167 Bulk Drugs Jobs - Page 2

To implement cGMP QC labo. pharma regulatory standards.• FDA of small molecule & analytical methods/equipment: GC, LC, ICP-MS, KF, LOD, ROI, optical rotation, RI, stability analysis, light obscuration, potentiometric titrations, spectroscopy

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

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.

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

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

Hiring For QC AM For Formulation Co in Khambhat Location Qualification: BSc / MSc / B.Ph / M.Pharm Exp : 8 to 18 Years CTC: Good Salary Experience in Formulation Is Must Send CV on sdpbharuch@gmail.com with Subject: QC Khambhat Share with Friends Required Candidate profile SDP HR SOLUTION 611, Golden Square, Beside DMART, Near ABC Circle, Bholav, Bharuch - 392001 Free Jobs !!1 Share with Your Friends & Colleagues!!!

Urgent Requirement in PHARMA Industry Experience persons wanted in R&D(RESEARCH & DEVELOPMENT) Department in BULK DRUGS (API), candidate should have good working experience in pharma industry. Qualification: B.SC /M.SC (Chemistry) Experience: 2-5Years Location: Jeedimetla , Hyderabad. Note: Only Male Persons Required. Contact: 8977333658.

Job description The primary role of an Expert Sales Executive is to ensure coverage plan of the said specialties on a regular basis to deliver scientific information and knowledge on Haleon products and relevant disease conditions, thereby adding value to the HCP. Role Ensure favorable recommendation in form of prescriptions by scientific promotion for Expert detailed brands for relevant specialty. Demonstrate effective Pre and Post Call Planning customized to specific HCP requirements. Understand territory performance data, build doctor & chemist profiles for effective territory management. Maintain and reconcile monthly inventory of all inputs and samples. Timely reporting as per systems & process laid out by the organization. High engagement with the GT team and other relevant. Regional stakeholders to ensure delivery of overall regional Business plan. Respond promptly to HCP queries within the individuals area of knowledge or seek support to resolve the same. Strict adherence to compliance protocols of the organization, including but not limited to reporting adverse events. Requirements: Desired Qualifications Science/Commerce graduate, B.Pharm/B.Sc/M.Pharm/MSc. Experience: 2-7 years of experience of working in a Pharma Location: Surat **Interested candidates can share their resume on pranitaa.x.prakashshetty@haleon.com Contact: 7418467771

#BDM hashtag#API hashtag#DrugIntermediate hashtag#BulkDrug Greetings from India Pharma People A leading API and Drug Intermediate major is looking for a Business Development Manager based at Mumbai The position would be responsible for B2B / Corporate Sales / Pharma Sales Product Listing Active Pharmaceutical Ingredient (API) Sales Po- Purchase Order Generation Competitive TOT/Agreement Sign off Ensure Competitive Market Share Bulk Sales / Vendor Management Candidates with relevant experience may please share their CV at ipp@indiapharmapeople.com or whatsApp at 9767790833 Regards Jai Hind Satish Sanhotra India Pharma People 9767790833

Role & responsibilities International Business Development and International Sales and export marketing in Pharmaceutical & Bulk Drugs, APIs Preferred candidate profile

Designation - Asst. Manager - Production - HOD Company - Leading Pharma Raw Material Mfg. Company Job Location - Dahej, Bharuch Qualification - B.E./ Diploma- Chemical / B.Sc. / M.Sc. Experience - Min. 10yrs. and above share with your friends. Required Candidate profile will be working in General Shift Must have experience in reaction, filtration, spray dryer, flash dryer Team Handling candidate from Chemical, Pharma, API, Cellulose, Bulk Drug, Pharma Intermediate

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 ]

Oversee and manage daily production activities Ensure adherence to cGMP and EHS guidelines Coordinate with cross-functional teams for smooth operations Optimize processes for efficiency and quality

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.

As an experienced professional with a minimum of 15+ years of relevant industry experience in API (Bulk Drugs), your role will involve leading, planning, and monitoring the day-to-day activities of the Warehouse. You will be responsible for maintaining API, Bulk drugs, and Chemical warehouses in compliance with ISO, cGMP, and regulatory guidelines. Your key responsibilities will include preparing and leading the department during Financial Audits, conducting Yearly Stock Audits, and maintaining Monthly Stock Statements. You will also be involved in the preparation of stores SOPs, monthly planning with production, and coordinating with the planning department. Furthermore, you will be accountable for ensuring warehouse security, maintaining accountability of inventory, and liaising with PCB. Your educational background should include a B.sc/M.sc in Chemistry (Mandatory) with an MBA qualification. If you are a dynamic professional seeking to make a significant impact in a challenging and rewarding environment, this opportunity based at the Factory location could be the ideal fit for you.,

Only for male candidates We are hairing for Chemists/Sr.Chemists/Manager/Ass.Manager 02 to 15 yrs(peptides) R&D CDMO:Sr.Executive/Executive(05 to 8 yrs) Roles and Responsibilitie Develop peptide-based products from concept to commercialization, ensuring compliance with regulatory requirements. Design, optimize, and scale up peptide synthesis processes using various techniques such as solid phase synthesis, solution phase synthesis, and enzymatic synthesis. Ensure timely delivery of high-quality products that meet customer expectations. Conduct research on new technologies and methodologies to improve productivity, efficiency, and quality of peptide production.

Role & responsibilities To receive operating instructions for the shift from Production Executive products. Ensure batch processing is carried out strictly in accordance with batch records and as instructed. Operates the process ensuring that all parameters are strictly followed and are within the specified limits. Responsible for maintaining Good House Keeping in all the areas of Production department. Ensure that the equipment's are always clean from outside. Follow GMP and Safety Instructions during the work. Ensure use of appropriate safety apparels while on work and should be aware of the location of fire fighting equipment and know operation. Shall be responsible for operating all the utilities, equipment's as per the operating instructions and ensure that the process parameters are strictly followed. Report immediately to the Executive / Officer any deviations observed during the operation. Preferred candidate profile We are looking for Male candidates to work for API Manufacturing industry . CLEAN ROOM activities - Majorly for freshers and Jr.officers . Current openings : 40Nos Designation : Freshers - BSC in chemistry / Diploma in chemical engineering only Junior officer : BSC in chemistry / Diploma in chemical engineering only Officer & Executive : BSC/MSC, BTech in Chemical Engineering Experience required : 0 to 5 years Any query ? Please reach out ramya_n@hikal.com

Recruiter Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy Role & responsibilities Operations Excellence (OE) Cost Productivity: Drive constraint / critical API projects • Drive throughput improvement projects on constraint/critical line • Identify scope of improvement short / long term capacity debottlenecks area. • Capacity challenges across units to support new and current business & filling requirements. • Ensure and plan the execution of improvement projects in co-ordination with Business / CI and manufacturing team. • Identify and managing scope for opportunity / improvement by analysing the trends of batches for continuous improvement. • Ensure HSE and cGMP practices are strictly followed during continues improvement projects. • Compilation of all completed projects and financial impact achieved for tracking of savings along with CFT alignment. Cost Productivity: Improvement & Tracking of Equipment Efficiencies Initiate OEE tracking of bottleneck lines to identify losses and drive improvement projects. • Tracking improvement projects related to Opex driven by Operational Excellence team in each unit/Block. • Cost Productivity: Improvement & Tracking of Product (SKU wise) Overall Yield (IL4 & IL6) • Prioritization of Top SKUs basis Volume & Value. • Compilation of all completed projects along with financial impact achieved for tracking of savings along with its alignment with site & central finance. Process Robustness • Improve process capability of products highlighted by units using DMAIC approach As per business need Capability Building - LSS Academy • LSS trainings to shop floor aspirants. • Creations of White belt & Green belt (LSSGB & LSSWB) • Deployment of LSS projects through DMAIC approach & different analytical. • Excel & PowerPoint first hand trainings to unit team • Meetings Simplification, though internal Dashboard Development and Visual Management Manufacturing 4.0 (Pegasus) Digital Transformation Use Cases • Initiate data collection, daily governance for sprint use cases OEE, cycle time etc. • Ensure 'AA' model for initial deployment of analytics use-cases. • AA-based process capability improvement for enabling 'golden batch' outcomes. • AA based cycle time variability reduction driving production improvement. • Digital-and-analytics led dynamic real-time manpower allocation. • PPDS (Production Planning & Detailed Scheduling) Implementation Pegasus Data & tech • Support and work with Data and tech lead to drive for Bottom-of-stack: unit-level interventions identification for high, medium high, medium low and low maturity units VIII. Mfg 4.0 Pegasus Mfg Tech & Auto • Support to execute the site specific project management for the aspiration for manufacturing technology upgradation (including automation),basis business need Review database / dashboards and performance review documents Tracking of Operations dashboard (Thoth) on monthly basis for Cipla and subsidiary units. o FTE/Kg o D2D o Cost/Kg Units o C Vs A o OEE o Mi-wave • Coordinate with HR and Finance to collate Manpower, Opex & Yield data. Employee engagement Conduction of Idea generation sessions all units. • Structured reward & recognition (digital / F2F platforms) for various cost productivity initiatives • Tracking of major Quality & Delivery deliverables through “Unit of the month” recognitions Manpower productivity Manpower optimization / repurposing by execution of various tools at shopfloor, such as OPE, DILO, OEE use case deployment. • Evaluate and recommend manpower asks request which is been raised by Unit. • Area/Equipment wise manpower plotting Manning Proposal Evaluation Recommendation on Capex proposals for asks raised by unit team – Basis Ask • Monitoring of Utilization & OEE monitoring area wise Coordinate for the execution of special projects across all units to ensure timely completion of Operational excellence initiatives. Drive and execute different projects related to automation, process, work simplification, establish processes, throughput improvement, yield improvement etc. that are identified based on business needs. • Supports cross functional teams on their continuous improvement journey by guiding them through an understanding of Lean Six-Sigma concepts, CI methodology, Kaizen events and other process improvements methods to drive key KPIs in cost, delivery, and quality. Support to Unit Team -Basis Ask Analysis of data • PPT • Energy and Water Projects • Internal Dashboard’s • Other Projects Drive – Short term/Long term Preferred candidate profile Preferably a Graduate in Chemical/Mechanical/Industrial Engineer 5-10 years in manufacturing excellence with knowledge of Lean manufacturing (Chemical/API Industry experience shall be an added advantage) Six sigma & Lean certifications like Green belt, Black belt Excellent Problem solving and analytical skills Quick Learner with interest in new technologies & Problem Solving challenging. Sound Process Engineering knowledge Good interpersonal & intrapersonal skills with ability to work in cross functional environment. Ability to form and lead CFT. Knowledge of basic statistical tools, applications, and data analysis Sound knowledge in Ms Office Tools (Excel, PPT and word file) Entrepreneurial Mindse Recruiter Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy

Recruiter Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy Role & responsibilities Operation, Maintenance, Control and Monitoring: Monitoring and implementing the preventive and breakdown maintenance of all the equipments & facilities of entire unit. Ensuring the availability of power supply to the plant without any interruption. Monitoring and supervising the operation and maintenance of substation equipments and facilities. Ensuring the implementation of preventive maintenance for critical electrical equipments such as HT breakers, LT breakers, PCC & MCC panels, protection relays, control panel, PDB, LDB, UPSDB, capacitor bank, harmonic filter diesel generator sets, uninterrupted power supply units, material hoist, EPABX system, passenger lifts, electrical stackers, CCTV camera, etc. Maintaining the optimized inventory of spares in engineering stores. Maintaining the availability of critical spares required to avoid major production delay. Reviewing and inspection of material inventory at engineering stores as per Purchase order. Initiating the request for maintaining the required inventory with coding in place for regular consumables items. Maintaining proper housekeeping and upkeep of engineering areas (substations, HT yard, MCC rooms, transformer yard, DG room, UPS room, DCS rooms, Calibration room, technical areas, hoist machine rooms, plant terrace, etc.) Executing the submission of CER / PR’s as per requirement with standard specification. Coordinating with purchase and vendors for clearing technical queries and release of PO Preparing of budget for Power Consumption, OPEX and CAPEX budget. Tracking and monitoring of budget on monthly basis. Analysing the increased variance against benchmarks and implementing the actions for controlling the same. Implementing the rectification of machinery breakdowns with minimum response time to avoid the impact on quality and productivity. Reviewing and monitoring of MTBF & MTTR for critical equipment as per benchmark. Encouraging team for the identification of various measures for controlling and reducing the available OPEX expenses by spare management and vendor development. Preparing the cost estimate for maintenance, major modification and project activities. Reviewing and checking the documents and records like daily log books, substation checklists, preventive maintenance records, calibration records, etc. Co-ordinating with concerned department in charges and heads for timely execution of engineering activities. Tracking to be done for all the activities as per plan. Preparation & sharing of reports like power consumption report, safety dashboard, CER tracking, CAPA tracking, OPEX report, MTBF report, etc. Identifying new technologies and vendor development for the system improvement and ease of operation and maintenance. Ensuring on-line bill processing against the availed services for the timely payment to vendor. Designing and selecting of tools, equipment’s, machinery, safety and protective devices as per the norms. Planning and Co-ordinating with contractors and vendors for the scheduling of maintenance activities. Ensuring close supervision while execution of critical task for maintaining the quality and safety standards. Providing the engineering support required for the modification / upgradation / changes as per requirement. Tracking and monitoring the timelines for the completion as per target. Planning and reviewing of planned preventive maintenance activities for the process and utility equipment’s as per SOP’s and approved schedule. Adhering and ensuring to meet the timelines for the completion of critical assignments related to project, modification and Safety Compliance. GMP: Implementing the tag numbering / coding of instruments as per the SOP. Adhering and implementing 100% compliance to the calibration of all measuring instruments of process and utility equipment’s as per schedule. Implementing departmental standard operating procedures (SOP) & protocols and addressing the suggestions / ideas for simplification and improvements. Preparing and updation of SOP / protocols as per the requirement and schedule. Implementing current good manufacturing practice (cGMP) for making continual improvement in quality management system. Adhering to the timely reporting and acknowledgement of non-conformances. Ensuring the timely completion of investigation with root cause analysis and appropriate CAPA in place. Following and execution of appropriate process validations, calibrations and qualification of equipment’s and facility under execution. Record and reports are made available. Ensuring the completion of scheduled vendor audit related to calibration laboratories. QMS: Implementing 100% compliance on QMS activities like process validations, calibrations and qualification of equipment’s, facility & IT networks under execution. Record and reports are to be maintained Operating software systems like SAP, DCS system, PLC System, LMS, Cipdox, trackwise, etc based on roles and rights provided in the applications. Maintaining the facility & equipment’s for all audit readiness. Monitoring and tracking of all the QMS tasks like, CR action, CAPA actions, deviations for timely closure. EHS: Ensuring and maintaining the plant hygiene, implementation of environment, health and safety policies and practices. Reviewing and extending the required technical support and resources for engineering services and facility management. Implementing and tracking the compliance of safety observations. Critical observations should be addressed immediately. Participating and preparing the risk assessments, hazops of non-routine maintenance activities, system, equipment and process. Preparation of Investigation report for safety incidences with root cause analysis and appropriate CAPA in place to avoid the re-occurrence. Learning and sharing to be ensured among the concerned team. Ensuring the timely investigation of safety incidences with root cause analysis and appropriate CAPA to avoid the re-occurrence. Learning and sharing should be ensured among the concerned team. Operating and reviewing the maintenance of EHS critical systems like Fire alarm system, Oxygen detection system, Hydrogen / Hydrocarbon gas detection system, NOVAC system, DSPA system, etc. Statutory: Maintaining the statutory compliance related to substation equipment’s and facility. Co-ordinating with electrical inspector, lift inspector and MSEDCL representative as per the requirement. Executing statutory legal compliances through compliance manager software. Training: Identifying and conducting trainings to engineers & contractors for their development and improvement in skills and knowledge through schedule training / external training. Energy Management EnMS: Reviewing and ensuring of Internal energy audits and tracking the action plan and compliance. Monitoring of daily power consumption along with investigation of variance with benchmark if any. Identifying and implementation of energy Saving Measures at unit level. Adhering to energy management system (EnMS) SOPs and related documents. Conduct or arrange energy audits and surveys, performance tests and investigations. Others: Performing any other allocated assignment after ensuring appropriate training is in place. Planning and execution of plant shutdown activities.

Role & responsibilities Operate and monitor critical equipment such as reactors, centrifuges, blenders, sifters, multi-mills, etc. Ensure strict compliance with cGMP guidelines during all stages of production. Maintain accurate and timely documentation in accordance with regulatory requirements, including handling of change controls, deviations, and batch records. Identify and escalate technical issues and implement corrective and preventive actions (CAPA). Coordinate with cross-functional teams (QA, QC, Maintenance) to ensure smooth plant operations. Adhere to standard operating procedures (SOPs) and safety protocols. Support process improvement initiatives to enhance productivity and efficiency. Key Skills & Competencies: Good understanding of chemical processes and API manufacturing. Hands-on experience with chemical plant operations and equipment. Strong documentation and problem-solving skills. Awareness of regulatory and compliance requirements.

Greetings! & very warm welcome to BEST-FIT Recruitment Riders, We are BEST-FIT Recruitment Riders feel immense pleasure to search and provide you with better carrier opportunities to aid you in achieving your aspirations. BEST-FIT Recruitment Rider is a highly specialized Recruitment & Executive Search Partner for Pharmaceutical, Biotech, CRO, Chemicals, Medical Devices & Turnkey Pharma Projects Engineering-Construction Design Sectors. We are searching & recruiting highly qualified professionals for Middle-Senior-Upper-Management and Executive jobs. (Eg: Managers, VP, President, CFO & CEO). Also offering customized recruitment services by Headhunting & Executive Search for Middle & Top management level professionals according to clients specific needs. We are BEST-FIT Recruitment Riders do exactly what our name tells. To know more about us please visit our website: www.bestfitrecruitment.co.in We would like to inform you that presently we have professional career opportunity matching to your profile with one of our esteemed client. Please see the following position summary: Client name: Leading name in Pharma & Agrochemicals intermediates Position: Projects Engineer - Chemicals Department: Chemicals Projects & Engineering Location: Jambusar, Gujarat Job Profile: Implementation of New Project for production of Bulk Drugs & Solvent Recovery. Equipment Sizing & Specifications to ensure production and Quality standards. Development of PFDS & P&IDS. Manage a Team member (Project department & contract labour), including Job allocation. Handling Process & Process Equipments. Provide critical assistance in expediting project activities To Provide technical inputs in Projects Planning, Projects Executive & scheduling products process. Assist in Troubleshooting & Problem solving for the existing facilities with involved in HAZOP and other Safety related studies. Project appropriate requisite documentation/ records. Desired Profile: BE / B.Tech / DME (Chemicals Engineering) with 1 to 4 yrs. experience in Chemical industrial project department. Experience in greenfield/brownfield projects in bulk/intermediate/specialty/fine chemicals, agrochemicals, or petrochemicals industry. Knowledge of chemical process equipment and utilities. Should have capability to manage Projects Management & Co-ordination effectively Skills in Projects Planning & Projects Executive. Expertise in Equipment Sizing, Development of PFDs & P&IDs etc. Project appropriate requisite documentation/ records. Sound understanding of EHS norms, HAZOP, risk assessment. Exposure to GMP / ISO / SHEQ systems. Strong project management and execution capability. Strong knowledge of project management principles Familiarity with project planning tools Understanding of safety regulations and statutory requirements. Familiarity with chemical plant operations, safety practices, and compliance standards. Good communication and cross-functional coordination skills. Analytical thinking and cost control mindset. Excellent coordination, communication, and problem-solving skills Shift work may be required depending on plant operations. Candidate who can join immediately would be added advantage. Good Team Handling Ability and Good Team Player. Recruiter Details: BEST - FIT Recruitment Riders G-7, Amrit Complex, Opp: Mahavir Jain Vidhyalaya & Jain Derasar, R.V. Desai Road, Near Goyagate Circle, Vadodara-390001, Gujarat, India Mobile: 07226009222 E-Mail: hrd@bfrr.in Website: www.bestfitrecruitment.co.in

The primary role of an Expert Sales Executive is to ensure coverage plan of the said specialties on a regular basis to deliver scientific information and knowledge on Haleon products and relevant disease conditions, thereby adding value to the HCP. Role Ensure favorable recommendation in form of prescriptions by scientific promotion for Expert detailed brands for relevant specialty. Demonstrate effective Pre and Post Call Planning customized to specific HCP requirements. Understand territory performance data, build doctor & chemist profiles for effective territory management. Maintain and reconcile monthly inventory of all inputs and samples. Timely reporting as per systems & process laid out by the organization. High engagement with the GT team and other relevant. Regional stakeholders to ensure delivery of overall regional Business plan. Respond promptly to HCP queries within the individuals area of knowledge or seek support to resolve the same. Strict adherence to compliance protocols of the organization, including but not limited to reporting adverse events. Requirements: Desired Qualifications Science/Commerce graduate, B.Pharm/B.Sc/M.Pharm/MSc. Experience: 2-7 years of experience of working in a Pharma Location: Surat, Valsad, Guna, Mehsana **Interested candidates can share their resume on pranitaa.x.prakashshetty@haleon.com Contact: 7418467771