Manufacturing Associate

Society for Conservation Biology; King of Prussia (Montgomery County); On-site; USD 55,000 - 75,000; Full time

Job summary

An innovative organization seeks a Downstream Associate Scientist / Manufacturing Associate for a 12-month position in King of Prussia. The role involves preparing buffer solutions, adhering to GMP standards, and ensuring compliance while documenting all manufacturing processes. Ideal candidates will have a Bachelor’s degree in a scientific field and 1+ years of relevant experience.

Qualifications

• 1+ years of cGMP experience required.
• Familiarity with protein purification process operations.
• Knowledge of cGMP guidelines and standards.

Responsibilities

• Preparation of buffer solutions and chromatographic separation.
• Completing daily manufacturing tasks per standard operating procedures.
• Documenting all manufacturing activities clearly and accurately.

Skills

Troubleshooting

Protein purification

Good Manufacturing Practices (GMP)

Documentation

Education

Bachelor of Science degree in Chemical Engineering, Biology, or Chemistry

Tools

Cytiva platform of purification equipment

Unicorn software

Job description

Job Title : Downstream Associate Scientist / Manufacturing Associate

Location : King of Prussia, PA 19406

Duration : 12 months (with possible extension to 18 months total)

Job Description :

• Preparation of buffer solutions, chromatographic separation, filtration and concentration operation, etc.
• Completing daily manufacturing tasks per standard operating procedures and batch document instructions.
• Documenting all manufacturing activities clearly and accurately.
• Ensures all production activities are completed in a safe and compliant manor.
• Maintain and prepare high quality documentation.
• Dispense large and small amounts of raw materials Perform CIP and SIP of product tanks
• Work with hazardous materials under the appropriate safety procedures.
• Familiarity with protein purification process operations and Good Manufacturing Practices (GMP) regulations.
• Bachelor of Science degree in Chemical Engineering, Biology, Chemistry, or other engineering or scientific field.
• 1+ years of cGMP experience. Knowledge of cGMP guidelines and standards.
• Knowledgeable of: Cytiva platform of purification equipment and Unicorn software.
• Able to troubleshoot.
• Ability to author, revise and/or support SOP's, change controls, deviations.