243 Batch Manufacturing Jobs - Page 3

1. Implementation and improvement in Quality Management System as per ISO 13485:2016. 2. Implementation & Formation of Standard Operating Procedure (SOP) & Protocols as per GMP. 3. Maintain complete documents of various departments like Site Master File, Device Master File with easy archival/retrieval. 4. Involve onsite into the calibration & Validation activities. Preparation of Calibration calendar and preventive maintenance. 5. Assist in preparation of Batch Manufacturing Record as per manufacturing and their review before release of the batch. 6. Giving line clearance before starting the New Batch.

Job Description: We are seeking a dedicated and skilled Production Officer to join our team. The ideal candidate should have a minimum of 1 year of experience in a regulatory-approved manufacturing plant, with hands-on experience in handling critical production equipment and knowledge of cGMP standards. Key Responsibilities • Operate and manage production equipment such as reactors, centrifuges, dryers, multi-mills, and other machinery used in manufacturing processes. • Oversee and ensure thorough cleaning of production areas, maintaining compliance with cleanliness and hygiene standards. • Monitor and maintain environmental conditions on the shop floor, ensuring adherence to regulatory and safety standards. • Implement and uphold basic current Good Manufacturing Practices (cGMP) in daily operations. • Assist in troubleshooting and resolving any production issues to ensure smooth workflow and minimize downtime. Qualifications and Skills • Experience: Minimum 1 year in a regulatory-approved plant. • Qualifications: Bachelors degree or diploma in a relevant field (e.g., B.sc. or M.sc. in Chemistry, Chemical Engineering, Pharmacy). • Technical Knowledge: Hands-on experience with equipment like reactors, centrifuges, dryers, and multi-mills. • cGMP Knowledge: Basic understanding of cGMP guidelines and regulations. • Teamwork: Ability to work effectively within a team and follow standard operating procedures. • Attention to Detail: Strong commitment to maintaining high standards in production and quality compliance.

Maintaining Quality Systems Ensuring cGMP compliance Prepare Batch Manufacturing Records Process Validation and Cleaning Validation Dossier Preparation and New Drug Applications Document Quality Risk activities Required Candidate profile Experience in GMP, ICH Q series and pharmaceutical quality systems Strong in documentation, audit preparedness and regulatory compliance

As an Assistant Manager/Manager- Quality Assurance, your responsibilities will include: - Reviewing and approving Standard Operation Procedures (SOP's) for all departments, ensuring timely completion of reviews and revisions according to the specified revision date. - Evaluating and approving analytical method validation protocols and reports, process method validation protocols and reports, water system validation protocols and reports, as well as equipment/instrument qualification protocols and reports. - Reviewing and approving raw material, packing material, semi-finished product, and final product specifications and test methods for analysis. Approving artwork and shade cards for printed packing material. - Overseeing and approving stability protocols and data. - Coordinating and supporting on-site audits conducted by customers and agencies, and implementing necessary corrective actions based on audit findings. - Developing, preparing, and implementing quality systems across the site. - Providing training to all staff members. - Reviewing and approving deviations, change control, and CAPA processes. - Planning and conducting internal audits for all departments. - Reviewing and approving batch manufacturing and batch packing records. - Ensuring the quality of manufactured products through an in-process quality assurance system. - Reviewing executed batch manufacturing records, batch packing records, finished product test reports with analytical data, and subsequently releasing batches for market distribution. - Ensuring data integrity compliance at the site. - Maintaining and improving product quality by conducting product, company, system, compliance, and surveillance audits, and investigating customer/market complaints. - Preparing FDA licensing documents, QA documents for export orders. - Creating quality documentation and reports by collecting, analyzing, and summarizing information and trends, including failed processes, stability studies, recalls, corrective actions, and re-validations. - Undertaking any additional responsibilities assigned by higher management as needed.,

Job Title: Quality Assurance Officers (4 Positions) Company: Nourish Pharmaceutical Pvt Ltd Location: Kheda, Gujarat Job Type: Full-time Nourish Pharmaceutical Pvt Ltd is a leading pharmaceutical company committed to delivering high-quality products. We're expanding our Quality Assurance team and looking for talented professionals to join us. Positions: 1. Quality Assurance Officer - Production 2. Quality Assurance Officer - QMS 3. Quality Assurance Officer - Validation & Qualification 4. Quality Assurance Document Control Officer Job Descriptions: 1. Quality Assurance Officer - Production - Key Responsibilities: - Ensure cGMP compliance in production areas - Manage and review Batch Manufacturing Records (BMRs), Batch Packaging Records (BPRs), and Master Formula Records (MFRs) in Pharma Cloud - Conduct in-process quality checks and documentation - Verify dispensing activities and line clearance - Collaborate with production team to ensure quality and compliance - Core Skills: - Attention to detail and analytical skills - Strong knowledge of cGMP, SOPs, and quality control procedures - Excellent communication and interpersonal skills - Experience & Qualification: - 0-3 years of experience in a similar role within the pharmaceutical industry - B.Pharm or M.Pharm degree in Pharmacy or a related field - Certification in quality assurance or a related field is an added advantage 2. Quality Assurance Officer - QMS - Key Responsibilities: - Manage deviations, CAPAs, and document handling - Ensure compliance with Quality Management System (QMS) standards - Conduct internal audits and facilitate external audits - Review and update SOPs, policies, and procedures - Collaborate with departments to ensure quality and compliance - Core Skills: - Strong analytical and problem-solving skills - Excellent communication and interpersonal skills - Ability to work independently and prioritize tasks - Experience & Qualification: - 1-3 years of experience in a similar role within the pharmaceutical industry - B.Pharm or M.Pharm degree in Pharmacy or a related field - Certification in quality assurance or a related field is an added advantage 3. Quality Assurance Officer - Validation & Qualification - Key Responsibilities: - Plan, coordinate, and execute validation and qualification activities - Ensure compliance with validation and qualification protocols - Review and approve validation reports and documentation - Collaborate with departments to ensure quality and compliance - Identify and mitigate risks associated with validation and qualification - Core Skills: - Strong knowledge of validation and qualification procedures - Excellent analytical and problem-solving skills - Ability to work independently and prioritize tasks - Experience & Qualification: - 1-5 years of experience in a similar role within the pharmaceutical industry - B.Pharm or M.Pharm degree in Pharmacy or a related field - Certification in validation and qualification or a related field is an added advantage 4. Quality Assurance Document Control Officer - Key Responsibilities: - Manage and maintain document control system - Implement and maintain change control system - Issue and maintain logbooks and records - Ensure plant and product documentation is accurate and compliant - Collaborate with QA team to ensure document accuracy and compliance - Core Skills: - Attention to detail and organizational skills - Basic knowledge of cGMP and quality control procedures - Excellent communication and interpersonal skills - Experience & Qualification: - 0-2 years of experience in a similar role within the pharmaceutical industry - B.Pharm, B.Sc or M.Pharm degree in Pharmacy or a related field - Certification in validation and qualification or a related field is an added advantage - All positions open for Fresher B.Pharm or M.Pharm degree in Pharmacy, Willingness to learn and grow in a quality assurance role How to Apply: If you're a motivated and detail-oriented individual with a passion for quality assurance, please submit your resume to info@nourishpharma.com

Interview For Production & QC Dept for API Pharma co in Bharuch on 29-08 at Dahej Qualification: Bsc/Msc Experience: 2 to 10 Years CTC: Up to 6 LPA EXP in API Is Must Send CV on sdpbharuch@gmail.com with Subject: Prod/QC Dahej No Job Charges Required Candidate profile Permanent Job Come Along with yr Friends Interview Venue: SDP HR Solution, 611, Golden Square Beside Dmart Near ABC Circle Bholav, Bharuch - 392001 Time : 9 to 3 Date : 29-08 Free Interview

Followings will be the core job responsibilities of the position holder: 1. Responsible for Operation, cleaning, and primary maintenance of compression machine, metal detector, Lifting and positioning device, IPQC instrument. 2. Responsible for recording of activity in logbooks, Batch manufacturing record & Responsible for complete documentation as required in the manufacturing of product and the cleaning of facilities and equipment, following cGMP s and good documentation practices. 3. To Ensure Area and equipment cleaning before line clearance as per standard procedures. 4. To perform all in-process checks and monitoring of all intermediate processes in compression. stage. To select recipes and set process parameters in PLC/SCADA compression ,IPQC instruments HMI & ensure its correctness before blender revolution. 5. Responsible for Issuance, utilization, cleaning, and retrieval of tooling s and machine change parts with its inventory. 6. Responsible for set up, changeover, and operation of various manufacturing equipment s but not limited to compression area. 7. Responsible for reporting and/or escalating any conditions or problems that may affect the quality or integrity of product to supervisor and HOD production. 8. Responsible for maintaining a neat, clean and safe working environment always and notifies supervisor immediately if any safety concerns, accidents or injuries are observed. 9. To ensure all in-process checks and monitoring of all intermediate processes, to check set process parameters in PLC/SCADA as per BMR before machine run in compression area. 10. Compliance of current Good Manufacturing Practices in the Hormone Facility & to follow GDP with data-integrity compliance. 11. To Complete the training and training record as per stipulated time. 12. Responsible for preparation and usage of Disinfectant and cleaning agent solution as per defined procedures. 13. To adhere to all Company policies, procedures, SOPs and Safety regulations. 14. To do overtime as needed & responsible for performing additional task, related duties as assigned.

Key Responsibilities: Continuous Process Verification (CPV): Collect, compile, and analyze process data from manufacturing batches. Monitor critical process parameters and quality attributes to ensure process consistency. Support trending and statistical analysis for process performance. Assist in identifying process deviations and recommending corrective actions. Data Entry & Management: Ensure accurate and timely entry of process and quality data into designated systems (e. g. , LIMS, SAP, Excel). Maintain data integrity and compliance with ALCOA+ principles. Generate periodic reports and dashboards for internal review. Scientific Document Review: Review batch manufacturing records, SOPs, protocols, and technical reports for completeness and accuracy. Ensure documents meet regulatory and internal quality standards. Collaborate with cross-functional teams (QA, QC, MSAT) for document approvals and updates.

Technician Granulation Job Purpose: To operate and monitor granulation equipment and processes in compliance with cGMP, SOPs, and safety standards, ensuring consistent production of high-quality pharmaceutical granules for tablet or capsule formulation. Key Responsibilities: Operate granulation equipment such as high-shear mixers, fluid bed dryers, oscillating mills, and blenders. Weigh, dispense, and mix raw materials as per batch manufacturing records (BMR). Monitor granulation parameters and adjust settings to maintain product quality. Perform in-process checks (e.g., moisture content, granule size) and document results accurately. Clean and maintain equipment and work areas as per SOPs. Execute machine changeovers and line clearance activities. Identify and report deviations or equipment malfunctions to the supervisor. Ensure compliance with cGMP, safety, and environmental regulations. Participate in continuous improvement and troubleshooting initiatives. Qualifications: ITI / Diploma / B.Sc or equivalent; technical diploma preferred. 4 6 years of experience in pharmaceutical manufacturing, preferably in granulation. Familiarity with cGMP, USFDA guidelines, and pharmaceutical documentation practices. Ability to read and interpret batch records and SOPs. Basic computer skills and understanding of production documentation. Preferred Skills: Attention to detail and strong documentation habits. Mechanical aptitude for operating and troubleshooting equipment. Team player with good communication skills. Forklift certification (if required for material handling).

Job Purpose: To operate and monitor granulation equipment and processes in compliance with cGMP, SOPs, and safety standards, ensuring consistent production of high-quality pharmaceutical granules for tablet or capsule formulation. Key Responsibilities: Operate granulation equipment such as high-shear mixers, fluid bed dryers, oscillating mills, and blenders. Weigh, dispense, and mix raw materials as per batch manufacturing records (BMR). Monitor granulation parameters and adjust settings to maintain product quality. Perform in-process checks (e.g., moisture content, granule size) and document results accurately. Clean and maintain equipment and work areas as per SOPs. Execute machine changeovers and line clearance activities. Identify and report deviations or equipment malfunctions to the supervisor. Ensure compliance with cGMP, safety, and environmental regulations. Participate in continuous improvement and troubleshooting initiatives. Qualifications: ITI / Diploma / B.Sc or equivalent; technical diploma preferred. 4 6 years of experience in pharmaceutical manufacturing, preferably in granulation. Familiarity with cGMP, USFDA guidelines, and pharmaceutical documentation practices. Ability to read and interpret batch records and SOPs. Basic computer skills and understanding of production documentation. Preferred Skills: Attention to detail and strong documentation habits. Mechanical aptitude for operating and troubleshooting equipment. Team player with good communication skills. Forklift certification (if required for material handling).

Hi Greetings form Avani consulting , We have job opportunity with Apimanufacturing (pharma company) for production department mysore location . we are going to conduct Walk -in interview in Bangalore on 30- august-2025 . Job Description for Production-Associate Position- Associate Work Experience Min 3-9 yrs in API Location Mysore Gender Any Qualification- B.Tech Chemical Engineering/M Sc and Bsc Chemistry /Diploma in chemical Engg Roles & Responsibility 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements. 2. To ensure gowning practices, entry / exit procedures, usage of PPEs are followed by team while in the department. 3. To ensure adherence of process instructions as per Batch Manufacturing Record and respective departmental procedures. 4. To ensure good housekeeping in the production shop floor. 5. To ensure compliance to cGMP, Safety, Health & Environment in delivering the product of intended Quality. 6. To ensure batch records on completion are reviewed for adequacy prior to hand over to QA for review, compliance & release / rejection. 7. To report deviations / incidents immediately upon occurrence and to conduct investigation in coordination with cross functional teams. 8. To ensure all document entries are performed online with legible, errors corrected with signature and date. 9. Monitoring and control of manufacturing environment and filling of daily log books. 10. To ensure preventive maintenance of equipment, calibrations of gauges / instruments are performed as per schedule & the outcome of verification is within control. 11. To ensure the sanitization activity is performed in the department. 12. To support QA in investigations related to OOS, Deviations, CAPA, Incidents, complaints or recalls, validations and any other support that would be required. 13. To ensure the raw material / Intermediates / API(s) are labelled at each stage of process and stored with appropriate segregation at recommended storage conditions ensuring no impact on product Quality. 14. To ensure that stocks are reconciled at regular intervals. 15. Any other assignment allocated by Production head. if interested please share updated resume and fill the details to 7327039030 or mona@avaniconsulting.com 1. Current CTC: 2. Expected CTC: 3 . Notice Period: 4. Total Experience 5. Current Location: 6. Preferred Location: 7. Reason for change: 8. Relevant years of experience in on roll :

Hi Greetings form Avani consulting , We have job opportunity with Api Manufacturing (pharma company) for production department mysore location. we are going to conduct Walk -in interview in Bangalore location on 30-Aug-2025. Job Description for Production-Associate Position- Associate Work Experience Min 3-9 yrs in API Location Mysore Gender – Any Qualification- B.Tech Chemical Engineering/M Sc and Bsc Chemistry /Diploma in chemical Engg Roles & Responsibility 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements. 2. To ensure gowning practices, entry / exit procedures, usage of PPE’s are followed by team while in the department. 3. To ensure adherence of process instructions as per Batch Manufacturing Record and respective departmental procedures. 4. To ensure good housekeeping in the production shop floor. 5. To ensure compliance to cGMP, Safety, Health & Environment in delivering the product of intended Quality. 6. To ensure batch records on completion are reviewed for adequacy prior to hand over to QA for review, compliance & release / rejection. 7. To report deviations / incidents immediately upon occurrence and to conduct investigation in coordination with cross functional teams. 8. To ensure all document entries are performed online with legible, errors corrected with signature and date. 9. Monitoring and control of manufacturing environment and filling of daily log books. 10. To ensure preventive maintenance of equipment, calibrations of gauges / instruments are performed as per schedule & the outcome of verification is within control. 11. To ensure the sanitization activity is performed in the department. 12. To support QA in investigations related to OOS, Deviations, CAPA, Incidents, complaints or recalls, validations and any other support that would be required. 13. To ensure the raw material / Intermediates / API(s) are labelled at each stage of process and stored with appropriate segregation at recommended storage conditions ensuring no impact on product Quality. 14. To ensure that stocks are reconciled at regular intervals. 15. Any other assignment allocated by Production head. if interested please share updated resume and fill the details to 7327039030 or mona@avaniconsulting.com 1. Current CTC: 2. Expected CTC: 3 . Notice Period: 4. Total Experience 5. Current Location: 6. Preferred Location: 7. Reason for change: 8. Relevant years of experience in on roll :

Role & responsibilities We are looking for candidates who has hands on work experience in the API manufacturing sector to handle API Production activities like intermediate , Clean room , Second line shift incharge role . Also we are hiring fresh graduates who have passed in 2020 and above . Preferred candidate profile Freshers - BSC /Diploma in Chemical Engineering (Only male ) Junior officer & Officer- BSC ,MSc in Chemistry

Job Purpose: To assist in daily production operations, ensure adherence to production schedules, and maintain product quality and safety standards while learning and developing core competencies in manufacturing processes. Key Responsibilities: Assist in monitoring daily production activities to meet production targets. Operate and supervise machinery as per SOPs (Standard Operating Procedures). Maintain records of production, materials, and equipment usage. Ensure compliance with safety, hygiene, and GMP (Good Manufacturing Practices) standards. Support in troubleshooting production issues and implement corrective actions. Participate in continuous improvement initiatives (e.g., 5S, Kaizen, Lean). Coordinate with quality control, maintenance, and warehouse teams. Learn and implement company policies, systems, and industry best practices. Report deviations, breakdowns, and production issues to senior staff. Assist in documentation work related to batch manufacturing records and reports.

Company: Leading Pharma Company(API manufacturing Unit) Location :Mysore Role: Production Associates Salary: up to 25% hike > Note: No Consulting Charges Roles & Responsibility for Production Associate 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements. 2. To ensure growing practices, entry / exit procedures, usage of PPEs are followed by the team while in the department. 3. To ensure adherence of process instructions as per Batch Manufacturing Record and respective departmental procedures. 4. To ensure good housekeeping in the production shop floor. 5. To ensure compliance to cGMP, Safety, Health & Environment in delivering the product of intended Quality. 6. To ensure batch records on completion are reviewed for adequacy prior to hand over to QA for review, compliance & release / rejection. 7. To report deviations / incidents immediately upon occurrence and to conduct investigation in coordination with cross functional teams. 8. To ensure all document entries are performed online with legible, errors corrected with signature and date.

Roles and Responsibility: Plan and execute manufacturing batches as per defined processes and SOPs. Conduct testing of raw materials, packaging materials, and finished goods. Prepare and maintain documents as per ISO 13485 requirements. Support process validation, troubleshooting, and improvements. Ensure compliance with ISO 13485, GMP, and regulatory requirements. Follow safety protocols and maintain a clean, safe working environment. Minimum Requirement: BSc in Chemistry or a related field. Additional certification (Masters degree or a PhD) is a plus Proficiency with Microsoft Office (Microsoft Excel, Microsoft Project) Knowledge of analytical chemistry principles (i.e. quality assurance and quality control) Extensive knowledge of techniques like distillation, crystallization and titration and hands-on experience with spectrometers and chromatographers

Hi, Greetings Walk in Invitation: We are having face to face interview on 30th Aug 2025 Saturday in Mysore Single Round Face to face Company : A leading Pharma API Unit - in Mysore Position - Production Department Associate Work Experience Min 3 yrs in API in current Hike would be appreciable on Current CTC Note: No Charges If interested drop your CV to Jyotsna - 7780363938|| jyotsna@avaniconsulting.com Thanks & Regards Jyotsna

Ipca Laboratories Ltd, Wardha is as API plant we are looking for Production Manager with below mentioned JD To ensure weekly / monthly production schedules as per plans. Monitor shift wise production and provide feedback to HOD on daily basis. To ensure smooth running of the plant, co-ordinate effective with maintenance department for any break down, utility, services etc. To co-ordinates with Q.C., Store, R&D, Inprocess lab for production related jobs. To ensure that production norms as per laid down procedure are achieved. Through optimum use of resources & report to HOD about the area requiring improvement. To prepare daily logbook containing functioning of the plant in all respects, covering shortage of manpower, incidents of indiscipline if any. To ensure that correct quantity & quality product is charged in safe way. Monitoring of step wise reactions & recording in batch card at the time of operation following cGMP norms. Proper maintenance of production records files & register. Carry out the production related job i.e. raw material, packing material, general material requisition and other requirement through supply chain management system. To identify areas of cost reduction and report to HOD and carry out all functions in cost effective manner. To carry out all operations as per Standard operating procedure. To keep watch on avoiding process deviation. To report all process deviation minor as well as critical through track wise system. To maintain production facilities in clean manner, to carry out disinfections activities in appropriate areas. To make sure that calibration of necessary equipment are done. To make sure that maintenance of equipment & plant is done as per schedule & recorded. To perform SCM & Track wise & validation activity. To ensure review of batch production and control record for its completion. To be a member of team for preparation of BPCR of new product related to plant and also time to time revision of existing BPCR when ever any change / amendment is done through track wise system. To responsible for investigating market complaint and OOS, OOT, Major deviation etc. To conduct the internal, online and self inspection audit as per schedule. To track the BPCR submission after completion of Batch. Manpower handling of respective area as a Plant Incharge. Qualification: B.E./ B. Tech Chemical candidates only. Experience : 18 to 30Years of experience. Interested candidates can sent their CV to jagpal.dewal@ipca.com

Role & responsibilities: 1. Prepare BMR for new products to be processed on the line 2. Raising material requisition for Vial processing & cartridge line to receive materials from stores 3. Update relevant SOPs & online BMR enteries. 4. SOPs preparation for Vial & cartridge processing area 5. Preparing samples as per customer requirements 6. Complete SAP entries for line activities 7. Checking NVPC records and submitting BMR to QA, 8. Other documentation, etc Preferred candidate profile: BE Mechanical/ BSc/ B. Pharm with 2-6 years of experience in Pharmaceutical/ Pharma packaging industry, SOP drafting, documentation, etc Perks and benefits: Transportation (free of cost) Subsidized Canteen facility Health Insurance Group Personal Accident Policy

1. Execute and monitor API manufacturing processes as per approved Batch Manufacturing Records (BMRs). 2. Supervise shift operations including manpower management and production output. 3. Ensure compliance with cGMP, safety, and EHS norms during operations. 4. Monitor critical process parameters and take corrective actions as needed. 5. Prepare and maintain production documentation BMR, logbooks, deviation reports, and incident reports. 6. Coordinate with QA, QC, Engineering, and Warehouse teams for smooth production flow. 7. Support validation and technology transfer activities. 8. Ensure timely availability of raw materials, solvents, and packing materials. 9. Participate in internal and external audits (USFDA, WHO-GMP, etc.). Identify areas of improvement for yield, efficiency, and process optimization

Designation - Manager - Quality Assurance Company - Leading Pharma Raw Material Mfg. Company Job Location - Dahej, Bharuch Qualification - B.Sc. / M.Sc. / B.E.- Chemical / B.Pharm Experience - Min. 8yrs. and above share with your friends Required Candidate profile company will provide transportation facility from Bharuch. Responsible for handling QA / GMP Related documentation QMS, Audit Preparation, Vendor Questionnaire, Market Compliant & Customer Compliance

Greetings from FocusR! If you are currently working in the Process Manufacturing industries, this is your chance to shift your career into the IT sector!!! Great opportunity of becoming an OPM Consultant (Oracle Process Manufacturing Consultant) Complete On-Job Training will be given by FocusR (with salary). Role: OPM Consultant - Domain Trainee Domain experience: 2-5 years Job location: Salem Notice period: Immediate - 30 Days Good experience to production process in the process manufacturing industry. Good understanding of how a process manufacturing industry runs. Should have strong knowledge of Production line/operations; uses of UOM; Routing and ingredients, Product, By-product, Co-product. Good understanding in Process Execution, Cost Management, Quality Management, and Product Development. End user in any ERP application. Willing to learn new concepts such as Oracle SCM, OPM. Excellent written and verbal communication skills. Should not have travel constraint. As we are investing huge capital on your training, we will not charge anything from you. hence, we prefer candidates who can work with FocusR for minimum duration of 30 months.

Hi, Greetings Walk in Invitation: We are having face to face interview on 30th Aug 2025 Saturday in Mysore Single Round Face to face Company : A leading Pharma API Unit - in Mysore Position - Production Department Associate Work Experience Min 3 yrs in API in current Hike would be appreciable on Current CTC Note: No Charges If interested drop your CV to Jyotsna [ 7780363938|| jyotsna@avaniconsulting.com ] Thanks & Regards Jyotsna

Greetings from Avani Consulting ! Hiring Production associates for API (Pharma Production ) Walkin drive face to face interview on 30th August'25 in Bangalore Company: a leading Pharma API Manufacturing company || Location - Mysore ( Nanjangud) Position- Associate || Work Experience Min 5-10 yrs in API if interested kindly share their updated resume with below details to priyanka@avaniconsulting.com or whatsapp to 9518220852 1. Current CTC: 2. Expected CTC: 3 . Notice Period: 4. Total Experience 5. Current Location: 6. Preferred Location: 7. Reason for change: Roles & Responsibility 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements. 2. To ensure gowning practices, entry / exit procedures, usage of PPEs are followed by team while in the department. 3. To ensure adherence of process instructions as per Batch Manufacturing Record and respective departmental procedures. 4. To ensure good housekeeping in the production shop floor. 5. To ensure compliance to cGMP, Safety, Health & Environment in delivering the product of intended Quality. 6. To ensure batch records on completion are reviewed for adequacy prior to hand over to QA for review, compliance & release / rejection. 7. To report deviations / incidents immediately upon occurrence and to conduct investigation in coordination with cross functional teams. 8. To ensure all document entries are performed online with legible, errors corrected with signature and date. 9. Monitoring and control of manufacturing environment and filling of daily log books. 10. To ensure preventive maintenance of equipment, calibrations of gauges / instruments are performed as per schedule & the outcome of verification is within control. 11. To ensure the sanitization activity is performed in the department. 12. To support QA in investigations related to OOS, Deviations, CAPA, Incidents, complaints or recalls, validations and any other support that would be required. 13. To ensure the raw material / Intermediates / API(s) are labelled at each stage of process and stored with appropriate segregation at recommended storage conditions ensuring no impact on product Quality. 14. To ensure that stocks are reconciled at regular intervals. 15. Any other assignment allocated by Production head Note: No Consulting Charges. Thanks & Regards Priyanka [ 9518220852 | priyanka@avaniconsulting.com ]

Ensure compliance with GMP & regulatory standards, oversee quality systems, audits & validations, manage QA team, review batch records, handle deviations/CAPA, support regulatory inspections, ensure product quality & safety across manufacturing.