Executive - Quality Control

Posted 6 Days Ago
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2 Locations
Junior
Pharmaceutical
The Role
The Executive - Quality Control is responsible for implementing quality control activities in pharmaceuticals, conducting analysis of materials and products, maintaining laboratory standards, and ensuring adherence to GMP and GLP guidelines. They will manage laboratory consumables and coordinate with production and warehouse for analytical activities.
Summary Generated by Built In

Position Title: Executive – Quality Control, Pharmaceuticals  

Job overview:

  • Implement quality control activities 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.

Responsibilities:                                                  

  • Analysis:

Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods and other samples.

Performing analysis of Stability, process validation samples, Cleaning Validation.

  • Good Laboratory Practice

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

Preparing SOPs and Formats and Analytical Test Record.

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

Arranging and observing Control Samples and maintaining record.

Participating in Investigation of 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, 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, spares, glassware and printed material.

  • Other

Coordinating with production, and warehouse for analytical activities

Compliance to HSE Requirements for QC laboratory.

Identifying and correcting unsafe conditions or behaviours 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.     

Requirements & Qualifications:

  • M.sc (Organic / Analytical Chemistry) / B. Pharm with 2-5 years of Experience as an analyst in similar industry
  • GMP & GLP knowledge
  • Good coordination & communication skills.  

What makes this position unique?

  • This position will provide good exposure to work in GMP/ GLP environment.

Location Information: Ankleshwar GIDC District: Bharuch State: Gujarat.

The Company
HQ: Dolní Měcholupy
3,360 Employees
On-site Workplace
Year Founded: 1999

What We Do

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 almost 5,000 unique talents bonded together by our mission to deliver high-quality and affordable medicines to people who depend on them every day. 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.

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