Job Description

Compensation & Details:

• 12 month extending contract
• Onsite in Malvern, PA
• $30-$34/hr - exact rate is based on several factors, including skills, experience, and education.
• Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law
• 10 PTO Days & 6 Sick Days

Required Skills & Experience

• Bachelor’s degree in Biology, Biotechnology, or a related scientific field.
• 1–2 years of experience in a laboratory setting working with multiple cell lines, preferably in a GMP-regulated environment.
• Strong understanding of aseptic techniques and cell culture practices.
• Excellent organizational skills and attention to detail.
• Effective verbal and written communication skills. -Ability to work independently and manage multiple priorities.

Nice to Have Skills & Experience

• Previous GMP experience
• Experience with cell counting instruments (e.g., NC200).

Job Description: We are seeking a motivated and detail-oriented QC Analyst to join our Clinical Release and Stability team. This role is primarily focused on cell line maintenance and cell handling within a laboratory environment. The ideal candidate will have strong aseptic technique, excellent organizational skills, and the ability to communicate effectively across teams. Key Responsibilities: -Perform routine cell line maintenance, including thawing, culturing, and monitoring of cell lines. -Ensure timely initiation of new cell lines and maintain accurate records of cell line schedules. -Operate and maintain laboratory equipment including: -NC200 Cell Counter -Biological Safety Cabinet (BSC) -Pipettes -Adhere to aseptic techniques and ensure full cleaning of the BSC between cell line changes. -Document all activities in compliance with GMP and internal quality standards. -Communicate effectively with team members and cross-functional partners to ensure smooth workflow and timely completion of tasks. -Support the Clinical Release and Stability team with additional QC testing as needed.

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