- Parexel (Providence, RI)
- …opportunity for an experienced and highly motivated professional to join our Global Regulatory Affairs team as a CMC Regulatory Affairs Senior/Consultant. This role ... small molecule products are developed and maintained in compliance with global regulatory requirements. The primary regions of responsibility include the United… more
- Prysmian (Lincoln, RI)
- …testing & improvements, manufacturability, feasibility, quoting activities, productivity enhancements, manufacturing process & equipment changes, new design ... establish list of alternate ingredients; maintain material recipes and mixing process parameters. + Identifies, documents, and verifies processing requirements for… more
- Cipla (Fall River, MA)
- …Identify areas for improvement in packaging activities and contribute to process enhancements. Support initiatives aimed at improving overall productivity through ... management / Dept. Head. Education QualificationsBachelor's degree in pharmaceutical sciences / electrical/ mechanical / production or related fields of… more
- Cipla (Fall River, MA)
- …and experience of GMP documentation required. Bachelor's degree in science , biochemistry, pharmaceutical engineering, Pharmaceutical Sciences , or related ... (may vary based on business needs) Reports To : Manufacturing Manager Salary Range: $62,400 - $75,400 Purpose: The...periodic review. Develop strategies and documents for cleaning and process validation of API equipment and products in compliance… more
- Cipla (Fall River, MA)
- …and experience of GMP documentation required. Bachelor's degree in science , biochemistry, pharmaceutical engineering, Pharmaceutical Sciences , or related ... (may vary based on business needs) Reports To : Department Head - Manufacturing Salary Range: $72,800 - $93,600 Job Overview Invagen Pharmaceuticals is searching for… more
- Cipla (Fall River, MA)
- …and Experience: Possess a minimum bachelor's degree in chemistry, Pharmaceutical Sciences , or related field of study from an accredited institution. Master's ... analytical development, Quality Control (QC), Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP)/Good Documentation Practices (GDP), etc. Technical Knowledge… more
- Syner-G BioPharma Group (Boston, MA)
- … engineering, process development, materials & engineering sciences , technology transfer, facilities/utilities/technical services, and manufacturing ... specifications, design, functional requirements, development, commissioning, and qualification of process equipment or systems for compliance with manufacturing … more
- Cipla (Fall River, MA)
- …the next products. Training and educating employees when necessary. Recording In- process entries into respective documents. Checking the Cleanliness of machines ... and Standard Operating Procedures (SOPs) as well as followcurrent Good Manufacturing Practices (cGMP), comply with legal regulations, monitoring the environment.… more
- Syner-G BioPharma Group (Boston, MA)
- COMPANY DESCRIPTION: Syner-G is a science -led, strategic partner for life science companies. We provide integrated regulatory and biopharmaceutical development ... post-market, along with operational strategy and support. With a global team of 400 employees across North America and...their journey to market. We are a leading life sciences consultancy committed to advancing human health by helping… more
- Merck & Co. (Boston, MA)
- …and strategic venture investments in healthcare as part of our Global Health Innovation fund. Together, we identify business critical opportunities, frame ... patient impactBring to bear experience in oncology (across discovery, translational sciences , development and commercialization) to identify capability gaps and ways… more
- ACROBiosystems Inc. (Boston, MA)
- ACROBiosystems is a worldwide leader in developing and manufacturing recombinant proteins and critical reagents/assays to support drug development and clinical ... in providing quality products and services and accelerating the process of therapeutic development. Our mission is to accelerate...aim to be a cornerstone company in the life science and healthcare industry. We value the fast growth… more
- Curia (Hopkinton, MA)
- Research Scientist II; Process Development Science in Hopkinton, MA Build your future at Curia, where our work has the power to save lives The Research Scientist ... II, Downstream Process Development Science will be responsible for...clients and colleagues via technical reports. Curia is a global contract development and manufacturing organization (CDMO)… more
- Olympus Corporation of the Americas (Westborough, MA)
- …Software as a Medical Device. + Demonstrated leadership in managing the global submission process for regulatory approvals across multiple markets. + ... the Digital Unit (DU). The DU is a high-growth, global innovation hub, focused on how digital technologies and...**Required:** + BS or comparable in engineering or life sciences required. + Minimum of 10 years of Regulatory… more
- Curia (Hopkinton, MA)
- …at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of ... development programs. In addition, the individual will collaborate closely with internal process development, manufacturing , and quality groups as well as… more
- Curia (Hopkinton, MA)
- …journals and texts at times beyond the "normal" working hours. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of ... microbiological testing (endotoxin, sterility and bioburden) for raw materials, in- process materials, intermediates and final product + Perform environmental… more
- Olympus Corporation of the Americas (Westborough, MA)
- …supports business objectives through: proactive monitoring and application of global regulatory requirements within the regional QMS; leading the governance ... of employee QMS awareness knowledge and application; lead quality sub-system process improvement projects to increase efficiency of the QMS through enhancing… more
- Takeda Pharmaceuticals (Boston, MA)
- …knowledge. **Job Description** **About the role** This senior individual contributor role in Global Manufacturing Science (GMSci) is the subject matter ... manufacturing strategies, applying deep drug substance expertise and direct manufacturing experience to support process design, scale-up, technology transfer,… more
- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **Title: Process Scientist - Global Manufacturing Science GMSci DP/PKG** **Location: Cambridge, MA** **About ... As a Process Scientist (Associate Director) - Global Manufacturing Science GMSci Drug...successful collaboration with: + Pharmaceutical Sciences . + Manufacturing Sciences + Global … more
- Saint-Gobain (Taunton, MA)
- …achieved, for our manufacturing facility in Taunton, MA for Saint-Gobain Life Sciences .** **Will Supervise second shift production - 3PM - 11:30PM. Will manage a ... only two companies in the world that is consistently recognized as both a top Global Employer and a Top 100 Global Innovator, but Saint-Gobain's remarkable story… more
- Takeda Pharmaceuticals (Boston, MA)
- … of new innovative medicines for our patients around the world through robust CMC processes. Global Manufacturing Science is a part of Global ... By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application… more
