Deskripsi Pekerjaan
We are representing a prestigious global pharmaceutical MNC that is establishing a new state-of-the-art manufacturing plant in Tuas, Singapore. This greenfield project represents a significant investment and commitment to innovation in pharmaceutical production. We are now seeking a highly motivated and meticulous Associate Technician (Production) to join the core operations team and play a pivotal role in the successful launch and ongoing operations of this world-class facility.
As an Associate Technician, you will be an integral part of the production unit, reporting to the Production Supervisor. Your primary responsibilities will encompass all aspects of production unit operations, from preparation and charging to reaction monitoring, sampling, and workup processes. You will ensure all activities comply with cGMP, SOPs, and safety regulations. You will have the opportunity to work with advanced manufacturing technologies and contribute to process optimization initiatives from the ground up.
Our client is a world-renowned pharmaceutical company with a strong pipeline of life-saving therapies. The new Tuas plant is designed to meet the highest standards of quality, safety, and sustainability. By joining this team, you will contribute to the production of essential medicines that improve patients' lives worldwide.
This role offers exceptional career development prospects, including comprehensive training on the latest pharmaceutical manufacturing processes. The successful candidate will become a Subject Matter Expert and may progress to senior technician or supervisory roles as the plant expands. We are looking for hands-on individuals eager to learn and committed to quality and safety.
Tanggung Jawab
- Perform production preparation activities including raw material staging and equipment setup.
- Execute charging of raw materials and intermediates as per batch instructions.
- Monitor and control reaction parameters such as temperature, pressure, and agitation.
- Conduct in-process sampling and perform basic analytical tests to ensure quality compliance.
- Carry out workup operations including filtration, distillation, drying, and milling.
- Maintain accurate batch records and documentation in compliance with GMP requirements.
- Ensure cleanliness and sanitation of production areas and equipment.
- Adhere to all safety protocols and contribute to a safe working environment.
Kualifikasi
- NITEC or Diploma in Chemical Engineering, Pharmaceutical Science, or related discipline.
- At least 1-2 years of experience in pharmaceutical or chemical manufacturing operations.
- Knowledge of cGMP and safety regulations in a manufacturing environment.
- Ability to work in shift patterns if required.
- Strong attention to detail and documentation skills.
- Good problem-solving skills and ability to work in a team.
- Physically fit to handle manual tasks and stand for long periods.
- Experience in new plant start-up or commissioning is an advantage.