Job Board | Assistants and Analysts – Sterile Pharmaceutical Production ( Zamudio )

The job board is aimed at people with different levels of qualification and experience, so we will value applications from:

• Professional Certificates related to manufacturing, conditioning, or the pharmaceutical industry.
• Intermediate or Higher Vocational Training in Biosciences, Laboratory, Pharmaceutical Product Manufacturing, Biotechnology, Chemistry, Microbiology or similar degrees.
• Complementary training in Good Manufacturing Practices (GMP/BPF).
• Previous experience in pharmaceutical, biotechnological, microbiological production, or other regulated production environments.
• Experience in the manufacture of biological products, active principles, vaccines, or microbiological processes.
• Handling of documentation and records associated with manufacturing processes.
• Computer skills at a user level.
• Knowledge of English, with a different required level depending on the position and responsibility.

The required level of experience will depend on the specific position, so we may value both profiles starting their professional career and professionals with consolidated experience in pharmaceutical production.

Previous experience in sterile pharmaceutical manufacturing and/or aseptic processes will be especially relevantly valued within this Job Board and will be one of the main criteria for prioritizing applications, especially for Analyst positions.

We will especially value practical experience in:

• Sterile pharmaceutical manufacturing and work under aseptic conditions.
• Aseptic handling of product, materials, and equipment.
• Work in cleanrooms and controlled environments.
• Compliance with access, clothing, and behavior rules in classified areas.
• Preparation of materials and components for production processes.
• Dosage, filtration, and handling of biological products or active principles.
• Preparation, cleaning, and sterilization of materials and equipment.
• Completion of manufacturing documentation and records in accordance with GMP/BPF.
• Rigorous following of standard operating procedures.
• Experience in the production of medicines, biological products, vaccines, active principles, or microbiological processes.

Experience in sterile manufacturing will be especially valued, but not necessarily exclusive for all professional levels, as we seek to build a pool that allows us to incorporate both experienced professionals and profiles with development potential.

We look for people who are rigorous, responsible, and quality-oriented, capable of working following established procedures and aware of the impact that each operation has on product quality and safety.

We will particularly value:

• Experience in the pharmaceutical industry.
• Experience in sterile manufacturing and/or aseptic processes.
• Experience working under GMP regulations.
• Experience in cleanrooms or controlled environments.
• Knowledge and application of aseptic handling techniques.
• Experience in the manufacture of biological products, vaccines, or active principles.
• Specific training or experience in microbiology for positions linked to bacterial production.
• Ability to work with precision and maintain adequate documentary traceability.
• Attention to detail and rigorous compliance with procedures.
• Ability to work in a team, responsibility, and orientation toward continuous improvement.

The opportunity to be part of a pharmaceutical company specialized in immunotherapy with allergens, working in a regulated and highly specialized industrial environment.

You will be able to develop your experience in pharmaceutical and biological manufacturing processes, integrating into teams where quality, GMP compliance, rigor, and product safety are part of our daily activity.

This Job Board will allow us to take your candidacy into account for future professional opportunities in accordance with your training, experience, and level of specialization.

At ROXALL, we are dedicated to the research, design, validation, manufacture, and distribution of anti-allergic vaccines within the immunotherapy with allergens sector.

Our Technical, R&D, and Clinical Trials center and our manufacturing plant are located in Zamudio. In a context of growth and development of our industrial activity, we want to continue incorporating talent into our Production teams.

We want to create a Job Board for Pharmaceutical Production Assistants and Analysts to identify professionals interested in joining our manufacturing teams in Zamudio in the face of future needs.

We are looking for profiles with different levels of training, specialization, and experience, from assistant positions to analysts with consolidated experience, to work in one of our production areas:

Depending on your training, experience, and professional level, you may participate in different stages of the production process:

• Preparation of materials and diluents.
• Dosage and filtration of bulks.
• Manufacture of individualized products.
• Manufacture of bulks.
• Labeling, tagging, and visual inspection.
• Conditioning and packaging.
• Completion of documentation and records associated with the manufacturing processes.

You may participate in the manufacture and processing of active principles and extracts, working with specific production equipment and applying aseptic handling techniques for materials in direct or indirect contact with the product.

Work also includes monitoring the correct state of equipment and facilities and communicating any incident or need for improvement detected during productive activity.

For profiles with specific training or experience in microbiology, we are looking for professionals who can participate in activities such as:

• Production of bacterial vaccines.
• Manufacture of bacterial concentrates and single components.
• Isolation, re-seeding, and identification of strains.
• Maintenance of strain collections.
• Preparation and control of materials and equipment.
• Verification, cleaning, and sterilization of materials.
• Stock and expiration management.
• Control and recording of environmental conditions in production areas.
• Completion of technical documentation in accordance with established procedures.