Aseptic Manufacturing Technician II (Day Shift)

ZipRecruiter; Philadelphia (Philadelphia County); On-site; USD 67,000; Full time

Job summary

Join a forward-thinking staffing provider specializing in scientific roles, where you will be responsible for hands-on cell processing in a biopharmaceutical environment. This role involves utilizing advanced bioreactor technology and performing critical aseptic techniques to ensure the highest quality in cell culture and downstream processing. You will thrive in a dynamic setting, contributing to both commercial and clinical applications while adhering to strict GMP standards. With a competitive salary and a comprehensive benefits package, this opportunity is perfect for those looking to advance their career in the biopharmaceutical industry.

Benefits

Medical insurance – PPO, HMO & HSA

Dental & Vision insurance

401k plan

Employee Assistance Program

Long-term disability insurance

Weekly payroll

Expense reimbursement

Online timecard approval

Qualifications

• Minimum of 1+ years of experience in biopharmaceutical GMP manufacturing.
• Experience with aseptic techniques and environmental monitoring.

Responsibilities

• Perform cell counts and operate cell wash and concentration machines.
• Conduct aseptic manipulations and environmental monitoring.

Skills

Cell culture

Downstream processing

Aseptic manipulations

Environmental monitoring

Tools

Single-use high-density bioreactors

Bio Safety Cabinets (BSCs)

Cell counting machines

Tube welders

Seal machines

Controlled rate freezers

Job description

Job Description

Overview:

This position is primarily responsible for hands-on cell processing using single-use high-density bioreactors, Bio Safety Cabinets (BSCs), cell count machines, cell wash and concentration machines, tube welders, and sealers for both commercial and clinical applications. Additional duties include environmental monitoring, cell culturing, and liquid transfers. The role mainly takes place in grade B (ISO7) and Grade A (ISO5) environments.

Duties:

1. Perform cell counts utilizing cell counting machines.
2. Operate cell wash and concentration machines.
3. Harvesting and seeding of single-use high-density bioreactors.
4. Conduct aseptic manipulations within Biological Safety Cabinets (BSCs).
5. Perform in-suite environmental monitoring during processing days.
6. Review documents in real-time, including Batch Records and Logbooks.

Qualifications:

Minimum of 1+ years of experience in biopharmaceutical GMP manufacturing operations, including cell culture and downstream processing. Experience with single-use high-density bioreactors, BSCs, cell counting machines, liquid transfers, tube welders, sealers, controlled rate freezers, and ISO7 gowning is required.

Why Choose R&D Partners?

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

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

Pay: $66,040

R&D Partners is a global staffing provider specializing in scientific, clinical research, and engineering roles. We offer opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.

R&D Partners is an equal-opportunity employer.