Calibration Analyst
at Taro Pharmaceuticals INC Canada
Brampton, ON, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 24 Oct, 2024 | Not Specified | 26 Jul, 2024 | 3 year(s) or above | Chemistry,Agilent,Writing,Msds,Testing,Chemicals | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
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Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
QUALIFICATIONS
- B. Sc. Chemistry or equivalent
- 3-5 years of laboratory experience
- Understanding of MSDS for safe handling of chemicals used in testing
- Ability to communicate with other team members on group tasks
- Ability to diagnose equipment issue and decide if the issue can be resolved internally or requires external service. All steps will be documented and procedures must be followed.
- Working knowledge of Empower software
- Experience with Waters and Agilent HPLCs
- Experience with Agilent GCs
- Multitasking ability including changing priorities as required
- Document report writing
- GMP guidelines
Responsibilities:
JOB PURPOSE
The main responsibility of this position is to maintain GMP compliance of all instruments and equipment assigned to the Metrology group.
DUTIES AND RESPONSIBILITIES
- Calibration/verification of instruments and equipment
- Review and revise calibration/verification procedures to remain compliant
- Work with internal customers to assist in the introduction of new equipment. This will include working with vendors as well as groups purchasing equipment.
- Creating test methods for verification of new equipment
- Interpretation of test results and creating a plan if additional testing is required
- Coordinating with third party contractors for repair and calibration appointments
- Complete all documentation following GMP guidelines and company SOPs
- Complete training as required by training matrix
- Document all steps performed in case of an NCI
- Complete requirements as related to Corrective and Preventive Actions (CAPA’s)
- Initiate Change Controls providing steps required and including other stakeholders
- Participate in Internal, Customer and Regulatory Audits.
- Order supplies required by group
REQUIREMENT SUMMARY
Min:3.0Max:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Brampton, ON, Canada