Executive Quality Control, Pharmaceuticals

Zentiva; Ankleshwar; On-site; INR 400,000 - 800,000; Full time

Job summary

Zentiva in Ankleshwar, Gujarat invites applications for Executive Quality Control in Pharmaceuticals. The role focuses on implementing QC activities in compliance with regulatory directives and HSE guidelines, using available resources to ensure consistent product quality for customer requirements.

Ideal candidates hold a Post Graduate in Science (Organic/Analytical Chemistry) with 1-5 years in chemical & instrumental testing labs, preferably from pharma.

Qualifications

• Post Graduate in Science (Organic or Analytical Chemistry) with 1-5 years in chemical & instrumental testing laboratory and exposure to GMP, GLP.
• Preferably from Pharma background only.

Responsibilities

• Perform sampling and analysis of raw materials, intermediates, finished products and related samples.
• Perform analysis of market complaints, Stability, process validation samples, and Cleaning Validation.
• Maintain calibration/maintenance of lab equipment and assist qualification of equipment.
• Manage reference standards, reagents, and chemicals; maintain laboratory records.
• Participate in investigations of out-of-spec results and retesting.
• Maintain laboratory data related to testing and validation activities.
• Coordinate with production and warehouse for analytical activities.
• Ensure compliance with HSE requirements for QC laboratory.
• Identify unsafe conditions and report hazards; assist on departmental projects.

Skills

Analytical ability

Trouble shootings

Co ordination

Communication

Education

Post Graduate in Science (Organic or Analytical Chemistry)

Job description

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

Testing

• Performing timely sampling and 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.
• Managing reference standards, working standards, laboratory reagents & chemicals.
• Arranging and observing Control Samples and maintaining record.
• Participating in Investigation of out of specification results, performing retesting.
• Maintaining laboratory raw data related to testing activity.

Validation

• Performing the validation exercise as per the protocol. Maintaining raw data related to validation.

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.