Aseptic Quality Manager - Toledo

Ethypharm; Toledo; Presencial; EUR 70.000 - 95.000; Jornada completa

Descripción de la vacante

Ethypharm is seeking an Aseptic Quality Manager to lead sterility assurance across the site and drive improvements in contamination control and environmental monitoring. You will partner with QC micro labs, manage media fills, and oversee aseptic processes to ensure compliant operations.

The role requires a Life Sciences bachelor’s degree and at least 2 years in pharmaceutical quality leadership, with strong familiarity with EU Annex 1, OOS/OOE investigations, and regulatory writing for audits.

Formación

• Bachelor’s degree in biology, pharmacy, biochemistry or related field.
• Minimum 2 years in a pharmaceutical quality leadership role, ideally in sterile manufacturing.
• Strong knowledge of aseptic processing, media fills, OOS/OOE investigations, and audits.

Responsabilidades

• Accountable for sterility assurance across site.
• Contamination control strategy and oversight of monitoring programs.
• Definition and implementation of environmental monitoring program; trend analysis.
• Partner with QC micro lab to develop monitoring and bioburden control strategies.
• Media Fill Program management: strategy, runs, and execution oversight.
• Aseptic behaviour definitions, training program development and gowning strategy.
• Sterilization processes support and strategy oversight.
• Risk assessments and improvement programs against current/future expectations.
• Environmental monitoring investigations (e.g., adverse EM trends).
• Review & approve major/critical deviations and change proposals with Sterility Assurance impact.
• Key involvement in audits with regulators/clients; collaboration on capital projects.
• Implement best practice and adapt to updated Annex 1 and related guidance.
• Support new product introductions requiring sterile operations.

Conocimientos

Sterility assurance

Environmental monitoring

Root cause analysis

Leadership

Technical writing

Audits & regulatory

Educación

Bachelor of Science in Life Sciences

Herramientas

Microbiology lab techniques

Environmental monitoring systems

Descripción del empleo

Ethypharm is a leading mid-sized global pharmaceutical company that manufactures and provides essential drugs, with a focus on hospital care, central nervous system (severe pain and addiction) and internal medicine. Our commitment is to improve patients' lives and make a positive impact on society and the environment.

Ethypharm has 1,700 employees dedicated to its various pharmaceutical activities, of which 1400 are in industrial operations. Our six production sites located in France, the UK, Spain, and China have expertise in injectables and complex oral solid forms.

With a global presence in 68 countries, the company markets its products directly in Europe and China, and has strategic partnerships in the EMEA, NA, LATAM and APAC markets.

Ethypharm works closely with the authorities and healthcare professionals to ensure that its medicines are used appropriately and that patients have access to them.

To find out more about Ethypharm, visit http://www.ethypharm.com and follow us on LinkedIn.

Aseptic Quality Manager

• Accountable for sterility assurance across site
• Contamination control strategy (leadership of the strategy: periodic review and update)
• Definition and implementation of environmental monitoring program. Management of trends and improvement of processes based on their results
• Parthership with QC micro lab to develop strategies of monitoring and bioburden control
• Media Fill Program (management of strategy, definition of runs, oversee of execution)
• Aseptic behaviour definition, development of training program and oversight (management). Definition of gowning strategy and cleaning processes
• Sterilization processes (suport to other departments to define sterilization strategy and oversight of execution)
• Risk assessments and improvement programs (implement/manage - against current and future expectations)
• Environmental monitoring investigations (i.e. Adverse EM trends, media fill failures)
• Review & approve any Major/Critical deviations and change proposals with Sterility Assurance impact for the assigned areas.
• Key part of audits with with regulators / clients
• Key part for new product introduction and for applicable capital projects (i.e. new lines/processes)
• Implementing best practice (i.e. ensuring understanding / compliance with updated Annex 1 - owning the transition and any risk assessments needed)
• Participant in audits to other sterile sites (CMOs) and suppliers providing microbiological service or sterile materials

Education:

• Minimum required education: Bachelor of Science Degree in relevant area; e.g. Biology, Pharmacy, Biochemistry or similar.

Experience:

• Minimum of 2 years experience in a pharmaceutical quality leadership function, preferably in a sterile manufacturing site.
• Microbiology experience is crucially required for this role. (Preferably, Micro Laboratory or Environmental monitoring experience, and ideally within a sterile pharmaceutical manufacturing facility).
• Detailed knowledge of aseptic processing, and ideally will have practical experience in an active aseptic manufacturing operation. Knowledge of aseptic process simulations (media fills)
• Experience in supporting/writting OOS/OOE/OOT and deviation investigations
• Experience in supporting internal and external laboratory audits

Knowledge, Skills and Abilities:

• Involvement in capital projects (new build/refurbishment of sterile lines) would be beneficial.
• Familiarity with EU Annex-1 and other regulations and guidance.
• Strong investigative skills, preferably familiar with Root Cause Analysis methods.
• Leadership experience, and supervisory experience is helpful.
• Shown expertise with audits and client-facing roles.
• Outstanding technical writing skills
• cGMP Compliance
• Strong sense of diplomacy and assertiveness
• Quality Judgement