Hybrid Sr. Executive – QC, Microbiology bei ZENTIVA

Position Title: Sr. Executive – QC, Microbiology  

Requirements & Qualifications:

• M.Sc. (Microbiology / Biotechnology) / B. Pharm with total 6-9 years of Experience in the microbiology laboratory of Pharmaceuticals & API & out of the total experience 3-4 years of Experience as a team leader
• GMP & GLP knowledge
• Knowledge of various applicable guidelines viz., USFDA, EU, Indian FDA, WHO, ICH
• Good coordination & communication skills.
• Conduct training to subordinate
• Knowledge of budgetary / procurement aspects
• Analytical Ability, Team building, troubleshooting
• Day to day planning of laboratory activities

Job overview:

• Implement quality control activities at Zentiva - 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:

Advanced knowledge, specifically on solid oral dosages & API’s;

• Microbial analysis of raw material and finished products, Microbial Monitoring of Controlled Area, Water samples and maintain proper documentation as per GLP and current guidelines.
• Sampling of Potable, Process and Purified Water as well as understanding of Water System
• Bacterial Endotoxin [LAL] Tests.

• Good Laboratory Practice

Knowledge of calibration & maintenance of lab. Equipment (viz., Balance, Incubator, Autoclave etc,. used in microbiology lab.) and performing qualification of laboratory equipment.

Preparing Microbiology laboratory documents, viz., SOPs, recording Formats, Analytical Test Record, Protocol & Report for Method validation & Equipment qualification

Handling of culture, media, laboratory reagents & chemicals.

Investigation of Laboratory incidents, out-of-specification / out-of-trend results

Review of laboratory raw data related to microbiology testing activity & Trending of data

Knowledge of QMS & e-tools, instrument software, and LIMS.

• Validation

Advance knowledge on Microbiology Analytical Method validation, cleaning validation, and computerized systems

• Others

Knowledge on HSE Requirements for QC laboratory.

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

Handling of projects as per the instruction of the department. Head to meet with the organizational objectives and priorities.

Identifying and planning requirements for laboratory consumables and monitoring the stock of chemicals, spares & glassware.

     What makes this position unique?

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

Location information: Ankleshwar, Gujarat India