Laboratory Technician - Analytical Development

Laboratory Technician - Analytical Development (Contract)

Join to apply for the Laboratory Technician - Analytical Development (Contract) role at Rentschler Biopharma

Advancing medicine to save lives. Together.

Thanks to many decades of experience and our passion for what we do, we make an essential contribution to the global availability of biopharmaceuticals, especially for patients with rare and serious diseases.

Rentschler Biopharma SE is a leading contract development and manufacturing organization (CDMO) focused exclusively on client projects. We offer customized full-service solutions for bioprocess development and the production of complex biopharmaceuticals. As a German family‑owned company with an international footprint and global reach, we combine experts, expertise and years of experience to develop best‑in‑class solutions – together with our clients.

Rentschler Biopharma has approximately 1,400 employees and is headquartered in Laupheim, Germany, with a site in Milford, MA, USA. In 2024, we joined the United Nations Global Compact, underlining our commitment to sustainability.

As an independent family‑owned company, we live by the motto:
Many hands, many minds – ONE TEAM! Open, respectful cooperation characterizes our working environment, where quality awareness, diligence and responsibility are our top priorities. With all the diversity of our talents in the Rentschler team, we pursue one vision together: advancing medicine to save lives.

• Perform routine laboratory preparation work including but not limited to daily calibration check of pH meters, pipettes, balances, and other equipment as necessary
• Perform laboratory Daily, Weekly, and Monthly housekeeping tasks in accordance with SOPs to maintain cleanliness and compliance within the lab
• Prepare reagents including mobile phases, buffers, and stock solutions
• Participate in aliquotation of validation samples and test materials
• Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, and cGMP regulations
• Participate in functions involving teams, which impact production, increase efficiency, solve problems, generate cost savings, and improve quality
• Additional routine tasks may be assigned as appropriate

• High School diploma and 3+ years of related experience, OR Associate Degree and 2+ years of related experience, OR Bachelor’s Degree
• Ability to work in a clean room environment
• Excellent organizational skills along with good written and verbal communication skills, and attention to detail
• Proficiency in GMP's and ability to follow instructions and work as a team member
• Proficiency in office tools is a plus

• Laboratory environment working with chemical reagents and analytical equipment
• Personal Protective Equipment must be worn as required
• Normal office working conditions: computer, phone, files, fax, copier
• Minimum travel required (Less than 10% domestic)

• Frequent lifting up to 10 lbs
• Frequent standing/walking to work in lab environment for extended periods
• Frequent sitting for extended periods to use computer

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Base Pay Range: $27/hr - $38/hr

40 hour/week

Seniority level:
Associate

Employment type:

Contract

Job function:
Science, Manufacturing, and Quality Assurance

Industries:
Biotechnology Research and Pharmaceutical Manufacturing