Job Description
The candidate is to support cradle-to-grave capital projects within the Pharmaceutical Industry (Biologics DS and DP). Typical projects include aseptic fill/finish/packaging, bioprocessing, facilities/utilities, Cleanroom, VHP and automation integration. Persons are Project Managers that have specific experience in an Pharma regulated environment.
Responsibilities
– Develops project objectives by reviewing project proposals and plans; conferring with management
– Determines/Develops project specifications by studying product design, and performance standards; completing technical studies; preparing cost estimates
– Provides timely engineering solutions to problems associated with project assignments
– Assist with Technical evaluations/project task on capital projects from the concept CAR funding stages through procurement, installation, start-up and commissioning
– Develops or assists with the development of project schedules by studying project plan and specifications; calculating time requirements; sequencing project elements
– Maintains project schedule by monitoring project progress; coordinating activities; resolving problems
– Controls project plan by reviewing design, specifications, and plan and schedule changes; recommending actions
– Controls project costs by approving expenditures; administering contractor contracts
– Prepares project status reports by collecting, analysing, and summarizing information and trends; recommending actions
– Maintains safe and clean working environment by enforcing procedures, rules, and regulations
– Maintains project records and documentation such as meeting minutes, specifications (URS, FRS, etc.), drawings (P&ID, schematics), change control, Preventative maintenance and calibration forms/data, etc.
– Maintains product and company reputation by complying with federal and state regulations (Health Authority)
– Contributes to team effort by accomplishing related results as needed
– Any other task as assigned by Supervisor/Manager.
About You :
– Bachelor’s Degree in Engineering (Chemical/Mechanical preferred)
– 5 – 15 years related work experience
– Pharmaceutical experience preferred especially in Biologics DS / DP
– CQV (Commissioning, Qualification and Validation) experience and knowledge is preferred.
– Instrumentation & Controls experience a plus
– GMP/cGMP knowledge a plus
– PMP certification a plus
– Self-motivated and capable of working in diverse team situations with company clients and maintaining a positive attitude towards project challenges.
– Bilingual in English (Written and Spoken) as well as in Indonesian (Written and Spoken).
– The Candidate must be based in Indonesia, preferably Indonesian Citizen.
Job Type: Contract
Contract length: 12 months
Salary: Rp10,000,000 – Rp15,000,000 per month
Ability to commute/relocate:
Jakarta: Reliably commute or planning to relocate before starting work (Required)
Experience:
Project Manager: 5 years (Preferred)
Project Coordinator: 5 years (Preferred)
Pharmaceutical Industry: 5 years (Preferred)
Commisioning, Qualification and Validation: 5 years (Preferred)
License/Certification:
PMP Certification (Preferred)