236 Api Manufacturing Jobs - Page 4

Department : IPR Designation : Officer /Executive / AM / Manager Experience : 2 - 10 years Qualification : MSc (Org. Chem)/M.Pharm Post Graduate Diploma in Patent Management (PGDPM) Location : Vadodara Role & responsibilities To conduct novelty and freedom to operate searches on various databases To prepare patent landscape by analyzing the patent claims and specifications To prepare disclosure of the ROS To retrieve, analyze and interpret the file histories of the patents To assist in patent drafting, filing and prosecution procedures Prepare preliminary reports for identifying new molecules or new opportunities Tracking the competitors patent(s) portfolio and updating the same To assist in drafting of Pre-grant or post-grant opposition(s) To assist in drafting and responding to customer queries To assist in the docket and record management To identify the polymorphism To search on various country patent databases to retrieve equivalent patent information(s), legal status etc.. in different countries. Preferred candidate profile Should be familiar with different patent law(s) particularly IN, USA & Europe Should have good technical skill and knowledge Should be expert in operating SciFinder and other database(s). Perks and benefits Canteen Facility Traspotation Facility Vadodara GMC/GPA/GTL For Social Security

• experience In Production manufacturing, operation, process safety and manpower management production planning, unit process in Chemical / API Intermediate Industry. • To ensure execution of production operations as per SOP. Required Candidate profile • To co-ordinate for internal GMP activities • Knowledge of GMP & GDP procedure to follow. • Monitoring production planning to meet production targets • Equipment handling.

Position Overview We are seeking a seasoned Operations Procurement - Deputy Manager to oversee the end-to-end procurement of raw materials essential for our CDMO manufacturing processes. This role demands a strategic thinker with a robust understanding of supply chain dynamics, supplier relationship management, and cost optimization. Key Responsibilities Vendor Management Supplier Identification & Evaluation : Identify and assess potential vendors, ensuring alignment with company standards and GMP compliance. Negotiation & Contracting : Negotiate Pricing , terms, and conditions with vendors, focusing on cost, quality, and delivery timelines. Supplier Relationship Management : Develop and maintain strong relationships with key vendors to ensure consistent material supply and address any performance issues. Procurement Operations Order Management : Oversee the creation and management of purchase orders, ensuring timely and accurate order fulfilment. Inventory Control : Monitor inventory levels to prevent stockouts or overstock situations, collaborating with PPIC teams to align material availability with production schedules. Compliance & Documentation : Ensure all procurement activities comply with internal policies and external regulations, maintaining accurate records of transactions. Cost Management & Reporting Cost Analysis : Conduct regular cost analyses to identify opportunities for cost reduction and process improvements. Budget Management : Assist in the preparation and management of procurement budgets, ensuring expenditures align with financial forecasts. Reporting : Generate and present regular reports on procurement activities, vendor performance, and cost savings initiatives to senior management. Cross-Functional Collaboration Internal Coordination : Collaborate with internal departments, including planning, production, quality assurance, WH and logistics, to ensure seamless material flow and address any operational challenges. Process Improvement : Identify and implement process improvements within the procurement function to enhance efficiency and effectiveness. Qualifications Education : Bachelors degree in chemistry , PG diploma in Supply Chain Management, or a related field. Experience : 68 years in procurement or supply chain roles, with a focus on raw materials procurement in CDMO / API manufacturing industry. Skills : Proficiency in procurement and inventory management software. Strong negotiation and communication skills. Ability to manage multiple priorities in a fast-paced environment. Preferred Experience Experience in sectors such as CDMO, Speciality chemicals, and API industry. Familiarity with ERP systems like Oracle & MS Office Knowledge of import/export regulations and international procurement practices.

Operate & maintain GC & HPLC instruments Analyze pharmaceutical samples using GC & HPLC techniques performing routine maintenance & troubleshooting Assist in developing & validating chromatography methods Record, analyze & report chromatography data Required Candidate profile Qualification required in B.Sc/M.Sc in chemistry Previous experience operating GC and HPLC instruments in a pharmaceutical or related industry Freshers can also apply

Job Title: Metallurgical Engineer Department: Quality / Production / R&D Reports To: Head of Department / Technical Manager Qualification: M.Tech in Metallurgy / Materials Science / Metallurgical Engineering from a recognized university. Job Purpose: To ensure selection, testing, and treatment of materials and welding processes are in line with industry standards and client specifications for oil & gas equipment manufacturing. To support production and quality teams in achieving robust metallurgical practices, enhancing product reliability, safety, and compliance. Key Responsibilities: Material Selection & Specification: Review project requirements and recommend suitable metals and alloys for pressure vessels, piping, valves, and other critical oil & gas equipment. Ensure materials comply with applicable standards (ASME, ASTM, API, NACE, etc.). Metallurgical Testing & Analysis: Plan and supervise destructive and non-destructive testing (DT/ NDT). Perform failure analysis and root cause investigation for rejected or failed components. Evaluate microstructure, hardness, grain size, and other metallurgical properties. Heat Treatment & Welding: Develop and monitor heat treatment procedures as per process requirements. Assist in qualifying welders, reviewing WPS/PQR, and ensuring welding processes meet industry standards. Process Improvement: Recommend process improvements for casting, forging, machining, welding, and surface treatment to improve material performance. Provide technical support for resolving metallurgical issues during fabrication or field complaints. Documentation & Compliance: Prepare metallurgical reports, inspection test plans (ITP), and maintain test records. Coordinate with third-party inspectors and clients for material approvals. Cross-Functional Coordination: Liaise with design, procurement, production, and quality teams to address metallurgical aspects in product lifecycle. Participate in technical discussions with suppliers and clients. HSE & Standards Compliance: Ensure all activities comply with company HSE policies and industry best practices. Stay updated with developments in metallurgy relevant to oil & gas industry applications. Strong knowledge of metallurgy of carbon steel, alloy steels, stainless steels, duplex steels, and corrosion-resistant alloys. Hands-on experience in metallurgical lab testing, heat treatment, welding metallurgy, and failure analysis. Familiarity with ASME, API, ASTM, NACE standards. Problem-solving mindset and attention to detail. Good communication and report-writing skills. Ability to work independently and collaboratively in a cross-functional team. 35 years preferred for mid-level roles in oil & gas equipment or heavy engineering industry.

Greetings!!!! We are seeking a dynamic and experienced Site Head to lead a CRAMS pharmaceutical manufacturing site . The role demands strategic leadership, cross-functional coordination, regulatory compliance, and operational excellence. Key Responsibilities: Oversee day-to-day site operations (production, QA/QC, engineering, supply chain) Ensure GMP compliance and regulatory readiness (USFDA, WHO, EU GMP) Lead cross-functional teams and drive business KPIs Client management for CRAMS / CDMO projects Lead tech transfer, scale-up, and capacity expansion projects 1. Site Operations Leadership Oversee day-to-day operations of the site (R&D, API/Formulation manufacturing, QC/QA, Engineering, EHS). Ensure smooth execution of contract research, development, and manufacturing projects. Monitor productivity, efficiency, and on-time delivery of client commitments. 2. Client & Business Interface Act as a primary on-site representative for client audits, visits, and project reviews. Support business development teams by providing technical and operational insights for new client onboarding or proposal discussions. 3. Regulatory & Compliance Oversight Ensure site operations meet global regulatory standards (USFDA, EMA, WHO, etc.). Lead regulatory inspections and client audits successfully. Enforce strong GMP , GLP , and EHS practices. 4. Strategic Execution Align site objectives with corporate strategy and CRAMS business goals . Drive capacity expansion, new technology adoption , or process improvements. Identify and eliminate bottlenecks in production or R&D delivery timelines. 5. Team & Leadership Management Lead a cross-functional team including manufacturing, QA/QC, R&D, engineering, SCM, HR. Focus on people development , succession planning, and team performance. Promote a strong culture of accountability, quality, and safety . 6. Financial & Cost Control Manage the site P&L (Profit & Loss) . Optimize resource utilization and control operating expenses. Identify and implement cost-saving initiatives without compromising quality. Desired Candidate Profile: Chemical Engineering 20+ years of experience in CRAMS / API industry Experience handling USFDA/EU GMP inspections Strong leadership, planning, and communication skills Interested candidates kindly share your updated cv to uma@bvrpc.com

1. Technology transfer activity End to End, lead role for ANK location. 2. Site transfer and Block transfer activities for ANK location. 3. Managing Tech. Transfer and Process Engg (TT and PE) team. 4. Ensure for smooth technology transfer from Research and development to plant with minimum concerns w.r.t. scale-up. 5. Coordination with desired stake holders for getting timely execution of plant validation campaign. 6. Smooth planning of lab demo and detailed studies on negative experiments, holding studies, identifying process criticalities, etc. w.r.t. Scale-up. 7. Freezing lab process w.r.t. Scale-up to avoid deviations at plant. 8. To manage for making EHS friendly process. 9. Detailed discussion and finalizing the process for all site transfer molecules. 10. Coordinate with team for equipment mapping at plant for new and site transfer molecules. 11. Planning, coordination, and effective communication for Execution of trial and validation batches at plant. 12. Exploring of new technologies and its implementation at plant. 13. Managing of smoothly performing related EHS studies including HAZOP and HAZAN studies for new / site transfer projects.

Formulation development of NCE projects, generic projects and line extension projects Preparation/review of literature summary and development report to the assigned product. Involve in execution and/or supervision of formulation development, process development and manufacturing of GMP batches of assigned product. Preparation/review of technical documents, which includes but not limited to MFC, BMR, BPR and Stability protocol following GDP. Representation in departmental audit Follow GxP (GMP, GDP etc.) for all processes and train the subordinates to follow the same. Execution and/or supervision of scale up/pilot scale batches in pilot plant under GMP condition. Preparation and/or review of technology transfer documents and technology transfer to manufacturing site, whenever required. Preparing/reviewing of QMS includes but not limited to change control, deviation, SOPs and OOS Communication with cross-functional team and client via mails, meetings and oral communication Responsibilities Qualifications -M. Pharm

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. To be kept good housekeeping in the production area during the shift I. To be verified weight and quality approved of the raw material issued by the ware house. J. Coordinate with the Executive production (shift In charge) for the smooth functioning of shift Production activity. K. To be ensure that safety procedure are followed during the production activity of shift. L. To be coordinate the executive production (shift In charge) to maintain cGMP and safe environment in the production area during the shift. M. Report the shift in charge for any deviation in the running process.

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.

Roles and Responsibilities Operate and maintain equipment such as centrifuges, reactors, distillation columns, filters (RO & DM Plant), dryers, bulk drugs handling systems, CGMP compliance systems. Ensure adherence to BMR guidelines during API manufacturing processes. Monitor and control process parameters to ensure quality production of APIs. Perform routine maintenance tasks on equipment and facilities to prevent breakdowns and optimize performance. Collaborate with cross-functional teams to resolve issues related to production operations. Desired Candidate Profile 3-7 years of experience in API manufacturing or pharmaceutical industry. Diploma/B.Sc degree in Chemistry or relevant field. Strong understanding of batch manufacturing records (BMR) principles and practices. Proficiency in operating various types of equipment including centrifuges, reactors, distillation columns, filters etc.

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.

Role & responsibilities Preparation and review of standard operating procedure. Monitoring of trend in the process and in the quality control. Preparation of Annual product quality review (APQR). Preparation of validation protocol & report. Reviewing of equipment qualification. To support the customer / regulatory audits. Follow up of CAPA. Handling of customer complaints. To support the preparation of new drugs endorsement / manufacturing license documents. Reviewing of stability data and monitoring of trend. Upkeep of documentation. Issue and control of documents. Issue batch production record. Issue and Retrieval of cleaning records. Review of batch production and equipment cleaning records. Documentation systems issue and control of documents. Upkeep of documentation. Issue of certificates photocopies to the user departments, with draw of obsolete copies and issue of uncontrolled copies whenever required. Checking the certificate of analysis prepared by quality control.

5-10 year Experience in Mechanical maintenance Department, Chemical/API Pharma Company. Location-Nandesari, Vadodara, Gujarat, India.

Should have good knowledge HPLC.

Responsibilities: Lead tech transfers from R&D to manufacturing sites Ensure compliance with regulatory requirements during TTO process Collaborate with cross-functional teams on project planning & execution

Manage day-to-day operations of lyophilization and aseptic production lines. Ensure compliance with cGMP , FDA , EMA , and other regulatory. Oversee equipment preparation , cleanroom operations , sterile filtration Oversee API manufacturing processes

Bulk Drug, API Production. SOPs, cGMP, Reactor, BMR Review, Raw Material Hydrogenation, batch production Key member of troubleshooting the production of an FDA license product In process checking on various intermediate steps Developing new production methods or improving existing ones to increase efficiency or quality of product maintenance and repairs of equipment used in production processes Active calculation batch reconciliation on various stages To be responsible for Batch start up activity, monitoring, calibration of balance and other instruction given by the Superior. To review technical documents like batch records, cleaning records, validation protocols, cleaning verification protocols. To be responsible for receiving raw materials to delivering the finished products. Conducting chemical analyses of new products to ensure that they meet safety standards Preparing and review of various document regarding manufacturing like SOP, Batch production records, Reconciliation record Preparation of daily production report Prepare safety manuals for operator, Provide training to operator for plant operation Monitoring of Preventive maintenance schedule and planning. Bulk Drug, API Production- High Potency Experience (Oncology) Isolator Handling Isolator cleaning Packing Oncology Product Documentation of Oncology Product SOPs, cGMP, Reactor, BMR Review, Raw Material Hydrogenation, batch production Key member of troubleshooting the production of an FDA license product In process checking on various intermediate steps Developing new production methods or improving existing ones to increase efficiency or quality of product

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 / Organic Chemistry with 4 to 5 years of experience In R&D Chemistry, product Development & Validation, operation, process & production planning, unit process, in Chemical Industry. Good knowledge of chemical reactions & chemistry. Required Candidate profile Performing the main PILOT PLANT / process validation tasks PILOT PLANT in best way possible. Good knowledge of chemicals, Equipment's, Glassware & machinery required in lab. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.Sc. / M.Sc. - Chemistry with 02 to 03 years of experience in Pharmaceutical Industries (API – Intermediates). Must be aware of the working conditions in an API / Intermediate unit. One who is able to handle all pharma reactors. Equipment handling. Required Candidate profile Monitoring production planning to meet production targets. To ensure that the production records are maintained and recorded at the time of performance. Knowledge of GMP & GDP procedure to follow. 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 / Organic Chemistry with 4 to 5 years of experience In R&D Chemistry, product Development & Validation, operation, process & production planning, unit process, in Chemical Industry. Good knowledge of chemical reactions & chemistry. Required Candidate profile Performing the main PILOT PLANT / process validation tasks PILOT PLANT in best way possible. Good knowledge of chemicals, Equipment's, Glassware & machinery required in lab. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.Sc. / M.Sc. - Chemistry with 02 to 03 years of experience in Pharmaceutical Industries (API – Intermediates). Must be aware of the working conditions in an API / Intermediate unit. One who is able to handle all pharma reactors. Equipment handling. Required Candidate profile Monitoring production planning to meet production targets. To ensure that the production records are maintained and recorded at the time of performance. Knowledge of GMP & GDP procedure to follow. Perks and benefits Negotiable - Depending Upon Candidate & Experience