Executive - Quality Control (OSD)

Why This Role Matters
Quality Control (QC) is a critical function in pharmaceutical manufacturing, ensuring that every batch of medicine meets stringent quality, safety, and regulatory standards before reaching patients. In the Oral Solid Dosage (OSD) segment, maintaining analytical precision and compliance is essential to uphold global pharmaceutical standards.
At Hetero, the Quality Control department plays a central role in ensuring product integrity through analytical testing, stability studies, and regulatory compliance. This opportunity is ideal for professionals with 3–9 years of experience in QC operations who are looking to advance their careers in a structured and compliance-driven pharmaceutical manufacturing environment.
Working in a high-capacity manufacturing unit like Unit-V, Jadcherla, provides hands-on exposure to sophisticated analytical instruments, regulatory inspections, and international quality benchmarks.

Job Description
Hetero is conducting a Walk-In Interview for experienced Quality Control professionals in the OSD (Oral Solid Dosage) segment. The company is hiring for Officer, Junior Executive, and Executive-level roles.
Selected candidates will be responsible for performing analytical testing, stability studies, documentation, and ensuring compliance with GMP and regulatory standards. The role requires strong technical expertise in analytical instruments and experience in pharmaceutical QC laboratory operations.

Key Features of the Role:
• Department: Quality Control (OSD)
• Designation: Officer / Jr. Executive / Executive
• Experience Required: 3 to 9 Years
• Mode of Hiring: Walk-In Interview
• Work Location: Unit-V, Jadcherla
• Exposure to regulatory-compliant manufacturing environment
• Opportunity to work with advanced analytical instrumentation

Responsibilities
• Perform analysis of raw materials, in-process samples, finished products, and stability samples
• Conduct sampling activities as per SOPs
• Handle and operate analytical instruments such as:
• HPLC (High Performance Liquid Chromatography)
• GC (Gas Chromatography)
• IP/FP testing (In-Process / Finished Product testing)
• MT (Method Transfer)
• MV (Method Validation)
• Conduct stability studies and maintain related documentation
• Prepare and review analytical reports in compliance with GMP standards
• Ensure laboratory documentation accuracy and audit readiness
• Follow regulatory guidelines and company SOPs
• Participate in internal and external audits
• Ensure timely completion of assigned testing activities
The role demands high analytical accuracy, regulatory awareness, and adherence to pharmaceutical quality standards.

Required Qualifications

Candidates must possess one of the following educational qualifications:
• Bachelor’s degree in Pharmacy
• Master’s degree in Pharmacy
• M.Sc (Relevant Chemistry / Analytical Chemistry / Pharmaceutical Sciences specialization preferred)

Educational Requirements:
A Bachelor’s or Master’s degree in Pharmacy or Science (Chemistry/Analytical Chemistry) is required. Candidates must have strong academic foundations in pharmaceutical analysis and laboratory practices.

Experience and Skills:

Experience:
• 3 to 9 years of experience in Quality Control within OSD manufacturing

Technical Skills:
• Hands-on experience with HPLC and GC
• Knowledge of sampling procedures
• Experience in IP/FP testing
• Exposure to Method Transfer (MT) and Method Validation (MV)
• Understanding of stability testing procedures
• Familiarity with GMP and regulatory documentation

Soft Skills:
• Strong attention to detail
• Analytical thinking and problem-solving ability
• Good documentation and reporting skills
• Ability to work in a team-based laboratory environment

Salary Insights:
Salary will be offered as per industry standards and will depend on experience, technical expertise, and interview performance.
Additional benefits may include:
• Exposure to regulatory audits
• Structured pharmaceutical manufacturing environment
• Career progression opportunities within Quality functions
• Professional development in analytical and compliance systems

Company Overview
Hetero is a globally recognized pharmaceutical company known for its strong presence in APIs and finished dosage formulations. The company operates advanced manufacturing facilities that comply with international regulatory standards.
The Unit-V facility in Jadcherla is part of Hetero’s large-scale manufacturing network, focusing on quality-driven pharmaceutical production with robust analytical and regulatory systems.

Walk-In Interview Details
Interview Date: 01 March 2026 (Sunday)
Interview Time: 09:30 AM to 03:00 PM
Work Location: Unit-V, Jadcherla, Telangana, India
Mode of Hiring: Walk-In Interview

Candidates are advised to carry:
• Updated Resume
• Educational Certificates
• Experience Certificates
• Latest Salary Slips
• Government ID Proof

FAQs

Q1: Is prior OSD experience mandatory?
Yes. Candidates must have experience in OSD Quality Control.

Q2: What instruments should candidates be experienced with?
HPLC and GC handling experience is essential.

Q3: Is this opportunity open to freshers?
No. This role requires 3–9 years of relevant QC experience.

Q4: What is the mode of hiring?
The recruitment process will be conducted through a walk-in interview.

Application Tip

• Highlight hands-on experience with HPLC and GC
• Mention exposure to stability studies and regulatory audits
• Clearly state experience in Method Transfer and Validation
• Be prepared to discuss analytical troubleshooting scenarios
• Carry all necessary documents for on-the-spot verification