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Quality Assurance MANAGER ( PHARMA)

We are looking for a highly skilled Quality Assurance Manager to lead and manage the Quality Assurance function in our Analytical Testing Laboratory . The ideal candidate will have extensive experience in handling critical audits, including USFDA , CAPA , GLP , WHO , NABL , and internal audits , and will play a key role in ensuring compliance with pharmaceutical regulatory requirements and industry best practices. This role demands expertise in maintaining robust quality systems, managing audits, and driving corrective and preventive actions (CAPA) to ensure the lab operates to the highest quality standards.

Key Responsibilities :

Quality System Management :

• Develop, implement, and maintain the Quality Management System (QMS) to comply with regulatory requirements (USFDA, WHO, NABL, GLP) and industry standards (ISO, ICH).
• Oversee the preparation and management of documentation including standard operating procedures (SOPs), batch records, test methods, and analytical reports to ensure compliance with regulatory standards.
• Implement risk management strategies to identify, assess, and mitigate quality-related risks within the testing laboratory.

Audit and Compliance Oversight :

• Lead and manage USFDA , WHO , NABL , GLP , and other regulatory audits, ensuring full preparedness and compliance.
• Coordinate and conduct internal audits to assess the effectiveness of the laboratory's quality system, identifying areas for improvement and ensuring alignment with company policies and regulatory standards.
• Ensure timely and effective resolution of audit findings by developing and executing Corrective and Preventive Actions (CAPA) in accordance with regulatory guidelines and company practices.
• Serve as the primary point of contact during external regulatory audits, inspections, and accreditation assessments.
• Collaborate with regulatory bodies and external stakeholders to ensure continuous improvement in quality and compliance.

CAPA Management :

• Lead the CAPA (Corrective and Preventive Action) process, ensuring thorough investigation and documentation of non-conformances, root cause analysis, and implementation of effective corrective and preventive actions.
• Track CAPA effectiveness and ensure corrective actions are sustainably integrated into the laboratory processes to prevent recurrence of issues.

Team Leadership & Training :

• Supervise, mentor, and train laboratory personnel on quality standards, testing protocols, regulatory compliance, and internal procedures.
• Conduct regular training sessions to ensure team competency in GMP, GLP, and audit readiness.
• Promote a culture of continuous quality improvement across the lab, encouraging proactive problem-solving and adherence to quality systems.

Regulatory Reporting & Documentation :

• Ensure accurate and timely reporting of analytical results, audit outcomes, CAPA documentation, and other quality metrics.
• Ensure all records are properly maintained to meet regulatory requirements, internal standards, and audit readiness.
• Prepare quality reports and metrics for senior management and regulatory submissions.

Testing Oversight & Review :

• Oversee the review and approval of analytical test results, ensuring compliance with specifications, regulatory guidelines, and SOPs.
• Investigate any discrepancies or out-of-specification (OOS) results and drive the resolution through root cause analysis and corrective actions.

Continuous Improvement & Risk Management :

• Identify and implement improvements to quality management processes, ensuring efficiency, compliance, and reliability of testing systems.
• Monitor emerging industry trends, regulations, and best practices, ensuring the laboratory’s practices remain at the forefront of industry standards.

Qualifications :

• Education : Bachelor's or Master’s degree in Chemistry, Biology, Pharmaceutical Sciences, or a related field. Certifications in Quality Management (e.g., Six Sigma, ISO 9001, or equivalent) or regulatory affairs are a plus.

Experience :

• Minimum of 15 years of experience in a Quality Management role within a pharmaceutical testing laboratory.
• Proven experience in managing and handling audits such as USFDA , WHO , NABL , GLP , CAPA , and internal audits .
• In-depth knowledge of regulatory standards and guidelines including GMP , GLP , FDA , EMA , and ICH .
• Experience leading CAPA investigations, root cause analysis, and implementing corrective/preventive measures.

Skills :

• Strong leadership skills with the ability to mentor and lead teams to achieve compliance and quality objectives.
• Excellent communication and interpersonal skills to interact effectively with regulatory authorities, senior management, and cross-functional teams.
• Detail-oriented with strong problem-solving skills and the ability to assess and mitigate risks effectively.
• Familiarity with laboratory instrumentation, analytical techniques, and pharmaceutical testing standards.
• Proficient in audit preparation, documentation review, and regulatory reporting.

How to Apply

Interested candidates may contact us or share their updated resume at the following email addresses:

/

Contact:

While applying, please mention “Application for QA Manager – Pharma Testing Laboratory” in the subject line.

Kindly include the following details along with your resume:

• Total Experience:
• Current CTC:
• Expected CTC:
• Notice Period:
• Current Location :
• Are you comfortable for relocation to Kolkata?

DESIGNATION

Technical Assistant for Forging shop

OVERVIEW

An opportunity for a mechanical engineer to supervise the forging department of a gas cylinder valve manufacturing company.

EDUCATIONAL QUALIFICATIONS

Bachelor’s degree or Diploma in Mechanical or Production Engineering

COMPETENCY

Knowledge and working experience on the followings

1. Knowledge on Forging process, forging equipment and Die design
2. Competency in engineering drawings

RESPONSIBILITIES

1. Supervising Forging Operation adherence to production and quality standards.
2. Monitoring forging set up, die preparation and forging parameters
3. Lead and guide forging operators
4. Enforce safety protocols

Perks and Benefits:

Commensurate with experience

Quality Assurance MANAGER-Pharma or Food /TIC Industry

We are looking for a highly skilled Quality Assurance Manager to lead and manage the Quality Assurance function in our Analytical Testing Laboratory . The ideal candidate will have extensive experience in handling critical audits, including USFDA , CAPA , GLP , WHO , NABL , and internal audits , and will play a key role in ensuring compliance with pharmaceutical regulatory requirements and industry best practices. This role demands expertise in maintaining robust quality systems, managing audits, and driving corrective and preventive actions (CAPA) to ensure the lab operates to the highest quality standards.

Key Responsibilities :

Quality System Management :

• Develop, implement, and maintain the Quality Management System (QMS) to comply with regulatory requirements (USFDA, WHO, NABL, GLP) and industry standards (ISO, ICH).
• Oversee the preparation and management of documentation including standard operating procedures (SOPs), batch records, test methods, and analytical reports to ensure compliance with regulatory standards.
• Implement risk management strategies to identify, assess, and mitigate quality-related risks within the testing laboratory.

Audit and Compliance Oversight :

• Lead and manage USFDA , WHO , NABL , GLP , and other regulatory audits, ensuring full preparedness and compliance.
• Coordinate and conduct internal audits to assess the effectiveness of the laboratory's quality system, identifying areas for improvement and ensuring alignment with company policies and regulatory standards.
• Ensure timely and effective resolution of audit findings by developing and executing Corrective and Preventive Actions (CAPA) in accordance with regulatory guidelines and company practices.
• Serve as the primary point of contact during external regulatory audits, inspections, and accreditation assessments.
• Collaborate with regulatory bodies and external stakeholders to ensure continuous improvement in quality and compliance.

CAPA Management :

• Lead the CAPA (Corrective and Preventive Action) process, ensuring thorough investigation and documentation of non-conformances, root cause analysis, and implementation of effective corrective and preventive actions.
• Track CAPA effectiveness and ensure corrective actions are sustainably integrated into the laboratory processes to prevent recurrence of issues.

Team Leadership & Training :

• Supervise, mentor, and train laboratory personnel on quality standards, testing protocols, regulatory compliance, and internal procedures.
• Conduct regular training sessions to ensure team competency in GMP, GLP, and audit readiness.
• Promote a culture of continuous quality improvement across the lab, encouraging proactive problem-solving and adherence to quality systems.

Regulatory Reporting & Documentation :

• Ensure accurate and timely reporting of analytical results, audit outcomes, CAPA documentation, and other quality metrics.
• Ensure all records are properly maintained to meet regulatory requirements, internal standards, and audit readiness.
• Prepare quality reports and metrics for senior management and regulatory submissions.

Testing Oversight & Review :

• Oversee the review and approval of analytical test results, ensuring compliance with specifications, regulatory guidelines, and SOPs.
• Investigate any discrepancies or out-of-specification (OOS) results and drive the resolution through root cause analysis and corrective actions.

Continuous Improvement & Risk Management :

• Identify and implement improvements to quality management processes, ensuring efficiency, compliance, and reliability of testing systems.
• Monitor emerging industry trends, regulations, and best practices, ensuring the laboratory’s practices remain at the forefront of industry standards.

Qualifications :

• Education : Bachelor's or Master’s degree in Chemistry, Biology, Pharmaceutical Sciences, or a related field. Certifications in Quality Management (e.g., Six Sigma, ISO 9001, or equivalent) or regulatory affairs are a plus.

Experience :

• Minimum of 12+ years of experience in a Quality Management role within a pharmaceutical testing laboratory.
• Proven experience in managing and handling audits such as USFDA , WHO , NABL , GLP , CAPA , and internal audits .
• In-depth knowledge of regulatory standards and guidelines including GMP , GLP , FDA , EMA , and ICH .
• Experience leading CAPA investigations, root cause analysis, and implementing corrective/preventive measures.

Skills :

• Strong leadership skills with the ability to mentor and lead teams to achieve compliance and quality objectives.
• Excellent communication and interpersonal skills to interact effectively with regulatory authorities, senior management, and cross-functional teams.
• Detail-oriented with strong problem-solving skills and the ability to assess and mitigate risks effectively.
• Familiarity with laboratory instrumentation, analytical techniques, and pharmaceutical testing standards.
• Proficient in audit preparation, documentation review, and regulatory reporting.

How to Apply

Interested candidates may contact us or share their updated resume at the following email addresses:

Contact: +

While applying, please mention “Application for QA Manager-Kolkata” in the subject line.

Kindly include the following details along with your resume:

• Total Experience:
• Relevant Experience in QA:
• Current CTC:
• Expected CTC:
• Notice Period:
• Current Location:
• Are you comfortable for relocation to Kolkata?

We're Hiring | Operations Manager

• 
  Location: Kolkat
• aProcess: Domestic Banking Proces

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Key Responsibilitie

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• PIsLead, mentor, and develop Team Leaders and frontline te
• amsMonitor productivity, quality, customer satisfaction, and process complia
• nceManage client expectations and stakeholder relationsh
• ipsIdentify improvement opportunities and implement process enhanceme
• ntsEnsure adherence to SLAs, operational metrics, and organizational polic

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Preferred Candidate Prof

• ile:
  Experience managing Domestic Banking/BFSI operations in a BPO enviro
• nmentStrong people management and stakeholder management s
• killsProven track record of delivering operational KPIs and business out
• comesExcellent communication, analytical, and problem-solving abil
• itiesGraduation is mand

• Develop, implement, and maintain quality assurance policies and procedures.
• Conduct internal audits of manufacturing processes and systems to ensure compliance.
• Analyze quality data, identify trends, and recommend corrective and preventive actions (CAPA).
• Collaborate with production, engineering, and R&D teams to resolve quality issues.
• Monitor product quality throughout the manufacturing lifecycle.
• Ensure compliance with relevant industry standards and regulations.
• Prepare quality reports and present findings to management.
• Participate in supplier quality assessments.
• Assist in the training of personnel on quality standards and procedures.
• Stay updated on industry quality trends and best practices.
• Manage documentation related to quality assurance activities.

• Bachelor's degree in Engineering, Science, or a related field.
• Minimum of 3 years of experience in Quality Assurance within a manufacturing environment.
• Solid understanding of Quality Management Systems (QMS), such as ISO 9001.
• Experience with statistical analysis tools and quality control techniques.
• Proficiency in data analysis and report generation.
• Excellent problem-solving and analytical skills.
• Strong communication and interpersonal skills, with the ability to work effectively with cross-functional teams.
• Detail-oriented and highly organized.
• Ability to work independently and manage multiple priorities.
• Familiarity with root cause analysis methodologies.

• Develop detailed daily, weekly, and monthly production schedules based on demand forecasts, sales orders, and inventory levels.
• Coordinate with sales, procurement, and production teams to ensure timely availability of raw materials and finished goods.
• Monitor production progress against the schedule and make necessary adjustments to address any deviations or potential delays.
• Optimize production sequences to maximize efficiency, minimize changeover times, and reduce waste.
• Maintain accurate production planning records and generate reports on production performance, forecast accuracy, and inventory status.
• Collaborate with the procurement team to ensure timely ordering of raw materials and packaging components.
• Identify potential production bottlenecks and work with relevant teams to implement solutions.
• Participate in demand planning meetings and provide input on production capacity and constraints.
• Ensure compliance with all company policies, quality standards, and safety regulations.
• Contribute to continuous improvement initiatives within the production planning and control function.

• Bachelor's degree in Supply Chain Management, Industrial Engineering, Business Administration, or a related field.
• Minimum of 3 years of experience in production planning or scheduling, preferably within the FMCG or consumer goods industry.
• Proficiency in using ERP systems (e.g., SAP, Oracle) and advanced Excel for planning and analysis.
• Strong understanding of inventory management principles, demand forecasting, and production scheduling techniques.
• Excellent analytical, problem-solving, and organizational skills.
• Good communication and interpersonal skills, with the ability to collaborate effectively across departments.
• Ability to work under pressure and meet tight deadlines.
• Detail-oriented with a commitment to accuracy.
• Experience with specific planning software (e.g., APS) is a plus.
• Proficiency in English; knowledge of Bengali is advantageous.

• Competitive salary and performance-based bonus opportunities.
• Comprehensive health insurance coverage.
• Company-sponsored retirement savings plan.
• Opportunities for professional development and training in supply chain management.
• A hybrid work model offering flexibility.
• Access to modern manufacturing facilities and planning tools in Kolkata .
• A supportive and team-oriented work environment.
• Paid time off and statutory benefits.

Our client, a leading player in the industrial manufacturing sector, is seeking a skilled Cost Accountant to join their finance team in Kolkata, West Bengal, IN . This role is essential for accurately tracking, analyzing, and reporting on production costs, ensuring profitability and efficiency in manufacturing operations. The ideal candidate will have a strong understanding of cost accounting principles, experience with manufacturing environments, and excellent analytical capabilities. This position requires on-site presence in Kolkata to work closely with production and finance teams. You will play a key part in optimizing cost management strategies and contributing to the financial success of our client's significant operations in the region.

• Develop and maintain cost accounting systems and standards.
• Analyze manufacturing costs, including direct materials, direct labor, and overhead.
• Prepare detailed cost reports, analyzing variances between standard and actual costs.
• Assist in the development of annual budgets and forecasts for manufacturing operations.
• Perform product costing, including job costing, process costing, and standard costing methods.
• Collaborate with the production team to identify opportunities for cost reduction and efficiency improvements.
• Participate in inventory valuation and control processes.
• Support internal and external audits related to cost accounting.
• Analyze the profitability of new products and projects.
• Ensure the accuracy and integrity of cost data used for decision-making.

• Bachelor's degree in Accounting, Finance, or a related field. Professional certifications (e.g., CMA, CA) are highly advantageous.
• 3-5 years of experience in cost accounting, preferably within a manufacturing environment.
• Solid understanding of cost accounting principles, methods, and systems.
• Proficiency in Microsoft Excel and experience with ERP systems (e.g., SAP, Oracle) is required.
• Strong analytical, problem-solving, and quantitative skills.
• Excellent attention to detail and accuracy.
• Good communication and interpersonal skills to work effectively with cross-functional teams.
• Ability to work independently and manage multiple tasks.
• Knowledge of inventory management and standard costing is essential.
• Must be based in or willing to relocate to Kolkata, West Bengal, IN .

Our client offers a competitive salary, comprehensive health benefits, and retirement savings plans. Employees benefit from paid time off and opportunities for professional development and training relevant to the manufacturing and accounting sectors. You will work in a structured environment with clear career progression pathways. The company culture emphasizes teamwork and continuous improvement, providing a supportive atmosphere for employees. This role offers a great opportunity to deepen your expertise in cost accounting within a stable and growing industry in Kolkata .