B Pharma Job at Cipla – Junior Officer – Production Role – Apply Now

Role : Junior Officer – Production (77038)

Requisition : ID 77038

Location : Goa, India

Department : Manufacturing

Employment Type : Permanent

Job Purpose:

Monitor and execute the production activities in an area during the shift by maintaining cGMP and safety norms to achieve production targets


  • Execute production activities in a shift by managing available resources to achieve production target
  • Maintain standard process parameters as per BMRs and other supporting documents for achieving production target and maintaining quality
  • Prepare manufacturing records and update online documentation to meet production and cGMP requirements
  • Follow safe work processes and ensure safety appliances are utilised during production activities in shifts to create a safe working environment
  • Execute production activities in a shift by managing available resources to achieve production target

Education Qualification : Bachelor in Pharmacy

Relevant Work Experience : 2 years of experience in pharmaceutical manufacturing


  • Communication Skills (clarity of thought, comprehension)
  • Likely potential for growth
  • Job / Product / Technical Knowledge / Pharma domain knowledge
  • Presentation & Interpersonal skills (If applicable)
  • Managerial or People Management skills
  • Safety awareness (If applicable)
  • Relevance of Previous Experience
  • Comprehension, Analytical & Problem solving abilities
  • Productivity & Result Orientation (If applicable)
  • Attitude
  • Qualification fitment
  • Sales drive (If applicable)
  • Personality traits (Individualistic / Team player, Out spoken, Maturity level etc.)


Explore Rasayanika for the Latest B Pharma Job at Cipla

Here are some interview questions and suggested answers for the role of Junior Officer – Production at Cipla:

  1. Can you briefly explain your understanding of cGMP (Current Good Manufacturing Practices) and its importance in pharmaceutical manufacturing?Answer: cGMP stands for Current Good Manufacturing Practices, and it is a set of regulations and guidelines enforced by regulatory authorities to ensure the quality, safety, and consistency of pharmaceutical products. In pharmaceutical manufacturing, adherence to cGMP is critical because it helps maintain product quality, reduces the risk of contamination, and ensures that pharmaceuticals meet regulatory standards. As a Junior Officer in Production, I understand that following cGMP is essential to achieve production targets while ensuring the safety and efficacy of the products we manufacture.
  2. How do you plan to manage available resources effectively to achieve production targets during your shift?                                                                    Answer: To effectively manage available resources for achieving production targets, I would start by assessing the production schedule and the number of personnel and equipment available during the shift. I would prioritize tasks, assign responsibilities, and ensure that everyone understands their roles. Regular communication and coordination with team members would be essential to keep the production process on track. Additionally, I would closely monitor progress, making adjustments as needed to optimize resource utilization and meet production goals efficiently.
  3. Could you provide an example of a situation where you had to strictly adhere to standard process parameters to maintain product quality? How did you handle it?                                                                                                                              Answer: In a previous role, I encountered a situation where a deviation from standard process parameters could have compromised product quality. It was essential to maintain the integrity of the process to meet production targets without compromising quality. I immediately alerted the relevant personnel, including supervisors and quality control teams, and documented the deviation. Together, we analyzed the situation, identified the root cause, and took corrective actions to bring the process back within the specified parameters. This experience highlighted the importance of strict adherence to process parameters to ensure product quality.
  4. How do you ensure a safe working environment during production activities, and what safety measures do you consider essential?                                            Answer: Ensuring a safe working environment during production activities is a top priority. I make sure that safety appliances, such as personal protective equipment (PPE), are readily available and that all team members are trained in their proper use. Regular safety briefings and reminders about safe work practices are essential. I also encourage a culture of reporting near misses or safety concerns to address issues promptly. Safety measures I consider essential include proper equipment maintenance, hazard identification, emergency response plans, and compliance with safety regulations and guidelines.
  5. Can you describe a situation where you had to deal with a challenging problem or unexpected issue during a production shift? How did you approach and resolve it?                                                                                                                Answer: During a production shift, I once encountered a sudden equipment malfunction that threatened to disrupt the entire production process. To address this issue, I immediately halted production, ensured the safety of the team, and notified maintenance and engineering personnel. While they worked on repairing the equipment, I organized a temporary work plan to minimize downtime. Once the equipment was fixed, we resumed production, closely monitored progress, and adjusted the schedule to meet the production target by working extra hours if necessary. This experience taught me the importance of quick problem-solving, effective communication, and adaptability in a production environment.



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