144 Api Production Jobs

The ideal candidate should have at least 3 years of experience of working in Pharmaceutical Production floor where the person is responsible for shift operations. The incumbent would typically be responsible for: Ensuring the targets are met keeping in mind safety and quality guidelines. Management and upkeep of facility, materials and manpower. Troubleshooting in operations, validations and equipment qualification Coordination with other functions like QC, QA, Warehouse among others. Knowledge and Adherence to SOPs , regulatory requirement Preparing Batch Manufacturing Records, Protocols, Reports, Investigation Reports, and Qualification Reports. Work on Continuous improvement Plans (like Capacity and Manpower Utilization, Product Cost Effectiveness, Effluent Control and Safety Improvement, etc.)

Responsibilities: Responsible for creating, maintaining, managing accurate & compliant production-related documentation. This role ensures that all documentation adheres to internal standards and external regulatory requirements.

Maintaining good housekeeping and cGMP in shop floor Preparation of New documents like BPCR and SOP Deviation , change control, OOS, activity and is compliance Plant keeps ready for audit Overall responsibility of cGMP Production should be achieved as per target. Equipment cleaning Log book and Solvent log Book to be maintained. BPCR arrangements for running batches. Review and completion of all documents like BPCR, Equipment logbook, and format as per SOP

1. Plan and execute production schedules, 2. Supervise granulation, blending, compression, and coating operations, 3. Strong knowledge of pharmaceutical manufacturing processes (API, DC granules, FDF), regulatory standards (GMP, WHO, USFDA)

Greetings! I am Priyanka. We are hiring QA Trainee / Officer Off roll for A leading API Manufacturing Company. Designation: 1. QA Officer/ trainee Off Roll Salary : Take way home [no benefits. no deduction] Location: Mysore Looking forward to hear from you. Note: No Charges Thanks & Regards Priyanka [ 9518220852 || priyanka@avaniconsulting.com ]

1. Daily Production Activities Operate and monitor production equipment under supervision. Ensure smooth running of production processes and support machine start-up/shutdown. Record production data accurately in logbooks. Assist in batch preparation and material handling. 2. Compliance & Safety Follow GMP/GLP guidelines and other industry regulations. Adhere to safety standards, including PPE usage and hazardous material handling. 3. Quality & Process Monitoring Conduct in-process checks (temperature, pressure, weight, volume). Identify and report deviations, abnormalities, or equipment malfunctions. Ensure proper storage and labeling of raw materials, intermediates, and finished goods. 4. Documentation & Reporting Maintain accurate production records, shift reports, and batch manufacturing records (BMR). Document equipment cleaning, usage, and preventive maintenance records. Assist during internal/external audits by providing required data. 5. Support & Coordination Collaborate with QC, Maintenance, and Warehouse teams. Assist senior staff in troubleshooting and minor equipment maintenance. Participate in training sessions and team meetings. 6. Continuous Improvement Learn and adapt to new production technologies. Suggest ideas for process improvement, waste reduction, and efficiency enhancement. Skills & Competencies Required: Technical Skills: Basic knowledge of production machinery and manufacturing processes (API). Understanding of GMP/GLP compliance. Basic computer skills for data entry and reporting.

Greetings! I am Priyanka. We are hiring QA Trainee / Officer Off roll for A leading API Manufacturing Company. Designation: 1. QA Officer/ trainee Off Roll Salary : Take way home [no benefits. no deduction] Location: Mysore Looking forward to hear from you. Note: No Charges Thanks & Regards Priyanka [ 9518220852 || priyanka@avaniconsulting.com ]

Job Responsibilities: Handling and monitoring the process in shifts. Following cGMP and Records updating (BPR, Data record, Machine running hours, Cleaning records) Manpower handling in shifts. Planning of shift activities & monitoring of shift activities. Supporting Pl ant- in-charges to achieve targets as per production plan. To follow ALCOA++ and data integrity procedures as per guidelines. Immediately reporting to plant in charge if any, abnormality noticed during the process and plant in the shift. To adhere cGMP (Q7 guidelines). Coordinating with QA, QC, Services department like electrical and mechanical, stores departments. To ensure good housekeeping and safety of men, material and machinery in the plant. To monitor overall plant parameters, equipment's and utilities. Any deviation during process report to superior and update the deviation related documents Trouble shooting in plant. To monitor the material movement during the shift hours. Proper communication during shift relieving & hand-overing. Receipt of Raw Materials & Material Management. Responsible for DM plant operation and Monitoring. To ensure to work collaboratively in all the shifts and with other departments. To contain, control the spills, salvaging of spills in his section.

Junior Executive/ Executive - Production (API) Job Criteria: B.E-B.Tech (Chemical Engg.) / M.Sc./B.Sc. 1 to 5 years of experience Job Role: Ensure that the products are manufactured as per the cGMP and handle critical equipment like reactor, centrifuge, blender, sifter, multi-mill, etc. Maintain documentation as per regulatory requirement like change control, deviations. Highlight technical problems and take corrective actions, and maintain safety practices. Technical Officer/ Junior Executive/ Executive-Production+Packing (OSD) Production Job Criteria: M. Pharm/B. Pharm/DME/ITI 2 to 7 years of experience Job Role: Manage granulation, compression, coating, pelletization and capsule filling area. Packing Job Criteria: M. Pharm/B. Pharm/DME/ITI 2 to 7 years of experience Job Role: Manage blister packing, bulk/bottle packing, documentation, Track and Trace and serialization. Technical Officer/ Junior Executive/ Executive- Production (Injectable) Job Criteria: M.Pharm/ B.Pharm/ Diploma/ITI 2 to 7 years of experience Exposure to aseptic practices and good documentation practices are must. Job Role: Handle manufacturing skids, Fedegari autoclaves ,Isolator, lyophilizers, vial washing and tunnel, vial/ ophthalmic /PFS filling and aseptic filtration, FFS, CIP/SIP, filters, microsphere refiner, active freeze drying System. Execute manufacturing activities as per SOP. Operation, cleaning, sterilization, qualification and maintenance of solution preparation systems.

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. Collaborate with production and quality teams to identify and resolve quality issues.

Hiring Quality Assurance Officer with 1 to 3 year experience. Should have sound knowledge of Production of Pharma/chemical industry Documenting and keeping records and assisting QA team for in depth analysis. Handling preventive action Required Candidate profile Review of Risk Assessment & investigation report. Should be Bsc in organic chemistry. nearby western line mumbai candidates will be preferred upto Boisar,Tarapur,Palghar district. Male candidates

Officer Production, Vapi, Gujarat Responsibilities: Equipment cleaning as per ECR/SOPs Ensure cGMP compliance Execute batch charging (BMR/BPR) Maintain records Complete BMR/BPR/ECR documentation Apply at talent@hireindians.com or call 8882212459. Required Candidate profile Qualifications & Skills: * B.Sc. / M.Sc. in Chemistry (Analytical/Organic/Industrial) or B. Pharma. * 1–4 years of experience in pharmaceutical formulation/API manufacturing.

Role & responsibilities To have sound Knowledge of API Production as Chemist Understanding of Reactor handling , BMR handling / BPCR Handling . Process handling, Documentation. handling the batches for distillation and monitoring in shifts as per Instruction of shift in charge. set up and adjust the machine as per batchs requirement . Preparing of Area for Audits Preferred candidate profile The candidate with API experience only Send mail with your CV attached in PDF and subject mentioning FOR POSITION OF PRODUCTION CHEMIST to jagpal.dewal@ipca.com

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

Candidate needs to handle all shop floor responsibilities of plant which includes batch and shift schedules preparation, planning and execution of batches, GMP documentation compliance, support in GMP audit compliance and investigation team

HE should be able to implement Pharmaceutical SOP for Production department with help of Manpower and Materials, Shift wise produciton as per schedule . Implementaton SOP on ground level under guildelines -SOP of GMP /FDI in various Produciton lines Required Candidate profile HE should be able to implement Pharmaceutical SOP for Production department with help of Manpower and Materials, Shift wise produciton as per schedule under guildelines of GMP-FDI for production

A Production Officer is responsible for carrying out shift production activities by following instructions from superiors like the AGM or Sr. Manager. A key part of the role is ensuring all raw materials and required batch sheets are available on time for planned batches. You will coordinate with the Engineering department for timely maintenance and with QC for in-process and finished product analysis. The position requires you to strictly follow GMP and safety norms, attend EHS training, and adhere to relevant Standard Operating Procedures (SOPs) . You will monitor and maintain stipulated parameters such as temperature, pH, and pressure during batch processing and record any observed abnormalities or deviations. You are responsible for preparing, checking, and reviewing production instructions and documents like BPCR, BCLR, MFC, and SOPs . The role includes producing APIs (Active Pharmaceutical Ingredients) and intermediates according to pre-approved instructions. You will ensure production facilities and equipment are clean, maintained, and calibrated, and will verify the environmental conditions of controlled areas. You are also responsible for managing and verifying the health and hygiene of contract workers and controlling their performance. In the absence of your reporting person, you will take responsibility for production activities and ensure that all ERP entries are correctly made and that subordinates are trained on the system.

Responsible for Supporting API plant operation in shift, handling equipment like- Reactor, Centrifuge, FBD, RMG, Sifter, MCM, Blender, VSM, Filter Etc, Maintain all parameters as per SOPs, trouble shooting, compliance of GMP, EHS & ISO norms etc Required Candidate profile M.Sc./B.Sc/Dip.Chemical with 4 to 8 yrs relevant working exp in API/Bulk Drug plant. Should be well Conversant with API mfg conversion reaction & unit operation. Must have work exp of GMP compliance. Perks and benefits Negotiable

Responsible for API Plant shift Oprn like batch charging,Reaction, extraction etc, Planning& Scheduling Prodn activities, maintain parameters as SOPs, Ensure GMP regulatory/EHS & ISO compliance, troubleshooting, documentation, SAP Entry, Manpower mgt Required Candidate profile BE-Chemical with 4 to 8 yrs relevant working exp in API plant. Should be well Conversant with API mfg conversion reaction & unit operation like filtration, drying, Batch/Continuous Distillation Column Perks and benefits Negotiable

Responsible for nutrition addition, harvesting, washing, homogenization, spray drying, packing. Shall check the maintenance of the department, premises, and equipment as per SOP and GMP norms.

We are looking for a meticulous Asst. Manager Production to lead production activities at Synnat Pharma Private Limited, ensuring seamless API manufacturing operations and adherence to the highest quality standards. As Asst. Manager Production, you will play a pivotal role in overseeing daily production activities, monitoring validation batches, and ensuring compliance with cGMP guidelines. Your responsibilities will include the preparation and review of production-related documents, coordination with cross-functional teams, and active participation in internal and external audits. You will also be responsible for identifying and resolving operational gaps, managing deviations and Out-of-Specification (OOS) incidents, and implementing Corrective and Preventive Actions (CAPA). With a strong focus on process optimization and continuous improvement, you will contribute to enhancing production efficiency and maintaining a facility that is always audit-ready. Your expertise in QMS (Quality Management Systems) and experience with ERP systems (SAP) will be crucial in driving operational excellence and ensuring the delivery of high-quality pharmaceutical products. Responsibilities: Oversee daily API production activities, ensuring compliance with established procedures and cGMP guidelines. Monitor validation batches, process parameters, and Batch Manufacturing Records (BMR/MBMR) for accuracy. Verify online BMRs and ensure compliance with regulatory and documentation standards. Coordinate with utility, QC, Stores, and Engineering teams to support seamless production operations. Supervise movement of finished products, intermediates, and recover solvents as per protocols. Identify and resolve operational gaps at the floor level to improve efficiency. Manage deviations, Out-of-Specification (OOS) incidents, and implement CAPA measures effectively. Ensure compliance with QMS and audit requirements; participate in internal and external audits. Prepare, review, and maintain accurate production documents, including validation protocols and training records. Develop preventive maintenance schedules, monthly production plans, and calculate raw material requirements. Train and mentor team members on production processes, compliance, and quality standards. Report production activities, deviations, and audit compliance to management while driving process improvements. General Expectations and Past Experiences: Strong understanding of API Manufacturing processes and cGMP guidelines. Demonstrated experience in preparing and reviewing production-related documents, including BMRs, validation protocols, and SOPs. Proven ability to manage and resolve deviations and Out-of-Specification (OOS) incidents effectively. Proficiency in using ERP Systems (SAP) for production planning, inventory management, and data analysis. Experience in participating in and contributing to successful internal and external audits. Strong leadership and communication skills with the ability to train and mentor production staff. In-depth knowledge of Cleaning Validation procedures and QMS (Quality Management Systems).

Responsibilities: * Ensure compliance with regulatory standards * Collaborate with cross-functional teams on new product launches * Develop API formulations using chemical expertise

As an Officer in API Production at Sun Pharmaceutical Industries Ltd, your primary responsibility will be to carry out batch operations in compliance with safety, cGMP, and SOP guidelines. You will be tasked with filling BPRs, maintaining online documentation, and ensuring data integrity accuracy. It is essential to uphold SOP compliance records and execute batch processing as per BPR and SOP requirements. Operating and handling equipment according to SOP, cleaning and sterilizing equipment, and conducting integrity testing of sterile grade filters are crucial aspects of this role. Furthermore, you will be responsible for planning the work of technicians, maintaining housekeeping in the designated work area to ensure product efficacy, purity, and safety. Effective communication with superiors and subordinates is key to carrying out work instructions accurately. Maintaining good housekeeping standards in the working area, personal hygiene, and executing tasks such as unloading sterilized articles and executing process simulations are essential duties in this role. Additionally, coordination with IPQA, QC, and Micro departments for PCO, Campaign changeover cleaning, and in-process sampling is required. You will also be involved in environmental monitoring of controlled and critical areas, reviewing calibration reports and trends, as well as calibration of sensors. Verifying critical routine operations, performing cleaning and sanitization activities as per SOP, completing assigned training on time, and maintaining shop floor discipline are integral parts of this position. Moreover, executing protocol-based activities, ensuring harmonious relationships among employees, and following proper handover procedures before leaving the workplace are critical responsibilities. Your role also involves documenting entries in respective SOPs, checking recorded entries, and upholding high standards of cleanliness and compliance throughout your work area.,

Position Summary Prepare breakfast and/or lunch offerings and assist with serving lines Participate in occasional catering functions Perform all positions within the kitchen, Opaa! Food Management, Inc operates in 8 states in the Midwest Our pay rates vary depending on state and position Please apply, and a Hiring Manager will discuss pay with you in more detail, Functions of the Job Essential Functions Production Assist with the set-up of serving lines daily and make sure that all food is held at the required temperature Milk coolers are stocked and ready for service, Assist in the preparation of foods in accordance with the menu plan and Opaa! recipes, as required Plan and prep ahead for the next day's menus, Operate slicers, mixers, grinders, and other equipment with proper certification, Keep work areas neat, clean, and organized, Clean kitchen and cafeteria areas including equipment and dishes, Keep inventory stock organized and practice First In/First Out (FIFO) procedures Keep cooler/storage racks clean and free from debris, Clean, monitor chemical usage, and maintain equipment in the dishwashing area Remove clean dishes from the machine and store them in serving areas, Requisition appropriate amounts of food and supplies through the Kitchen Manager, Prepare bread, cakes, cookies, and other baked goods as required by the menu plan Present to customers in an appealing manner, Batch cooking to maintain a quality product and excellent food presentation, Set up serving/bar lines and ensure all food is held at the proper temperatures Clean and restock items as needed, Serve items as needed with proper serving sizes and utensils Quality presentation and hospitality are required, Keep serving lines/condiments supplied with food items, napkins, silverware, and dishes as needed to customers, Compliance Prepare foods for meal service in strict compliance with the menu plan and Opaa! recipes, Convert and follow a standardized recipe to ensure a consistent, high-quality product, Recognize a Reimbursable Meal and follow the Meal Pattern according to HHFKA and CACFP regulations, Keep and Maintain accurate daily production records per grade group as planned, Follow HACCP processes and procedures with daily, weekly, and monthly food safety logs Record temperatures of all hot and cold food, Obey safety rules as outlined in Opaas ?Safety Procedure Manual? and exercise caution in all work activities, Report any unsafe working conditions to the appropriate supervisor Participates in the safety incentive program, Participate in the ?Daily Dish?, Attend all required meetings and in-services Complete the required yearly continued training hours according to HHFKA, Demonstrate and promote Opaa!s Core Values of ?Always Act in the Best Interest of the Students, Schools, and Communities We Serve?, ?Be Honest?, ?Have a Passion to Serve Others?, and ?Commit to Continuous Improvement?, Maintain strict compliance with the Opaa! Food Management, Inc Timekeeping Policy Administrative Handle customer monies at service time, as required Make changes as well as run a cash register or computer Require that only reimbursable meals are allowed through the POS system, Complete necessary paperwork, tray counts, and meal reconciliation tasks on a daily basis, Submit all hours worked by clocking in and out in ADP or by submitting an edit sheet for any missing time Notify DNS 24 hours in advance of inability to cover an assigned shift In the event of an emergency, notify the DNS as soon as it is administratively feasible, Other duties as assigned, Physical/Visual Activities or Demands Physical/visual activities or demands that are commonly associated with the performance of the functions of this job, While performing the duties of this job, the employee is frequently required to stand, walk, sit, squat, climb, balance, kneel, crawl, push, pull, grasp, feel, taste, smell, talk, hear, and reach with hands and arms, The employee must exert over 60 pounds of force occasionally and/or be able to frequently lift, carry, push, pull, or otherwise move objects up to 25 pounds, Specific vision abilities required by this job include concentrated attention, depth perception, the ability to bring objects into sharp focus, and color vision, Working Conditions Working conditions commonly associated with the performance of the functions of this job: Inside and outside working conditions, Frequently works around moving mechanical parts and is frequently exposed to wet and/or humid conditions and extreme heat, Occasionally exposed to toxic or caustic chemicals and extreme cold, The noise level is usually loud, Education Position Qualifications High School Diploma or GED, preferred; or up to one-month related experience, training, or equivalent combination of education and experience Language Skills Ability to read and comprehend simple instructions, short correspondence, and memos Ability to write simple correspondence Ability to effectively present information in one-on-one and small group situations to customers, clients, and other employees of the organization, Mathematical Skills Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, commons fractions, and decimals Ability to compute rate, ratio, and percent and to draw and interpret bar graphs, Reasoning Ability Ability to apply commonsense understanding to carry out detailed but uninvolved written or oral instructions Ability to deal with problems involving a few concrete variables in standardized situations, Machines, Tools, Equipment, And Work Aids Dishwasher, Steamer/Kettle, Mixer, Oven, Stove, Fryers, Slicer, Thermometers, Gauges, Knives, Box Cutters, Meal Counting Software, Desktop PCs, Calculator, Telephone, Fax, Scanner, Copier, Printer, Opaa! is committed to creating a diverse environment and is proud to be an equal-opportunity employer All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status,

1. API synthetic process tech transfer to plant and scale-up at plant. 2. BMR and scale-up documents preparation. 3. Process Validation 4. Plant batch trouble shooting 5. Production of API at plant. Required Candidate profile 1. Knowledge of process development and tech transfer 2. API plant working experience 3. Working experience in pharma company with good production knowledge. 4. Knowledge of GMP