Start Date
Immediate
Expiry Date
23 Dec, 26
Salary
50000.0
Posted On
24 Sep, 26
Experience
12 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
Yes
Skills
Industry
Pharmaceutical Manufacturing
Duties:
- You will be Working as part of the Quality Assurance team on site ensuring products are manufactured, stored and packaged in accordance with cGMP.
- Support the development of GMP training packages and delivery of training
- Participate in the preparation and review of procedures and batch documentation
- Perform audits of all departments to agreed schedule
- Ensure the quality system at Genzyme is effectively implemented and maintained
- Ensure practises meet cGMP requirements
Job Requirements:
- Acts as Quality Point person for systems / processes providing guidance / feedback on quality issues
- Perform timely review of documentation / investigations /reports highlighting and assisting in the resolution of concerns commensurate with the risk
- Work with relevant departments to ensure timely closure of quality actions / findings
- Actively contribute to continuous improvement initiatives.
- Conduct duties in a safe manner and report all safety issues or concerns
- Maintain work area to good housekeeping standards
- Ensure attendance at place of work when required
- Support team in achieving team goals/targets
- Attend team meetings as required
- Actively contribute to continuous improvement initiatives
- Measure and report RFT / trend data and work with departments to resolve recurring issues
- Participate in internal supplier and regulatory audits and key quality initiatives as appropriate
- Perform critical/ constructive review of procedures and practices
- Support investigation of deviations ensuring all product deviations are closed prior to product release
- Ensure compliance to cGMP at all times
Qualifications & Experience
- Third Level qualification (degree in science or related discipline preferred).
- Minimum of 2 years’ experience in a similar role
- Experience working in a GMP environment is required
- Very good knowledge of cGMP in a regulated environment • Excellent accuracy and attention to detail
- Excellent interpersonal skills
- Good presentation skills
- Working knowledge of computer packages
- Flexible approach – comfortable with on-going change
Personal Characteristics:
- Takes personable responsibility for their actions
- Excellent attention to detail.
- Good communicator who is comfortable to work as part of a team
- Focused on achieving results
How To Apply:
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Duties:
- You will be Working as part of the Quality Assurance team on site ensuring products are manufactured, stored and packaged in accordance with cGMP.
- Support the development of GMP training packages and delivery of training
- Participate in the preparation and review of procedures and batch documentation
- Perform audits of all departments to agreed schedule
- Ensure the quality system at Genzyme is effectively implemented and maintained
- Ensure practises meet cGMP requirements
Job Requirements:
- Acts as Quality Point person for systems / processes providing guidance / feedback on quality issues
- Perform timely review of documentation / investigations /reports highlighting and assisting in the resolution of concerns commensurate with the risk
- Work with relevant departments to ensure timely closure of quality actions / findings
- Actively contribute to continuous improvement initiatives.
- Conduct duties in a safe manner and report all safety issues or concerns
- Maintain work area to good housekeeping standards
- Ensure attendance at place of work when required
- Support team in achieving team goals/targets
- Attend team meetings as required
- Actively contribute to continuous improvement initiatives
- Measure and report RFT / trend data and work with departments to resolve recurring issues
- Participate in internal supplier and regulatory audits and key quality initiatives as appropriate
- Perform critical/ constructive review of procedures and practices
- Support investigation of deviations ensuring all product deviations are closed prior to product release
- Ensure compliance to cGMP at all times
Qualifications & Experience
- Third Level qualification (degree in science or related discipline preferred).
- Minimum of 2 years’ experience in a similar role
- Experience working in a GMP environment is required
- Very good knowledge of cGMP in a regulated environment • Excellent accuracy and attention to detail
- Excellent interpersonal skills
- Good presentation skills
- Working knowledge of computer packages
- Flexible approach – comfortable with on-going change
Personal Characteristics:
- Takes personable responsibility for their actions
- Excellent attention to detail.
- Good communicator who is comfortable to work as part of a team
- Focused on achieving results
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