Manager - IPQA (OSD)

PeopleStrong; Daman; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

PeopleStrong in India is seeking a Deputy Manager - Inprocess Quality Assurance (OSD) to oversee in-process QA for oral solids, manage samples, verify rejections and destructions, and ensure SOP compliance on the shop floor.

The role includes coordinating validation, reviewing batch records, and monitoring systems and equipment while driving continuous improvement within the QA team.

Qualifications

• In-process QA for oral solids.
• Sample management and traceability responsibilities.
• Verification of online rejection and destruction processes.
• Review and ensure compliance with Standard Operating Procedures.

Responsibilities

• Carry out in-process quality assurance activities on the shop floor.
• Coordinate and execute validation and qualification activities.
• Review batch records and related documents for accuracy and compliance.
• Monitor compliance to systems and processes through regular shop-floor rounds.
• Review recipe and audit trails for process equipment to ensure integrity.
• Provide guidance and on-the-job coaching to the QA team and drive capability development.
• Identify and implement continuous improvement initiatives and adopt best practices.

Job description

Position : Deputy Manager - Inprocess Quality Assurance (OSD)

1) In-process Quality Assurance (Oral Solids)

Partake in controlling, implementing, executing the activities of Quality Assurance.

To carry out sample management.

Verification of online rejection and destruction if any.

Co-ordination and execution of validation and qualification activities.

To check the compliance and execution of Standard Operating Procedures.

To review the batch records and other related documents.

Monitor compliance to systems & processes by frequent shop-floor rounds.

Monitor compliance of the recipe and audit trail review of process equipments.

2. APQR (Annual Product Quality Review)

Monitoring and execution of continued process verification (CPV) of critical process parameter (CPP).

Review of Annual Product Quality Review and necessary corrective action.

To carry out Control sample management.

Destruction and Annual Product Review (Performing and checking) of control sample on monthly basis.

Jointly investigate the significant change, Out of Calibration (OOC), out of specification result (OOS), Out of trend (OOT) with the user department & review the recommended CAPA to ensure closure.

5. Audit Compliance and Walk through

Carry out Self-Inspection along with representative departments and tracking of compliance closure with appropriate evidence.

Provide functional and technical guidance to the team through on the job coaching and support them in capability development.

Identify and recommend continuous improvement initiatives and adopt best practices.

Keep self and team updated to developments and advances in his field of work.