Panacea Biotec Pharma Ltd. has announced a new recruitment opportunity for experienced pharmaceutical professionals in its Production Department. The company is inviting applications for the position of Production Executive from candidates who have hands-on experience working in a sterile injectable manufacturing facility.

This recruitment opportunity is particularly suitable for pharmaceutical professionals with 3 to 8 years of relevant experience in injectable manufacturing operations. Candidates meeting the required eligibility criteria can submit their updated CV through the official email address mentioned in the recruitment notification.

Job Overview

Particulars Details

Company Name

Panacea Biotec Pharma Ltd.

Position

Production Executive

Department

Production / Sterile Injectable Manufacturing

Experience Required

3–8 Years

Industry

Pharmaceutical Manufacturing

Manufacturing Area

Sterile Injectables

About Panacea Biotec Pharma Ltd.

Panacea Biotec is a pharmaceutical and biotechnology company engaged in the development and manufacturing of pharmaceutical products and vaccines.

The organization operates pharmaceutical manufacturing facilities where trained professionals work across production, quality, engineering, research, and other technical functions.

This recruitment drive provides an opportunity for experienced sterile manufacturing professionals to explore a career opportunity in the pharmaceutical production sector.

Position Available

Job Title: Production Executive

The selected candidate will be expected to work in pharmaceutical production operations associated with sterile injectable manufacturing.

Candidates should possess relevant industry experience and practical knowledge of sterile manufacturing processes, pharmaceutical documentation, Good Manufacturing Practices (GMP), and regulatory compliance requirements.

Experience Required

Applicants should have 3 to 8 years of relevant professional experience.

The recruitment notification specifically states that candidates must have experience working in a sterile injectable manufacturing facility.

Experience in injectable manufacturing is mandatory.

Candidates without relevant sterile injectable manufacturing experience may not be considered for this position.

Eligibility Criteria

Interested candidates should carefully review the following eligibility requirements before submitting their applications:

Candidates must have relevant experience working in a sterile injectable manufacturing facility.

Applicants should possess 3–8 years of relevant industry experience.

Practical experience in injectable manufacturing operations is mandatory.

Candidates should understand GMP requirements and pharmaceutical production procedures.

Knowledge of sterile area practices, contamination control, production documentation, and regulatory compliance will be beneficial.

Only candidates meeting the required sterile injectable manufacturing experience criteria should apply.

Key Responsibilities of a Production Executive

Although detailed job responsibilities are not specified in the recruitment advertisement, professionals working as Production Executives in sterile injectable manufacturing facilities typically handle:

Monitoring and executing sterile manufacturing activities according to approved Standard Operating Procedures (SOPs) and Batch Manufacturing Records (BMRs).

Ensuring compliance with cGMP, Good Documentation Practices (GDP), data integrity principles, and regulatory requirements.

Supervising manufacturing activities such as equipment preparation, compounding, filtration, filling, sealing, and other sterile production operations, depending on the assigned manufacturing area.

Reviewing production documents and ensuring that manufacturing records are completed accurately and contemporaneously.

Participating in deviation investigations, Corrective and Preventive Actions (CAPA), change controls, and manufacturing process improvements.

Coordinating with Quality Assurance, Quality Control, Engineering, Warehouse, and other departments to maintain smooth manufacturing operations.

Ensuring compliance with sterile area behavior, gowning procedures, environmental monitoring requirements, and contamination control practices.

Skills Required for Sterile Injectable Production Professionals

Candidates applying for Production Executive positions should ideally have technical knowledge of:

Current Good Manufacturing Practices (cGMP): Understanding regulatory requirements governing pharmaceutical manufacturing operations.

Aseptic Processing: Knowledge of sterile handling practices and contamination prevention during manufacturing operations.

Sterile Area Practices: Understanding personnel movement, material transfer, gowning qualification, and cleanroom behavior.

Pharmaceutical Documentation: Experience maintaining BMRs, equipment logbooks, SOP records, and other GMP documents.

Deviation and CAPA Management: Basic understanding of deviation investigations, root cause analysis, and corrective and preventive actions.

Data Integrity: Familiarity with ALCOA+ principles and accurate documentation practices.

Contamination Control: Understanding microbial contamination risks and controls implemented within sterile manufacturing facilities.

How to Apply

Interested and eligible candidates should prepare an updated professional CV highlighting their experience in sterile injectable manufacturing operations.

Applicants may send their CV to:

Email: rajnithakur@panaceabiotec.com

Candidates should clearly mention the position they are applying for in the email subject line.

Suggested Email Subject:

Application for Production Executive – Sterile Injectable Manufacturing

Before submitting the application, candidates should verify that their CV clearly mentions their injectable manufacturing experience, current designation, total years of experience, present organization, and relevant technical skills.

Important Note for Applicants

The recruitment advertisement clearly specifies that only candidates with relevant sterile injectable manufacturing experience should apply.

Applicants should carefully verify their eligibility and application details before sending their CV. Candidates are also advised to rely on official company communications for subsequent recruitment updates and never pay money to unauthorized individuals claiming to guarantee employment.

Technical FAQs

1. What technical experience is mandatory for the Production Executive position?

Candidates must have practical experience working in a sterile injectable manufacturing facility. Experience in injectable manufacturing is explicitly stated as mandatory in the recruitment notification.

2. What are the critical GMP requirements in sterile injectable manufacturing?

Critical GMP requirements include validated manufacturing processes, qualified equipment, proper personnel gowning, environmental monitoring, contamination control, accurate documentation, data integrity, deviation management, and strict adherence to approved SOPs.

3. What is aseptic processing in pharmaceutical manufacturing?

Aseptic processing involves manufacturing and handling sterile pharmaceutical products under controlled conditions designed to prevent microbial, particulate, and endotoxin contamination. It requires qualified cleanrooms, trained personnel, validated processes, environmental monitoring, and strict adherence to sterile practices.

4. What documents should a Production Executive understand in injectable manufacturing?

A Production Executive should be familiar with Batch Manufacturing Records (BMRs), Batch Packaging Records (BPRs), SOPs, equipment logbooks, cleaning records, deviation reports, CAPA records, change controls, and other GMP-related documents.

5. What is the role of contamination control in sterile manufacturing?

Contamination control is essential for maintaining product sterility and patient safety. It includes facility and equipment design, cleaning and disinfection, personnel gowning, environmental monitoring, material movement controls, aseptic practices, and investigation of microbial or particulate excursions.