About the role
AI summarisedSenior Associate Quality Control I (Chemistry) role at Amgen in Singapore Manufacturing - Tuas.
BiotechOnsiteQuality
Key Responsibilities
- Senior Associate Quality Control I (Chemistry) 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.
Requirements
- Master’s degree in Chemistry, Biochemistry or related technological field OR Bachelor’s degree in Chemistry, Biochemistry or related technological field and 2 years of directly related experience OR Associate’s degree in Chemistry, Biochemistry or related technological field and/or 4 years of directly related experience OR High school diploma in Chemistry, Biochemistry or related technological field / GED and 6 years of directly related experience Preferred 4 years of relevant professional work experience within the pharmaceutical or biopharmaceutical industry and laboratory testing experience preferred.
- Strong knowledge and understanding of GMP pharmaceutical production, pharmaceutical plant operation and associated testing methods.
- Strong technical knowledge in and experience with the following QC Chemistry/ Biochemistry/ Raw material testing methods and equipment is required: Immunosorbent Assay/Cell based Bioassay: Potency, Host Cell Proteins, ELISA Chromatography: UPLC, HPLC, LC-MS, GC-HS General Chemistry: Capillary Electrophosis, LOD, Autotitration, KF, Optical Rotation, FT-IR, Conductivity, TOC, pH, wet chemistry Ability to preempt issues and disruptions to lab operations and develop mitigation actions Problem solving skills with the ability to apply logic, utilize technical knowledge and assess data to troubleshoot issues and derive appropriate GMP decisions and solutions Experience in laboratory asset management, method qualification and transfers Ability to coach, mentor and/or cross train staff within core technical areas Good communication skills (technical writing and verbal communication/presentation) Interact effectively with cross functional team and ability to work well in teams Ability to manage multiple simultaneous activities in a rapidly changing environment 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.