Zentiva

Executive - Quality Control

Zentiva  •  Ankleshwar, IN (Onsite)  •  16 days ago
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Job Description

JOB TITLE

Executive Quality Control, Pharmaceuticals

JOB PURPOSE

Generic

Implement quality control activities for Pharmaceuticals at Ankleshwar adhering to regulatory / global quality guidelines 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 Ethics.

REQUIREMENTS

Education / Experience

Post Graduate in Science (Organic Chemistry )

2-4 years in chemical & instrumental testing laboratory with exposure to GMP, GLP.

Technical skills &

Competencies / Language

  • Analytical ability
  • Trouble shootings
  • Co ordination
  • Communication
  • Leadership

KEY ACCOUNTABILITIES

Testing and release

Planning of timely sampling and analysis and review of raw material, bulk product, intermediates, finished goods, packing material and other samples for Pharmaceuticals.

Performing analysis of Raw Material Samples received from new vendors for Pharmaceuticals.

Good Laboratory Practice

Planning for calibration & maintenance of lab. Equipment and assisting for the qualification of laboratory equipment.

Reviewing pharmacopeias for specification preparation.

Preparing SOPs and Formats and Analytical Test Record.

Managing reference standards, working standards, laboratory reagents & chemicals.

Reviewing and observing Retention Samples and maintaining record.

Investigating out of specification results, retesting and review the analysis records.

Maintaining & reviewing laboratory raw data related to testing activity.

Validation

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

Management of laboratory Consumables

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

Co ordination

Coordinating with production, and warehouse for analytical activities.

Other

Compliance to HSE Requirements for QC laboratory.

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

Carrying out any other assignments or projects as per the instruction of the Dept. Head to meet with the organizational objectives and priorities.

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Zentiva

About Zentiva

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

Industry
Chemicals & Materials
Company Size
1,001-5,000 employees
Headquarters
Prague 10, CZ
Year Founded
1488
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