Position Overview
Senior QA Specialist – Valencia (on‑site). 3–5 years of experience in Quality Assurance within the pharmaceutical industry.
Responsibilities
* Support the effective execution and oversight of Quality Assurance activities, contributing to the maintenance of the Quality Management System, documentation management, deviation handling, CAPA follow‑up, audit readiness, and regulatory compliance.
* Support Deputy QP‑related activities when required.
* Implement, maintain, and continuously improve the Quality Management System in line with GMP requirements and internal procedures.
* Manage and maintain QA documentation, including SOPs, work instructions, templates, records, and other controlled documents.
* Review quality records and provide quality oversight of manufacturing and associated operations.
* Ensure compliance with approved procedures and applicable regulatory requirements.
* Participate in the management of deviations, incidents, non‑conformities, change controls, and CAPAs.
* Support investigations, root cause analysis, and follow‑up of corrective and preventive actions.
* Support preparation, coordination, and follow‑up of internal audits, external audits, customer audits, and regulatory inspections.
* Monitor compliance with applicable pharmaceutical regulations, GMP standards, and internal quality policies.
* Collaborate cross‑functionally to ensure quality requirements are integrated into daily operations and decision‑making.
* Support the design and delivery of training related to GMP, quality procedures, and compliance standards.
* Contribute to the monitoring of quality KPIs and continuous improvement initiatives within the QA area.
Qualifications
* University degree in Pharmacy, Chemistry, Biotechnology, Health Sciences, or a related field.
* 3–5 years of experience in Quality Assurance within the pharmaceutical industry.
* Previous experience in GMP‑regulated manufacturing environments.
* Solid knowledge of Quality Management Systems (QMS).
* Experience in quality documentation management.
* Knowledge of deviations, CAPAs, change controls, and non‑conformities.
* Experience supporting audits, inspections, and inspection readiness.
* Knowledge of root‑cause analysis and pharmaceutical QA operations.
* Fluent Spanish and English.
* Knowledge of or exposure to Deputy QP responsibilities will be highly valued.
* FDA knowledge is a plus.
What We Value in You
Customer centricity, speed with quality, adaptability to change and flexibility, innovation, leadership and teamwork, effective communication, growth mindset, business orientation, compliance, integrity, and sustainability.
What We Expect You to Do
* Act with a strong quality and compliance mindset in all activities.
* Demonstrate rigor, accuracy, and discipline in documentation and QA processes.
* Collaborate effectively with cross‑functional stakeholders.
* Escalate quality risks and compliance concerns in a timely and constructive manner.
* Balance operational agility with quality and regulatory requirements.
* Show accountability, ownership, and reliability in assigned responsibilities.
* Promote continuous improvement, integrity, and teamwork across the organization.
Benefits
* Permanent contract.
* Adaptable working hours.
* Free on‑site cafeteria.
* On‑site parking.
* Professional development and continuous training.
Selection Process
* Initial contact by phone or email.
* 1 or 2 interviews (on‑site or virtual) with HR and the Technical Management team.
* Ongoing communication about application status.
Do you think this role is not for you? If this opportunity is not the right fit for you at the moment, we encourage you to stay tuned for future opportunities at BioNanoPharma and share this role with people in your network who may be interested.
Equal Opportunities Commitment
At BioNanoPharma, we are committed to fostering an inclusive and diverse workplace and to providing equal opportunities for all candidates. We do not discriminate on the basis of gender, gender identity or expression, ethnicity, nationality, religion, sexual orientation, disability, age, or any other characteristic protected by applicable law.
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