, 40 hours per week
Position: QA Junior Support
PharmEng Technology is a leading provider of innovative technology solutions for the pharmaceutical industry. We are seeking a highly motivated and detail-oriented individual to join our team as a QA Junior Support. This is a full-time position, working 40 hours per week.
Responsibilities:
- Provide support to the Quality Assurance team in ensuring compliance with regulatory requirements and company standards
- Assist in the preparation, review, and maintenance of quality documentation, including SOPs, batch records, and validation protocols
- Participate in internal and external audits and assist in implementing corrective and preventive actions
- Collaborate with cross-functional teams to ensure timely completion of quality tasks and projects
- Conduct routine checks and inspections to ensure adherence to quality standards
- Support the investigation and resolution of quality issues and deviations
- Maintain and update quality databases and systems
- Stay current with industry regulations and best practices to ensure compliance and continuous improvement
Requirements:
- Bachelor's degree in a scientific or related field
- 1-2 years of experience in quality assurance, preferably in the pharmaceutical industry
- Knowledge of FDA regulations and GMP guidelines
- Strong attention to detail and ability to multitask and prioritize in a fast-paced environment
- Excellent communication and interpersonal skills
- Proficient in Microsoft Office and experience with quality management systems
- Ability to work independently and in a team setting
At PharmEng Technology, we value diversity and are committed to equal employment opportunities for all individuals. We offer a competitive salary and benefits package, as well as opportunities for growth and development within the company.
If you are a self-motivated and passionate individual looking to start your career in quality assurance, we encourage you to apply for this exciting opportunity. Join our team and be a part of our mission to improve the quality of healthcare through innovative technology solutions.
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).
