To ensure that all production activities are carried out in compliance with the cGMP requirements by strictly adhering to the standard operating procedures and good documentation practicesEnsures all team members strictly comply with cGMP procedures and immediately calls attention and corrects any member deviating proceduresAdherence to safety, health, hygiene and environmental measuresCandidates having on hand experience in pharmaceutical sterile formulation AreaCandidates having an sound knowledge on PCS-7 Automation systemCandidates shall be able to perform following activities as per Standard Operating Procedures below and having a sound knowledge on cGMP
a) Monitoring of cleaning activities with correct disinfectant and frequency
b) Monitoring and recording area differential pressure, temperature and relative humidity
c) Performing CIP and SIP OF Mobile Vessel
d) Performing Automation Formulation System (PCS-7) of Formulation Vessel, Filtration Skids and Transfer Vessel
e) Ensure cleanliness and sterilization of Formulation Vessel and Transfer Vessel
f) Preparation of solution according to the different batches and the production plan for vials / cartridgesComply in any other general SOPs and EOPs that related to production activities in PDPResponsible for documentation specifically on preparation, review and revision of BMR, SOP’s, EOP’s, ECC’sResponsible to fill in the required data in batch record online with correct GDP9 Ensure completeness of batch record before submitted to QADirectly involved and having a knowledge on qualification and validation of equipment and processIdentification and raising deviation, change control and compiling other related documents in coordination with QAClosely coordinates with the different department QA, QC, Warehouse, Instrumentation and Automation, and Maintenance for achieving the day to day production targetsCandidates having a knowledge on SAP system
Candidate must possess at least a Bachelor's Degree, Post Graduate Diploma, Professional Degree, Biology, Chemistry, Science & Technology, BioTechnology, Engineering (Bioengineering/Biomedical) or equivalentRequired skill(s) Fill Finish, Aseptic Environment, Grade A cleanroomAt least 2 year(s) of working experience in the related field is required for this positionApplicants must be willing to work in NusajayaPreferably Senior Executives specializing in Engineering - Chemical or equivalentApplicant must willing take on routine 3 shift with2 off days per week
Or you may send your updated resume/CV to
Shortlisted candidate will contact within 2 weeks time
Salary:MYR 3,500 - 6,500
Deadline:01st Mar 2020
In 2012, with more than 35 years of success behind it, Biocon, India's largest biotech company set up their first overseas plant in Johor Bahru, Malaysia – Asia’s largest integrated Insulin manufacturing facility. With an investment of about USD 275 million, it is the highest foreign investment in Malaysia’s biotech sector till date and currently employs about 570 professionals in a state-of-the-art facility.
The attached document speaks about the journey and the many challenges and milestones encountered along the way. It talks of the Human Capital strategy of the company and how the Malaysia story is embedded in the same.
There were several steps which led to the success and many of them were differentiated with innovative ideas and sharp business acumen.
Biocon Malaysia offers an excellent career opportunity for biotech professionals.
If you want to be a part of a Company that constantly creates history and consistently earns more accollades for its innovations and other significant accomplishments and contributions, then we invite you to be a part of the BIOCON FAMILY! Apply to join us today.
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