What Jobs are available for Sun Pharma in Delhi?

We are looking for a highly skilled and experienced QA/QC Civil Engineer with a strong background in the construction of substations , overhead transmission lines (OHTL) , underground cable works , and building infrastructure . The ideal candidate should have SEC approval and be capable of enforcing quality standards, ensuring compliance, conducting inspections, managing documentation, and supporting continuous improvement in line with project requirements.

Candidates with prior Saudi or GCC experience strongly preferred

Key Responsibilities:

• Maintain and manage quality documentation, including system manuals, national/international standards, technical data sheets, ITPs, and client specifications.
• Monitor and inspect civil activities, from raw material acceptance through to final testing, commissioning, and handover.
• Develop and implement quality procedures, inspection checklists, and method statements related to civil works.
• Conduct root cause analysis and lead corrective/preventive actions for civil-related non-conformities.
• Ensure project quality requirements are met in compliance with PQP, ITPs, PTS, MOS, checklists, and applicable codes and standards.
• Perform internal quality audits to verify adherence to QMS requirements.
• Coordinate closely with project stakeholders including construction managers, project managers, vendors, third parties, and the TQM team.
• Provide technical guidance to the construction team for improvement in quality performance and compliance.
• Review and prepare project quality documents and ensure complete documentation (QA/QC dossiers) at project close-out.
• Monitor and report KPIs related to Quality Costs, NCRs, lessons learned, and trends in project performance indicators.
• Review project technical submittals to ensure alignment with quality and specification requirements prior to implementation.
• Maintain detailed QA/QC logs and reports, including NCR logs, proactive logs, calibration records, inspection logs, and lessons learned for reporting to the TQM department.
• Understand and interface across multi-disciplinary engineering functions and ensure all are reflected in QA/QC deliverables.

Minimum Qualifications & Experience:

• Bachelor’s Degree in Civil Engineering or equivalent.
• Minimum 8+ years of QA/QC experience in substation, building, and infrastructure projects , including OHTL and underground cable work .
• Experience with SEC or Aramco projects is mandatory or strongly preferred .
• Strong knowledge of civil quality control procedures, inspection techniques, and material verification methods.
• Familiarity with ISO 9001:2015 (QMS) standards. Certification as Internal Auditor or Lead Auditor is preferred.
• Proficient in interpreting civil engineering drawings, specifications, and technical standards.

Note: This job is located in KSA

• Developing and implementing robust quality control plans and procedures for all manufacturing processes.
• Leading and managing the quality control team, providing guidance, training, and performance evaluations.
• Establishing key performance indicators (KPIs) for quality and monitoring performance against targets.
• Conducting regular internal audits of manufacturing processes and quality systems to ensure compliance and identify areas for improvement.
• Analyzing quality data, identifying root causes of defects, and implementing corrective and preventive actions (CAPA).
• Collaborating with R&D, production, and engineering teams to ensure product design and process capabilities meet quality standards.
• Managing supplier quality, including audits and performance monitoring.
• Staying updated with industry best practices, new technologies, and regulatory changes related to quality management.
• Championing a quality-focused culture throughout the organization.
• Preparing detailed quality reports for senior management.
• Utilizing digital tools for remote team management, data analysis, and collaboration.

• Bachelor's degree in Engineering (Mechanical, Industrial, or Chemical) or a related field. Master's degree is a plus.
• Minimum of 7 years of experience in quality control and assurance within a manufacturing environment.
• Proven experience in developing and implementing Quality Management Systems (e.g., ISO 9001, Six Sigma, Lean Manufacturing).
• Strong understanding of statistical process control (SPC) and other quality tools.
• Excellent leadership, communication, and interpersonal skills, with the ability to manage a remote team effectively.
• Proficiency in quality management software and data analysis tools.
• Experience with remote collaboration platforms and tools.
• Strong analytical and problem-solving abilities.
• Ability to travel occasionally if required for specific audits or team meetings, though the role is primarily remote.
• Demonstrated ability to drive continuous improvement initiatives.

• Lead and manage the daily operations of the pharmaceutical Quality Control laboratory.
• Develop, validate, and implement analytical methods for testing raw materials, intermediates, and finished products according to pharmacopoeial and regulatory standards (e.g., USP, EP, IP).
• Supervise and train QC analysts, ensuring adherence to standard operating procedures (SOPs) and safety guidelines.
• Perform complex analytical testing using various instrumentation such as HPLC, GC, UV-Vis, FTIR, dissolution testers, and Karl Fischer titrators.
• Review and approve analytical data, batch records, and stability study reports.
• Investigate out-of-specification (OOS) results and deviations, determining root causes and implementing corrective and preventive actions (CAPAs).
• Ensure the proper calibration, maintenance, and qualification of laboratory equipment.
• Maintain laboratory compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
• Participate in regulatory inspections and internal audits.
• Collaborate with R&D, Production, and Quality Assurance departments to resolve quality issues and support product development.
• Contribute to the continuous improvement of QC processes and systems.
• Stay updated on the latest scientific advancements and regulatory guidelines in pharmaceutical quality control.

• Master's degree or Ph.D. in Pharmaceutical Sciences, Chemistry, or a related field.
• Minimum of 7-10 years of progressive experience in pharmaceutical Quality Control.
• Proven experience in leading and managing a QC laboratory team.
• Expertise in analytical method development, validation, and transfer.
• Hands-on experience with various analytical instruments and techniques relevant to pharmaceutical testing.
• Thorough understanding of GMP, GLP, and regulatory requirements.
• Strong knowledge of pharmacopoeias (USP, EP, IP).
• Excellent analytical, problem-solving, and decision-making skills.
• Strong leadership, communication, and interpersonal abilities.
• Proficiency in laboratory information management systems (LIMS) is a plus.
• Detail-oriented with a strong commitment to quality and accuracy.

• Supervise the daily operations of the quality control laboratory.
• Develop and implement QC testing procedures and protocols.
• Train and mentor QC technicians on testing methods and equipment operation.
• Conduct inspections of raw materials, in-process products, and finished goods.
• Analyze quality data and identify trends or deviations from standards.
• Investigate quality complaints and implement corrective and preventive actions (CAPA).
• Ensure compliance with GMP, HACCP, and other relevant quality standards.
• Maintain accurate records of all quality control activities.
• Collaborate with production and R&D teams to resolve quality issues.
• Manage laboratory equipment calibration and maintenance schedules.

• Bachelor's degree in Chemistry, Food Science, Microbiology, or a related scientific field.
• Minimum of 4 years of experience in quality control within the manufacturing sector, preferably consumer goods.
• Proven experience with quality management systems (e.g., ISO 9001).
• Strong knowledge of GMP and statistical process control (SPC).
• Excellent leadership, communication, and problem-solving skills.
• Proficiency in laboratory techniques and instrumentation.
• Ability to work effectively in a fast-paced manufacturing environment.
• Experience with regulatory compliance in the food or consumer goods industry.

• Develop, implement, and manage the company's quality control system.
• Oversee all incoming, in-process, and final product inspections and testing.
• Lead a team of quality control personnel, providing training and supervision.
• Analyze quality data and trends to identify root causes of defects and implement corrective actions.
• Ensure compliance with ISO 9001 standards and other relevant industry regulations.
• Collaborate with production and engineering teams to resolve quality issues and improve processes.
• Manage supplier quality and conduct audits of incoming materials.
• Maintain accurate quality records and documentation.
• Develop and deliver quality training programs for staff.
• Drive continuous improvement initiatives within the quality control department.

• Bachelor's degree in Engineering, Manufacturing Technology, or a related field.
• Minimum of 6 years of experience in quality control or quality assurance within a manufacturing setting.
• Proven experience in implementing and managing quality management systems (e.g., ISO 9001).
• Strong understanding of statistical process control (SPC) and quality tools.
• Experience with various inspection and testing techniques.
• Excellent leadership, team management, and problem-solving skills.
• Strong analytical and data interpretation abilities.
• Effective communication and interpersonal skills.
• Experience with calibration and metrology is a plus.
• Knowledge of Six Sigma or Lean Manufacturing principles is advantageous.

• Perform a variety of analytical tests on pharmaceutical raw materials, intermediates, and finished products.
• Operate, calibrate, and maintain laboratory instruments such as HPLC, GC, UV-Vis, FT-IR, and dissolution testers.
• Analyze test results, interpret data, and prepare accurate analytical reports.
• Ensure all testing is conducted in compliance with GMP, GLP, and relevant pharmacopoeial standards.
• Investigate and document any Out-of-Specification (OOS) results or deviations.
• Participate in method validation and transfer activities.
• Maintain laboratory inventory and ensure adequate stock of reagents and consumables.
• Assist in internal and external audits by providing necessary documentation and explanations.
• Train and mentor junior laboratory personnel.
• Contribute to process improvement initiatives to enhance laboratory efficiency and quality.

• Master's degree in Chemistry, Pharmaceutical Sciences, or a related field.
• Minimum of 5 years of experience in pharmaceutical quality control analysis.
• Extensive hands-on experience with analytical instruments (HPLC, GC are essential).
• Thorough knowledge of IP, BP, USP, and other relevant pharmacopoeias.
• Strong understanding of GMP and GLP principles.
• Excellent documentation, data interpretation, and problem-solving skills.
• Ability to work independently and as part of a team.
• Good communication skills.