Upstream Bioprocess Scientist (Ambr250) - Malvern

Eurofins PSS Insourcing Solutions; Malvern (Chester County); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

A biotechnology company in Malvern, PA is looking for a full-time role in upstream process development. Candidates with a Bachelor's or Master's degree in biopharmaceutical, biotechnology, or pharmaceuticals are encouraged to apply. Responsibilities include performing development utilizing the Ambr250 system, conducting lab work, maintaining records, and ensuring compliance with cGMP practices. The role offers flexible shifts and benefits, including life insurance, 401(k) matching, and paid time off. Join a leading company making a difference in scientific advancements.

Qualifications

• Bachelors or Master’s degree in biopharmaceutical, biotechnology or pharmaceutical required.
• Broad knowledge in upstream process development and hands-on experience.
• Authorization to work in the United States indefinitely without restriction or sponsorship.

Responsibilities

• Perform Upstream process development utilizing the Ambr250 Satorius system.
• Perform duties in a protocol-driven work, such as cell culture, and running Ambr bioreactors.
• Support lab work associated with development and scale-up projects.
• Organize records, capture results into data sheets, and contribute to technical reports.
• Assist with lab upkeep and organization efforts, including waste disposal.
• Conduct, analyze and report data in accordance with departmental requirements.
• Record experimental data and maintain accurate laboratory notebooks.
• Comply with cGMP practices.
• Analyze and present data in a professional format.
• Demonstrate clear verbal and written communication.
• Follow appropriate SOPs and internal documentation requirements.

Job description

A biotechnology company in Malvern, PA is looking for a full-time role in upstream process development. Candidates with a Bachelor's or Master's degree in biopharmaceutical, biotechnology, or pharmaceuticals are encouraged to apply. Responsibilities include performing development utilizing the Ambr250 system, conducting lab work, maintaining records, and ensuring compliance with cGMP practices. The role offers flexible shifts and benefits, including life insurance, 401(k) matching, and paid time off. Join a leading company making a difference in scientific advancements.