Assistant Manager- Quality Control, Chemistry

3.1.

Adhere to current GMP guidelines

3.2.

Following ALCOA+++ practices during documentation and related activities 3.3.

Compliance to local and international HSE norms

3.4.

Regulatory compliance

3.5.

ISO 14000 related activities

3.6.

Regular Pharmacopoeia and regulatory requirement review for compliance 3.7.

To participate in any regulatory/Customer inspection takes place at the site 3.8.

Training of self and subordinates on quality and HSE systems

4.1.

Preparing protocol and report for Analytical Method validation, cleaning validation and performing / organizing the validation exercise as per the protocol. 5.

Management of laboratory Consumables

5.1.

Identifying and planning requirement for laboratory consumables and monitoring the stock of chemical, glassware and printed material.

5.2.

Maintaining stock of laboratory chemicals in line with budget

Co ordination

6.1.

Coordinating with production, and warehouse for analytical activities.

7.1.

Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations.

7.2.

Carrying out any other assignments or projects as per the instruction of the Dept.

Head to meet with the organizational objectives and priorities.

7.3.

Performing internal quality audit as a “Qualified Internal Auditor” during internal Quality Audit abiding the internal quality audit schedule.

7.4.

Train the subordinate for laboratory related jobs.