144 Api Production Jobs - Page 2

Job Title: Plant / Factory Head API (Cephalosporin) Manufacturing Location: Udaipur, Rajasthan Experience: Minimum 10+ years in pharmaceutical industry with at least 10 years in Plant/Factory leadership roles Qualification: B.Tech / Diploma in Chemical Engineering (Mandatory) Job Purpose We are seeking an experienced and result-oriented Plant/Factory Head to lead our API (Active Pharmaceutical Ingredient) manufacturing facility (specializing in Cephalosporin group) at Udaipur. The role requires strong expertise in pharmaceutical chemical operations, plant management, compliance, and cross-functional leadership to ensure smooth, safe, and compliant operations while achieving business objectives. Key Responsibilities Lead and manage end-to-end operations of the API manufacturing plant (Cephalosporin group). Drive operational efficiency, productivity, and cost optimization while maintaining quality and safety standards. Ensure compliance with cGMP, FDA, WHO, and other regulatory norms . Oversee plant functions including production, QA/QC, engineering, utilities, EHS, and maintenance . Implement best practices in chemical process safety, EHS, and sustainable manufacturing. Develop strategies for continuous improvement, automation, and technology adoption in plant operations. Manage production planning, budgeting, and resource allocation to meet business goals. Lead, mentor, and develop large cross-functional teams. Coordinate with senior management and corporate teams for strategic decision-making. Ensure successful handling of regulatory and customer audits with zero non-compliance findings. Monitor and review plant performance through KPIs and prepare MIS reports. Desired Candidate Profile B.Tech/Diploma in Chemical Engineering (Mandatory). Minimum 10+ years of experience in pharmaceutical chemical/API manufacturing, including leadership of large teams. Strong exposure to API (Cephalosporin group preferred) with proven expertise in handling large-scale pharma chemical operations. In-depth knowledge of cGMP, regulatory requirements, EHS, and chemical process safety. Excellent leadership, problem-solving, and decision-making skills. Strong interpersonal skills with the ability to influence, manage, and motivate diverse teams. Demonstrated ability to drive operational excellence and innovation.

Seeking a IPQA Executive to ensure skincare products meet regulatory, safety & quality standards. Work closely with manufacturing, R&D, and QC teams. Requirement: 2+ years of QA experience, preferably in cosmetics or pharma manufacturing. Required Candidate profile Skincare manufacturing & QC expertise Knowledge of FDA, GMP, ISO regulations Attention to detail & procedural compliance Strong analytical, problem-solving & com skills Ability to work with GMP proces

Eligibility: Experience : 0-2 Years Position: Shift Chemist Departments: API Production Qualification: M.Sc, Diploma, B.Sc, B.Pharm Documents to Carry (Photocopies): Resume All Educational Certificates Previous Organizations Relieving Letters Current Offer / Increment Letter Last 3 Months Payslips Aadhar & PAN Card Must be willing to work in shift operations

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.

Execute and monitor production activities as per SOPs and cGMP guidelines. Ensure compliance with safety, health, and environmental regulations during production operations. Handle day-to-day production activities for API and intermediate products. Required Candidate profile B.Sc. / M.Sc. (Chemistry) / B.E / B.Tech. (Chemical Engineering) with 2 to 7 years in API or Intermediates Manufacturing Strong knowledge of API / Intermediates manufacturing processes.

Experience in section LCMS/ PSD/ HPLC/ GC/ Method Validation. Interview will be held in Pune location. Required Candidate profile 2 to 5 years of experience in section LCMS/ PSD/ HPLC/ GC/ Method Validation.

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

Production (Oral) / Solvent Recovery Plant Chemist/Officer/ Executive B.Sc. (Chemistry) / M.Sc. (Chemistry) / Diploma Chemical / B. Tech. Chemical 2-10 years of relevant experience Quality Control Chemist/Officer/ Executive B. Pharma/ B. Sc.(Chemistry) / M. Sc.(Chemistry) 2-10 years of relevant experience QA / Micro Chemist/Officer/ Executive B. Pharma / M. Sc.(Chemistry) M. Sc.(Micro)/B. Tech. Biotech 2-10 years of relevant experience Engineering Operator/ Fitter/ Electrician/Technician ITI-Fitter/Elec./Inst & RAC 2-10 years of relevant experience Supervisor/ Officer / Engineer/Executive Dip. in Mech./Inst./Elect. Engg. & B. Tech. Mech./Inst./Elect. Engg. Please Note: Eligible and interested candidates may bring their latest CVs, passport size photograph and salary proof. Preference will be given to candidates having exposure of regulatory inspections . As per job requirements, candidate might have to work in the shifts. No TAIDA will be given. Contact : For any query, please contact on +91-1762-532598, +91-6284702108 & email : hr@neclife.com

Role & responsibilities QA/Qc Trainee (off roll) Preferred candidate profile Preferred Skills: 1. Knowledge of API manufacturing processes and regulations. 2. Familiarity with quality management systems (QMS) and audit processes. 3. Strong communication and interpersonal skills. Key Responsibilities: 1. Assist in conducting audits and inspections of production areas, warehouses, and laboratories. 2. Support the QA team in reviewing and updating SOPs, Batch Records, and other quality documents. 3. Participate in deviation investigations, CAPA implementation, and change control processes. 4. Collaborate with production and quality teams to identify and resolve quality issues. 5. Learn and implement GMP, GLP, and regulatory guidelines (e.g., USFDA, WHO, ICH). 6. Assist in documentation, record-keeping, and data management. 7. Support internal audits, regulatory inspections, and compliance activities.

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

Key Responsibilities Execute daily production operations as per approved SOPs, BMR/BPR, and production plan. Handle manufacturing processes, equipment operations, cleaning, and changeover activities. Prepare, review, and maintain production documentation (BMR, BPR, logbooks, and SOPs). Ensure adherence to cGMP, GDP, and EHS standards across production processes. Actively participate in QMS activities deviations, CAPA, change controls, incident handling. Coordinate with QA, QC, Engineering, and Warehouse for smooth batch execution. Assist in audit preparation (internal, regulatory, and customer audits) with proper documentation. Monitor yield, productivity, and process improvements to minimize batch rejections. Ensure proper training and compliance of operators/technicians on SOPs and safety practices.

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.

We are looking for a dynamic and detail-oriented Production Manager to join our team at our chemical. Manufacturing facility in Bharuch. Production processes, ensuring operational efficiency, and maintaining safety and quality standards. Required Candidate profile Bachelor's Degree/Diploma in Chemical Engineering or related field. 1 to 3 years of experience in production management within the chemical industry.

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

Freshers, Here's Your Chance to Begin Your Career! Eligibility Criteria: Qualification: Diploma-chem/ B.Sc-Chem/ M.Sc-Chem Age: 20 to 23 Years Pass out Year: 2023 / 2024 / 2025 Minimum 50% aggregate in all academics Documents to Carry: Resume Copies of all educational certificates Xerox of Aadhar and PAN card Department: API Production Note: Candidates must be willing to work in shift operations.

Minimum 15 years in API & OCTG Products and Line Pipes as per API Specifications, Finishing Carbon Steel API Product, Plan and issue required materials from stores in advance to maintain quality. quality systems as per ISO 9001 / API Spec. Q1

Role & responsibilities Execute daily production activities for oncology formulations (oral solids / injectables) as per approved batch manufacturing records. Ensure compliance with cGMP, GDP, EHS, and regulatory guidelines at all stages of production. Handle and monitor highly potent active pharmaceutical ingredients (HPAPIs) with appropriate containment measures. Operate and maintain manufacturing equipment such as granulators, compression machines, coating machines, aseptic filling lines, lyophilizers, etc. Coordinate with QA/QC, engineering, and warehouse teams for smooth execution of production plans. Perform in-process checks and ensure documentation in line with SOPs. Adhere to cleaning and sanitation procedures to prevent cross-contamination. Assist in process validation, technology transfer, and new product introductions. Monitor and control wastage of materials and utilities. Maintain production records, logbooks, and batch documents accurately

Role & responsibilities QA/QC Officer Preferred candidate profile Preferred Skills: 1. Knowledge of API manufacturing processes and regulations. 2. Familiarity with quality management systems (QMS) and audit processes. 3. Strong communication and interpersonal skills. Key Responsibilities: 1. Assist in conducting audits and inspections of production areas, warehouses, and laboratories. 2. Support the QA team in reviewing and updating SOPs, Batch Records, and other quality documents. 3. Participate in deviation investigations, CAPA implementation, and change control processes. 4. Collaborate with production and quality teams to identify and resolve quality issues. 5. Learn and implement GMP, GLP, and regulatory guidelines (e.g., USFDA, WHO, ICH). 6. Assist in documentation, record-keeping, and data management. 7. Support internal audits, regulatory inspections, and compliance activities.

Role & responsibilities QA/Qc Trainee (off roll) Preferred candidate profile Preferred Skills: 1. Knowledge of API manufacturing processes and regulations. 2. Familiarity with quality management systems (QMS) and audit processes. 3. Strong communication and interpersonal skills. Key Responsibilities: 1. Assist in conducting audits and inspections of production areas, warehouses, and laboratories. 2. Support the QA team in reviewing and updating SOPs, Batch Records, and other quality documents. 3. Participate in deviation investigations, CAPA implementation, and change control processes. 4. Collaborate with production and quality teams to identify and resolve quality issues. 5. Learn and implement GMP, GLP, and regulatory guidelines (e.g., USFDA, WHO, ICH). 6. Assist in documentation, record-keeping, and data management. 7. Support internal audits, regulatory inspections, and compliance activities.

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 ]

Role & responsibilities Knowledge of operation of plant equipments, handling materials and monitoring the process as per BPR in shifts. Develop Skill to physically operate various plant equipments and fix minor equipment problems. Follow and strictly adhere to cGMP as per SOP and online recording of required data in BPR, Equipment and cleaning status records. To ensure good house-keeping and safety of men, material and machineries in the plant as per SOP. Ensure personal hygiene as required under cGMP and strictly adhere to it. To contain, control the spills, salvaging of spills in the plant. To regularly monitor in shift duty, the overall plant parameters, equipments and utilities. Reporting any deviation during process to superior and immediate update of the deviation related documents Trouble shooting in plant To ensure proper receipt and movement of material to and from the plant during the shift hours. To maintain good inter personal relationship in shop floor and with other departments.

Role & responsibilities Operation of all production equipments, execution and monitoring the process as per BMR during shift hours. To perform all the calibration activities for W.B and holding tanks receivers as per SOP and maintain calibration records as updated. To monitor overall plant parameters & utilities. To control the spills, salvaging of spills in the plant. To ensure personal hygiene inside the plant. To ensure all the chemicals are handled as per MSDS. Ensure to maintain documentation in plants with respect to BMR, cleaning records, all production related log books.