OBJECTIVE:
- To define a uniform, controlled procedure for handling any change in personnel, including change of role, resignation, or interdepartmental transfer.
- To ensure continuity of responsibilities, proper documentation, and compliance with GMP and company policies.
- To prevent loss of information, unauthorized access, or interruption in GMP activities during personnel changes.
SCOPE:
- This SOP applies to all employees of Caisa Pharma, including permanent, contractual, trainees, and temporary personnel.
- This SOP covers promotions, demotions, job role changes, resignations, and transfers between departments.
RESPONSIBILITIES:
Human Resource Department (HR):
- Responsible for managing all personnel changes as per this SOP.
- To ensure handover, documentation, and access control changes are completed.
Respective Department:
- Department Heads shall support the handover process and validate the completeness of activities.
Information Technology (IT):
- IT shall update system access upon HR instruction.
Quality Assurance (QA) Dept:
- QA shall ensure GMP responsibilities are transferred properly for personnel working in GMP areas.
DEFINATIONS:
- Role Change: Any change in designation, responsibilities, or reporting structure.
- Resignation: Voluntary separation from employment initiated by the employee.
- Transfer: Movement of an employee from one department or location to another within the company.
- Handover: Formal transfer of responsibilities, documents, and in-process work.
PROCEDURE:
Personnel Role Change (Promotion / Demotion / Responsibility Modification)
- Department Head shall raise a request for a role change with justification through email or discussion with Management.
- HR shall review qualification, experience, performance, and competency for the new role.
- HR shall prepare a revised Job Description (JD) and obtain approvals.
- Employee shall acknowledge and sign the new JD.
- HR shall update personnel records, organization chart, and HR master list.
- IT shall update system access as per the new role.
Personnel Transfer (Inter-Departmental / Intra-Departmental)
- Department Head shall request a transfer with justification and expected date through email or discussing with Management.
- HR shall verify resource availability in receiving department.
- HR shall coordinate discussion with both departments.
- Employee shall complete pending work, ongoing documentation, and material handover.
- Department Head shall certify that handover is complete.
- HR shall issue internal transfer approval.
- HR shall update JD if required.
- IT shall modify access rights and assign new access where required.
Personnel Resignation / Separation:
- Employee shall submit a resignation letter or email to Department Head and HR.
- Department Head or HR shall acknowledge resignation and inform concerned Department Head.
- Employee shall serve notice period as per company policy unless waived.
- A complete handover shall be performed, including:
-
- Ongoing tasks
- Documents and SOPs
- Keys, and ID cards
- Data, laptops, storage devices
- GMP documentation (if applicable)
- Department Head shall certify handover completion.
- HR shall arrange exit interview and clearances with all concerned departments.
- IT shall deactivate system access, email, and software rights.
- HR shall close personnel file and record separation in HR system.
- QA shall ensure no pending GMP responsibilities remain open (e.g., deviations, CAPA, training gaps).
Handover Requirements:
- Handover must be done before the effective date of resignation, transfer, or role change.
- All handover notes must be clear, signed, and acknowledged by both giving and receiving personnel.
- For GMP areas, the handover must include batch records, logs, controlled documents, open activities, and operational status.
- HR shall verify completion before approving final change.
System Access and Security Control:
- IT/Admin shall modify access rights only upon written instruction from HR.
- Upon resignation, all access shall be revoked on the last working day.
- For transfers, previous access shall be removed and new access granted based on job role.
- QA shall review access rights for GMP-relevant systems (LIMS, ERP, documentation systems).
Document and Record Update Requirements:
HR shall update:
- Employee master data
- Reporting structure
- Organization chart
- JD file
- Training matrix
QA shall update:
- Training files
- GMP competency documentation
- Authorized signature list
- Departmental responsibility charts
Notification and Communication:
- HR shall communicate personnel changes to:
-
- Department Heads
- IT
- QA
- Security
- Finance (for final settlement or revised salary)
-
- HR shall update attendance and payroll systems when needed.
Training:
- All employees shall be trained on this SOP.
- Newly appointed or transferred personnel shall receive additional training for new responsibilities as applicable.
REFERENCES:
NA
RECORDS:
| Sr No. | Title | Document No. |
| 1 | Exit Interview Form | F/HR008/001 – 00 |
| 2 | No Dues Clearance Form | F/HR008/002 – 00 |
| 3 | Access issuance / modification / deactivation form | F/HR008/003 – 00 |
REVISION HISTORY.
| Amendment Date: | Update Summary | Version No. |
| NA | New SOP | 01 |