Executive - Quality Control (LCMS)

Posted 18 Hours Ago
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Ankleshwar, Bharūch, Gujarāt
Junior
Pharmaceutical
The Role
The role involves implementing quality control for pharmaceuticals, performing timely analysis of samples, maintaining laboratory equipment, preparing SOPs, and ensuring compliance with global quality and safety guidelines. It requires coordination with production and warehouse for analytical activities and participation in investigations of out of specification results.
Summary Generated by Built In

Generic 

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. 

KEY ACCOUNTABILITIES 

Testing 

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

Performing analysis of market complaints, Stability, process validation samples, Cleaning Validation of Pharmaceuticals.  

Good Laboratory Practice 

Performing 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. 

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. 

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   

Position required through experience in LCMS.

REQUIREMENTS 

 

Education / Experience 

Post Graduate in Science (Organic or Analytical Chemistry ) 

1-3 years in a Pharmaceutical Company. 

Technical skills & 

Competencies / Language 

  • Analytical ability  

  • Trouble shootings 

  • Co ordination 

  • Communication 

Behavioural Competencies 

(LEAD and others) 

  • Accountability, Authenticity, Collaboration, Courage and Trust 

Top Skills

Lcms
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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