DURATION - 6 MONTHS - ONSITE POSITION - SHIFT - FRI, SAT, SUN 6PM - 6AM + 1 DAY EVERY OTHER WEEK + MANDATORY OVERTIME.



Recommend SOP and batch record changes as needed

Review proposed SOP revisions and provide feedback to management

Real-time audit of batch records in the production suites for completeness, documentation, calculation errors and conformance to critical process parameters

Perform room and equipment clearances per procedure following cleaning conducted by production.

Perform microbial swabbing of equipment and room surfaces for environmental monitoring.

Maintain a full understanding of all client SOPs and policies along with all cGMP and CFR guidance that are applicable to the manufacturing of solid oral dosage pharmaceutical products.

Perform routine testing of in-process and finished product samples including particle size, bulk density, moisture analysis, appearance, and AQL testing real-time.

Moni...