88 Pharmaceutical Production Jobs - Page 3

Recruiter Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy Role & responsibilities The responsibilities are Operations, Control and Monitoring 1. Improving, continuous reviewing and up gradation of existing production SOPs and work systems to ensure their strict implementation in respective block. 2. Resolution and identification of maintenance related activities of equipment and facility and making sure those are closed appropriately 3. Executing proposed changes in product, process or equipment and facility. 4. Preparing production plan and supervising the API and Intermediate batches as per production plan. 5. Ensure facility upkeep is maintained all the time. 6. Any other assignment given by management. 7. Communicating concerns with cross functional and service departments. 8. Control and monitor departmental opex budget. 9. Monitoring and controlling of effluent generation from manufacturing block. 10. Periodic review and monitoring of inventory in coordination with unit stores and supply chain. 11. Executing and monitoring of validation of new product, CIP, AVD with the help of cross functional team. 12. Implementation of new technology w.r.t. process equipments or facility. 13. Supporting quality assurance team for DMF submission. 14. Executing and supervising training, validation, qualification and calibrations protocols. 15. To perform visual inspection and certification of cleaned equipment after product change over cleaning as per standard operating procedure. cGMP: 1. Following departmental standard operating procedures (SOP) and providing suggestions for SOP simplification and any other improvements. 2. Making sure all the documents and checklist are verified before and after manufacturing. 3. Ensuring retention and destruction of records are maintained in a department. 4. Verifying status labelling of accessories, in-process instruments, containers, area & equipment 5. Performing contemporaneous (on time) document entries. QMS / OTHER SOFTWARE SYSTEMS: 1. Operating software systems like SAP, Quality Management System, Track wise system, Cipdox software, PR approval, LMS, Ariba, PPDS and E-Track system etc. based on roles and rights provided in the applications. 2. Compiling Annual product quality review along with quality assurance department and other CFT. 3. Participating and contributing to investigation for any non-conformance along with CFT. EHS: 1. Following Environment, Health and Safety policies and practices. 2. Making sure personnel health, hygiene and organisation practices are followed. 3. To conduct risk analysis of product, system, equipment, process as per standard procedure. Training 1. Attaining training as per training need and providing training to sub-ordinates through available software of Learning Management System (LMS). Energy Management system (EnMS) 1. Participating in EnMS audits & Leadership rounds. Preferred candidate profile B.Tech Chemical with minimum 10 years of API production experience including experience to handle a block/section in a API plant.

Roles and Responsibilities Prepare and review batch records for API production runs to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to resolve issues related to product quality and process optimization. Develop and maintain knowledge of current Good Manufacturing Practices (cGMP) guidelines and industry standards.

Shenoy Hospital is looking for Sr.Pharmacist / Incharge to join our dynamic team and embark on a rewarding career journey Dispense medications and provide pharmaceutical care to patients. Advise patients and healthcare providers on the proper use of medications. Manage pharmacy inventory and ensure the availability of essential drugs. Ensure compliance with pharmaceutical regulations and standards. Maintain accurate patient records and medication histories. Provide training and support to pharmacy staff. Good communication skills Atleast 2 to 3 years of experience as Pharmacist Must be Qualified B.Pharmacy/D.Pharmacy with Certified P

Position Overview: We are looking for a Sr. Manager will be responsible for leading and managing end-to-end multiple API production blocks. The role requires ensuring optimal productivity, quality, cost control and regulatory compliance in alignment with cGMP standards. This position plays a critical role in driving continuous improvement, cross-functional coordination, and operational excellence within the production unit.. Key Responsibilities: Oversee daily production activities to ensure efficiency, quality, and cost-effective management of resources. Develop and implement production schedules based on inventory / market requirements / capacity constraints and provide feedback accordingly. Deployment of manpower & supervisor as per production requirement. Monitor and adjust production processes as necessary to meet production targets and quality standards. Ensure all production batch records are completed and signed off on time. Responsible or keeping production facilities clean and appropriately disinfected. Responsible for the validation protocols and reports are completed and signed. Responsible for qualification of new and modied facilities, when appropriate and equipment. Responsible for maintaining and updating the documents related to the Production activities. Ensure smooth production under EHS & cGMP compliance. Ensure for reporting of all production deviations and evaluation of the same. Ensure process problems /deviations are solved and rectified within a set of time frame, co-ordination/follow up with all the departments like R&D, MSTG, QC, QA, Engineering & Stores. Institute operational controls, monitor the key characteristics, carry out root cause analysis for the non-conformity and take CAPA. Responsible for self-inspection of the area w.r.t EHS and production systems. Responsible for training all the employees of production. Responsible for preventive maintenance is executed as per the planned schedule. Responsible for analyzing the time cycle of each batch and taking corrective actions if any deviations are observed. Responsible for any optimization initiative across the production blocks. Ensure that the yield, % solvent recovery and quality of APIs and Intermediate products are as per the standard norms. Analyze production costs and recommend strategies to reduce costs and improve Profitability. Responsible for monthly RM requirement and weekly RM schedule. Responsible for performing of Internal audit. Responsible for water consumption, effluent generation as per the set norms. Responsible for controlling hazardous waste generation. Identification of Risks & Hazards, Environmental aspects & evaluation and review the same. Responsible for any other work assigned by senior management in the absence of Site Head/ Unit Head. Qualifications and Experience: Analytical Skills and Communication Basic understanding of pharmaceutical or chemical industry Strong organizational, multitasking abilities, time management skills Company Website :- www.scllifesciences.com

Role & responsibilities : Prepare and review documentation such as SOPs, BMRs, and logs with attention to detail and good command of English. SHARE RESUME TO hrd@stedmanpharma.com / 9786920463 Preferred candidate profile : Education: B.Pharm / M.Pharm / M.Sc. (Chemistry, Biotechnology, Microbiology) / B.Tech or B.E. in Chemical Engineering or related fields. Freshers or recent graduates looking to start their career in pharmaceutical production Basic understanding of GMP , manufacturing processes, and safety protocols Good written and verbal communication skills in English (especially for documentation purposes) Attention to detail, willingness to learn, and ability to work in a team Open to working in production environments and learning practical applications Available for a full-time, 6-month paid internship

Production Officer specially for Effervescent tablets production Effervescent Tablets: Maintain low relative humidity (maximum of 25% or less) and moderate to cool temperatures (25 Required Candidate profile C) to prevent product degradation and sticking to machinery

Roles and Responsibilities Collaborate with cross-functional teams to resolve issues related to product development, manufacturing processes, and regulatory compliance. Ensure adherence to cGMP guidelines and company policies throughout all aspects of production chemistry operations.

B.tech, Instrumentation or Electronics, min 5-7 years experience in chemical /pharma or manufacturing industry, Key skills in PLC programming, industrial automation, equipment upgradation, new lines setup etc & HVAC systems. SAP preferred. Required Candidate profile Core skills in industrial process equipment, automation, PLC programming, HMI etc . Diploma holders can also be considered.

Present suitable promoted products Liaise with and persuade targeted doctors to prescribe our products utilizing effective selling skills and performing cost-benefit analysis Provide product information and deliver product samples Required Candidate profile Familiarity with databases, statistics, product lines and latest medical issues Negotiation and sales skills Highly motivated and target driven with a proven track record in sales Perks and benefits Health insurance Retirement plans Paid time off

Project Role : Software Development Lead Project Role Description : Develop and configure software systems either end-to-end or for a specific stage of product lifecycle. Apply knowledge of technologies, applications, methodologies, processes and tools to support a client, project or entity. Must have skills : Manufacturing Engineering MES Good to have skills : NAMinimum 7.5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Pharmasuite MES Architect, you will be responsible for designing, developing template based MES recipes in Rockwell FactoryTalk PharmaSuite (FTPS) to support pharmaceutical manufacturing processes. You will collaborate with cross-functional teams to ensure efficient recipe authoring and seamless integration with automation and enterprise systems while adhering to regulatory and industry standards. Roles & Responsibilities:-Develop MES recipes using Rockwell FTPS, ensuring compliance with industry best practices.-Design and implement building blocks for reusable recipe structures.-Work closely with process engineers and manufacturing teams to map end-to-end pharmaceutical processes, with a focus on biologics.-Ensure compliance with pharmaceutical regulations (GMP, GxP, 21 CFR Part 11).-Participate in the full MES lifecycle, from design and validation to deployment and support.-Perform recipe testing, troubleshooting, and validation in alignment with SDLC (Software Development Life Cycle) methodologies.-Collaborate with DCS teams to ensure seamless MES-DCS integration for automated manufacturing.-Support and maintain MES systems in a validated state, ensuring high availability and performance.-Provide technical expertise in MES implementation and contribute to continuous improvements in manufacturing processes.Must-Have Skills: -MES experience in life sciences manufacturing, specifically with Rockwell FTPS.-Hands-on experience in MES-DCS integration for process automation.-Knowledge of ERP and Data Historian integration with MES.-Hands-on experience in recipe authoring, building block development, and validation.-Strong understanding of pharmaceutical manufacturing, especially biologics. Professional & Technical Skills: -Knowledge of SDLC and pharmaceutical regulations (GMP, GxP, 21 CFR Part 11).-Experience in executing at least one full MES lifecycle project with demonstrated results.-Good communication skills to collaborate with cross-functional teams. Additional Information:-Minimum 5 to 7.5 years of experience in MES recipe design and deployment in pharmaceutical manufacturing.-This position is based at our Kolkata, Bengaluru, Pune, Mumbai, Chennai, Hyderabad and Ahmedabad office.-A full-time 15 years of education is required. Qualification 15 years full time education

Requirement for B.sc/Msc Chemistry, BioChem, Microbilogy, Dip/BE/Btech Chem/Petro/Biotechnology / Bpharm / Mpharm Location - Chennai/Kovai/Cuddalore/Pondy Field - Pharma/Water Treatment/Paint/Chemical Industry Designation - QC / P Chemist /Lab Asst

Looking for Retired Production machine operator in Pharma industry , who can teach sterile and Non sterile, through VR (Virtual reality) We are knowledge partners of LSSSDC, https://lsssdc.in ,LSSSDC and Biological E. Ltd are offering skilling, Hyd

Role & responsibilities Excels in managing the quality inspection & release programs for company's Pharma products and leading validation, qualification, QA, analysis & sampling of Raw Materials (API & Formulation) and Packaging Material. Expertise in driving QMS/QC Activities - OOS, Deviation, Change Control, Risk Assessment, Investigations, RCA, CAPA, Audits, Equipment Calibration & Validation on the shop floor for ensuring adherence to GMP and Regulatory Compliance.

Data Search & Analysis on the drug discovery and development Creating technology reports Kindly provide minimum two references with resume Required Candidate profile Keen interest in drug discovery, API Good Knowledge of organic chemistry Good Communication Skills

Embark on a Global Growth Journey: Production Chemist Location: Hyderabad, India Company: Lactonova No of Positions : 3 Industry: Nutraceuticals & Pharmaceutical Formulations If youre ready to revolutionize the Nutraceuticals and Pharmaceutical Formulations space, this is your opportunity to lead and grow with us as a Production Chemist Job description Developing and optimizing production processes for pharmaceutical formulation based on client requirements Conducting experiments and trials to determine the best production process for chemicals Creating and maintaining detailed records of the production process, including batch records, protocols, and reports Monitoring production processes to ensure they meet quality standards and product specifications Troubleshooting and resolving issues related to the production process Maintaining equipment used in the production process and coordinating maintenance activities with the maintenance team Conducting safety audits and maintaining a safe working environment Identifying opportunities for process improvements and implementing changes to increase efficiency and productivity Providing technical support to production teams and resolving production-related issues Strong analytical and problem-solving skills Excellent communication and interpersonal skills What Sets You Apart: Experience: Minimum 3 years in Production Chemist within Pharmaceutical Formulations or Nutraceutical industries. Qualification Bsc Chemistry, Msc Chemistry Language Proficiency: Fluent in English and Hindi (Additional languages are a bonus). Why This Opportunity is Special: Global Impact: Join a forward-thinking, globally recognized leader in the Nutraceutical and Pharmaceutical Formulations space. Collaborative Culture: Work in an entrepreneurial environment that values innovation and results. Unlimited Growth Potential: Be a key player in shaping the future of wellness and redefine industry standards. How to Join Us: Ready to Lead and Inspire? Take the leap and send your CV and cover letter to [ hra@lactonova.com , +91 6303037351]. Lets grow together, make an impact, and lead the future of wellness in Nutraceuticals and Pharmaceutical Formulations.

New Client Acquisition & Business Development: • Minimum 3+ years of proven experience in sales and business development within the Pharmaceutical raw materials Domestic B2B API , Excipients sales Reach me@ 8687773611 Required Candidate profile • Strong network within pharmaceutical companies in Hyderabad, Bangalore, Chennai & Pondicherry is a plus! • Experience with pharma raw material distributors/manufacturers is preferred

Operating and maintaining equipment Monitoring production processes Monitor production processes, identifying and reporting any issues Maintain accurate and complete records of production activities Ensuring adherence to quality standards and GMP Required Candidate profile Previous experience in API pharma manufacturing or a similar industry Ability to operate and maintain equipment Knowledge of GMP and other relevant regulations is essential

Role & responsibilities production chemist Preferred candidate profile pharma experience, API, BULK DRUG,GMP, GLR,SSR,CENTRIFUSE,BPR,

Production Chemist required for a pharma company at kundli, sonipat Qualification- B. pharma Exp- min 7 yrs salary- upto 60k Wtsapp me resume at 8295842337- MR. Bansal

We are seeking a Fresher Pharmaceutical Production Executive to join our pharmaceutical production team. In this role, you will assist in the manufacturing process of pharmaceutical products, ensuring that all production activities comply with safety, quality, and regulatory standards. This is an excellent opportunity for someone looking to start their career in pharmaceutical production and contribute to the production of high-quality medicines Oversee production processes, ensure GMP compliance, and maintain batch records.

We are seeking a Fresher Pharmaceutical Production Executive to join our pharmaceutical production team. In this role, you will assist in the manufacturing process of pharmaceutical products, ensuring that all production activities comply with safety, quality, and regulatory standards. This is an excellent opportunity for someone looking to start their career in pharmaceutical production and contribute to the production of high-quality medicines Oversee production processes, ensure GMP compliance, and maintain batch records.

We are seeking a Fresher Pharmaceutical Production Executive to join our pharmaceutical production team. In this role, you will assist in the manufacturing process of pharmaceutical products, ensuring that all production activities comply with safety, quality, and regulatory standards. This is an excellent opportunity for someone looking to start their career in pharmaceutical production and contribute to the production of high-quality medicines Oversee production processes, ensure GMP compliance, and maintain batch records.

We are seeking a Fresher Pharmaceutical Production Executive to join our pharmaceutical production team. In this role, you will assist in the manufacturing process of pharmaceutical products, ensuring that all production activities comply with safety, quality, and regulatory standards. This is an excellent opportunity for someone looking to start their career in pharmaceutical production and contribute to the production of high-quality medicines Oversee production processes, ensure GMP compliance, and maintain batch records.

We are seeking a Fresher Pharmaceutical Production Executive to join our pharmaceutical production team. In this role, you will assist in the manufacturing process of pharmaceutical products, ensuring that all production activities comply with safety, quality, and regulatory standards. This is an excellent opportunity for someone looking to start their career in pharmaceutical production and contribute to the production of high-quality medicines Oversee production processes, ensure GMP compliance, and maintain batch records.

We are seeking a Fresher Pharmaceutical Production Executive to join our pharmaceutical production team. In this role, you will assist in the manufacturing process of pharmaceutical products, ensuring that all production activities comply with safety, quality, and regulatory standards. This is an excellent opportunity for someone looking to start their career in pharmaceutical production and contribute to the production of high-quality medicines Oversee production processes, ensure GMP compliance, and maintain batch records.