ALTEN Portugal, a leading force in the IT, Engineering and Life Sciences industries. We are currently seeking a dedicated and detail-oriented QC Analyst/Reviewer.
ALTEN Group
Within 30 years, ALTEN has become leader in both outsourced Engineering and IT Enterprise Services. ALTEN, composed of 54,000 employees (88% engineers), carries out complex and highly technical projects throughout the value chain of 6,500 clients, the most prestigious companies in all sectors of industry, services and telecommunications. We work with key actors in the Aeronautics & Space, Defense & Naval, Security, Automotive, Rail, Energy, Life Sciences, Finance, Retail, Telecommunications and Services sectors.
Do you want to work in exciting projects at renowned clients? At ALTEN we believe that knowing and meeting the expectations of our consultants is a key factor in our success. Our consultants make the difference. Do you want to make the difference too?
We are seeking a highly motivated QC Analyst/Reviewer to join our Quality Control team. The successful candidate will play a key role in analytical method validation, ensuring compliance with regulatory standards, and aligning test methods with international pharmacopeias (e.g., USP, EP, BP, JP).
Key Responsibilities:
* Perform method validation, transfer, and verification in compliance with ICH guidelines and regulatory requirements.
* Conduct detailed comparison of analytical methods against international pharmacopeias (USP, EP, BP, JP) to ensure alignment and regulatory compliance.
* Execute a range of QC laboratory tests including HPLC, GC, dissolution, UV, and other compendial methods.
* Prepare, review, and approve validation protocols, reports, and related technical documentation.
* Support investigations, deviations, CAPAs, and change controls related to QC methods.
* Collaborate cross-functionally with R&D, Quality Assurance, and Regulatory Affairs.
* Maintain high standards of data integrity and ensure compliance with GMP.
Qualifications:
* Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or related discipline.
* 2+ years' experience in a QC laboratory within the pharmaceutical industry.
* Strong knowledge of method validation and pharmacopeial requirements (USP/EP/BP/JP).
* Hands-on experience with HPLC, GC, UV, dissolution, and related techniques.
* Familiarity with GMP, ICH, and regulatory guidelines.
* Excellent attention to detail, organizational, and documentation skills.
Location: Sintra, Portugal (On-site).
Why Join Us?
* Possibility to work with cutting-edge technology in the Life Sciences industry
* Collaborative and dynamic work environment
* Possibility to join a top-leading company in the industry
* Continuous trainings
* Possibility to join different and interesting projects
If you want to embrace in a new and challenging opportunity and are excited about the opportunity to contribute to our team, we want to hear from you Please submit your resume and cover letter detailing your relevant experience and qualifications.