Inteldot has over 14 years in the life science industry with allocations a cross Puerto Rico the United Sates Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.
Overview:
We are seeking a Quality Compliance Auditor to serve operations in the regulated industry. The selected candidate will be responsible for ensuring that all services provided under the contract align with applicable regulatory requirements client policies and industry best practices.
Requirements:
- ISO Lead Auditor 9001 or 13485
- Internal Auditor experience
- Strong Background in Quality and Compliance (ISO related)
- Regulated Environment Experience
- Knowledge in: Supplier Quality management CAPA Investigations Management Review Complaints Risk Management Validation/CS
Qualifications:
- Bachelors degree in Life Sciences Engineering or related field.
- Minimum 5 years of compliance experience in a regulated environment (GxP FDA ISO).
- Strong analytical organizational and communication skills.
- Bilingual (English/Spanish) preferred.
Inteldot has over 14 years in the life science industry with allocations a cross Puerto Rico the United Sates Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico. Overview:We are seeking a Quality Compliance Auditor to serve operations in the regulated industr...
Inteldot has over 14 years in the life science industry with allocations a cross Puerto Rico the United Sates Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.
Overview:
We are seeking a Quality Compliance Auditor to serve operations in the regulated industry. The selected candidate will be responsible for ensuring that all services provided under the contract align with applicable regulatory requirements client policies and industry best practices.
Requirements:
- ISO Lead Auditor 9001 or 13485
- Internal Auditor experience
- Strong Background in Quality and Compliance (ISO related)
- Regulated Environment Experience
- Knowledge in: Supplier Quality management CAPA Investigations Management Review Complaints Risk Management Validation/CS
Qualifications:
- Bachelors degree in Life Sciences Engineering or related field.
- Minimum 5 years of compliance experience in a regulated environment (GxP FDA ISO).
- Strong analytical organizational and communication skills.
- Bilingual (English/Spanish) preferred.
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