Monday, August 24, 2015

Pharma technician @ Merck

Message Classification: Restricted


pharma technician (12 hours rotating shift)

 

Interested applicants please send your resume to Mr Wong Kok Keong at kok.keong.wong@merck.com.

 

JOB PURPOSE

 

·         Perform manufacturing operations per production schedule in compliance with cGMP and achieve the operational objectives.

 

·         Meet Site’s safety, health and environmental (SHE) performance objectives through compliance with site SHE rules.

 

·         Ability to carry out basic shopfloor trouble shooting, initiate RTPS sheet and participate in solution development and implement.

 

 

MAIN RESPONSBILITIES

 

Manufacturing Excellence

 

Routine Operation

 

  • Responsible for completing all assigned activities, ensuring accurate documentation completion on modules.
  • Meet performance metrics of the assigned operations.
  • Provides accurate information to visual boards.
  • Responsible for maintaining good facility housekeeping.
  • Effectively communicates during shift handover.
  • Responsible for conducting On-The-Job training for staff as required, could include being a technical skill trainer.

 

 

Non Routine Operation / Campaign turnaround Activities

 

  • Performs equipment cleaning/maintenance/calibration and setup at least either two modules in Tablet Manufacturing/Nasonex Operation or 3 modules in DPI and supports equipment cleaning for all operations.
  • Responsible to perform OQ/PQ and support IQ when assigned.

 

 

Incident, Event, Atypical

·         Provide detailed information for all events and atypical to assist in notification /investigation.

·         Responsible to carry out basic shop floor trouble shooting and escalate to next appropriate level when required.

·         Support in data collection to assist investigations.

 

 

Continuous Improvement

  • Actively participate in Kaizen events in operations in accordance with Kaizen plans when assigned.
  • Provide improvement feedback based on understanding of lean tools and techniques.

 

 

 

Financial Stewardship

  • None

 

 

Quality / SHE Stewardship

 

Quality

  • Ensures manufacturing related activity is completed according to established procedures and all associated documentation is completed to a high standard.

 

Safety, Health & Environment

  • Ensures compliance to all Safety and cGMP requirements and participates as ERT team member when assigned.

·         Participates in and supports the implementation of actions for all Incident Investigations and Audits.

·         Highlights “Near Miss” and other improvement ideas for work environment.

 

 

 

People Excellence

 

People Management

·         Use Tier process and other opportunities to engage positively with others to improve both communication + teamwork skills.

·         Share technical knowledge + feedback to other as opportunity/training occurs.

 

Self

  • Exhibit a positive attitude and provide constructive feedback & solutions to issues /opportunities in the work place.
  • Responsible to participate in improvement project and actively generate ideas.
  • Develops and updates on career path with manager, which is aligned with Performance Management Process.
  • Ensures both operational knowledge and technical skills are maintained and compliant against individual training requirements.

 

 

 

ACCOUNTABILITIES

DIRECT IMPACT ($)*

INDIRECT IMPACT ($)*

 

NA

 

NA

 

NA

       * (only if applicable)

 


 

SUPERVISORY RESPONSBILITIES:

No. of direct reports:

Total: __0__ direct
(Refers to the no. of staff reporting directly to this position)

No. of indirect reports:

Total: __0__ indirect
(Refers to total number of staff reporting to this position’s direct reports)

 

(The headcount figure is subjected to ±10% fluctuation in view of changing business needs.)

 

 

 

PROFILE:

Qualification:

·         A Diploma or a Technical school graduate Science / Engineering with strong back ground in operation and maintenance in pharmaceutical/API chemical manufacturing experience.

·         Must be will to work in 12 hours rotating shift (day/night).

 

 

Experience:

·         3 to 5 years of hands-on experience.

 

 

Leadership, Professional and Functional Competencies*

·         Refer to Career Framework Competency Model.

 

 

Other Personal Attributes*:

·         Strong back ground in operation of chemical/pharmaceutical systems including hands on experience.

·         Experience in safety procedures/practices.

·         Familiarized with cGMP working environment.

·         Has a good writing and communication skill.

·         Understanding of lean tools and techniques including Work Standards, Kanban, 5S and Visual management.

·         Has the capability to train people on operations.

 

 

 

*(Including competencies found in career maps as applicable)

 

 

 

 

 

 

Wednesday, August 12, 2015

Laboratory Technician @ Santoku BASF Pte. Ltd.

Message Classification: Restricted


Company: Santoku BASF Pte. Ltd.

Position available: Laboratory Technician

 

·         QC & QA functions of process, product and analytical results;

·         Routine analysis of raw material, product, process samples including external analysis services;

·         Perform tests and in-house validations in accordance with established methods;

·         Review data quality in accordance with established guidelines/criteria;

·         Perform routine maintenance and troubleshooting of laboratory equipment;

·         Inventory control of chemicals and consumable materials;

·         Perform quality documentation and data management to ensure compliance to relevant standards;

·         Assist superiors in QC, QA functions and projects.

Interested candidates please send resumes to bernard@santokubasf.com.sg

 

 

QA Department
Santoku BASF Pte Ltd
35 Tuas West Avenue Singapore 638433