Cipla is a multinational pharmaceutical and biotechnology company renowned for its commitment to affordable and accessible healthcare. With a strong presence in over 80 countries, Cipla has been a trusted name for decades. Working at Cipla means being part of a culture that values quality, integrity, and patient-centric innovation. A production job at Cipla is a step towards a stable and rewarding career in the pharmaceutical manufacturing sector.
Job Description: Junior Operator Production
Here is a detailed breakdown of the Junior Operator Production role at Cipla’s Rangpo plant.
Job Title: Junior Operator Production
Division/Department: Production
Location: Rangpo, Sikkim, India
Job Purpose
The primary purpose of this role is to execute production operations in strict compliance with safety and Good Manufacturing Practices (GMP) requirements to achieve manufacturing targets during a shift.
Key Responsibilities & Accountabilities
The Junior Operator will be responsible for the following key areas:
- Efficient Production Execution:
- Operate machinery efficiently, without errors or deviations, following Standard Operating Procedures (SOPs).
- Perform all unit operations and processes as per the Batch Manufacturing Record (BMR).
- Optimize the use of available resources like manpower and materials to meet shift targets.
- Quality & Process Improvement:
- Maintain equipment and facility as per SOPs, ensuring audit readiness at all times.
- Identify and rectify deficiencies in the area or errors in documents.
- Suggest ideas to optimize processes, enhance production, and reduce waste.
- cGMP Documentation:
- Maintain accurate and timely online documentation, including BMR and supporting records.
- Ensure 100% data integrity by checking all documents before submission.
- Safety & Training:
- Adhere to all cGMP and safety guidelines personally and ensure compliance from workmen.
- Conduct training for workmen on equipment operation, safety, and housekeeping.
- Ensure proper usage of Personal Protective Equipment (PPE) and report any safety near-misses immediately.
Key Skills and Competencies
- Technical Knowledge: Understanding of pharmaceutical unit operations and machinery.
- Attention to Detail: Critical for maintaining GMP and error-free documentation.
- Problem-Solving: Ability to identify issues and suggest improvements.
- Teamwork & Communication: Essential for smooth inter-shift coordination and training.
Eligibility Criteria
- Education Qualification: Diploma in Pharmacy (D.Pharm) or Diploma in Mechanical Engineering.
- Work Experience: 0 to 2 years of experience in a manufacturing organization. Freshers from the pharmaceutical industry are encouraged to apply.
