
Synovia Pharma PLC, a subsidiary of Beximco Pharmaceuticals Limited
Career Opportunity at Synovia Pharma PLC
Executive, Quality Systems

We are looking for dynamic individual to work with our Quality Systems team.
Key Responsibilities:
- Preparation of Site Validation Master Plan (SVMP) and execute accordingly with team.
- Preparation of protocol, report and co-ordinate for Process Validation
- Perform Cleaning Validation of equipment
- Facility, Utility & Equipment Qualification in terms of Installation qualification, Operational qualification including commissioning and Performance qualification.
- Transport Validation of bulk product, cold chain product and finished product as per requirement.
- Computerized System Validation.
- Monitor the Temperature mapping of storage area according to scheduled qualification plan.
- Prepare Site Training Plan yearly and follow up the achievement target according to plan schedule with team approach. Facilitate and design effective training program for employees to implement cGMP on Site.
- Prepare and Review SOP and conduct Training.
Desired Profile:
Experience: 1-3 Years hands on experience in Validation and Qualification.
Skills and Competencies:
- Must have strong attention to detail and a high level of accuracy
- Work-ethics, due diligence, can peruse to others towards a required point of view.
- Highly motivated and result-oriented.
- Ability to manage multiple priorities
- Sound knowledge of Qualification, Validation, GMP and regulatory guidelines.
- Excellent communication and inter-personal skills.
Job Location: Tongi (Synovia Site)
Application Instructions
Last date of application: December 27, 2023 |