16 Pharma Manufacturing Jobs

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. Prior experience in FDA-inspected environments or India GMP-compliant plants would be highly beneficial. Additionally, familiarity with batch records, deviation analysis, OOS/OOT, and audit trails is essential. Exposure to computer vision or AI-based inspection tools is a definite advantage. As a Project Lead, you will collaborate with the OneOrg.ai product and tech team to execute pilot proposals, work closely with client teams to ensure adoption and results, and ensure alignment with FDA, WHO-GMP, and CDSCO standards throughout the project. Your role will involve defining, driving, delivering, and exiting projects, leaving behind a usable, scalable AI asset once success is achieved. The compensation for this role will be project-based, with defined milestones (Use Case, Pilot, Success, Exit). Successful pilots may lead to long-term or repeat engagements, with the opportunity for a bonus upon enterprise conversion. This role offers a unique experience where you have full ownership of projects, measurable impact through working pilots, and the chance to shape how AI enters the shop floors of pharma manufacturing. Join us at OneOrg.ai and be part of building India's first AI brain for pharma manufacturing, exploring innovative use cases such as visual inspection of blister packs using computer vision, batch deviation risk prediction, GMP document intelligence, and operator behavior detection. If you have a strong consulting mindset, a passion for driving value, and are comfortable working in a hands-on, outcome-driven tech environment, we would love to have you on our team.,

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, coordinating with QA/QC for quality assurance, and batch release. Additionally, you will be tasked with monitoring efficiency, minimizing downtime, implementing process improvements, handling audits, documentation, and regulatory inspections, as well as leading and motivating plant staff to ensure training and performance standards are met. This is a full-time, permanent position with benefits such as Provident Fund and a performance bonus. The work schedule will be during day shifts. The ability to commute or relocate to Pune, Maharashtra, is required for this role. If you are a seasoned professional in pharma manufacturing with strong leadership skills and a dedication to ensuring quality and compliance, we invite you to apply for this challenging and rewarding opportunity as a Plant Manager in Pharma Manufacturing.,

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 person.,

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 approach is crucial for the success of both customers and the company. The job is based in Hyderabad and requires working from the office for 5 days a week. The ideal candidate should have experience working with manufacturing companies, with an added advantage if they have experience in Pharma manufacturing. A background in accounting is also essential for this role. To apply for this position, interested candidates are required to submit their resumes along with an explanation of why they are suitable for the role. Relevant work or project experience should also be included in the resume. Resumes can be sent to careers@lorhanit.com.,

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 implementation and optimization of SAP S/4 HANA within our organization. Reporting directly to the CIO, you will be responsible for driving strategic initiatives, streamlining processes, and ensuring the successful integration of SAP S/4 HANA across all departments. Additionally, 10-12 people will report to this position, in addition to the outsourced partner. Key Result Areas 1. 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. 2. 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. 3. 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 streamline workflows, enhance efficiency, and drive productivity gains. 4. Change Management: Lead change management efforts to drive user adoption and acceptance of SAP S/4 HANA across the organization. Develop and execute comprehensive change management plans, including training programs and communication strategies. 5. Vendor Management: Manage relationships with SAP implementation partners, consultants, and vendors. Ensure adherence to project scope, deliverables, and service level agreements (SLAs) to achieve successful outcomes. 6. Technical Expertise: Serve as a subject matter expert on SAP S/4 HANA functionality, capabilities, and best practices. Provide guidance and support to internal teams on system configuration, customization, and integration requirements. 7. Risk Management: Identify and mitigate project risks and issues to minimize potential disruptions to implementation timelines and objectives. Proactively address challenges and obstacles to ensure the successful delivery of SAP S/4 HANA projects. 8. Continuous Improvement: Drive a culture of continuous improvement within the SAP team and across the organization. Monitor key performance indicators (KPIs) and metrics to evaluate the effectiveness of SAP S/4 HANA implementation and identify areas for enhancement. Qualifications & Experience: Bachelor's degree in finance, Business Administration, Information Technology, or a related field. Proven record of accomplishment of at least 5 years in successfully leading SAP S/4 HANA implementation projects in a mid-sized organization, with additional pharmaceutical industry experience being a significant advantage. Extensive experience of at least 5 years in finance, accounting, or related fields, with a deep understanding of financial processes and systems. Advanced knowledge of SAP S/4 HANA modules, functionality, and configuration options. Certification in SAP S/4 HANA or relevant SAP modules preferred. Strong leadership skills with the ability to inspire, motivate, and mentor cross-functional teams. Ability to thrive in a fast-paced, dynamic environment and manage multiple priorities simultaneously. Excellent communication, interpersonal, and stakeholder management skills. Experience with change management, business process optimization, and project management methodologies

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 necessary Personal Protective Equipment (PPE) during shop-floor operations. Your responsibilities will also include identifying unsafe conditions or acts, reporting safety-related incidents promptly, following instructions from previous shifts or managers diligently, and reviewing/updating shop-floor documents in a timely manner. Additionally, you will be responsible for maintaining cleanliness, ensuring good housekeeping in designated areas, and coordinating with relevant departments for equipment maintenance, calibration, and batch execution. To qualify for this role, you should hold a B.Sc/M.Sc in Chemistry or B.Tech in Chemical Engineering. The job is a full-time position based at Piramal Enterprises Limited in Digwal, Medak, Telangana. Don't miss the opportunity to apply for this position with Job ID 5381 before the deadline on 07/22/2025, 04:31 AM.,

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 /Software Problems with the support of FMS team at the site and Corporate teams. 5. Management of Quality informatics, Laboratory Applications Chromatography (CDS)/Non-Chromatography (Non-CSD) such as Waters Empower, Chromeleon , Lab-X etc. 6. Management of Manufacturing informatics such as Data Loggers, PLCs, SCADA & DCS systems. 7. L1 support to all global application like EDMS, LMS, Trackwise, SAP-HANA, and LIMS. 8. Contribute for preparation of IT SOPs, CSV - Computer system qualification & validation, Maintain IT regulations & compliance, regulatory audit support. 9. To perform and participate in QMS activities such as Change Controls (CCRs), Incidents, Deviations and Corrective & Preventive Actions (CAPAs). Follow-up to close all CCR/Deviation/Investigation/CAPA related to all infra system in a timely manner. 10. To support Implementation of site-based projects and Global projects at the site. 11. Coordination with internal and external stakeholders for various application support and project execution. 12. Understanding of IT security policies, domain policies, malware and antivirus. 13. Procurement & payment process management. 14. People Management process for IT Team Educational Qualification: BE/B. Tech, MCA, BCA, MSc.-IT, BSc.-IT, Graduation + PGDCA. Skills: IT Infrastructure Management, CSV Support, IT regulatory requirements, Quality Informatics and Manufacturing Informatics. Experience: 7 - 8 Years in IT Operations, Preferably in Pharma Manufacturing.

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 knowledge in QA Documation He/ She should have 3-5 years of experience with B. Pharm./ M. Pharm./ educational qualification. Candidate should possess excellent verbal and communicational skills.

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 and handle a fast-paced environment. Benefits: Competitive salary based on qualifications and experience. Opportunities for professional growth and development. Health insurance coverage. Employee discounts on pharmaceutical products. Friendly and inclusive work environment.

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 knowledge in QA Documation He/ She should have 3-5 years of experience with B. Pharm./ M. Pharm./ educational qualification. Candidate should possess excellent verbal and communicational skills

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. Production Head, UDFDA Approved, Pharma Manufacturing

The ideal candidate will have hands-on experience in HR operations within the pharma sector, with a good understanding of HR policies, statutory compliance, and employee engagement practices