QC Officer / Senior Executive

Sri Ambikare Pharma; Jadcherla; On-site; INR 500,000 - 700,000; Full time

Job summary

Sri Ambikare Pharma Pvt. Ltd. in Jadcherla, Telangana, invites a skilled QC Officer/Senior Executive to strengthen our Quality Control team. You will test raw materials, in-process samples, and finished products, ensuring compliance with GMP and regulatory standards.

The role requires hands-on experience with analytical instruments (HPLC, GC, UV, IR), strong documentation, and a collaborative approach to meet strict timelines in a fast-growing pharma environment.

Qualifications

• 2–8 years of experience in pharmaceutical Quality Control.
• Hands-on experience with analytical instruments such as HPLC, GC, UV, and IR is preferred.
• Knowledge of GMP, SOPs, and laboratory documentation.

Responsibilities

• Perform testing of raw materials, intermediates, in-process samples, and finished products as per approved specifications.
• Operate analytical instruments such as HPLC, GC, UV, IR, and dissolution apparatus, as applicable.
• Follow GMP, SOPs, laboratory safety, and data integrity requirements.
• Prepare and maintain analytical worksheets, test reports, and laboratory records.
• Report abnormal results, deviations, and OOS results to the QC Manager.

Skills

Quality Control

HPLC

GC

UV/Vis

IR

GMP

SOPs

Data integrity

Documentation

Teamwork

Education

B.Sc./M.Sc. Chemistry or B.Pharm/M.Pharm

Tools

HPLC

GC

UV

IR

Dissolution Apparatus

Job description

product range :- OSD - pellets and granules

Employment Type: Full-Time, Permanent

Educational Qualifications: B.Sc. / M.Sc. Chemistry or B.Pharm / M.Pharm,

About the Company.

We're Growing. Come Grow With Us.

Every great pharmaceutical company starts with a vision, and at Sri Ambikare Pharma Pvt. Ltd., we're proud to see that vision becoming a reality—one milestone at a time.

As a fast-growing pharmaceutical startup, every day brings new opportunities to learn, innovate, and build something meaningful. From setting up our state-of-the-art manufacturing facility and establishing robust Formulation R&D (FR&D) and Analytical R&D (AR&D) capabilities to navigating the exciting journey of regulatory approvals and pharmaceutical licensing, we are laying the foundation for a world-class manufacturing organization.

Our goal is clear: to build a quality-driven facility that meets the highest global regulatory standards, including the path toward USFDA-compliant manufacturing.

As we continue expanding, we're looking for passionate professionals who want to be part of this exciting journey.

About the Role.

We are looking for a skilled and experienced QC Officer / Senior Executive to join our Quality Control team. The candidate will be responsible for testing raw materials, in-process samples, and finished products while

ensuring compliance with pharmaceutical quality standards and GMP requirements.

Key Responsibilities

• Perform testing of raw materials, intermediates, in-process samples, and finished products as per approved specifications.
• Operate analytical instruments such as HPLC, GC, UV, IR, and dissolution apparatus, as applicable.
• Perform wet analysis and stability sample testing as required.
• Prepare and maintain analytical worksheets, test reports, and laboratory records.
• Follow GMP, SOPs, laboratory safety, and data integrity requirements.
• Support instrument calibration, qualification, and maintenance activities.
• Report abnormal results, deviations, and OOS results to the QC Manager.
• Support laboratory investigations and maintain proper documentation.
• Ensure timely completion of testing activities and coordinate with the QC team.

Required Skills and Experience

• 2–8 years of experience in pharmaceutical Quality Control.
• Hands-on experience with analytical instruments such as HPLC, GC, UV, and IR is preferred.
• Knowledge of wet analysis, dissolution, and stability testing is an advantage.
• Good understanding of GMP, SOPs, and laboratory documentation.
• Strong analytical skills, attention to detail, and teamwork.
• Understand applicable SOPs, GMP requirements, and laboratory safety procedures within the first month.
• Independently perform assigned routine QC tests within two months after completing the required training and competency assessment.
• Maintain accurate records and report abnormal results promptly.