Process Development Senior Associate

**Process Development Senior Associate**

**Amgen Singapore Manufacturing**

**HOW MIGHT YOU DEFY IMAGINATION?**

Amgen is one of the world’s leading independent biotechnology companies. For over 4 decades, Amgen has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics, but has invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. Japan and Asia Pacific (JAPAC) is the fastest growing region in Amgen. Now we are hiring a **Process Development Senior Associate **in **Amgen Singapore Manufacturing**.

**Process Development Senior Associate**

**Live**:
**What you will do**

**Responsibilities**:

- Responsible for providing scientific and technical support for commercial production and testing of synthetic drug substance
- Support new product introduction, troubleshooting and improvement of existing and new processes run at the Amgen Singapore Manufacturing site
- Assess initiatives associated to analytical method improvements and optimizations
- Responsible for the development and preparation of laboratory-based experiments to support method transfers, qualifications & validations, analytical support to small scale model interrogation, investigations, and process improvements
- Responsible for planning procedures for defined projects, including timelines, milestones, methodological approaches, expected results and necessary resources
- Supports cross-functional teams of scientists and engineers through project challenges and implement advance scientific experiments, which contribute to the successful completion of goals and/or projects
- Responsible for experimentation in the lab to resolve technical issues observed during transfer / testing and manufacturing at large and laboratory scales

All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities

**Win**:
**What we expect of you**:
**Qualifications**:

- Master’s degree in Science, Engineering or related technological field
- Bachelor's Degree in Science, Engineering or related technological field and 2 years of directly related experience OR
- Associate degree in Science, Engineering or related technological field and 6 years of directly related experience OR
- Diploma in Science, Engineering or related technological field and 8 years of directly related experience
- At least 4 years of relevant work experience in the commercial manufacturing environment within the pharmaceutical industry and regulated environments (i.e. cGMP, OSHA, EPA) is preferred
- Subject matter expert for analytical and organic Chemistry
- Good knowledge of state-of-the-art technologies, emerging scientific and regulatory directions for synthetic processing, product attributes and testing
- Display basic knowledge of the manufacturing practices, regulatory requirements, scientific properties and risks associated with synthetic processing and knowledge of different synthetic processing platforms (i.e. reaction, concentration, crystallization, isolation, drying)
- Experience in working closely with scientific, quality control and manufacturing disciplines across clinical and commercial operations
- Good understanding of synthetic product quality attributes, analytical control strategies and analytical methods/technologies used in synthetic manufacturing
- Good understanding and hands-on experience with qualification, transfer and validation of methods (LC, GC, KF titration, etc.) used in release, in-process and stability testing to analyze or to characterize synthetic drug substance, product variants and process related impurities
- Experience and display knowledge in setting up laboratory-based experiments and implementing studies to support manufacturing
- Experience in collaborating and building solid working relationship across departments, with diverse and remote staff and with external collaborators
- Display project management, planning and organizational skills
- Ability to independently uncover and resolve issues associated with the development and implementation of scientific projects
- Strong interpersonal, written and oral communication skills for the timely documentation, presentation, and discussion of scientific results in a fast-paced, multi-disciplinary, team-based environment
- Familiarity with documentation in a highly regulated environment
- Ability to provide solutions to a large variety of technical problems

**Thrive**:
**What you can expect of us**

As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.
- Vast opportunities to learn and move up and across our global organization
- Diverse and inclusive community of b