Executive - Quality Control, Pharma

Zentiva Group; Ankleshwar; On-site; INR 600,000 - 900,000; Full time

Job summary

Executive – Quality Control in Ankleshwar, India, will implement QC activities in alignment with regulatory and global quality directives and HSE guidelines. The role involves sampling, analysis, and validation tasks to ensure consistent product quality meeting customer requirements.

The candidate will work with GMP/GLP standards, handle analytical instruments, prepare SOPs, and coordinate with production for QC activities while maintaining compliant laboratory records.

Qualifications

• M. Sc (Organic / Analytical Chemistry) or B. Pharm with 5-8 years as analyst in Pharmaceuticals / API industry.
• GMP & GLP knowledge is essential.
• Experience in analytical method validation, validation of cleaning processes and knowledge of QA/QC practices.

Responsibilities

• Perform sampling and analysis of raw materials, bulk products, intermediates and finished goods.
• Conduct analysis of Stability, process validation samples, and Cleaning Validation.
• Operate and maintain lab instruments (HPLC, GC, UV/IR, dissolution tester, auto-titrator, polarimeter).
• Prepare SOPs, formats, and analytical test records; manage reference standards and laboratory reagents.
• Assist in investigations of out-of-specification results and maintain lab data.

Skills

Analytical ability

Coordination & communication

LIMS & QMS knowledge

GMP & GLP knowledge

Education

M.Sc (Organic / Analytical Chemistry)

B.Pharm

Tools

HPLC

GC

UV spectrophotometer

IR spectrophotometer

Dissolution tester

Auto-titrator

Polarimeter

Job description

Executive - Quality Control, Pharma### Executive - Quality Control, PharmaPresenta candidatura: India / Ankleshwar: Full time: Offerta pubblicata oggi: R2469814**Position Title:** **Executive – Quality Control****Qualification and Experience:**M. Sc (Organic / Analytical Chemistry) / B. Pharm with 5 - 8 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge**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 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, and Cleaning Validation.Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc.* **Good Laboratory Practice**Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment.Knowledge on the preparation of SOPs and Formats and Analytical Test records.Managing reference standards, working standards, laboratory reagents & chemicals.Arranging and observing Control Samples and maintaining the record.Participating in the Investigation of out-of-specification results.Maintaining laboratory raw data related to testing activity.* **Validation**Performing Analytical Method validation, cleaning validation as per the protocol.* **Other**Coordinating with production and the warehouse for analytical activitiesCompliance 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 instructions of the Department. Head to meet with the organizational objectives and priorities. **Requirements*** GMP & GLP knowledge* Good coordination & communication skills.* Analytical ability* Knowledge on LIMS & QMS**What makes this position unique?*** This position will provide good exposure to work in GMP/ GLP environment.**Location information:** Ankleshwar, Gujarat, India