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Specialist Cleaning Validation (M/F/D)

2+ years
Not Disclosed
10 Jan. 24, 2025
Job Description
Job Type: Full Time Education: B.Sc,M.Sc,B.Pharma,M.Pharma,LifeScience Graduates Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Specialist Cleaning Validation (m/f/d)

Location: Freiburg, Germany
Job Type: Full-Time (Temporary for 2 Years)
Posted: 1 Day Ago
Job ID: 4924834


Purpose and Values

At Pfizer, we are dedicated to breakthroughs that change patients' lives. Every day, we strive for innovations that make the world healthier. Our mission is driven by our core values, guiding us on what we need to achieve for patients and how we do it.


Role Overview

We are looking for a Specialist in Cleaning Validation to join our team at the Freiburg site. The position involves creating and reviewing cleaning validation protocols, monitoring quality systems, and ensuring compliance with GMP regulations. The successful candidate will contribute to the continuous improvement of cleaning validation processes, participate in projects, and handle coordination tasks across departments.


Key Responsibilities

Cleaning Validation and Documentation

  • Create and review cleaning validation and verification protocols for pharmaceutical production and packaging equipment.
  • Ensure the approval of documentation and monitor the approval process.
  • Perform periodic reviews and maintain templates and master data in the area of cleaning validation.
  • Oversee the status of validation and coordinate meetings between planning and laboratory teams.

Process Improvement and Quality Monitoring

  • Continuously improve cleaning validation processes to enhance efficiency and ensure compliance, using software-based solutions.
  • Contribute to projects and special tasks while coordinating cleaning validation activities.
  • Monitor the quality system for cleaning validation and assist in audits by authorities and customers.
  • Contribute to the creation, maintenance, and compliance of quality systems such as SOPs, master plans, and validation concepts under GMP regulations.

Collaboration and Training

  • Work closely with other teams to ensure smooth execution of cleaning validation processes.
  • Assist in presenting cleaning validation-related topics during audits and regulatory inspections.

Required Qualifications

Education and Experience

  • A background in a technical or pharmaceutical profession or experience in relevant fields.
  • A minimum of two years of professional experience in pharmaceutical manufacturing.
  • Ideally, knowledge of quality systems related to cleaning validation or hygiene monitoring.
  • Familiarity with GMP-compliant documentation processes.

Skills and Expertise

  • Proficient in the use of MS Office (Word365) and other common software tools.
  • Ability to work independently, with a structured and self-organized approach.
  • Strong communication skills and ability to work effectively in teams.
  • Attention to detail and commitment to continuous improvement.

What We Offer

  • The chance to be part of an innovative team at one of our most advanced production sites.
  • Career growth and development opportunities.
  • Comprehensive employee health management programs.
  • Attractive company pension plans.
  • Subsidized canteen.

Application Process

If you are passionate about contributing to breakthroughs in healthcare, we encourage you to apply online. Please submit your full application, including a cover letter, resume, and certificates, along with your earliest possible start date and salary expectations.

Pfizer is committed to equal opportunity employment and ensures a fair and non-discriminatory recruitment process in line with local regulations. We welcome applicants from all backgrounds and are an inclusive employer.


Diversity and Inclusion

Pfizer strives to create an inclusive work environment and provides reasonable accommodations for applicants with disabilities. We encourage you to showcase your talents, knowing that we will make adjustments to support your application and career journey.


This role offers a great opportunity for professionals looking to contribute to high-quality pharmaceutical manufacturing while developing their career in an innovative and supportive environment.