214 Api Production Jobs - Page 7

Roles and Responsibilities Only for male candidates Department requirements - Production, solvent recovery plant, Technical service dept, Warehouse, Quality assurance, Quality control, R&D, AR&D, DQA, RA and HR Ensure compliance with GMP guidelines and regulatory requirements for API manufacturing. Oversee bulk drug production, quality control, and warehousing operations. Develop and implement effective QA/QC procedures to ensure product quality and purity. Collaborate with cross-functional teams to resolve issues related to active pharmaceutical ingredients (APIs) and bulk drugs. Conduct regular audits and inspections to maintain high standards of quality assurance.

Job Responsibilities: A. To be take and hand over charge of shift at shop floor. B. To ensure the adherence of SOP and cGMP during the manufacturing operation in the plant. C. To prepare Raw material requisition slip in the every first shift based on daily production planning and submit to the warehouse department. D. To be fill the online documents of production like BMR, Usage log book of equipments, weighing Scale calibration etc during the shift. E. To be dispose the Hazardous waste as per the SOP during the shift. F. To ensure the safety of persons and equipments in the plant during the shift. G. To be ensuring that before starting the production, equipments are cleaned as per SOP. H. T...

Role & responsibilities 1. To procure Raw materials from Ware house 2. Perform the Operations in accordance to the established SOPs and cGMP and capture the data in relevant documents. 3. To maintain for Good documentation practise at work place 4. To ensure the entry of batch related details in ERP. 5. To execute batches every day as per the Production planning schedule. 6. To arrange for Quality testing of in-process, intermediate & finished goods as per SOP.

Experience in API pharma Perform all QC activity as per defined SOP and document it on time. To assist the Head QC in investigation of OOS results. To maintain the stability chamber for temperature, humidity, and recording.

Roles and Responsibilities Ensure compliance with GMP guidelines during API manufacturing processes. Operate centrifuges, reactors, and other equipment safely and efficiently. Maintain clean room design principles to prevent contamination. Monitor bulk drug production lines for quality control purposes. Collaborate with team members to achieve production targets.

M.Sc. Chemistry / M. Tech. Chemical Engineering with 5 to 10 years of experience in process / production department of synthetic organic manufacturing unit. Managing of production. Managing production planning to meet production targets. Required Candidate profile Managing manpower & monitoring timely execution of various jobs for targets within time frame. To ensure the time cycle of all stages of production. To prepare SOP related to production department. Perks and benefits Negotiable - Depending Upon Candidate & Experience

M.Sc. Chemistry / M. Tech. Chemical Engineering with 5 to 10 years of experience in process / production department of synthetic organic manufacturing unit. Managing of production. Managing production planning to meet production targets. Required Candidate profile Managing manpower & monitoring timely execution of various jobs for targets within time frame. To ensure the time cycle of all stages of production. To prepare SOP related to production department. Perks and benefits Negotiable - Depending Upon Candidate & Experience

M.Sc. Chemistry / M. Tech. Chemical Engineering with 5 to 10 years of experience in process / production department of synthetic organic manufacturing unit. Managing of production. Managing production planning to meet production targets. Required Candidate profile Managing manpower & monitoring timely execution of various jobs for targets within time frame. To ensure the time cycle of all stages of production. To prepare SOP related to production department. Perks and benefits Negotiable - Depending Upon Candidate & Experience

M.Sc. Chemistry / M. Tech. Chemical Engineering with 5 to 10 years of experience in process / production department of synthetic organic manufacturing unit. Managing of production. Managing production planning to meet production targets. Required Candidate profile Managing manpower & monitoring timely execution of various jobs for targets within time frame. To ensure the time cycle of all stages of production. To prepare SOP related to production department. Perks and benefits Negotiable - Depending Upon Candidate & Experience

M.Sc. Chemistry / M. Tech. Chemical Engineering with 5 to 10 years of experience in process / production department of synthetic organic manufacturing unit. Managing of production. Managing production planning to meet production targets. Required Candidate profile Managing manpower & monitoring timely execution of various jobs for targets within time frame. To ensure the time cycle of all stages of production. To prepare SOP related to production department. Perks and benefits Negotiable - Depending Upon Candidate & Experience

M.Sc. Chemistry / M. Tech. Chemical Engineering with 5 to 10 years of experience in process / production department of synthetic organic manufacturing unit. Managing of production. Managing production planning to meet production targets. Required Candidate profile Managing manpower & monitoring timely execution of various jobs for targets within time frame. To ensure the time cycle of all stages of production. To prepare SOP related to production department. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Recruiter Details Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy Role & responsibilities 1. Ensure compliance of applicable legal & statutory requirements related to Environment, Occupational Health and Safety Management system. 2. Liaising with Directorate of Industrial Safety & Health (DISH) office, PECO, Fire department, District supply officer, MPCB, CPCB need basis for legal requirements. 3. Ensure effective implementation of Environment, Occupational Health and Safety Management system. 4. Ensuring initiation, planning & support for trainings, examine the effective of training. 5. To advise concerned department heads for implementation of Environment Health and Safety p...

Job Objective : 1. Excellent team player/leader can efficiently motivate the subordinates to achieve the set targets within stipulated time. 2. Proficiency in written and oral communication skills. 3. Ensuring best in class quality and timely project execution 4. Strong initiative in decision making and owing up of responsibilities. 5. Strongly believe in turnaround of Business, systems and procedures with an integration of internal skill set along with outstanding team building. Job Role: 1. All activities related to production and monitoring the process as per SOPs. 2. Communicate day to day process deviations and breakdowns of the equipment to concerned persons. 3. Check and implement the...

Preferred candidate Profile: Only for Male candidates. Shift Incharge: 06 to 10yrs Chemist : 0yrs to 5yrs

Role & responsibilities: Person skilled in analytical handling, VQ, APQR, QMS. Preferred candidate profile we have requirements 2-5 year's for Chemist and 10-12 year's for Asst. Manager. Only for male candidates.

Eligibility: Experience : 2-3 Years Position: Shift Chemist Departments: API Production Qualification: M.Sc, Diploma, B.Sc, B.Tech Chemical 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

Review DCS alarms. Ensure that batch charging and other manufacturing operations are strictly in accordance with the BMR/SOP and align with current GMP practices. Maintain manufacturing records online, ensuring compliance with data integrity practices. Collect samples of intermediate/in-process materials and send them to the IPQC/QC lab. Enter and verify production-related inputs in the SAP system. Review and ensure the generation of PISCADA reports. Transfer finished goods using the "Finished Goods Transfer Note." Monitor and ensure minimum stock levels of consumables, logbooks, and status labels. Ensure preventive maintenance of all equipment according to the schedule. Coordinate with serv...

To handle DCS as operator. Ensure batch charging & other manufacturing operations should be strictly as per BMR/SOP & in line with current GMP practices. To maintain manufacturing records online & should comply data integrity practices. To take out sample of intermediate/in-process material and send to IPQC/QC lab. To ensure the production related inputs in SAP system. To be check and ensure the PISCADA reports generation & review of DCS alarms. Transfer finished goods through Finished Goods Transfer Note. To Check and ensure minimum stock of consumables, Logbooks & status labels. Ensuring preventive maintenance of all equipment as per schedule. Co-ordinate with service departments (QA, QC, ...

Job Description: Operate, monitor, and optimize chemical production processes. Prepare chemical batches according to Standard Operating Procedures (SOPs). Ensure quality control through in-process testing. Coordinate with Quality Assurance (QA) and R&D teams for process improvement and new product trials. Maintain production documentation, including batch records, logbooks, and reports. Adhere to safety protocols, chemical handling procedures, and environmental regulations. Troubleshoot equipment malfunctions and process deviations. Support in scaling up lab-scale processes to full-scale production. Monitor inventory levels of raw materials and reagents. Train and guide plant operators and j...

Lead research and development of APIs, excipients, and formulations. Optimize existing formulations and explore new product ideas. Conduct laboratory research, testing, and documentation. Collaborate with QC, production, and regulatory teams. Required Candidate profile Min 10 years of R&D experience in the pharmaceutical sector. Strong knowledge of formulation science, GMP, and regulatory norms. Skilled in analytical techniques, lab procedures, and instrumentation.

Hi, Greetings from Avani Consulting!!! Walk in Invitation: We have job opportunity with API Manufacturing Plant for Associate /Sr. Associate Production Profile for Mysuru Loaction. Interview Location BANGALORE We are having face to face interview on 21st June Saturday in Bangalore.- Single Round Face to face Company : A leading Pharma API Unit - in Mysore Position - Production Department Associate /Sr. Associate Work Experience Min 5 yrs in API in current Salary 20% to 25 % hike on current CTC. Note: No Charges If interested drop your CV to Shweta Gupta [ 7015954549|| shweta@avaniconsulting.com ] Thanks & Regards Shweta Gupta

Role & responsibilities Graduate engineer + having 5 to 7 years Exp. Of training documentation and implementation Capable to organise training related to management system Standard .prepare quality manual and system procedures, co-ordinate with department for completing & implementing the work related to audit. To conduct MRM & internal audit as per requirement of API, ISO 9001-14001 standard. To prepare record of internal audit ,data analyses .To review the quality environment and health and safety policy periodically and endure safety management system is effectively implemented and maintain to the requirement of customer standards. The work related to audit.

1. Should be handle instrument activity of project 2. Should know the cGMP awareness related to project 3. Document Handling (DQ,IQ,PQ) Kindly share your updated CV on sneha.shinde@embio.co.in & kchoudhary@embio.co.in

Maintaining Good housekeeping in workplace as per cGMP Equipment Operation and cleaning should be followed as per SOP Receipt and storage of raw material in day stock area for the batch as per Material Requisition slip Carry out the process as per manufacturing & packing record instruction All safety rules/precaution to be followed strictly in manufacturing area In process checks and documentation should be followed as per procedure Maintaining cGMP standards, ISO 9001, ISO 14001 & HACCP standards in the plan Make sure that the production facilities are clean and when appropriate disinfected Ensure that the premises and equipment are maintained and records kept in respective area Responsibil...

JOB DESCRIPTION: Maintaining work place-good housekeeping as per cGMP Operating and cleaning of equipment as per SOP Receipt and storage of raw material in day stock area for the batch as per request slip Carry out the process as per LMR and operation verification All safety rules/precaution to be followed strictly Execution of the production schedules for current and coming months Coordinating internal /external audits and maintaining relevant documents In process checks to be done and documented in presence of supervisor Maintaining cGMP standards, ISO 9001, ISO 14001 & HACCP standards in the plan Making sure that the premises and equipment are maintained and records kept Responsibility in...