Manufacturing Associate III - Buffer & Media Prep Sun-Wed 1st Shift

Join to apply for the Manufacturing Associate III - Buffer & Media Prep (3 month Contract; Sun-Wed 1st Shift) 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.

• Key areas of responsibility include but not limited to operating the glass washer and autoclave, weigh & dispense, preparation of buffer and media, and supporting manufacturing teams as needed
• Perform operations of the following (may be applicable to commercial scale product, development studies, clinical material or validation activities)
• Operate manufacturing process equipment to perform various manufacturing production steps
• Proficient operating inside of a BSC, sampling, and performing with aseptic techniques
• Monitor and record batch parameters, including computer data entry. Complete relevant paperwork following GDP/GMP guidelines
• Troubleshoot process problems and respond to alarms. Provide information for unplanned events, including entering data into event management software
• Order, receive and distribute supplies into production area as needed
• Demonstrate procedures as a part of training sessions for other team members; may schedule department or process activities which could involve coworkers
• Participate on Continuous Improvement Teams
• May perform other duties as assigned. (During Production Processing these activities may increase)
• Knowledge of laboratory and pharmaceutical production equipment included but not limited to autoclaves, glass washer, process tanks, and analytical equipment
• Familiar with standard troubleshooting approaches (problem statement, root cause analysis, corrections, etc.)
• May be required to train others as needed
• Knowledge of bioreactor and chromatography preferred but not required
• Such additional responsibilities as the Company may also assign

• With high school diploma:
  Normally requires 6+ years of related experience required or an associate degree in Life Sciences/Engineering field. Biotech Certificate preferred
• With Bachelor’s degree:
  Normally requires 4+ years of related experience.
• Good with Microsoft Office – Outlook, Word, Excel
• Proficiency in a variety of mathematical disciplines and able to work with both the metric and USA standards of measurement, and military time
• Able to read and follow detailed written instructions and have good verbal/written communication skills
• Able to write legibly and grammatically correct entries on records
• Good interpersonal skills and be able to work effectively and efficiently in a team environment
• Ability to meet schedule required; this position may include shift, weekend, holiday work and overtime at times, as dictated by the 365-day per year production schedule

• Personal Protective Equipment must be worn as required
• May require lifting amounts of 25 lbs
• Manufacturing operations tasks requires operator to regularly remain on feet for shift
• Pushing buffer containers ranging from 50L to 200L
• Sitting for periods of 2 to 3 hours
• Ability to work in a clean room environment and comply with hygiene standards and use of special garments. Additionally, personal protective equipment must be worn due to safety requirements

• PPE as required
• May require lifting amounts of 25 lbs
• Manufacturing operations tasks requires operator to regularly remain on feet for shift

• Mid-Senior level

• Contract

• Manufacturing, Production, and Quality Assurance

• Biotechnology Research and Pharmaceutical Manufacturing