Aseptic Processing Technician (1st shift) - Level I - II

Society for Conservation Biology; Philadelphia (Philadelphia County); On-site; USD 10,000 - 60,000; Full time

Job summary

A leading company in Philadelphia is seeking an Aseptic Processing Technician for the 1st shift. This role involves executing aseptic procedures in a cleanroom environment while adhering to strict quality and safety standards. The technician will collaborate with team members to ensure efficient production and maintain compliance with GMP regulations. Ideal candidates will have research experience in aseptic techniques and a quality mindset. This is a contract-to-hire position offering competitive pay based on experience.

Qualifications

• Research experience with aseptic techniques required.
• 0-2 years in biopharmaceutical-based GMP manufacturing operations.

Responsibilities

• Complete training and maintain documentation.
• Ensure compliance with quality standards and safety guidelines.
• Perform materials stocking and kit preparation.

Skills

Aseptic Techniques

Teamwork

Quality Mindset

Education

Research Experience

0-2 Years Experience in GMP

Tools

Microsoft Excel

Microsoft Word

Microsoft Outlook

Job description

Aseptic Processing Technician (1st shift) - Level I - II

Aseptic Processing Technician (1st shift)

Philadelphia, PA - onsite

$27 per hr - $31.75 - depending on level

1st shift is 7am - 5:30pm - Tuesday - Friday

6 month CONTRACT TO HIRE

Essential Functions and Responsibilities

• Complete training sessions and ensure training documentation is maintained.
• Proficiently carry out procedures to achieve a consistent, error-free execution of daily job assignments
• Work as part of a team to produce each lot accurately and fully complete batch records, forms, and documentation.
• At all times, understand and comply with quality standards and safety guidelines.
• Perform materials stocking, kit preparation, reagent preparation, cleaning activities, and equipment maintenance.
• Identify errors and report them promptly to lab management. Participate in root cause analysis and implement corrective actions.
• Adheres to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs), including Good Documentation Practices (GDP).
• Must adhere to the clients core values, policies, procedures, and business ethics.
• Comply with Safety SOPs, SDS sheets, and laboratory procedures per company policy and OSHA regulations.
• Perform miscellaneous duties as assigned.

Required Education, Skills, and Knowledge

• Research experience with aseptic techniques - MUST HAVE and must be on resume
• Demonstrated technical knowledge of aseptic processing in cleanroom environments.
• Cell culture or cell line experience
• 0-2 years of experience in biopharmaceutical-based GMP manufacturing operations
• Able to read, write and understand English, and be proficient in Microsoft (Excel, Word, Outlook).
• Able to accurately perform basic math, including fractions, decimals, and percentages.
• Able to work effectively with team members and show initiative to assist others on the team.
• Able to work successfully in a fast-paced, team-oriented environment.
• Quality mindset, familiar with 21 CFR Part 11 and standard GxP best practices and FDA regulations.

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