Quality Assurance Specialist at Project Delivery Partners

Madrid, Community of Madrid, Spain -

Full Time

Start Date

Immediate

Expiry Date

26 Sep, 26

Salary

0.0

Posted On

28 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

GMP Compliance, Batch Record Review, Internal Auditing, CAPA Management, Validation Protocols, Regulatory Alignment, Analytical Thinking, Written Communication, Verbal Communication, QA Software Proficiency

Industry

Pharmaceutical Manufacturing

Description

PharmEng / Efor is a leading pharmaceutical and biopharmaceutical consulting company committed to providing innovative solutions to the challenges facing our industries. We pride ourselves on our dedication to quality, safety, and excellence in everything we do. As we continue to grow, we are seeking a highly qualified and motivated Quality Assurance Specialist to join our team. The QA Specialist will ensure that all products, processes, and documentation comply with regulatory standards such as FDA, EMA, and GMP. This role is vital to maintaining product safety, efficacy, and quality throughout the manufacturing lifecycle. Responsibilities: Monitor and enforce GMP compliance across manufacturing and laboratory operations. Review batch records, SOPs, and validation protocols to ensure accuracy and regulatory alignment. Conduct internal audits and inspections to identify non-conformances and recommend corrective actions. Investigate deviations, CAPAs, and complaints to ensure timely resolution and documentation. Support regulatory submissions and inspections by preparing documentation and participating in audits. Train staff on quality procedures and compliance standards. Maintain and update QA documentation systems including change controls and risk assessments. Qualifications Bachelors degree in Pharmacy, Chemistry, Biology, or related life sciences field. 4+ years of QA experience in a pharmaceutical or biotech environment. Strong knowledge of GMP, ICH Q10, FDA, and EMA regulations. Experience with quality systems, CAPA management, and validation documentation. Skills Exceptional attention to detail and analytical thinking. Strong written and verbal communication skills. Proficiency in QA software and documentation tools. Ability to work independently and in cross-functional teams. Join us: If you are a dedicated and highly motivated individual with a passion for ensuring the highest standards of Engineering and Quality in the Pharmaceutical Industry, we encourage you to apply. PharmEng / Efor offers a dynamic and inclusive work environment, competitive compensation, and opportunities for professional growth. Be part of our team and contribute to the success of our industry-leading solutions. PharmEng / Efor is an equal opportunity employer and welcomes applicants from all backgrounds. Thank you for your consideration and application! We review all resumes and submissions, however, due to the high volume of applications we receive, only approved candidates will be contacted.

Responsibilities

The QA Specialist ensures all products and processes comply with FDA, EMA, and GMP regulatory standards. Key duties include monitoring manufacturing operations, conducting internal audits, and managing deviations and CAPAs.