Chemist II at Boston Scientific Corporation Malaysia

Galway, Connacht, Ireland -

Full Time

Start Date

Immediate

Expiry Date

20 Mar, 26

Salary

0.0

Posted On

20 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Chemistry, Quality Systems, cGMP, Test Method Development, Validation, Gas Chromatography, Analytical Testing, Equipment Calibration, Regulatory Audits, Technical Guidance, Documentation, Data Trending, Laboratory Management, Training, Process Validation, Software Applications

Industry

Medical Equipment Manufacturing

Description

Primary Commitment to patient safety and product Quality. Understands and comply with all the regulations governing the quality systems. Delivery of key Quality and Performance Objectives. Maintenance of laboratory scorecards and trackers. Ensure compliance with mandatory training requirements and ensure that your training records are up to date and compliant to cGMP. Your responsibilities may include test method development and validation, raw material, in process, finished product and Stability testing. Complete documentation associated with testing/ method development & Validation/ equipment qualification in a timely manner. Ensure all analytical testing is carried out as defined in the Quality System. Perform equipment calibration and qualification as required. Review of all laboratory Quality Systems to ensure compliance to cGMP. Participate in Regulatory, Internal (Auditor/Auditee) and Vendor audit programs as required. Provide training (induction/ on the job/ procedures and updates), technical guidance / trouble shooting to laboratory staff including review of associated training records. Review and approval of Laboratory results and documentation, as required the trending and charting of data. Perform and assist with additional duties as may be directed by your direct line manager. Proficient in the use various software application utilized in the laboratory. Create, review and approve change requests as required. Creation of purchase requisitions for laboratory equipment and consumables. Management of laboratory spend and approval of vendor invoices. Management of laboratory inventory and supplies and ordering of same. Manage laboratory training process and maintenance to training status. Provide analytical support to process validations. Participate on VIP and Continuous project teams as required. NFQ Level 8 (240 credits) in Science, Chemistry or a relevant discipline Min. 3-5 years' experience in a similar role ideally in medical devices Strong experience in Gas Chromatography would be an advantage Good technical capabilities, communication skills, teamwork abilities and initiative. Proven ability to work well as part of a team & on own with minimum supervision.

Responsibilities

The Chemist II is responsible for ensuring patient safety and product quality by complying with quality system regulations and delivering key quality objectives. Responsibilities include testing, method development, documentation, and participation in audits.