| Location | Charles City, Iowa |
| Job Type | Full-time |
| Industry | Biotechnology/Pharmaceuticals |
| Company Size | 1,000 to 1,499 employees |
| Year Founded | 1981 |
| Website | http://www.cambrex.com |
As a Process Engineer II, you’ll build on your chemical engineering experience while continuing to receive mentorship from senior engineers and scientists who support your professional growth. In this role, you’ll operate with increasing independence, contributing your expertise across all stages of bringing new products from the laboratory to full-scale batch manufacturing. You’ll gain hands-on experience with diverse processes and unit operations such as reactions, distillation, extraction, filtration, and drying, while also beginning to lead small to moderate projects.
As part of a global contract development and manufacturing organization, you’ll have the opportunity to collaborate directly with pharmaceutical clients worldwide and to work on multiple processes each year. This position offers clear pathways for career development, whether you choose to specialize in technical expertise, project leadership, or operations. Over time, you’ll have opportunities to advance into roles as a subject-matter expert, project manager, or operations leader — making a lasting impact on both the industry and patients worldwide.
Responsibilities:Draft the conceptual process design for individual chemical steps including: scaling calculations for unit operations, equipment selection, and determination of operating parameters.
Lead process reviews for operability, safety, and quality.
Provide technical information directly to external clients and internal stakeholders.
Lead and participate in production campaigns for single chemical steps through planning, technical analysis, and in-person observation.
Develop process understanding and recommend improvements through process modelling and the analysis of production and laboratory data.
Perform quality investigations and corrective action / preventative action implementation.
Conduct process improvement projects to reduce cycle time, increase yield, and improve quality.
Draft manufacturing documents: process flow diagrams, batch records, validation protocols, standard operating procedures, quality investigations, campaign reports
Qualifications / Skills::Cambrex is an innovative life sciences company with a refreshingly human approach. Driven by passion, our pharmaceutical products, expertise and technologies accelerate our customers’ small molecule therapeutics into markets across the world.
With over 35 years of active pharmaceutical ingredient (API) development and manufacturing expertise, a growing team of more than 1,200 experts and a strong presence in the USA and Europe, we are tried and trusted across branded and generic API markets.