In Nanonol Technologies we’re #hiring!

Nanomol Technologies, S.L. is a privately owned company delivering advanced solutions and technologies to obtain high-added value products by particle design and nanoformulation together with advanced cGMP particle characterization services.

We are looking for a Quality Assurance Technician. She/He will be dedicated to our Particle Characterization Unit to set up and monitor policies for GMP and ISO17025 compliance for our laboratory processes. For that she/he will work under the guidance of the Quality Assurance Manager. She/He also will collaborate in the implementation of a Quality Management System of a European partnership involving our company, joining a Quality Assurance international team.  

Responsibilities:

Implementation, maintenance and continuous improvement of a Pharmaceutical Quality Management System (PQMS) for cGMP particle characterization laboratory in Nanomol Technologies:

• Management of Deviations, CAPAs (Corrective Action Preventive Action), claims and complaints, Control Changes, Personnel Training, Validation Master Plan (VMP), process validation, Risk Analysis, Out Of Specifications (OOS) results, equipment qualification, analyst supervision, Certificate of Analysis (CoA) release.
• Document elaboration and management.
• Prepare internal and external audits.
• Monitoring of CFR21 compliance of informatic system.
• Report timely to manager, director and CEO-level.

Collaboration in the implementation of a Quality Management System of a European Association related to the contract development and manufacturing of nanomedicines, with internal and external collaboration with Nanomol’s QA team and QA managers of the association:

• Document elaboration and management.
• Prepare internal and external audits.
• Engage with organization (all levels) to acquire relevant inputs and ensure Quality compliance.
• GMP supplier qualification.
• Report timely to manager and director level.

Requisites:

• Essential: Degree in Pharmacy.
• Essential: Proven experience in Quality department roles (Quality Assurance or Quality Control), a minimum of two years, in a GMP-accredited Pharmaceutical Laboratory.
• Good working knowledge of current requirements for Good Manufacturing Practices.
• Fluent in English and Spanish. 

*Those applicants not fulfilling the two essential requisites (Degree in Pharmacy and Proven experience in Quality department roles) will be discarded.  

Valuable:

• Experience in particle characterization techniques (Laser Diffraction, DLS, Microscopy techniques) and HPLC analysis.
• Experience in Pharmaceutical Production Roles. Preferred in liquid, sterile, and lyophilized forms.
• Experience in ISO17025.
• Experience in Analytical Development, Technology Transfer or Regulatory Affairs.

Desired Skills:

• Excellent collaboration skills in multicultural teams.
• Ability to work independently fulfilling established timelines.
• Attitude of continuously striving for excellence.
• Flexibility to adapt to strategic needs.
• Strong organizational and interpersonal skills.

What we offer:

• Join a growing SME with a highly motivated and qualified team.
• Interact with several roles in the organization and outside.
• Challenging role with significant learning opportunities.
• Starting salary according to experience, revisions according to performance.
• Flexible working hours with partial home office available in the company.
• Job location: Bellaterra - Barcelona, Spain.
• Job Type: Full-time.

The application file should be sent to direccio@nanomol-tech.com and contain:

1. CV

2. Cover letter

3. Two reference names and their contact information