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QA Manufacturing Specialist(m/w/x)
Description
As a QA Manufacturing Specialist, you will ensure product quality by monitoring manufacturing processes, conducting audits, and providing on-the-floor training. This role involves real-time oversight, documentation review, and supporting compliance with GMP standards.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Strong background in quality assurance within pharmaceutical or regulated manufacturing environment
- •Solid understanding of GMP (Good Manufacturing Practices)
- •Good understanding of aseptic process and its core requirements
- •Excellent communication and coaching skills
- •Ability to make sound decisions and manage deviations in a fast-paced setting
- •Collaborative spirit and passion for ensuring compliance and product integrity
Work Experience
approx. 1 - 4 years
Tasks
- •Perform real-time quality assurance support on the shop floor
- •Monitor adherence to GMP practices during critical manufacturing steps
- •Witness and verify critical process steps and in-process controls
- •Document line clearances before manufacturing operations
- •Review manufacturing processes for compliance with batch records and SOPs
- •Ensure proper material handling, labeling, and segregation during production
- •Identify and report deviations or abnormal events on the shop floor
- •Support or lead impact assessment and documentation of deviations
- •Coordinate with QA and production leadership for timely resolution
- •Review completed batch manufacturing records for accuracy and compliance
- •Assist operators with proper GMP documentation practices
- •Verify logbooks, equipment use records, and cleaning records
- •Observe interventions during aseptic operations for compliance
- •Support environmental monitoring and cleanroom behavior compliance
- •Conduct routine walkthroughs and spot checks for GMP standards
- •Participate in internal audits and regulatory inspections
- •Provide on-the-job coaching and GMP guidance to operators
- •Reinforce good documentation practices and quality culture
- •Provide input into root cause analysis based on observations
- •Support implementation of corrective and preventive actions
Languages
English – Business Fluent
Benefits
Retirement Plans
- •Competitive pension fund plan
Bonuses & Incentives
- •Annual bonus
Other Benefits
- •Financial and non-financial benefits
- ten23 healthFull-timeOn-siteExperiencedVisp
- Lonza
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QA Manufacturing Specialist(m/w/x)
The AI Job Search Engine
Description
As a QA Manufacturing Specialist, you will ensure product quality by monitoring manufacturing processes, conducting audits, and providing on-the-floor training. This role involves real-time oversight, documentation review, and supporting compliance with GMP standards.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Strong background in quality assurance within pharmaceutical or regulated manufacturing environment
- •Solid understanding of GMP (Good Manufacturing Practices)
- •Good understanding of aseptic process and its core requirements
- •Excellent communication and coaching skills
- •Ability to make sound decisions and manage deviations in a fast-paced setting
- •Collaborative spirit and passion for ensuring compliance and product integrity
Work Experience
approx. 1 - 4 years
Tasks
- •Perform real-time quality assurance support on the shop floor
- •Monitor adherence to GMP practices during critical manufacturing steps
- •Witness and verify critical process steps and in-process controls
- •Document line clearances before manufacturing operations
- •Review manufacturing processes for compliance with batch records and SOPs
- •Ensure proper material handling, labeling, and segregation during production
- •Identify and report deviations or abnormal events on the shop floor
- •Support or lead impact assessment and documentation of deviations
- •Coordinate with QA and production leadership for timely resolution
- •Review completed batch manufacturing records for accuracy and compliance
- •Assist operators with proper GMP documentation practices
- •Verify logbooks, equipment use records, and cleaning records
- •Observe interventions during aseptic operations for compliance
- •Support environmental monitoring and cleanroom behavior compliance
- •Conduct routine walkthroughs and spot checks for GMP standards
- •Participate in internal audits and regulatory inspections
- •Provide on-the-job coaching and GMP guidance to operators
- •Reinforce good documentation practices and quality culture
- •Provide input into root cause analysis based on observations
- •Support implementation of corrective and preventive actions
Languages
English – Business Fluent
Benefits
Retirement Plans
- •Competitive pension fund plan
Bonuses & Incentives
- •Annual bonus
Other Benefits
- •Financial and non-financial benefits
About the Company
ten23 health
Industry
Pharmaceuticals
Description
The company is a human-centric strategic partner for the pharmaceutical industry and biotech start-ups, focusing on the development and testing of medicines.
- ten23 health
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