molecular diagnostics, pharma ... Deliver and control new methods, workflows, and manufacturing protocols for oligonucleotide ...

Enpro

Manufacturing Engineer

Santa Rosa, CA · On-site

$79K - $102K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Support business unit goals and objectives, quality initiatives, continuous improvement initiatives ... Excellent fundamentals of engineering concepts (tolerance analysis), statistical process control ...

Enpro Industries

Manufacturing Engineer

Santa Rosa, CA · On-site

$79K - $102K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Support business unit goals and objectives, quality initiatives, continuous improvement initiatives ... Excellent fundamentals of engineering concepts (tolerance analysis), statistical process control ...

All JobsQuality Control Pharma JobsQuality Control Pharma Jobs in Santa Rosa, CA

Quality Control Pharma information

See Santa Rosa, CA salary details

$14

$22

$32

How much do quality control pharma jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for quality control pharma in Santa Rosa, CA is $22.92, according to ZipRecruiter salary data. Most workers in this role earn between $19.71 and $25.24 per hour, depending on experience, location, and employer.

What is quality control in the pharmaceutical industry?

Quality Control (QC) in the pharmaceutical industry refers to the processes and procedures used to ensure that pharmaceutical products meet required standards of quality, safety, and efficacy. QC professionals test raw materials, in-process samples, and finished products using various analytical techniques to verify that they comply with regulatory specifications. The goal is to detect and prevent defects, ensuring that only products that pass rigorous standards are released to the market. QC is essential for maintaining public health and regulatory compliance in the pharmaceutical sector.

What are the key skills and qualifications needed to thrive as a quality control professional in the pharmaceutical industry?

To thrive as a Quality Control professional in pharma, you need a strong background in chemistry, biology, or a related science, along with knowledge of Good Manufacturing Practices (GMP) and relevant regulations. Familiarity with laboratory instruments (e.g., HPLC, GC), LIMS software, and quality assurance certifications such as ASQ or ISO standards is typically required. Attention to detail, analytical thinking, and effective communication help professionals excel in ensuring product quality and regulatory compliance. These skills ensure that pharmaceutical products are consistently safe, effective, and compliant with industry standards.

What are some of the common challenges faced by quality control professionals in the pharmaceutical industry?

Quality Control professionals in pharma often face challenges such as staying updated with evolving regulatory standards, managing tight timelines for product release, and ensuring accuracy in complex analytical testing. They must also coordinate closely with production and R&D teams to address any discrepancies or deviations quickly. Maintaining meticulous documentation and effectively handling audits are essential parts of the role, making attention to detail and strong communication skills particularly important.

What is the difference between Quality Control Pharma vs Quality Assurance Pharma?

AspectQuality Control PharmaQuality Assurance Pharma
Primary FocusTesting and inspecting raw materials, in-process, and finished products for complianceDeveloping and maintaining quality systems and processes to prevent defects
CertificationsGMP, GLP, relevant laboratory certificationsGMP, ISO 9001, quality management system certifications
Work EnvironmentLaboratories, testing facilitiesQuality departments, documentation, audits
Common Employer RolesPharmaceutical companies, contract labsPharmaceutical companies, regulatory agencies

While both roles aim to ensure product quality, Quality Control Pharma focuses on testing and inspection, whereas Quality Assurance Pharma emphasizes establishing systems and processes to prevent issues. Understanding these differences helps in choosing the right career path or job focus within the pharmaceutical industry.

Is quality control pharma a good career?

Quality Control Pharma involves testing and inspecting pharmaceutical products to ensure they meet safety and quality standards. It offers stable employment, opportunities for advancement, and requires attention to detail, knowledge of laboratory techniques, and often certifications such as GMP training.

What is the role of quality control in pharma?

The role of quality control in pharma involves testing and inspecting raw materials, in-process samples, and finished products to ensure they meet safety, efficacy, and quality standards. QC professionals use analytical techniques and follow Good Manufacturing Practices (GMP) to identify and prevent defects, supporting regulatory compliance and product consistency.

What are popular job titles related to Quality Control Pharma jobs in Santa Rosa, CA?

For Quality Control Pharma jobs in Santa Rosa, CA, the most frequently searched job titles are:

What job categories do people searching Quality Control Pharma jobs in Santa Rosa, CA look for?

The top searched job categories for Quality Control Pharma jobs in Santa Rosa, CA are:

What cities near Santa Rosa, CA are hiring for Quality Control Pharma jobs?

Cities near Santa Rosa, CA with the most Quality Control Pharma job openings:

Quality Control Pharma jobs near you
Infographic showing various Quality Control Pharma job openings in Santa Rosa, CA as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 20% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $47,682 per year, or $22.9 per hour.

Manufacturing Engineer

Stark Pharma Solutions Inc

Santa Rosa, CA • On-site

$79K - $102K/yr

Contractor

Re-posted 2 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Manufacturing Engineer position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Position: Manufacturing Engineer

Location: Santa Rosa, CA or Irvine, CA (Onsite)

Duration: Long Term
Experience: 5+ Years
 

Job Overview

We are seeking an experienced Manufacturing Engineer to support manufacturing operations, process optimization, and new product introduction within a regulated medical device environment. The ideal candidate will have expertise in manufacturing process development, validation, continuous improvement, and quality systems while collaborating with cross-functional teams to drive operational excellence.

Key Responsibilities

  • Develop, optimize, and support manufacturing processes to improve quality, efficiency, and productivity.
  • Troubleshoot production issues and implement corrective and preventive actions.
  • Lead process validation (IQ/OQ/PQ) and equipment qualification activities.
  • Support New Product Introduction (NPI) and transfer products into manufacturing.
  • Prepare and maintain manufacturing documentation, including SOPs, work instructions, and validation protocols.
  • Drive continuous improvement initiatives using Lean Manufacturing, Six Sigma, SPC, and Root Cause Analysis.
  • Support CAPA, NCR, Change Control, Risk Assessments (FMEA), and deviation investigations.
  • Collaborate with Quality, R&D, Production, Supply Chain, and Regulatory teams to resolve manufacturing challenges.
  • Ensure compliance with FDA 21 CFR Part 820 (QMSR), ISO 13485, GMP, and company quality standards.

Required Qualifications

  • Bachelor's degree in Mechanical, Manufacturing, Biomedical, Industrial Engineering, or a related field.
  • 5+ years of Manufacturing Engineering experience in the Medical Device industry.
  • Strong knowledge of FDA 21 CFR Part 820/QMSR, ISO 13485, and GMP.
  • Experience with IQ/OQ/PQ, process validation, equipment qualification, and NPI.
  • Hands-on experience with CAPA, NCR, Change Control, FMEA, and Root Cause Analysis.
  • Knowledge of Lean Manufacturing, Six Sigma, SPC, and DFM principles.
  • Strong analytical, documentation, communication, and problem-solving skills.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com