Zentiva is hiring for the role of Executive Quality Control, Pharmaceuticals at Ankleshwar, Gujarat, India. This opportunity is suitable for candidates with a postgraduate background in Science and 1-4 years of experience in a pharmaceutical company, especially in quality control laboratory activities.
Job Details
| Company | Zentiva |
| Position | Executive Quality Control, Pharmaceuticals |
| Department | Quality Control |
| Location | India / Ankleshwar; Ankleshwar |
| Employment Type | Full time |
Job Description
The selected candidate will implement quality control activities for Pharmaceuticals at Ankleshwar while adhering to regulatory and global quality directives and HSE guidelines. The role focuses on optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements, while living Group’s Values and Code of Ethics.
Key Responsibilities
Testing
- Perform timely analysis of raw material, bulk product, intermediates, finished goods and other samples for Pharmaceuticals.
- Perform analysis of market complaints, Stability, process validation samples, and Cleaning Validation of Pharmaceuticals.
Good Laboratory Practice
- Perform calibration and maintenance of lab equipment and assist for the qualification of laboratory equipment.
- Review pharmacopeias for specification preparation.
- Prepare SOPs and Formats and Analytical Test Record.
- Manage reference standards, working standards, laboratory reagents and chemicals.
- Arrange and observe Control Samples and maintain records.
- Participate in investigation of out of specification results, retesting and review the analysis records.
- Maintain and review laboratory raw data related to testing activity.
Validation
- Prepare protocol for Analytical Method validation, cleaning validation and perform the validation exercise as per the protocol.
Management of Laboratory Consumables
- Identify and plan requirement for laboratory consumables and monitor the stock of chemical, spares, glassware and printed material.
Coordination
- Coordinate with production and warehouse for analytical activities.
Other Responsibilities
- Comply with HSE requirements for QC Laboratory.
- Identify and correct unsafe conditions or behaviors and promptly report other potentially hazardous situations.
- Carry out any other assignments or projects as per the instruction of the Dept. Head to meet organizational objectives and priorities.
Qualification
- Post Graduate in Science (Organic or Analytical Chemistry)
- Analytical ability
- Trouble shootings
- Co ordination
- Communication
- Behavioural competencies: Accountability, Authenticity, Collaboration, Courage and Trust
Experience
- 1-4 years in a Pharmaceutical Company.
How to Apply
Interested candidates can apply online through the official Zentiva Workday application link given below.