Ajanta Pharma is Hiring for Production, QC and QA Officers

Ajanta Pharma Ltd. is conducting a walk-in interview for experienced pharmaceutical professionals for its US FDA approved OSD formulation facility at Paithan, Dist. Chhatrapati Sambhajinagar, Aurangabad, Maharashtra. The company is looking for candidates with relevant exposure in regulated plant environments and hands-on experience in production, quality control and quality assurance functions.

Ajanta Pharma Ltd. is a specialty pharmaceutical company engaged in development, manufacture and marketing of quality finished dosages in domestic and international markets. The current hiring drive is suitable for candidates who have worked in OSD manufacturing, packing, QC analysis, analytical QA, IPQA, documentation and validation-related activities.

1. Production Officer / Sr. Officer

Job Overview

Responsibilities

• Handle OSD manufacturing operations such as granulation, compression, coating, pellet coating and capsule filling.
• Work in primary and secondary packing sections as per approved procedures.
• Maintain and follow documentation requirements for regulated manufacturing operations.
• Support shop-floor compliance, production tracking and process execution in line with plant systems.

Qualifications

• B. Pharm / M. Pharm

Key Skills and Experience Required

• 03 to 06 yrs. experience for OSD manufacturing operations.
• Experience in primary and secondary packing section.
• Knowledge of Pas | X, SCADA and E-log.
• Knowledge of track and trace and e-BMR.

2. Quality Control Officer / Sr. Officer

Job Overview

Responsibilities

• Perform analysis of FP, IP, PV and stability samples.
• Support method validation and method transfer activities.
• Participate in investigation activities under QMS.
• Handle and operate analytical instruments as required for QC laboratory work.

Qualifications

• B. Pharm / B.Sc / M. Sc.

Key Skills and Experience Required

• 03 to 05 yrs. experience in Quality Control.
• Experience in analysis of FP, IP, PV and stability samples.
• Experience in method validation and method transfer and Investigation (QMS).
• Experience of handling of various instruments – HPLC, LIMS.

3. Quality Assurance Officer

Job Overview

Responsibilities

• Support IPQA activities in manufacturing and packing sections.
• Review and maintain batch-related documentation and in-process compliance records.
• Assist in equipment qualification and validation activities for facility and utility systems.

Qualifications

• B. Pharm / M. Pharm

Key Skills and Experience Required

• 02 to 03 yrs. experience in IPQA manufacturing and packing section.
• Knowledge of SCADA equipment and PAS | X batch records.
• Qualification of Equipment with SCADA, facility and utility and Validations.

4. Quality Assurance Officer / Sr. Officer

Job Overview

Responsibilities

• Handle Analytical QA activities and review analytical reports.
• Perform online review of chemical and microbiological testing.
• Support GLP function and qualification of instruments with software.
• Work on laboratory investigations and QMS-related activities.

Qualifications

• B. Pharm / M. Pharm / M.Sc.

Key Skills and Experience Required

• 03 to 05 yrs. experience in Analytical QA and review of analytical reports.
• Hands on LIMS software, Openlab, LC solution.
• Working knowledge of QMS, change control, CAPA, incident, deviation, Market complaints.

Candidate Preference

• For all positions, candidates having exposure to regulatory requirements of documentation cGMP/CGDP and worked in regulated plants shall be preferred.

Walk-In Interview Details

How to Apply

If unable to attend interview, forward your updated CV at:

CV.ptn@ajantapharma.com