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2 - 4 years

3 - 6 Lacs

Pune

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Preferred candidate profile Looking for a candidate with 2 to 4 years of work experience as QC analyst /AQA reviewer in reputed pharma companies. Should have Knowledge of handling/analytical data review of HPLC, FTIR, UV spectrophotometer, KF Autotitrator, Dissolution apparatus. Have Basic knowledge of CGMP, GDP, Data integrity. Should have Basic knowledge of OOS (Out of specification), OOT (Out of rend), OOC (Out of calibration).

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2 - 7 years

3 - 5 Lacs

Jadcherla

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Naukri logo

** VEDIO CALL INTERVIEW ** Roles and Responsibilities Perform CSV (Computer System Validation) tasks for new systems implementation. Ensure compliance with GMP regulations during software validation processes. Conduct software validation activities according to GAMP guidelines. Key Skills : Good Exposure on CSV,PLC, Software Validation in pharmaceutical industry, SAP,LIMS Qualification, TRIMS,NICHELONS,HVACMS/BIMS,EMPOWER,ELMS. ** Preferred male candidate only. Interested candidate can share their resumes below mail id: sonali.n@hetero.com/9100408534. Job Location : Unit V, Hetero Labs limited, Jadcherla, Hyderabad.

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2 - 7 years

1 - 3 Lacs

Palghar

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Seeking a IPQA Executive to ensure skincare products meet regulatory, safety, and quality standards. Work closely with manufacturing, R&D, and QC teams. Requirement: 2+ years of QA experience, preferably in cosmetics or pharma manufacturing. Required Candidate profile Skincare manufacturing & QC expertise Knowledge of FDA, GMP, ISO regulations Attention to detail & procedural compliance Strong analytical, problem-solving & com skills Ability to work with GMP proces

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3 - 6 years

10 - 20 Lacs

Hyderabad

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Job summary We are seeking an individual to perform the Preventive Maintenance and Break Down Maintenance of Analytical Equipment's present in Quality Control . Roles & Responsibilities To perform the preventive and breakdown maintenance of analytical equipment's or Instruments like HPLC, UPLC, GC-HSS, Dissolution Test Appratus, Titrators, FTIR, UV-VIS Spectrophotometer,.... To update the preventive maintenance plan whenever addition of instruments or match the calibration schedule. To prepare the task lists for all analytical equipment's and update them in SAP. To perform the preventive maintenance as per the PM schedule. To make sure of closing the generated PM orders in SAP after performing the PM. To ensure that the instruments / equipment are used with utmost care and as instructed in the relevant SOP. To attend the breakdown's and close notification or order of the instrument /equipment after the Completion of breakdown maintenance. To be a part of investigating the incidence related to instrument Responsible for the maintaining of required spares for all instruments in warehouse. To get the quotations for the required spares and services for the maintenance of the instruments. To generate the purchase requisitions for the required spares and services. To perform the PM in the given frequency within the given period. Adhering to the allotted shift schedule with right time. If any changes prior permission shall be taken from Group leader. Qualification Educational qualification: An B.Tech. or any Degree in Instrumentation, Mechanical, Electronics, Electrical. Required Work experience : 3 to 6 years Skills & attributes: Technical Skills • Hands-on Experience on maintenance of Waters HPLC (Arc, e2695), Agilent HPLC (1200, 1260 Infinity), Agilent GC-HSS (7890, 8890, 7897, G1888), Dissolution Testers (Electrolab, Sotax), Metrohm Titrators. • Working experience in a cGMP (Current Good Manufacturing Practice) environment, with a special emphasis on Good Documentation Practices (GDP). • Basic knowledge in SAP usage Behavioural skills • Prioritizes effective communication and demonstrates a performance-oriented mind-set. • Effective verbal and written communication skills. • Performance-oriented approach, consistently striving for high standards. • Demonstrates flexibility in working shifts and a clear understanding of team dynamics. Additional Information About the Department Quality Control Formulations For more details, please visit our career website at https://careers.drreddys.com/#!/

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Exploring GMP Jobs in India

The good manufacturing practice (GMP) job market in India is thriving with numerous opportunities for job seekers looking to build a career in this field. GMP professionals play a crucial role in ensuring that pharmaceutical, food, and other industries comply with quality standards and regulations to produce safe products for consumers.

Top Hiring Locations in India

  1. Mumbai
  2. Bangalore
  3. Hyderabad
  4. Delhi
  5. Pune

These cities are known for their strong presence in the pharmaceutical and manufacturing industries, making them hotspots for GMP job opportunities.

Average Salary Range

The salary range for GMP professionals in India varies based on experience and location. Entry-level positions can expect to earn around INR 3-5 lakhs per year, while experienced professionals can command salaries ranging from INR 8-15 lakhs per year.

Career Path

A typical career path in the GMP field may start as a Quality Control Officer, progress to Quality Assurance Manager, and eventually lead to roles such as Quality Head or Compliance Director. Continuous learning and certifications can further accelerate career growth in this domain.

Related Skills

In addition to expertise in GMP, professionals in this field are often expected to possess skills in regulatory compliance, quality management systems, risk assessment, and audit processes.

Interview Questions

  • What is GMP and why is it important in manufacturing? (basic)
  • Can you explain the difference between GMP and GDP (Good Distribution Practice)? (medium)
  • How do you ensure compliance with GMP regulations in a manufacturing facility? (medium)
  • What are the common challenges faced in maintaining GMP standards and how do you address them? (medium)
  • Describe a situation where you had to handle a GMP violation. How did you resolve it? (advanced)
  • How do you stay updated with the latest developments in GMP regulations? (basic)
  • What role does documentation play in GMP compliance? (basic)
  • How do you conduct risk assessments in the context of GMP? (medium)
  • Can you walk us through your experience with GMP audits? (medium)
  • How do you handle deviations from GMP standards in a production process? (advanced)
  • What steps would you take to implement GMP in a new manufacturing facility? (medium)
  • How do you ensure that all employees in a manufacturing facility are trained on GMP requirements? (basic)
  • Describe a successful GMP improvement project that you led. (advanced)
  • How do you prioritize tasks to ensure GMP compliance while meeting production deadlines? (medium)
  • What measures do you take to prevent cross-contamination in a manufacturing environment? (medium)
  • How do you communicate GMP requirements to different stakeholders within an organization? (basic)
  • Can you provide an example of a GMP non-conformance and how you addressed it? (advanced)
  • How do you handle changes in GMP regulations and incorporate them into existing processes? (medium)
  • What role does technology play in ensuring GMP compliance? (basic)
  • How do you ensure that suppliers and vendors adhere to GMP standards in the supply chain? (medium)
  • Describe a situation where you had to make a difficult decision to maintain GMP compliance. (advanced)
  • How do you conduct root cause analysis for GMP deviations? (medium)
  • What strategies do you use to create a culture of quality and compliance in an organization? (medium)
  • How do you assess the effectiveness of GMP training programs for employees? (medium)
  • Can you provide examples of key performance indicators (KPIs) that you use to measure GMP compliance? (advanced)

Closing Remark

As you explore GMP job opportunities in India, remember to showcase your expertise, experience, and readiness to adapt to the evolving regulatory landscape. By preparing thoroughly and demonstrating your commitment to quality and compliance, you can position yourself as a valuable asset in this dynamic field. Good luck with your job search!

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