GMP Jobs

Hiring: Plant Head - Pharma Location: Chennai Experience: 15-20 Years Industry: Pharmaceutical / Pharma ManufacturingTalent Zone Consultant is hiring an experienced Plant Head to lead end-to-end pharmaceutical manufacturing operations, ensure regulatory compliance, and drive plant efficiency, quality, and productivity.Key Responsibilities:Oversee overall pharmaceutical plant operations and production activities.Ensure compliance with GMP, WHO-GMP, USFDA, and regulatory standards.Manage production planning, quality assurance, and manufacturing processes.Drive operational excellence, cost optimization, and productivity improvements.Lead production, engineering, quality, and maintenance teams.Ensure adherence to safety, hygiene, and environmental standards.Manage audits, inspections, CAPA, and regulatory documentation.Drive plant capacity utilization and continuous improvement initiatives.Key Skills: Pharma Manufacturing, Plant Operations, GMP, WHO-GMP, USFDA, Production Management, Quality Assurance, CAPA, Regulatory Compliance, Operational Excellence, Lean Manufacturing

Key ResponsibilitiesImplement, maintain, monitor, and continuously improve the Quality Management System.Ensure compliance with applicable Good Manufacturing Practices (GMP), regulatory requirements, and internal quality procedures.Prepare, review, revise, and maintain Standard Operating Procedures (SOPs), quality manuals, policies, and other controlled documents.Coordinate internal audits, external audits, customer audits, and regulatory inspections, as applicable.Manage deviations, non-conformances, investigations, root cause analysis, and Corrective and Preventive Actions (CAPA).Oversee document control, change control, training records, and quality-related documentation.Coordinate with Quality Control (QC), Production, Stores, Engineering, and other departments to address quality issues.Monitor compliance with approved procedures and ensure timely closure of audit observations and corrective actions.Support quality risk assessments and periodic reviews of the Quality Management System.Maintain audit trails, compliance records, and other quality documentation.Assist in investigating customer complaints and product quality issues, where applicable.Prepare quality reports and support management reviews and continuous improvement initiatives.Guide team members on QMS requirements, documentation practices, and quality procedures.

The Draft is an ISO 9001:2015 certified bakery and caf with FSSAI registration. We are looking for a Food Safety & Quality Executive to take charge of our hygiene, safety and quality systems. You will make sure every product leaving our kitchen and bakery meets food safety regulations and our own quality standards.

We are seeking a dedicated Manufacturing Chemist with 5 to 11 years of experience to work full-time in our Raipur facility. In this role, you will be accountable for producing various pharmaceutical products, including tablets, capsules, ointments, syrups, and veterinary liquids and powders, in compliance with batch manufacturing records (BMR), standard operating procedures (SOP), and good manufacturing practices (GMP).Key responsibilities include operating production equipment and maintaining accurate batch records, ensuring that all production processes adhere to safety and hygiene standards. You will also collaborate closely with the quality assurance and quality control teams to ensure consistency and quality in production activities. To succeed in this role, you should hold a graduate degree, and strong attention to detail is essential. You will need excellent communication skills to coordinate effectively with colleagues and other departments. Prior experience handling production equipment and an understanding of quality control processes will be advantageous. Ensuring compliance with safety regulations and maintaining a clean working environment will also be critical. This position requires working from the office at our Siltara location. All interested candidates must be male, as specified in the job requirements. If you have a passion for manufacturing and quality assurance in the pharmaceutical industry, we invite you to apply.

### Job Description - Manufacturing Chemist* Handle manufacturing of Tablets, Capsules and External Preparations.* Follow BMR, SOPs, GMP and Schedule M requirements.* Supervise dispensing, granulation, blending, compression, coating and capsule filling.* Handle ointment/cream manufacturing and filling operations.* Maintain manufacturing records and process parameters.* Ensure cleanliness, hygiene and line clearance.* Coordinate with QA/QC for in-process checks.* Report deviations and manufacturing issues to the Production Head.* Ensure safe and efficient production as per quality standards.

We are preferring experience candidate, however we are looking for Bsc/Msc/Diploma Pharma, B Pharma or any Other Graduate who has worked in pharmaceutical Api or Formulation factory or lab on all different level including production , Quality Assurance, Testing, Documents, Machine Handling, Glp, Quality Assurance , Quality Control, Analyst etc.

1. In-Process & Line Quality Control Perform regular, hourly online sampling and visual checks directly on active conveyor belts. Verify critical parameters: fluid absorbency capacity, strip/wing sealing integrity, dimensions, and unit weight. Enforce strict Line Clearance protocols during raw material changeovers and product variant shifts. 2. Documentation & Compliance Management Maintain real-time shop floor QC logs, batch registers, and daily quality shift reports. Ensure operations conform to Good Manufacturing Practices (GMP) and ISO standards. Track raw material rejection rates and monitor waste management logs.

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.

Key Responsibilities Sample Analysis: o Conduct chemical and physical analysis of raw materials, intermediates, and finished products using standard laboratory techniques. Perform stability studies and report observations. Documentation: o Maintain accurate and detailed laboratory records as per Good Documentation Practices (GDP). o Prepare and review analytical reports, COAs (Certificates of Analysis), and lab protocols. Compliance & Safety: o Ensure compliance with Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and regulatory guidelines. o Follow laboratory safety protocols and maintain a clean and organized workspace. Equipment Maintenance: o Calibrate and maintain laboratory instruments and troubleshoot issues as needed. o Ensure timely preventive maintenance of equipment. Quality Assurance: o Identify and report out-of-specification (OOS) results and participate in root cause investigations. o Assist in preparing for internal and external audits. Continuous Improvement: o Participate in validation activities and method development as required. o Contribute to process improvements in QC procedures.

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

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.

Salary: Take home / net - Rs 50000 to 75000 pm plus bonus, leave encashment and PFGood work environment_________________________________Candidates can mail (rankandfile94@yahoo.co.in) or whatsapp (97 6996 4647) following details 1. Resume2. Present Salary3. Notice period_________________________________Required:Diploma/ BE - Mech/ Production Engg with minimum 12 years experience in Projects/ Engineering/ Maintenance in API / Bulk Drugs / Intermediates industry;Good knowledge of basic chemistry and chemical processesMust be familiar with cGMP protocols/ procedures with respect to maintenance functionExperience of handling Jr Engr / maintenance technicians desirableAge profile: 35 to 50 yearsCall/ contact urgentlySHOBANARank & File consultantsBrief job profile:Independently responsible for maintenance of Plant & Utility equipments such as rotating and static equipmentAssist in other engg activities like expansion, modification, project activitiesCoordinate with mechanical, electrical & civil contractors for routine & project activities_________________________________About the Organisation:Our client is an established SSI unit manufacturing niche API & intermediate products for export/ global markets;It has a modern manufacturing unit at Taloja;The co has ambitious growth plans and has developed new molecules through in-house R&D which will be marketed in domestic and global markets;

Job DescriptionThe HPLC Analyst will perform chromatographic analysis of pharmaceutical raw materials, in-process samples, and finished products according to approved analytical methods.Key ResponsibilitiesOperate and maintain HPLC instruments.Perform assay, impurity, and other applicable analytical tests.Prepare samples, mobile phases, and reagents.Review chromatograms and document analytical results.Follow approved methods, laboratory SOPs, and data-integrity practices.Report abnormal results and assist with laboratory investigations.Requirements2-4 years of hands-on HPLC experience in a pharmaceutical laboratory.Relevant qualification in Chemistry, Pharmacy, or a related discipline.Knowledge of analytical method execution and laboratory documentation.

We are looking for a Quality Assurance Quality Control Engineer to join our team in Boisar West. This is a full-time position, requiring candidates with 1 to 7 years of experience in quality assurance and control.Key Responsibilities:- Conduct Quality Inspections: Carry out regular inspections of products and processes to ensure they meet defined quality standards and specifications.- Develop Test Plans: Create comprehensive test plans and procedures that outline the methods for testing products and processes for quality compliance.- Analyze Quality Data: Collect and analyze quality data to identify trends and areas for improvement, ensuring that corrective actions are taken when needed.- Collaborate with Teams: Work closely with production and engineering teams to implement quality control measures and address any quality-related issues effectively.- Documentation Management: Maintain accurate records of quality control activities, inspections, and results, ensuring all documentation is updated and compliant with industry standards.- Training and Guidance: Provide training and support to staff on quality assurance procedures and best practices to foster a culture of quality within the organization.Required Skills and Expectations:The ideal candidate should have a strong understanding of quality control processes and tools. Attention to detail and strong analytical skills are essential for identifying defects and ensuring compliance. Excellent communication skills are necessary for collaborating with team members and documenting findings. Familiarity with quality management systems and relevant industry standards will be an advantage. A proactive attitude towards problem-solving and a commitment to continuous improvement is expected.

We are preferring experience candidate, however we are looking for Bsc/ Msc/ Diploma Pharma, B Pharma or any Other Graduate who has worked in pharmaceutical Api or Formulation factory or lab on all different level including production , quality assurance, testing, documents, machine handling, glp, quality assurance , quality control, analyst etc.

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.

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.