JOB TITLE : Executive Quality Control, Pharmaceuticals
JOB PURPOSE: Implement quality control activities for Pharmaceuticals at Ankleshwar adhering to regulatory / global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet with customers’ requirements, living Group’s Values and Code of Ethics.
Education / Experience: Post Graduate in Science (Organic or Analytical Chemistry) 1 - 5 years in chemical & instrumental testing laboratory with exposure to GMP, GLP.
Preferably from Pharma background only.
Technical skills & Competencies / Language · Analytical ability · Trouble shootings · Co ordination · Communication
Behavioural Competencies: Accountability, Authenticity, Collaboration, Courage and Trust
Key Responsibility :
1. Testing
1.1. Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods and other samples for Pharmaceuticals.
1.2. Performing analysis of market complaints, Stability, process validation samples, Cleaning Validation of Pharmaceuticals.
2. Good Laboratory Practice
2.1. Performing calibration & maintenance of lab. Equipment and assisting for the qualification of laboratory equipment.
2.2. Managing reference standards, working standards, laboratory reagents & chemicals.
2.3. Arranging and observing Control Samples and maintaining record.
2.4. Participating in Investigation of out of specification results, performing retesting.
2.5. Maintaining laboratory raw data related to testing activity.
3. Validation
3.1. Performing the validation exercise as per the protocol. Maintaining raw data related to validation.
4. Management of laboratory Consumables
4.1. Identifying and planning requirement for laboratory consumables and monitoring the stock of chemical, spares, glassware and printed material.
5. Co ordination
5.1. Coordinating with production, and warehouse for analytical activities.
6. Other
6.1. Compliance to HSE Requirements for QC laboratory.
6.2. Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations.
6.3. Carrying out any other assignments or projects as per the instruction of the Dept. Head to meet with the organizational objectives and priorities.
Zentiva is a Pan-European Platform developing, manufacturing and providing high-quality and affordable medicines to more than 100 million people in Europe. Zentiva has 4 wholly owned manufacturing sites and a broad network of external manufacturing partners to ensure supply security. We offer solutions in key therapeutical areas like Cardiology & Circulation, Diabetes, Oncology, Respiratory, CNS and focus on expanding our portfolio in self-care. The company is Private Equity owned, delivering sustainable double-digit growth, with an ambitious 5-year plan for further strong (organic and inorganic) growth across Europe.
We are a team of more than 5,000 unique talents bonded together by our purpose to provide health and wellbeing for all generations. We want Zentiva to be a great place to work, where everyone feels welcomed and appreciated and can be their true selves contributing to the best of their ability.
Data protection: It’s not just a checkbox – it’s our commitment! Please visit our Privacy Notice https://www.zentiva.com/gdpr/privacy-notice
