Shop Floor Oversight: Conduct regular monitoring of manufacturing and packaging operations to ensure compliance with Good Manufacturing Practices (GMP).
In-Process Checks: Perform physical inspections and testssuch as weight variation hardness and friabilityat defined intervals during production.
Line Clearance: Verify and authorize the Line Clearance before starting any new batch to prevent cross-contamination or mix-ups.
Documentation Review: Audit Batch Production Records (BPR) and Batch Packaging Records (BPR) in real-time to ensure data integrity and accuracy.
Environmental Monitoring: Monitor controlled environments checking parameters like temperature humidity and pressure differentials in production areas.
Sampling: Collect representative samples of raw materials intermediates and finished products for laboratory analysis and stability testing.
Deviation Management: Identify document and report any deviations or non-conformances on the floor assisting in root cause investigations.
Equipment Validation: Ensure all processing equipment and weighing scales are properly calibrated and labeled with their current status.
Standard Operating Procedures (SOPs): Ensure all personnel strictly follow established SOPs and provide on-the-job training where necessary.
Regulatory Compliance: Act as a quality gatekeeper to ensure the facility remains audit-ready for inspections by bodies like the FDA MHRA or WHO.
Required Experience:
Intern
Shop Floor Oversight: Conduct regular monitoring of manufacturing and packaging operations to ensure compliance with Good Manufacturing Practices (GMP).In-Process Checks: Perform physical inspections and testssuch as weight variation hardness and friabilityat defined intervals during production.Line...
Shop Floor Oversight: Conduct regular monitoring of manufacturing and packaging operations to ensure compliance with Good Manufacturing Practices (GMP).
In-Process Checks: Perform physical inspections and testssuch as weight variation hardness and friabilityat defined intervals during production.
Line Clearance: Verify and authorize the Line Clearance before starting any new batch to prevent cross-contamination or mix-ups.
Documentation Review: Audit Batch Production Records (BPR) and Batch Packaging Records (BPR) in real-time to ensure data integrity and accuracy.
Environmental Monitoring: Monitor controlled environments checking parameters like temperature humidity and pressure differentials in production areas.
Sampling: Collect representative samples of raw materials intermediates and finished products for laboratory analysis and stability testing.
Deviation Management: Identify document and report any deviations or non-conformances on the floor assisting in root cause investigations.
Equipment Validation: Ensure all processing equipment and weighing scales are properly calibrated and labeled with their current status.
Standard Operating Procedures (SOPs): Ensure all personnel strictly follow established SOPs and provide on-the-job training where necessary.
Regulatory Compliance: Act as a quality gatekeeper to ensure the facility remains audit-ready for inspections by bodies like the FDA MHRA or WHO.