Senior Director, Drug Substance Manufacturing - Waltham, MA

+The Senior Director, Drug Substance Manufacturing is responsible for leading GMP drug substance manufacturing, process performance qualification (PPQ), ensuring commercial supply, and overseeing all CMC activities related to Fab-oligonucleotide conjugates (drug substance).+ · +R ...

++We are seeking an accomplished Senior Director to lead all outsourced drug substance manufacturing operations. · The ideal candidate has deep technical understanding of peptide drug development experience with synthetic and recombinant manufacturing techniques for peptides. · I ...

We are seeking an accomplished and strategic Senior Director, Drug Substance Development and Manufacturing to lead and oversee all outsourced drug substance manufacturing operations. · ...

We are seeking an accomplished and strategic Senior Director Drug Substance Development Manufacturing lead oversee all outsourced drug substance manufacturing operations. · This key leadership role accountable driving technical excellence across manufacturing lifecycle including ...

We are seeking an accomplished and strategic Senior Director Drug Substance Development Manufacturing to lead oversee all outsourced drug substance manufacturing operations. · The ideal candidate is an experienced leader with a deep technical understanding of peptide drug develop ...

We are seeking an accomplished and strategic Senior Director, Drug Substance Development and Manufacturing to lead and oversee all outsourced drug substance manufacturing operations. · ...

As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. · Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. · ...

As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. · Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. · ...

Be a hero for our rare disease patients. At Ultragenyx, we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to do. · ...

+Job summaryThis position is responsible for development and drug substance manufacturing activities of new and existing products at external Contract Manufacturing Organizations CMOs. · +ResponsibilitiesAct as the drug substance subject matter expert and manage external DS devel ...

We are focused on developing best-in-class medicines for people living with autoimmune and rare diseases. Leveraging our team's expertise in antibody discovery and engineering we have created a robust pipeline of differentiated investigational therapeutic candidates for well-vali ...

Opportunity awaits those up to the challenge of developing transformative therapies across a broad range of debilitating diseases. · Serve as technical expert on internal/external projects (process implementation, validation, tech transfer). · ...

We are seeking a Director of Quality Control to lead and execute the QC strategy across our clinical-stage pipeline. · ...

Developing transformative therapies for debilitating diseases as part of the Process development team. · ...

+ Work with hazardous materials inside laboratory environments+ Stage, weigh, sample, and transfer materials+ Maintain manufacturing spaces in good operation including cleaning reactors · + Follow Standard Operating Procedures in support of cGMP activities · + Other assigned ta ...

The Associate Director, Stability is a self-motivated individual who works as a member of an integrated team at Ardelyx contracting, designing, managing, and evaluating stability studies at contractors for both drug substance and drug product. · ...

Perform hands-on execution of purification, filtration and formulation activities to develop scalable downstream processes for biologics. · ...

Cambrex is seeking an Associate Scientist to join its team in Waltham, MA. The successful candidate will have a passion for working in a fast-paced environment and experience working in a chemistry research lab. · ...

The Associate Director, Stability is responsible for managing stability studies at contractors for drug substance and drug product. The individual should have experience with ICH and cGMP guidelines and ability to contribute to regulatory filings. · Develop strategic direction of ...

The Staff Technical Project Engineer - Automation plays a leading role in delivering automation, data, and digital transformation projects across Thermo Fisher Scientific's Drug Substance manufacturing network.This senior engineer will own and drive complex automation and data in ...