Position: QA Support
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.
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
Qualifications:
- 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
Contract Details:
- Temporary contract with potential for extension
- Full-time position, 40 hours per week
- Competitive salary and benefits package
- Location: Madrid, Spain
If you are a dedicated and motivated individual with a passion for quality assurance in the pharmaceutical industry, we encourage you to apply for this exciting opportunity. Join our dynamic team and make a positive impact on the healthcare industry. Apply now!
PharmEng Technology, now part of Efor Group, leader in Compliance Engineering, is a leading provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes.
As part of Efor’s global network of 3,000 experts across 12 countries, we are better equipped than ever to deliver innovative and comprehensive solutions tailored to the unique needs of clients worldwide. This integration strengthens our ability to combine global expertise with local proximity, positioning PharmEng as a strategic partner for the industry’s most prominent players.
Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique challenges.
At PharmEng Technology by Efor, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives, developing customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs.
Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical, and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).
