Job Description
Join to apply for the QA Support role at PharmEng Technology
Join to apply for the QA Support role at PharmEng Technology
Company Overview
PharmEng Technology is a leading global provider of pharmaceutical consulting and project management services. With over 20 years of experience, we have a proven track record of helping pharmaceutical companies achieve compliance, improve efficiency, and reduce costs. Our team of experts is dedicated to providing innovative solutions and exceptional customer service to our clients.
About The Job QA Support
Position: QA Support
Company Overview
PharmEng Technology is a leading global provider of pharmaceutical consulting and project management services. With over 20 years of experience, we have a proven track record of helping pharmaceutical companies achieve compliance, improve efficiency, and reduce costs. Our team of experts is dedicated to providing innovative solutions and exceptional customer service to our clients.
Position Overview
We are currently seeking a QA Support professional to join our team in Madrid, Spain. This is a temporary position with the potential for extension based on project needs. The QA Support will be responsible for providing support to the Quality Assurance team and ensuring compliance with regulatory requirements.
Key Responsibilities
- Assist with the development, implementation, and maintenance of quality systems and procedures
- Conduct internal audits to ensure compliance with company policies and regulatory requirements
- Support the review and approval of SOPs, change controls, and other quality documents
- Participate in the development and execution of training programs for employees
- Collaborate with cross-functional teams to identify and resolve quality issues
- Assist with the preparation and hosting of regulatory inspections
- Keep up-to-date with industry regulations and guidelines to ensure compliance
- Bachelor's degree in a scientific or related field
- Minimum of 2 years of experience in a quality assurance role within the pharmaceutical industry
- Knowledge of GMP regulations and guidelines
- Strong attention to detail and ability to work independently
- Excellent communication and interpersonal skills
- Fluent in Spanish and English
- Temporary contract with potential for extension
- Full-time position, 40 hours per week
- Competitive salary and benefits package
- Location: Madrid, Spain
- Seniority level Entry level
- Employment type Full-time
- Job function Quality Assurance
- Industries Pharmaceutical Manufacturing
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