GMP Jobs

Job Duties & ResponsibilitiesSr. No. Job Duties & Responsibilities1 Perform testing of Raw Materials, Finished Goods, and In-Process Materials and report analytical results accurately.2 Handle and operate analytical instruments such as HPLC, UPLC, GC, ICP, DSC, XRD, and PSA.3 Carry out calibration of analytical instruments as per the master calibration schedule.4 Investigate analytical errors/deviations, identify root causes, and implement corrective and preventive actions (CAPA).5 Prepare laboratory SOPs, analytical study reports, and related technical documentation.6 Execute method validation activities and prepare validation protocols and reports.7 Review analytical chemistry testing records for raw materials, stability samples, and finished products for compliance and accuracy.8 Prepare and review specifications, methods of analysis, and analytical development reports.9 Ensure compliance with quality systems, laboratory procedures, and regulatory guidelines.10 Discuss daily work plans with supervisors/managers and mentor junior laboratory personnel.11 Participate in project meetings and prepare weekly and monthly progress reports for management review.12 Perform routine laboratory activities including equipment maintenance, chemical inventory management, and laboratory housekeeping.13 Maintain strict IP confidentiality and comply with all related data privacy and company policies.

We are looking for a Granulation Operator to join our team in Sanand, Ahmedabad. In this role, you will be responsible for operating and maintaining granulation equipment to support the manufacturing process.As a Granulation Operator, your key responsibilities will include:1. **Operating Equipment**: You will operate granulation machines according to specified procedures to ensure high-quality output.2. **Monitoring Processes**: You will monitor the granulation process to detect any irregularities, making adjustments as necessary to maintain production standards.3. **Quality Control**: You will perform routine inspections and tests on granulated materials to ensure they meet quality specifications.4. **Cleaning and Maintenance**: You will be responsible for cleaning the machines and work areas, performing basic maintenance to ensure optimal functioning of the equipment.5. **Record Keeping**: You will maintain accurate records of production data, equipment performance, and any issues encountered during the process.To be successful in this role, you should have a background in mechanical or production processes, preferably with 1 to 3 years of experience. An I.T.I. certification is required. You must exhibit attention to detail, strong problem-solving skills, and a commitment to safety protocols. Excellent communication skills are also essential for collaborating with team members and reporting to supervisors. Your ability to work effectively in a fast-paced environment will be important for meeting production targets.

Designation :- IPQA Officer-Quality AssuranceExperience:- 1 Years To 3 Years Injectable Background Mandatory Salary:- As Per InterviewGender:- MaleJob Location:- Boisar, Maharashtra Industry:- Manufacturing Company

JD - Sr. Manager/ Chief ManagerLocation: Gonde, NashikExperience: 12-15 Years of experience in similar type of industry, Pharmaceutical or Perfume glass Bottle Manufacturing industryQualification: B.E/ B.Tech, Graduate from science background with MBA from reputed university.Role & Responsibilities Review performance against operating plans and approve necessary improvements or corrective actions. Production Planning, Scheduling &Control. Oversee the entire production cycle, from raw material management to finished goods. Enhance in the targeted percentage of glass-to-glass yield & OEE over the last year. Minimize the Production losses, monitor yield, Improvement projects and ensure adherence to established production stan monitor Sops, and best practices. Review and approve departmental budgets, ensuring effective control of spending. Optimize labor, material utilization, and engineering efficiency. Ensure availability and maintenance of required production resources and equipment. Develop, implement, and maintain reporting systems related to production performance and metrics. Provide timely and accurate reports on production activities, deviations, and achievements. Ensure strict compliance with GMP, safety regulations, and good housekeeping standards. Monitor adherence to all company policies, procedures, and regulatory requirements. Drive a safety-focused culture across the production team. Improve product quality and quantity within planned schedule while maintaining cost. Define duties, responsibilities, and accountability for all direct subordinatesMaintain effective communication within the department and with cross-functional stakeholders. Support the implementation of manufacturing and organizational plans aligned with the Operations Master Plan. Collaborate effectively with internal managers and external stakeholders to meet production goals. Lead continuous improvement initiatives to enhance productivity, reduce waste, and improve operational efficiency Perform additional duties as assigned with flexibility and willingness.Important Competencies Production Planning Execution Implementation of TPM & GMP lean manufacturing implementation by using of TPM Kaizen 5S Project ManagementKey Skills Strategic Production Planning SAP- S 4 HANA Team Management Proficient in Excel Time Management & analytical skillsProcess Knowledge

We are seeking dedicated API Plant Operators for our facility in Nandesari GIDC, Vadodara. The ideal candidates will support manufacturing operations, ensuring strict adherence to GMP and SOP guidelines. This full-time position involves operating various equipment, monitoring process parameters, and maintaining accurate documentation. It's an excellent opportunity for junior and trainee operators, as well as freshers with relevant qualifications. Join our team to kickstart a rewarding career in the API and pharmaceutical industry

Job Title: Quality Control Executive / InspectorLocation: Ahmedabad , ChangodarExperience: 12 years of quality control experience in manufacturing, pharma, or medical devices.Job Summary:The Quality Control Executive/Inspector ensures that raw materials, in-process items, and finished products meet defined quality standards and regulatory requirements. The role involves inspection, testing, documentation, and collaboration with production and quality teams to maintain product quality and compliance.Key Responsibilities:Inspect raw materials, in-process products, and finished goods for quality compliance.Perform visual, dimensional, and functional checks using inspection tools.Conduct required product tests and analyze results against specifications.Identify defects, deviations, and non-conformities and report findings.Maintain accurate inspection and test documentation.Support quality audits and ensure compliance with ISO, GMP, and internal standards.Collaborate with production and QA teams to resolve quality issues and drive improvements.Qualifications & Skills:Bachelors degree in Quality, Engineering, Life Sciences, or related field.Knowledge of ISO/GMP standards.Strong attention to detail, analytical skills, and problem-solving ability.Proficiency with inspection tools (calipers, micrometers, gauges).

Hiring Alert: ISO Coordinator (Manufacturing Industry Nagpur)Location: Nagpur, MaharashtraDepartment: Quality / OperationsExperience: 25 yearsQualification: Bachelors degree in Engineering, Business, or related fieldKey Responsibilities:A) ISO CoordinationDevelop, implement, and monitor Quality Management Systems (QMS).Maintain documentation and records as per ISO 9001 standards.Coordinate and support internal & external audits for ISO compliance.Conduct employee training on ISO procedures and corrective actions.Manage supplier audits and maintain approved vendor lists.B) MIS Data Creation & ManagementPrepare and maintain daily, weekly & monthly MIS reports.Build dashboards and performance tracking tools (Google Sheets / Excel).Analyze shop floor KPIs and drive process improvements.Automate repetitive reporting tasks to enhance accuracy & efficiency.Present visual reports and insights to management teams.C) Shop Floor CoordinationCollaborate with Production & Quality teams to capture real-time data.Monitor Plan vs Actual status and identify process bottlenecks.Track dispatch and monthly revenue reports.Required Skills:Hands-on experience with ISO standards & audit process.Certification in ISO 9001 / Quality Management Systems preferred.Advanced Excel / Google Sheets skills (Pivot, VLOOKUP, automation).Familiarity with Google Data Studio or Power BI is an advantage.Strong analytical, coordination, and communication abilities.Salary: Based on experience & interviewJoining: Immediate preferred

Engineer (Mechanical) ISO & GMP DocumentationHalol, Gujarat Full-time On-siteAbout the Role:We are looking for a Mechanical Engineer with experience in technical documentation related to ISO and GMP standards. The role involves ensuring compliance, maintaining records, and supporting plant operations with a strong focus on safety and process improvements.Key Responsibilities: Prepare, review, and maintain documentation as per ISO & GMP requirements. Support validation and qualification activities of mechanical systems. Assist in audits, CAPA implementation, and internal quality compliance. Work closely with cross-functional teams for equipment installation, calibration, and preventive maintenance. Ensure all maintenance and modification activities are carried out safely and as per SOPs.Required Skills & Qualifications: Diploma / B.E. / B.Tech in Mechanical Engineering. 2-5 years of experience in documentation related to ISO/GMP standards (preferably in process or manufacturing industries). Strong understanding of technical drawings, SOPs, and maintenance procedures. Excellent communication and documentation skills.Why Join Us: Be part of a process-driven and quality-focused engineering team. Exposure to compliance and validation systems in a growing organization. Opportunity for continuous learning and professional development.

Candidate should be aware about Analytical instruments, Chemical testing, Knowledge of GMP & ISO documentation.

Prepare daily and weekly production schedules in coordination with production, QA/QC, and store departments. Monitor production progress and adjust plans as per actual output or delays. Coordinate with the stores and purchase team to ensure timely availability of raw materials and packaging materials. Track material consumption and prepare usage reports for RM and PM. Assist in maintaining inventory levels and raise requirements in advance to avoid line stoppage. Communicate with the quality department to plan batches as per sampling/testing timelines. Ensure proper documentation of batch planning, material requisitions, and issuance records. Actively participate in shop floor planning and line allocation based on machine availability. Support in capacity planning, equipment loading, and manpower forecasting. Work closely with ERP/MRP systems for production and inventory planning entries.

Key Responsibilities:Implement and monitor QA systems (as per GMP/ISO/FDA guidelines).Conduct internal audits and support external audits (regulatory & client).Review and approve SOPs, batch records, and quality documents.Investigate and document deviations, CAPA, OOS, and change controls.Coordinate with production, QC, and regulatory teams for compliance.Ensure training and qualification of QA team members.Maintain records and documentation per regulatory standards.

Below JD Details for Junior Position:1. Experience in API / Intermediates manufacturing company 2. Working as per SOP and follow the safety protocols3. Working experience in GMP environment4. Maintaining Documentation / BMRBelow JD Details for Senior Position: Manufacturing activities as per production plan for API / Intermediates Production as per GMP & SOP Review BMR Ensure safety and other precautions during plant and RM handling Ensure quality of products as per specification Handling of manpower in shifts

We are looking for an experienced and dynamic General Manager to lead our plant operations at Manhalli Village, Bidar. The ideal candidate will bring strong leadership, technical expertise, and operational management experience in the Chemical or Pharmaceutical manufacturing sector to drive productivity, safety, and compliance.Key Responsibilities:Lead overall plant operations including production, quality, maintenance, and safety.Develop and implement strategies to optimize manufacturing efficiency, reduce costs, and enhance product quality.Ensure compliance with regulatory and statutory requirements (GMP, ISO, EHS, etc.).Oversee resource planning, budgeting, and team management.Foster a culture of continuous improvement and operational excellence.Coordinate with R&D, supply chain, and quality assurance departments to meet production targets.Monitor key performance indicators and implement corrective actions when needed.Lead audits and ensure readiness for customer and regulatory inspections.Required Skills and Competencies:Strong knowledge of chemical or pharmaceutical manufacturing processes.Proven leadership skills in managing cross-functional teams.Excellent communication, decision-making, and organizational abilities.Deep understanding of GMP, EHS, and other industry compliance standards.Ability to drive productivity and build high-performing teams.Experience in DCS operated plant is an advantage and a plus point to the candidate.

Machine Operation:Set up, operate, and monitor food processing machines according to production specifications.Adjust machine settings (e.g., temperature, pressure, flow rates) to optimize performance and ensure product quality.Product Quality and Safety:Monitor production processes and products for quality and consistency.Ensure compliance with food safety regulations and standards (e.g., HACCP, GMP).Inspect finished products to identify any defects or issues.Maintenance and Troubleshooting:Perform routine maintenance and cleaning of machinery.Troubleshoot equipment malfunctions and coordinate repairs when necessary.Training and Supervision:Train and mentor junior machine operators on best practices and safety protocols.Supervise and guide the work of junior operators.Continuous Improvement:Contribute to continuous improvement efforts by identifying areas for process optimization.Participate in the development of new recipes and cooking techniques.Documentation and Reporting:Maintain accurate production logs and reports.Report any observed quality issues or malfunctions.Safety:Follow safety protocols and adhere to workplace regulations.

Understanding and implementing QMS and GMP concepts.Referring issues to senior Production staffPerforming day to day activities related to dispensing from stores and verification at different stagesResponding to other ad-hoc queries from other personnel in the company, after consultation with other production Staff.Performing supervision and manufacturing related activities at various stages.

We are seeking a motivated and detail-oriented Chemical Analyst to join our team. As an analyst, you will support our team in conducting chemical tests, analyzing samples, and maintaining lab equipment. The ideal candidate must have foundational understanding of chemistry principles and laboratory procedures, to apply their knowledge in a professional laboratory environment. The role requires attention to detail, a strong commitment to safety standards, and the ability to collaborate with senior team members.Key Responsibilities: Chemical Analysis & Testing:Perform routine chemical tests and analyses on raw materials, in-process samples, and finished products to ensure they meet the required specifications. Data Documentation & Reporting:Record and document results in a clear and organized manner, ensuring accuracy in all data entries. Prepare reports for senior analysts or supervisors with findings, conclusions, and recommendations. Sample Preparation & Handling:Prepare and handle chemical samples by following established lab procedures. This includes weighing, mixing, and maintaining proper sample storage conditions. Lab Equipment Maintenance & Calibration:Maintain, calibrate, and troubleshoot laboratory equipment and instruments. Ensure proper use of equipment and adherence to all safety guidelines. Method Development & Validation Support:Assist in the development and validation of new chemical analysis methods, under the guidance of senior analysts. Contribute to method improvements based on findings from experimental tests. Adherence to Safety & Quality Standards:Follow all safety guidelines and laboratory protocols. Ensure compliance with health, safety, and environmental regulations. Maintain a clean, organized, and safe working environment at all times. Collaboration & Communication:Work closely with senior analysts and lab managers to troubleshoot problems, analyze trends, and implement improvements.

QA Manager / Asst QA Manager Responsibilities:-To handle calibration & validation activities at site.Preparation & review of Technical Documents like Site Master File, Validation Master Plan, Qualifications & Validation Protocols, Validation Reports, Master Formulas, Batch Manufacturing & Packing Records, Policies, Manuals Work Instructions, general and standard specifications and testing procedures & Standard Operating Procedures.To prepare, review & report annual product reviews & product stability reports.To investigate complaints, deviations, quality incidents and non-conformances and ensure implementation of CAPA.To control IPQC activities in production and packing of finished products.To handled external audits like regulatory audits and vendor audits.To indent QA requirements.To approve (sanction) leaves of QA department personnel..To conduct internal audits as per current Good Manufacturing Practices (cGMP) requirements.To issue Corrective Action & Preventive Action and to do follow up for effective implementation of Corrective Action & Preventive Action.To review and approve out of specification, quality incident, deviation, change control, validation documents.To Review and Release manufactured batch.Revision of SOPs & it's integration with Corporate Documents.Act as the pollution prevention, waste minimization and energy team member where applicable.Implementation of Quality Management System & Environment Management System requirements as applicable to IPQC function.To conduct training on Good Manufacturing Practices/Good Laboratory Practices in coordination with Human Resources department.Vendor development, evaluation & assessment of suppliers through auditsTo review Batch Manufacturing Records.To perform gap & risk analysis.To handle change controls.

Job Title: Production Shift In-charge Location: Nandesari, VadodaraPositions: 2 Education: B.Sc. / M.Sc. / Diploma in Chemical Engineering.Experience: 5-10 years of working experience in an API (Active Pharmaceutical Ingredient) and intermediate plant, with a strong understanding and practical application of GMP (Good Manufacturing Practices)Job Summary:We are seeking a highly motivated and experienced Production Shift In-charge to join our team for Pharmaceutical Company. The successful candidate will be responsible for overseeing and managing all production activities during their assigned shift, ensuring efficient operation, adherence to quality standards, and compliance with all safety and regulatory requirements. This role requires a strong leader with proven experience in pharmaceutical manufacturing, specifically in API and intermediate production.Key Responsibilities:Shift Management: Lead and supervise a team of production operators and technicians during the assigned shift. Plan and organize daily production activities to meet targets and schedules. Allocate tasks and responsibilities to team members effectively. Monitor production processes and troubleshoot any issues that arise. Ensure smooth shift transitions and effective communication with incoming/outgoing shifts.Production Operations: Oversee the manufacturing of APIs and intermediates, ensuring processes are followed according to batch production records and standard operating procedures (SOPs). Monitor raw material consumption, in-process parameters, and finished product quality. Optimize production efficiency and minimize waste. Coordinate with other departments such as Quality Control, Quality Assurance, Maintenance, and Stores to ensure seamless operations.Quality and Compliance (GMP): Ensure strict adherence to Good Manufacturing Practices (GMP) and other relevant regulatory guidelines. Oversee the accurate and timely completion of all production documentation, including batch records, logbooks, and deviation reports. Identify and report any deviations, non-conformances, or quality incidents, and participate in investigations. Implement corrective and preventive actions (CAPA) as required. Ensure equipment and facility are maintained in a state of readiness and compliance.Safety and Environment: Promote and enforce a strong safety culture within the production area. Ensure all team members follow safety procedures and use appropriate personal protective equipment (PPE). Report any safety hazards or incidents promptly. Ensure compliance with environmental regulations.Team Development: Provide training and guidance to production operators and technicians. Foster a positive and productive working environment. Conduct performance evaluations and provide feedback to team members.Reporting: Prepare daily, weekly, and monthly production reports. Communicate production status, challenges, and achievements to management.Skills and Qualifications: Proven leadership and supervisory skills in a manufacturing environment. In-depth knowledge of API and intermediate manufacturing processes. Strong understanding and practical application of GMP, GLP, and other relevant pharmaceutical regulations. Excellent problem-solving and decision-making abilities. Strong communication (verbal and written) and interpersonal skills. Ability to work effectively in a fast-paced, dynamic environment. Proficiency in using relevant computer software for data entry and reporting. Ability to work flexible shifts, including nights, weekends, and holidays, as required.

JOB DUTIES AND RESPONSIBILITIES1 To monitor shift activities, plan and ensure timely production completion activities as per plan and dispatch thereby ensuring optimal utilization of resources and esuring quality standards being maintained at all time.2 To ensure timely conducting Production Batches as per requirement, keeping productivity and quality norms in place.3 Expertise in implementing cost saving measures to achieve substantial reduction in terms of man days, production cost, raw materials and energy consumption.4 Set daily/weekly/monthly objectives as per production planning.5 Check production output according to specifications.6 DCS operations/ trouble shooting & data recording.7 Prepare reports on performance and progress.8 Record all the production reports BMR/quality records/failure analysis/plant waste generation/management etc.9 Train new employees and follow procedures.10 Ensure plant strict safety guidelines as per company standards/guidelines11 RM/PM planning & issuance from warehouse.12Maintain plant housekeeping & maintain required standards in all the production areas.13 Planning, organizing, directing and running optimum day-to-day operationsOther DetailsQualification : BE/B Tech Chemical, M.Sc in ChemistryGender : MaleJob Location : SaykhaIf any candidates is suitable for this opening please sent me your updated profile on this mail id.Sheetal Tanwar

Job Title: Executive/Sr ExecutiveDepartment: QAExperience Required: 5 to 10 yearsSalary - 4-7 LpaJOB DUTIES AND RESPONSIBILITIES (Please Mention In Below Table)1 Manage release of product batches, including owning the QA product release workflow in SAP.2 Lead and supervise a team of QA professionals to perform operations as described above.3 Review and approve Deviation and Laboratory Investigations4 Review and approve Purchase Specifications and Analytical Standards5 Review and approve Issue Reviews and CAPA6 Assist with Non-Conformance Investigations and provide guidance in identifying potential product impact and determination of final product disposition7 Review and update Standard Operating Procedures (SOPs) for GMP compliance8 Follow all regulatory guidelines, cGMP guidelines, Environmental Health and Safety regulations as required by the job function Review validation protocols and completed documents, including process qualification protocols for validations of commercial processes.9 Work to create an environment of open communication, participation and information-sharing within and between teams within QA and throughout facility

AM QC Chemist for Agro chemical Industry In Saykha,Bharuch, GujaratJob Title: Executive/Sr ExecutiveDepartment: QCExperience Required: 5 to 10 yearsSalary - 4-7 LpaJOB DUTIES and RESPONSIBILITIES (Please Mention In Below Table)1 Perform the testing of Raw Material/Finished goods/In process materials and report the results.2 Handle the analytical instruments like HPLC, UPLC, GC, ICP, DSC, XRD, PSAetc3 Calibration of the Analytical instruments as per the master calibration schedule4 Investigate the analytical error/deviations during analysis and find out the root cause. propose appropriate corrective and preventive action for the same10 Discuss work plan on daily basis with supervisor/ manager and Mentor junior lab personnel11 Participate in project meetings and prepare weekly and monthly reports and submit to Manager12 Regular lab duties including equipment maintenance, chemical inventory and lab clean-up13 Maintain strict IP Confidentiality and adhere to all related data privacy policies

Develop and match new color shades as per customer or sample references. Perform visual and instrumental color matching using tools like spectrophotometer, colorimeter, etc. Adjust formulations to achieve color accuracy in paints, plastics, textiles, inks, or cosmetics. Maintain shade standards and color records for all matched formulations. Conduct lab trials and prepare drawdowns for approvals. Coordinate with production and QC to ensure shade consistency in batch scale-up. Handle customer shade complaints or re-matches, providing timely solutions. Work with software like Color iMatch, Datacolor, X-Rite, or equivalent tools. Ensure adherence to *quality and color tolerance parameters Maintain safety, housekeeping, and compliance with company standards.