Job Opportunity: Production and Quality Control Professionals at Neuland Laboratories Limited

Summary

Neuland Laboratories Limited, a globally recognized leader in the pharmaceutical manufacturing sector, is seeking experienced professionals to join our dynamic team in Hyderabad. We are currently hiring for multiple openings across our Production, Quality Control, and Production Documentation departments. If you are a dedicated professional with a background in the pharmaceutical industry and a drive for excellence, we invite you to apply and contribute to our mission of providing high-quality healthcare solutions.

About Neuland Laboratories Limited

Established in 1984, Neuland Laboratories Limited has evolved into a powerhouse in the pharmaceutical industry. Headquartered in Hyderabad, India, and publicly listed, we are renowned for our expertise in the manufacturing of Active Pharmaceutical Ingredients (APIs). As an end-to-end solutions provider for the global pharmaceutical industry’s chemistry needs, we pride ourselves on innovation, regulatory compliance, and a commitment to quality that saves lives.

At Neuland, we believe our people are our greatest asset. We provide an environment that fosters professional growth, technical expertise, and collaborative problem-solving.

Available Positions

We are currently inviting applications from talented individuals for the following roles:

1. Production Department

• Experience Required: 2 to 8 years
• Key Responsibilities: Overseeing daily manufacturing operations, ensuring compliance with SOPs and cGMP guidelines, managing batch production records, and maintaining safety protocols on the shop floor.

2. Quality Control (QC) Department

• Experience Required: 3 to 8 years
• Key Responsibilities: Conducting analytical testing of raw materials, in-process samples, and finished goods using advanced instrumentation (HPLC, GC, etc.). Ensuring all testing is conducted in strict accordance with quality standards and regulatory requirements.

3. Production Documentation

• Experience Required: 5 to 8 years
• Key Responsibilities: Managing the lifecycle of production documentation, ensuring accurate data integrity, preparing and reviewing batch manufacturing records (BMRs), and maintaining comprehensive records for regulatory audits.

Candidate Requirements

• Educational Background: A degree or diploma in Pharmacy, Chemistry, or a related field.
• Industry Experience: Prior experience in a pharmaceutical manufacturing environment is mandatory.
• Compliance Awareness: Strong knowledge of regulatory requirements, safety standards, and documentation practices.
• Skills: Ability to work in shifts, attention to detail, strong analytical skills, and the capability to work effectively within a team-oriented environment.

Why Join Neuland Laboratories?

Joining Neuland Laboratories means becoming part of a publicly listed organization with a legacy of excellence spanning four decades. We offer a challenging work environment where you can sharpen your technical skills, gain exposure to complex manufacturing processes, and play a vital role in the global pharmaceutical supply chain.

How to Apply

We are looking for motivated candidates who are ready to take the next step in their career. To apply for any of the above positions, please send your updated resume via WhatsApp to 8179538447.

When submitting your application, please ensure you include the following mandatory details in your message:

• Full Name
• Current Organization
• Present CTC (Cost to Company)
• Expected CTC

Please note: Only shortlisted candidates will be contacted for further rounds of the selection process. Ensure your resume highlights your relevant experience in alignment with the specific department requirements mentioned above.

Neuland Laboratories Limited is an equal opportunity employer. We encourage all qualified candidates to apply and join us in our commitment to “Quality and Reliability.”