
Aseptic Process Specialist
4 days ago
Job Title: Validation Specialist
This role is responsible for ensuring the integrity of our manufacturing processes through effective validation and qualification. You will work closely with cross-functional teams to develop, execute, and document validation protocols and reports.
You will be responsible for analyzing results, identifying areas for improvement, and recommending corrective actions. Your expertise in aseptic techniques, validation methodologies, and regulatory guidelines will be essential in maintaining compliance with cGMP and other industry standards.
In this role, you will have the opportunity to work on complex projects, collaborate with stakeholders, and contribute to the development of our validation master plan. If you are a detail-oriented professional with a strong analytical mindset and excellent communication skills, we encourage you to apply.
Key Responsibilities:
- Develop, execute, and document validation protocols and reports
- Analyze results and identify areas for improvement
- Recommend corrective actions and implement changes as needed
- Maintain compliance with cGMP and other industry standards
- Collaborate with cross-functional teams to achieve project goals
Required Skills and Qualifications:
- Bachelor's/Master's degree in Pharmacy, Biotechnology, Microbiology, or related field
- Strong analytical and problem-solving skills
- Excellent communication and documentation skills
- Ability to manage multiple priorities and meet deadlines
- Proficiency in QMS tools and software
Benefits:
- Opportunity to work on complex projects
- Collaborative team environment
- Professional growth and development opportunities
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