28 Pharma Manufacturing Jobs

As an Application Support Engineer for Werum PAS-X MES, your role involves being an expert in PAS-X system administration and configuration, with a particular focus on versions 3.1.8, 3.2.1, and 3.30. You will need to have a good technical architecture experience in PAS-X, including understanding of application and web server, database architecture, interfaces, and server log analysis. Your key responsibilities will include: - Supporting MES integration with Level 2, Level 3, and Level 4 systems. - Creating SQL scripts and understanding DB schema for database expertise. - Troubleshooting PAS-X related technical issues such as scale integration and printer/scanner problems. - Performing IT co...

As a Senior FICO professional with Lorhan IT Services, you will be responsible for leveraging your 10+ years of relevant experience to support our 120+ active customers across APAC, MENA, AnZ, and USA. Your primary focus will be on working with manufacturing companies, with an added advantage if you have experience in Pharma manufacturing. Being from an accounting background, you will play a crucial role in developing and delivering SAP Digital Core and Digital Transformation Services to help our customers increase operational efficiencies. Key Responsibilities: - Utilize your expertise in FICO to provide solutions and services in application development, system integration, and managed serv...

As a Senior Manager-IT at the Mumbai location, your role involves leading the design, configuration, and implementation of SAP PP, QM, and PM modules. Your responsibilities include: - Leading the implementation of SAP PP/QM/PM modules across all Sun Pharma plants - Reviewing and overseeing the work of third-party vendor support teams - Collaborating closely with the business team to understand and deliver new requirements - Ensuring all deployments adhere to GxP processes with a focus on validation activities - Providing technical configuration expertise for SAP PP/QM/PM modules - Overseeing and guiding the team in handling SAP PP/QM/PM rollout projects - Utilizing ABAP debugging skills to t...

As a Senior Manager-IT at the Mumbai location, you will be responsible for leading the design, configuration, and implementation of SAP PP, QM, and PM modules. Your key responsibilities will include: - Leading the implementation of SAP PP/QM/PM modules across all Sun Pharma plants - Reviewing and overseeing the work of third-party vendor support teams - Collaborating closely with the business team to understand and deliver new requirements - Ensuring all deployments adhere to GxP processes with a focus on validation activities - Providing technical configuration expertise for SAP PP/QM/PM modules - Overseeing and guiding the team in handling SAP PP/QM/PM rollout projects - Utilizing ABAP deb...

We are seeking an experienced and proactive Maintenance Executive to join our Pharma manufacturing facility The ideal candidate will be responsible for overseeing the maintenance and reliability of equipment, facilities, and utilities in the factory The role involves developing and implementing preventive maintenance programs, troubleshooting issues, and ensuring the uninterrupted operation of production processes.

You are a seasoned Ignition SME/Solution Architect with over 4 years of hands-on experience in Ignition by Inductive Automation and 10+ years in IT/OT systems integration. Your role will involve architecting and deploying scalable Industrial IoT (IIoT) solutions across manufacturing environments, focusing on going beyond traditional SCADA implementations. Your deep expertise in OT systems, MQTT protocol, UNS design, and ISA-95 contextualization, along with a proven track record of template-driven, reusable solution delivery across multiple sites, will be crucial for success. - Lead the architecture, design, and deployment of IIoT solutions using Ignition Perspective, MQTT, and edge computing...

We are seeking an experienced and proactive Maintenance Executive to join our Pharma manufacturing facility The ideal candidate will be responsible for overseeing the maintenance and reliability of equipment, facilities, and utilities in the factory The role involves developing and implementing preventive maintenance programs, troubleshooting issues, and ensuring the uninterrupted operation of production processes

As a Business Development Manager for the life-science & Medical communications sector or Pharma manufacturing, your role involves: - Leading the overall business development activities and being accountable for revenue generation. - Growing the current business from existing clients in the Life-sciences, medical communications sector, or Pharma manufacturing. - Developing new business opportunities through existing and new clients, exploring new avenues of business streams. - Contributing effectively to Pre-Sales by providing strategic and timely solutions. - Using consultative selling expertise to understand and address customer needs, building long-term partnerships. - Implementing brand ...

Oversee complete Production & Manufacturing operations at the Pharmaceutical Formulation Unit Ensure smooth execution of batch manufacturing for OSD (Tablets, Capsules, Dry Syrups) Ensure compliance with FDA regulations and GMP guidelines Monitor production efficiency, process optimization & manpower management Coordinate with QA, QC, and Regulatory teams for smooth operations Handle regulatory audits, validation, and documentation processes OSD Manufacturing Tablets, Capsules, Dry Syrups FDA Approval & Regulatory Compliance (WHO-GMP, Schedule M preferred) Production Planning & Process Optimization Team Leadership & Manpower Management

SAP Implementation Leadership: Lead the planning, execution, and management of SAP S/4 HANA implementation projects from initiation to completion. Ensure alignment with organizational goals, timelines, and budgetary constraints. Financial Expertise: Utilize your strong background in finance to understand and address the unique financial requirements and challenges of the organization. Collaborate with finance teams to develop and implement solutions that optimize financial processes within SAP S/4 HANA. Business Process Optimization: Identify opportunities for business process improvement and optimization through the implementation of SAP S/4 HANA. Work closely with cross-functional teams to...

As a qualified candidate for this position, you should ideally hold a B.Tech degree, and an MBA qualification would be considered advantageous. With at least 5 years of experience in pharma manufacturing and quality, specifically in a consulting firm, you have gained valuable insights and expertise in the industry. Your primary responsibilities will revolve around implementing, managing, and developing Digital Quality Solutions within the pharmaceutical sector. This includes hands-on experience with various tools such as LIMS, Empower, and LMS. You will be expected to collaborate closely with the business stakeholders to grasp their requirements and effectively document project scopes, inclu...

As a Project Lead at OneOrg.ai, you have the exciting opportunity to expand the AI Superbrain into the realm of pharma manufacturing. In this role, you will play a crucial part in transforming digitization from a future plan to a regulatory and business imperative. Your main responsibility will be to identify high-impact AI use cases within manufacturing, such as visual deviation detection, batch yield variance, and SOP non-compliance, and lead short-cycle projects to deliver visible value to clients. Ideally, you should have 8-15 years of experience in pharma manufacturing, QA/QC, or GMP automation, with deep exposure to GMP documentation, audit trails, batch monitoring, and deviations. Pri...

As a Plant Manager in Pharma Manufacturing located in Baddi, you will bring over 10 years of experience in pharma manufacturing with a minimum of 3 years in a leadership role. Holding a degree in B.Pharm, M.Pharm, B.Sc, or B.Tech (Chemical/Pharma) will qualify you for this position. Your primary responsibility will be to oversee all plant operations, including production, quality, maintenance, and compliance. You will be accountable for ensuring timely, cost-effective, and GMP-compliant manufacturing processes. Your key responsibilities will include managing day-to-day manufacturing activities according to the production plan, ensuring compliance with cGMP, WHO-GMP, and regulatory norms, coo...

You are looking for an experienced Tele Marketing Executive with knowledge of the pharmaceutical industry. Preferably, the candidate should have work experience in a PCD Pharma Company or Pharma Manufacturing company. Salary is not a constraint for the right candidate. This is a full-time, permanent position with benefits including cell phone reimbursement and paid time off. The work schedule is during day shift hours with a performance bonus offered. The ideal candidate should have a Bachelor's degree and a total of 2 years of work experience, including 2 years in sales and 1 year in pharmaceutical sales. Proficiency in Hindi and English languages is preferred. The work location will be in ...

The job opening at Lorhan IT Services is for a Senior FICO professional with 10+ years of relevant experience. Lorhan IT Services caters to over 120 active customers in regions like APAC, MENA, AnZ, and the USA by offering services in application development, system integration, and managed services. The company has developed strong solutions in digital and SAP over the last 20 years, focusing on SAP Digital Core and Digital Transformation Services. They aim to help enterprises enhance their business processes for better ROI and efficiency. Employees at Lorhan IT Services prioritize building strong customer relationships while maintaining a risk mitigating and compliance-driven culture. This...

Prefer Immediate joiners Position Summary As the Head of SAP, you will play a pivotal role in driving the organization towards digital transformation and operational excellence. Your vision will be to leverage SAP S/4 HANA as a catalyst for innovation, efficiency, and strategic growth. By implementing best-in-class solutions and optimizing business processes, you will empower our teams to unlock their full potential and deliver exceptional value to our customers and stakeholders. Your leadership will be instrumental in shaping the future of our organization, positioning us as a leader in the industry and driving sustainable success in an ever-evolving landscape. You will lead and oversee the...

As a Production Associate at PPL Digwal, your primary responsibility will be to perform production activities in compliance with GMP and Safety standards. You will report directly to the Manager of Production and collaborate with internal stakeholders such as QC, QA, SCM, and Safety departments. With 4-8 years of experience in manufacturing (API) according to Pharma Manufacturing GMP requirements, you will play a crucial role in ensuring EHS continual improvement by participating in activities like emergency mock drills, training sessions, and permit to work procedures. It is essential to follow all site safety requirements, exhibit positive behavior in safety culture transformation, and use...

Raise laboratory Change control, incidents, deviations and LI wherever applicable. Review of Instrument qualification and scheduled calibration planner. Ensure proper laboratory analysis as per MOA and current product specification.

Hi, We are having an opening for Manager - Location IT lead at our Ahmednagar / Baroda/ Taunsa location Job Summary : The Job holder will be responsible for all aspects of frontend IT support including IT infrastructure, Application support, Quality IT, Manufacturing IT, and CSV. Additionally, ensure compliance with regulatory requirements, support audits, manage IT-related procurement and handle payment processes for the site. Areas Of Responsibility : 1. The Job holder will ensure the smooth IT operations at the site. 2. Management of IT Infrastructure, Inventory for hardware and software. 3. Backup-Restoration, Archival-Retrieval of electronic data. 4. Resolving on going Hardware /Softwar...

04 to 05 Years Experience of QA Documentation . Should be able to conduct IPQA independently. Responsible for Line clearance In-process of all activities. Responsible for review, compilation and closing of Batch manufacturing records and Batch Packing records. Responsible to follow, Good Documentation Practices, Good Manufacturing Practices to ensure the quality standards of company. Verification & monitoring of shop floor activities from dispensing to dispatch. Responsible for manufacturing compliance. Responsible for preparation of relevant SOPs. Monitoring & verification of log books at manufacturing blocks for compliance Desired Candidate Profile The candidate should have adequate knowle...

Handling of Quality management system like Market complaints, Change Control, Deviations, OOS, OOT, Incidents, CAPA, Self-Inspection, Vendor Qualification. Review and Approval BMR/BPRs, Prepare of Standard Operation Procedure, Process Validation, Hold Time Study Protocol and Reports, Annual Product Quality Review & trending, Cleaning validation. Qualification/ requalification of Equipments. Release of Finished Product, Continuous Process Verification, Trainings etc.

Responsibilities: Dispense prescription medications with accuracy and attention to detail. Provide excellent customer service, addressing inquiries and concerns. Collaborate with healthcare professionals to ensure optimal patient care. Maintain proper inventory levels and assist in stock management. Adhere to all relevant legal and ethical guidelines in pharmaceutical practices. Requirements: Bachelor's degree in Pharmacy from a recognized institution. Registered Pharmacist with the appropriate state licensing authority. Strong attention to detail and accuracy in dispensing medications. Excellent communication skills and customer-centric approach. Ability to work collaboratively in a team an...

Role & responsibilities 1. Performing Stability analysis, Method transfer and Method Validation. 2. Preparation and review of Method Transfer Protocols, Validation protocols and all related protocols, procedures and reports. 3. To carry out analytical method development, method validation and testing of impurities in finished products on LCMS/MS and GCMS/MS 4. FG (HPLC) 5. Preparation, review of departmental SOPs and training of analysts. 6. Calibration and validation of instruments equipments. 7. Review and maintenance of all logbooks in the department. 8. Procurement of columns, chemicals/ reagents/ solvents and standards for Stability analysis, Method Transfer and Method Validation.

We are seeking a highly skilled and experienced Production Head to join our team at ABC. The ideal candidate will have a solid background in pharmaceutical manufacturing within USFDA approved plants. The Production Head will be responsible for overseeing all aspects of production, ensuring maximum efficiency of the workforce and yield of materials. They will play a crucial role in planning and executing production programs to meet delivery schedules while also considering previous orders.

04 to 05 Years Experience of QA Documentation . Should be able to conduct IPQA independently. Responsible for Line clearance In-process of all activities. Responsible for review, compilation and closing of Batch manufacturing records and Batch Packing records. Responsible to follow, Good Documentation Practices, Good Manufacturing Practices to ensure the quality standards of company. Verification & monitoring of shop floor activities from dispensing to dispatch. Responsible for manufacturing compliance. Responsible for preparation of relevant SOPs. Monitoring & verification of log books at manufacturing blocks for compliance Desired Candidate Profile The candidate should have adequate knowle...