Lowongan Kerja PT Ciba Vision Batam

Info Lowongan Kerja Batam, With worldwide headquarters in Atlanta, Ciba Vision is a global leader in the research, development and manufacturing of optical and ophthalmic products and services, including contact lenses and lens care products. Ciba Vision products are available in more than 70 countries worlwide. We invite suitable candidates to apply for the following position :

QC Supervisor

Kepulauan Riau - Batam

Responsibilities:

• Supervise and lead QC team to ensure smooth day to day manufacturing operation. Maintain procedure and implement Good Manufacturing Practices (GMP) 

Requirements:

• Candidate must possess at least a Bachelor's Degree in Engineering / Science.
• At least 2 year(s) of working experience in the related field.
• Familiar with quality activities.
• Experience with GMP / GDP implementation would be an advantage.
• Able to use statistical tools and spreadsheet.
• Able to work on shift and long hours. 
• Applicants must be willing to work in Batam.

Quality System - CAPA Specialist

Kepulauan Riau, Riau

Responsibilities:

• Perform complaint and failure investigation according to Corporate and International Standards and Requirements. The investigation must be conducted in timely manner with good quality standard; thorough, in-depth root cause analysis, including corrective and preventive actions. Review customer complaint report, trends and respond customer’s complaints with complete investigation report.

Requirements:

• Degree holder from Science or Engineering.
• 3 to 5 years experience, peferably from pharmaceutical or Medical Device Industries
• Good understanding in cGMPcompliance, proficient in advanced quality investigation techniques
• Good investigation and technical report writing skills in English.

Quality/e-Compliance Engineer

Batam (Kepulauan Riau), Riau

Responsibilities:

• Facilitate and support definition, implementation and monitoring of Computerized Systems. Responsible for Computerized System Validation approval and provide an independent oversight to minimize the company’s risk exposure in compliance with applicable laws, regulations, policies and procedures (global and site) for Computerized System. Assess compliance against any associated Computerized System Validation standard or guidlinethrough audit or other means as appropriate.

Requirements:

• Degree holder from Science, Engineering or IT
• 2 to 3 years experience, preferably in Pharmaceutical or Medical Device Industries.
• Experience with all phases of computerized system (software and infrastructure) validation and qualification. 
• Thorough knowledge of ISO, cGMP’s, GLP’s, 21 CFR Part 11 and 820 requirements. 

Please email your resume to: hr.recruit@cibavision.com