Lowongan Production Manager Reagent di PT Virtue Diagnostics Indonesia

This position is responsible for reagent manufacturing overall management including setting up process, technical transfer, process validation and mass production to support new product introduction (NPI) launch and product supply for market in timely manner

Responsibilities:

- General 

• As a member of the site leadership team, provide advise on key and operations related issues, initiative and strategy for continually improving the site operations performance.
• Work closely with cross functions team to solve technical and product supply issues

- Manufacturing Management

• Responsible for overall reagent manufacturing management from material requisitioning to finish goods stock in warehouse.
• Deliver technical support for sales and service team to solve product issue from customer’s site. 
• Participate in NPI design process and design review meeting as manufacturing representative to provide input related to product requirement and review product producibility.
• Set up appropriate manufacturing process according to design output, and leads process and product validation.
• Responsible for technical transfer external parties, through cooperation with internal and external stakeholders.
• Support on site audit for new product registration, together with Quality and RA team.
• Responsible for monitoring manufacturing process and continuously optimize it to deliver stable products.
• Build a lean culture within reagent manufacturing department to improve efficiency & productivity and reducing cost  

- Leadership & People Management 

• Create an environment of strong team spirit, motivate and inspire teams to achieve ambitious goals in the short, mid, and long term to support business growth.
• Drive collaboration of cross functions teams and business units within the organization.
• Manage performance and talent development for all direct functional reports, and qualify them in a timely manner

- Cost Management 

• Control budget and departmental costs, headcount and CAPEX towards the set targets.
• Periodically evaluates workload and expense in the department, and continue to optimize cost control and department‘s productivity and competitiveness

- Other relevant duties as assigned

Qualifications:

• Bachelor Degree in Pharmacy/Pharmacist, Biology, Engineering, Life Science or related. 
• Minimum 6 years or more relevant quality working experience in a decision making role in related industry.
• Solid understanding of the regulation in the medical device industry.
• Experienced in quality system setting up a base on ISO 9001, ISO 13485 and GMPs. 
• Preferred hands on medical products’ processing and production. 
• Strong interpersonal, oral and written communication skills in Bahasa and English, with the ability to effectively communicate with all levels of the organization.
• Willing to work in Cikarang