Job Description

Duties:

• Perform daily GMP Quality Control laboratory testing activities at the facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations.
• Perform environmental monitoring of the cleanroom areas as scheduled.
• Perform data analysis and result reporting of microbiology assays to support product lot release with adherence to turnaround times.
• Act as subject matter expert (SME) on one or more assays and train new laboratory personnel.
• Support generation and revisions of documentation, such as SOP, protocols and reports, deviations, laboratory investigations, CAPAs, and change control

Qualifications:

• Bachelor’s degree in a relevant discipline (biological sciences or equivalent)
• 3-8 years of experience in the pharmaceutical industry within a Quality Control role; experience with cell therapy products is a plus.
• Hands on experience in bioburden, endotoxins, mycoplasma, gram stain, environmental monitoring, and sterility techniques

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

Pay Scale:

$85,000 – $93,600 ( Dependent on Experience)

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.

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