Cadila Pharmaceuticals Hiring Quality Junior Officer Ankleshwar

Cadila Pharmaceuticals Recruitment Notification

Cadila Pharmaceuticals, a leading name in the pharmaceutical industry, is hiring a Quality Junior Officer for its manufacturing facility in Ankleshwar, Gujarat, India. This role offers an excellent opportunity for professionals in quality assurance and quality control to advance their careers in a reputable organization. Qualified candidates with relevant educational backgrounds and experience in GLP, HPLC analysis, and CGMP compliance are encouraged to apply.

About Cadila Pharmaceuticals

With decades of experience delivering high-quality pharmaceutical products, Cadila Pharmaceuticals is recognized for its innovation and adherence to stringent quality standards. Its Ankleshwar facility is pivotal in manufacturing and quality assurance, offering professionals an environment to learn and grow.

Role Overview: Quality Junior Officer

Location: Ankleshwar, Gujarat
Department: Quality Assurance and Control
Job Code: 18004902

As a Quality Junior Officer, you will ensure compliance with Good Laboratory Practices (GLP), perform detailed analyses, and uphold the integrity of quality processes. This position requires hands-on experience with HPLC, LIMS modules, and cGMP systems.

Key Responsibilities

• To maintain and adhere to the GLP and safety procedures in the laboratory.
• To perform the analysis as per work allocation and record the results in a work sheet (protocols) for raw materials, packing materials, intermediates, APIs, stability, etc., as per the current specification and method of analysis.
• To work as an analyst and maintain the CFR 21 Part 11 compliance by following laid down procedures.
• To perform all the HPLC-related analysis and perform the online documentation for In-process, intermediate, finished products & returned goods / raw materials Hold time, stability study, / working standard analysis as per laid-down specifications & test procedures, SOPs, as per work allocation, and report the analysis data in LIMS modules and report to Section Head or QC Head.
• To ensure that every specification and method of analysis used is the right product/material code.
• To follow the instruction of shift/section in charge for analysis/planning.
• To report QI/NQI/OOS/OOT deviation/ddiscrepancy in laboratory analysis to QC-in-charge and initiate QI/NQI/OOS/OOT deviation.
• Responsible for performing calibration of laboratory instruments as per schedule and laid down SOPs with documentation and update of instrument calibration status tag.
• To record and ensure all the entries and results are in line with current specifications and STPs.
• To ensure all column performance and column entry are maintained in column logbooks.
• To maintain instruments log books properly as per analysis.
• To acquire training from the concerned person to update the cGMP system and update technical knowledge.
• To maintain reference/working standard/impurity standard usage records.
• To maintain the instrument history record.
• Joint analysis with A.R. laboratory personnel during analytical method transfer on HPLC.
• Preparation of stability protocols and stability reports.
• To perform analysis of stability samples as per stability schedule
• Daily monitoring and recording of temperature and humidity of refrigerator/working standard chamber and laboratory area.
• Perform holding time study of intermediates and preparation of reports.
• Inform and Investigate OOS results in RM/Intermediates/APIs
• Ensure CFR 21 part -11 compliance and follow good chromatography practices during analysis, integration and reviewing of on-line and off-line chromatographic analysis to
• Maintain proper data integrity.
• To ensure no spillage of lab. Chemicals/solvents
• To prepare mobile phase/solution for analysis as per requirement to avoid wastage of lab chemicals and reagents/solvents.
• To coordinate with the store department to obtain prior information of urgent analysis of raw materials.

Candidate Qualifications

Educational Requirements

• Bachelor’s or Master’s Degree in Pharmacy or Natural Sciences.

Experience

• 1–3 years of experience in quality assurance or control in a pharmaceutical environment.
• Proficiency in handling analytical tools, such as HPLC, and regulatory databases like LIMS.

Skills and Attributes

• Basic knowledge of worldwide cGxP regulations.
• Strong communication and organizational skills.
• Hands-on experience in stability studies, calibration processes, and analytical reporting.

How to Apply?

Candidates meeting the above qualifications are encouraged to apply online by visiting the official Cadila Pharmaceuticals career portal:
Apply Here

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