Job Description
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.
Duties and Responsibilities - Review and approval of cGMP analytical data comparing results to internal and customer specifications, SOPs, and established standards to ensure accuracy and quality of data
- Works collaboratively with QC team members and cross functional teams for timely resolution of quality issues to achieve project goals
- Support Product Release activities ensuring timelines are met
- Work on problems of diverse scope in which analysis of data requires evaluation of identifiable factors
- Identify and resolve issues with assistance from Data Review team
- Review of LIRs
- Support all data integrity initiatives and strive for right first time
- Make daily decisions about the quality of data based on biochemical knowledge and compliance background
- Revise, create SOPS and/or test forms as required
- Assists with metrics for trending and reporting as required, stability and QC analytical data
- Task and team-oriented, analytical, organized, detail-oriented, self-motivated and ability to multitask
- Exceptional communication and interpersonal skills
- Assists in training of new hires and retraining of QC laboratory staff, as needed
- Assist/mentor QC new hires on cGMP/GDP
- Strong knowledge of QC analytical equipment and software required
- Strong communications skills - written and verbal
- Able to prioritize workload to meet stringent timelines
- Provide timely status updates to Management upon request
- Proficient with MS Outlook, Word, Excel and PowerPoint, and other electronic systems
- Performs other duties as assigned
Qualifications - B.S. in Chemistry, Biology, Chemical Engineering, or related biological sciences
- 3+ years in a cGMP analytical laboratory environment
- HPLC, PA800, CS2500, SDS Page
- LIMS, EMPOWER
- cGMP experience
Working Conditions - Personal protective equipment must be worn in the laboratories according to Rentschler safety requirements
- Will interact with other departments
- Pace may be fast and job completion demands may be high
- Not a hybrid position, work must be performed on site
Physical Requirements - May be required to stand for long periods of time while performing review of lab logbooks, equipment, lab documentation
- Must be able to walk distances between labs, offices, departments
- Must be able to work safely in a lab environment
- PPE as required
Job Tags
Contract work,