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QC Stability Consultant (Biotechnology)

R&D Partners
Redwood City, CA, United States
$124.8K-$145.6K a year
Temporary

Biotechnology company is hiring a QC Stability Consultant to oversee the stability program to ensure safety, efficacy and quality of products throughout their shelf life.

This role involves managing stability studies, analyzing data, and ensuring compliance with regulatory requirements. This is a 12-month contract.

Responsibilities

  • Stability Program Management
  • Oversee the design and execution of stability studies including protocol development, sample management, and data collection.
  • Implement best practices and innovative solutions to enhance efficiency of stability studies.
  • Analyze stability data to assess product performance and identify trends.
  • Prepare stability reports for regulatory submissions.
  • Work closely with R&D, Quality Assurance, Manufacturing, and Regulatory Affairs teams to ensure alignment of stability studies.

Qualifications

  • Bachelors, Masters, or PhD in Chemistry, Biochemistry, Pharmaceutical Sciences
  • 8-10 years of experience in Quality Control or Stability role within pharmaceuticals or biotechnology industry
  • Strong knowledge of GMP, ICH Guidelines, and regulatory requirements for stability testing

Salary

$124,800-$145,600

Why Choose R&D Partners?

As an employee, you have access to a comprehensive benefits package including :

  • Medical insurance PPO, HMO & HSA
  • Dental & Vision insurance
  • 401k plan
  • Employee Assistance Program
  • Long-term disability
  • Weekly payroll
  • Expense reimbursement
  • Online timecard approval

R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering.

We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.

R&D Partners is an equal-opportunity employer.

8 days ago
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