Responsibilities
● Be responsible for the calibration of both GMP and non-GMP equipment according to SG requirements.
● Participate in and execute projects to create calibration plans in line with project timelines.
● Manage 3rd-party calibration services, coordinating with the production and utility teams to meet their schedules and shutdown periods.
● Issue calibration job plans from the Maximo system in a timely manner and coordinate with users to schedule suitable times for calibration.
● Operate the Maximo system to maintain calibration master data.
● Assist in drafting or updating SOPs, URS, or other required documents.
● Perform other tasks as assigned by leadership.
Requirements
● Diploma or higher qualification in instrumentation, automation, Pharmaceutical Engineering, or other related specialties; candidates with equivalent work experience is plus.
● Ability to quickly learn GMP related knowledge and all related calibration requirement and code.
● Possess good communication ability and comprehension ability.
● Display a good working attitude, strong work ethic, and willingness to follow leadership directives.
● Be open to accepting temporary work assignments, including overtime on weekends or weekdays, and other roles as required.
● Able to work independently with limited supervision in a fast-paced environment.
● Possess good multi-tasking and prioritization skills.
Career development
● Through complete systematic training, you will quickly grow to be a calibration engineer and a subject matter expert of calibration.
● A performance-oriented promotion system, diverse and comprehensive challenges in a cGMP manufacturing environment, and career advancement incentives will all contribute to your career development.
● Explore your management potential, grow with the team, and light up the growth plan of life.
