pharmaceutical engineer

Jobsvale Rudram Placement

Position: Maintenance Engineer (Male) Industry: Pharmaceutical Experience: 6+ Years Qualification: Mechanical Engineer Salary: Up to ₹70,000 (As per Experience) Working Hours: 9:00 AM to 6:00 PM Weekly Off: SundayKey Skills &amp; Responsibilities:<ul><li>Preventive and breakdown maintenance planning &amp; execution</li><li>Utility operations and equipment handling</li><li>GMP documentation and SOP compliance</li><li>Equipment calibration and validation support</li><li>HVAC/AHU requalification activities</li><li>Team supervision and coordination</li></ul>Benefits: Transportation, Lunch Facility, PF, Gratuity, Bonus 7 Sick Leaves, 7 Casual Leaves, 18 Earned Leaves (after 6 months)Apply Now: adm.jobsvale@gmail.com Contact: 7211188860Job Types: Full-time, PermanentPay: ₹60,000.00 - ₹70,000.00 per monthBenefits:<ul><li>Food provided</li><li>Leave encashment</li><li>Provident Fund</li></ul>Work Location: In person

Maintenance Engineer ( Pharma Industry )

Smart Vision Technical Services

Job SummaryWe are seeking a highly experienced and entrepreneurial Pharmaceutical Manufacturing Professional to establish, commission, and independently run a medicine production unit in Oman. The role involves complete responsibility from project planning and regulatory approvals to production, quality compliance, and commercial readiness.The ideal candidate will act as a founding leader for the manufacturing unit, with strong technical, regulatory, and operational expertise.Key ResponsibilitiesProject Setup &amp; Plant Establishment<ul><li>Lead end-to-end setup of a pharmaceutical manufacturing facility in Oman.</li><li>Plan factory layout, utilities, HVAC, clean rooms, and production flow as per GMP standards.</li><li>Coordinate with consultants, contractors, equipment suppliers, and utility providers.</li><li>Oversee installation, qualification, and validation of machinery and systems.</li></ul>Regulatory &amp; Compliance<ul><li>Manage regulatory approvals and licensing with Oman Ministry of Health (MOH) and relevant authorities.</li><li>Ensure compliance with Oman GMP, WHO-GMP, and international pharmaceutical standards.</li><li>Prepare and submit documentation for site registration, product registration, and inspections.</li><li>Handle audits, inspections, and corrective action plans.</li></ul>Production &amp; Operations<ul><li>Establish SOPs for manufacturing, packaging, storage, and distribution.</li><li>Plan and manage production schedules to meet quality, cost, and delivery targets.</li><li>Ensure efficient use of manpower, materials, and equipment.</li><li>Monitor yields, deviations, and continuous improvement initiatives.</li></ul>Quality Assurance &amp; Quality Control<ul><li>Set up and manage QA/QC departments.</li><li>Implement quality management systems including documentation control, change management, deviation handling, and CAPA.</li><li>Ensure batch release, stability studies, and product lifecycle compliance.</li><li>Maintain strict adherence to data integrity and quality standards.</li></ul>Supply Chain &amp; Vendor Management<ul><li>Identify and approve raw material, API, and packaging suppliers.</li><li>Negotiate procurement contracts and ensure reliable supply chains.</li><li>Manage inventory, warehousing, and expiry control.</li></ul>Commercial &amp; Business Support<ul><li>Support management in product selection, costing, and pricing strategies.</li><li>Coordinate with marketing and distribution teams for product launches.</li><li>Ensure cost-efficient operations and profitability of the manufacturing unit.</li></ul>Team Building &amp; Leadership<ul><li>Recruit, train, and manage production, QA, QC, engineering, and support staff.</li><li>Build a strong GMP-compliant culture across the organization.</li><li>Conduct performance reviews and continuous training programs.</li></ul>Key Skills &amp; Competencies<ul><li>Strong knowledge of pharmaceutical manufacturing processes.</li><li>Deep understanding of GMP, regulatory compliance, and audits.</li><li>Proven project management and plant setup experience.</li><li>Leadership ability to run operations independently.</li><li>Strong documentation, analytical, and problem-solving skills.</li><li>Ability to liaise with regulators, consultants, and international partners.</li></ul>Qualifications &amp; Experience<ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in Pharmacy, Pharmaceutical Sciences, or Chemical Engineering.</li><li>10&ndash;20 years of experience in pharmaceutical manufacturing.</li><li>Proven experience in setting up a new pharma plant (greenfield or brownfield).</li><li>Prior experience in GCC / Middle East regulatory environment is a strong advantage.</li><li>Experience with WHO-GMP / MOH audits preferred.</li></ul>Reporting ToManaging DirectorCompensation<ul><li>Competitive senior-level salary</li><li>Performance-based incentives</li><li>Long-term leadership and growth opportunity</li></ul>Job Type: Full-timePay: RO800.000 - RO1,500.000 per month

Head – Pharmaceutical Manufacturing / Plant Head

Tibbi Pvt LTD

WE ARE HIRING: Production Pharmacist and Supply Chain ExpertCompany: Aesthetic Group Location: Lahore Industry: Aesthetic Group Job Type: Full-timeAbout the CompanyA well-known Aesthetic Group is looking for a company dedicated to manufacturing high-quality skin care products. We are seeking a Production Pharmacist to join our manufacturing team.Job SummaryThe Production Pharmacist will be responsible for supervising and managing daily manufacturing operations. The ideal candidate will ensure that all production activities are performed in strict compliance with cGMP (Current Good Manufacturing Practices), safety protocols, and regulatory guidelines, while ensuring timely achievement of production targets.Key ResponsibilitiesProduction Supervision: Supervise manufacturing processes (Granulation, Compression, Coating, Encapsulation, or Liquid/Syrup preparation) to ensure efficiency and quality.Documentation: Maintain accurate and timely Batch Manufacturing Records (BMR), logbooks, and Standard Operating Procedures (SOPs).Compliance: Ensure strict adherence to cGMP, GLP, and EHS (Environment, Health &amp; Safety) standards during production.Process Control: Perform in-process quality checks (IPQC) to monitor weight variation, hardness, friability, and disintegration time.Resource Management: Manage production staff, ensuring discipline, proper gowning, and adherence to hygiene standards.Coordination: Collaborate with Quality Assurance (QA), Quality Control (QC), and Warehouse departments for smooth material flow and product release.Machine Maintenance: Coordinate with the engineering department to ensure production machinery is calibrated and functioning correctly.Requirements &amp; QualificationsEducation: Pharm-D (Doctor of Pharmacy) from a PEC/Pharmacy Council recognized university Licensure: Valid registration with the Pharmacy Council (Category A) Experience: 1&ndash;3 years of experience in a pharmaceutical production environmentSkills:Strong knowledge of DRAP regulations and cGMP guidelines Familiarity with production machinery (Tablet Press, FBD, Blister Packaging, etc.) Leadership and team management skills Proficiency in MS OfficeJob Type: Full-timeApplication Question(s):<ul><li>what is your Current/Last Salary?</li><li>what is your salary expectations?</li><li>Does, Monday to Friday working days suits you ?</li></ul>Education:<ul><li>Middle School (Preferred)</li></ul>Experience:<ul><li>pharmacist: 3 years (Preferred)</li></ul>Work Location: In person

Production Pharmacist and Supply Chain Expert

lifecraft engineering

ABOUT USBuilding Excellence Through Pharmaceutical InnovationAt Lifecraft Engineering, we don&rsquo;t just build pharmaceutical systems we craft trust, precision, and progress. Driven by innovation and a commitment to global quality and regulatory excellence, we create turnkey solutions that empower the healthcare world to move forward with confidence. Our mission is simple yet powerful: to engineer the future of wellness and help industries touch more lives with reliability, integrity, and purpose.Job description<ul><li>Sourcing and Evaluation:</li></ul>Identifying, evaluating, and qualifying vendors for electrical components, control panels, relevant items.<ul><li>Technical Expertise:</li></ul>Possessing strong technical knowledge of electrical components and systems used in pharmaceutical engineering.<ul><li>Negotiation:</li></ul>Negotiating prices, terms, and delivery schedules with suppliers to achieve cost savings and maintain quality.<ul><li>Procurement Process Management:</li></ul>Managing the entire procurement process, including creating purchase orders, tracking orders, and ensuring timely delivery.<ul><li>Quality Assurance:</li></ul>Ensuring that all purchased materials as pharmaceutical engineering meet the required quality standards and specifications with<ul><li>Documentation and Record Keeping:</li></ul>Maintaining accurate records of all procurement activities, including quotations, purchase orders, and supplier information.<ul><li>Compliance:</li></ul>Ensuring as per pharmaceutical engineering compliance with company policies, industry standards, and relevant regulations.<ul><li>Collaboration:</li></ul>Working closely with engineering, production, planning, and other departments to understand their material requirements.<ul><li>Market Research:</li></ul>Conducting market research to stay informed about new technologies, products, and pricing trends.Required Skills:<ul><li>Technical Knowledge: Solid understanding of electrical components, control systems, and relevant industry standards.</li><li>Negotiation Skills: Ability to negotiate effectively with suppliers to achieve favorable terms.</li><li>Communication Skills: Excellent written and verbal communication skills.</li><li>Organizational Skills: Strong organizational and time management skills.</li><li>Problem-Solving Skills: Ability to identify and resolve procurement-related issues.</li><li>Computer Skills: Proficiency in MS Office Suite (especially Excel) and experience with ERP systems.</li></ul>Qualifications and Experience:<ul><li>Bachelor's degree in Engineering or a related field.(pharmaceutical engineering )</li><li>Min 2-3 yrs proven experience in procurement, preferably within the electrical or pharmaceutical engineering industry.</li><li>Knowledge of industry standards and regulations related to procurement</li></ul>Job Type: Full-timePay: ₹18,323.84 - ₹30,522.26 per monthBenefits:<ul><li>Health insurance</li><li>Provident Fund</li></ul>Work Location: In person

Assistant Purchase Engineer

Soho Dragon

<div>SoHo Dragon represents a tech-driven, AI-native pharmaceutical company that&rsquo;s shaping the future of healthcare. We&rsquo;re looking for a mid-to-senior-level Data Engineer to play a key role in building and optimizing data solutions. 
You&rsquo;ll work with Snowflake and Dagster as your core tools, while also leveraging Terraform, GitHub Actions, and Databricks to deliver scalable, high-impact data pipelines. 
Start date: ASAP

Contract duration: 2-6 months</div>

Data Engineer

Sushen Medicamentos

ORGANIZATIONAL DETAILSCompany: Sushen Medicamentos Pvt. Ltd. Department: Maintenance &amp; Engineering Location: Ahmedabad, Gujarat Reports To: Assistant Manager - Maintenance / Maintenance and Projects Head Position Type: Full-Time, Permanent Experience Level: 4-5 Years (Mandatory: EU GMP Approved Plant Experience)ABOUT SUSHEN MEDICAMENTOSSushen Medicamentos Pvt. Ltd. is a leading pharmaceutical services company with global operations, specializing in:<ul><li>Pharmaceutical Project Management Services (PMS): Comprehensive turnkey solutions for manufacturing infrastructure</li><li>Contract Development and Manufacturing Organization (CDMO): Specialized manufacturing services with expertise in effervescent tablets and solid dosage forms</li></ul>Operating under stringent regulatory standards including cGMP, WHO-GMP, USFDA, and EMA compliance, Sushen is committed to delivering pharmaceutical excellence globally.POSITION SUMMARYThe Maintenance Engineer - Solid Oral Dosage will be responsible for ensuring optimal performance, reliability, and regulatory compliance of all equipment and systems used in solid oral dosage (tablets, capsules, effervescent tablets) manufacturing operations. This role requires hands-on technical expertise in maintaining sophisticated pharmaceutical manufacturing equipment while adhering to EU GMP standards.The ideal candidate will have proven experience working in EU GMP approved pharmaceutical plants with a strong foundation in either electrical or mechanical engineering, applied specifically to solid dosage manufacturing environments.KEY RESPONSIBILITIESEquipment Maintenance &amp; Reliability<ul><li>Perform preventive and corrective maintenance on solid oral dosage manufacturing equipment including:</li><li>Tablet compression machines (rotary tablet presses, single/multi-station presses)</li><li>Capsule filling machines (automatic/semi-automatic)</li><li>Granulation equipment (high shear granulators, fluid bed processors)</li><li>Blenders and mixers (V-blenders, double cone blenders, bin blenders)</li><li>Coating machines (film coating pans, sugar coating equipment)</li><li>Milling and sieving equipment</li><li>Tablet dedusters and metal detectors</li><li>Effervescent tablet manufacturing equipment</li><li>Material handling systems (conveying, vacuum transfer)</li><li>Troubleshoot equipment breakdowns and implement rapid corrective actions to minimize production downtime</li><li>Monitor equipment performance parameters and identify potential failure points</li><li>Maintain equipment logs, maintenance records, and history cards as per GMP requirements</li><li>Coordinate with equipment vendors for specialized maintenance and technical support</li></ul>Electrical/Mechanical Systems ManagementFor Electricals :<ul><li>Maintain electrical control panels, motor control centers (MCCs), and variable frequency drives (VFDs)</li><li>Troubleshoot PLC-based control systems, HMI interfaces, and SCADA systems</li><li>Ensure proper functioning of interlocks, safety circuits, and emergency stop systems</li><li>Maintain power distribution systems, lighting, and electrical safety systems</li><li>Handle electrical calibration and instrumentation maintenance</li></ul>For Mechanicals :<ul><li>Maintain mechanical drive systems, gearboxes, bearings, and transmission components</li><li>Manage hydraulic and pneumatic systems including compressors, valves, and cylinders</li><li>Perform alignment, balancing, and vibration analysis of rotating equipment</li><li>Maintain cooling systems, lubrication systems, and material handling mechanisms</li><li>Handle mechanical modifications and upgrades to existing equipment</li></ul>EU GMP Compliance &amp; Documentation<ul><li>Execute all maintenance activities in strict compliance with EU GMP guidelines</li><li>Maintain comprehensive documentation including:</li><li>Preventive maintenance schedules and execution records</li><li>Breakdown reports and corrective action records</li><li>Equipment qualification documents (IQ/OQ/PQ)</li><li>Change control documentation</li><li>Deviation and CAPA records related to equipment</li><li>Standard Operating Procedures (SOPs) for maintenance activities</li><li>Support qualification and validation activities for new equipment installations</li><li>Participate in regulatory audits and inspections, providing technical documentation and explanations</li><li>Ensure maintenance activities do not compromise product quality or GMP compliance</li><li>Follow cleanroom protocols and hygiene requirements during maintenance in production areas</li></ul>Utilities &amp; Support Systems<ul><li>Support maintenance of critical utilities serving solid dosage manufacturing:</li><li>Compressed air systems (instrument air, plant air)</li><li>HVAC systems maintaining environmental conditions in production areas</li><li>Dust extraction systems (for tablet compression, coating, granulation areas)</li><li>Vacuum systems</li><li>Clean utilities (purified water systems as applicable)</li><li>Monitor utility parameters and ensure consistent supply to manufacturing operations</li><li>Coordinate with utilities team for planned shutdowns and emergency situations</li></ul>Continuous Improvement &amp; Technical Support<ul><li>Identify opportunities for equipment reliability improvement and efficiency enhancement</li><li>Participate in root cause analysis for recurring equipment failures</li><li>Contribute to CAPA (Corrective and Preventive Actions) related to equipment issues</li><li>Support technology transfer and scale-up activities for new products</li><li>Assist in preparation of technical specifications for new equipment procurement</li><li>Maintain spare parts inventory and coordinate timely procurement of critical components</li></ul>Safety &amp; Compliance<ul><li>Follow all electrical/mechanical safety standards and lockout-tagout (LOTO) procedures</li><li>Ensure compliance with industrial safety regulations and EHS requirements</li><li>Use appropriate Personal Protective Equipment (PPE) and ensure team compliance</li><li>Participate in safety training programs and incident investigations</li><li>Maintain housekeeping standards in maintenance workshops and work areas</li></ul>REQUIRED QUALIFICATIONSEducation<ul><li>Bachelor's degree in Electrical Engineering OR Bachelor's degree in Mechanical Engineering (B.E./B.Tech)</li></ul>Experience<ul><li>Total Experience: 4-5 years in maintenance engineering roles</li><li>Mandatory Requirement: Minimum 3 years of hands-on experience in EU GMP approved pharmaceutical manufacturing plants</li><li>Solid Dosage Experience: Proven experience maintaining solid oral dosage (tablets/capsules) manufacturing equipment</li><li>Pharmaceutical Industry: Strong understanding of pharmaceutical manufacturing environment and cGMP requirements</li></ul>Technical SkillsCore Technical Competencies:<ul><li>Strong troubleshooting and diagnostic skills for pharmaceutical manufacturing equipment</li><li>Hands-on experience with tablet compression, capsule filling, granulation, and coating equipment</li><li>Understanding of process flow in solid oral dosage manufacturing</li><li>Proficiency in reading and interpreting technical drawings, P&amp;IDs, electrical schematics, and mechanical drawings</li><li>Knowledge of preventive and predictive maintenance methodologies</li></ul>GMP &amp; Regulatory Knowledge<ul><li>Thorough understanding of EU GMP requirements for pharmaceutical manufacturing</li><li>Knowledge of equipment qualification (IQ/OQ/PQ) processes</li><li>Familiarity with change control, deviation management, and CAPA systems</li><li>Understanding of cleanroom classifications and environmental monitoring</li><li>Documentation practices as per GMP guidelines</li></ul>PREFERRED QUALIFICATIONS<ul><li>Experience with effervescent tablet manufacturing equipment</li><li>Experience with regulatory inspections (WHO GMP, EU GMP)</li><li>Understanding of pharmaceutical validation protocols and regulatory requirements</li></ul>CORE COMPETENCIESTechnical Competencies<ul><li>Equipment troubleshooting and problem-solving</li><li>Preventive and breakdown maintenance execution</li><li>Technical documentation and record-keeping</li><li>Equipment performance analysis</li><li>Vendor coordination and management</li></ul>Quality &amp; Compliance<ul><li>EU GMP compliance mindset</li><li>Attention to detail and documentation rigor</li><li>Process understanding and quality consciousness</li><li>Regulatory awareness</li><li>Risk assessment capabilities</li></ul>Professional Competencies<ul><li>Analytical and logical thinking</li><li>Time management and prioritization</li><li>Team collaboration</li><li>Communication skills (verbal and written)</li><li>Learning agility and adaptability</li><li>Safety consciousness</li><li>Ownership and accountability</li></ul>Job Types: Full-time, PermanentPay: ₹40,000.00 - ₹60,000.00 per monthWork Location: In person

Maintenance Engineer - Solid Oral Dosage

KYRA INTERNATIONAL PVT LTD

Role SummaryWe are looking for a skilled AutoCAD 2D Design Engineer with experience in pharma machinery design. The candidate will be responsible for preparing detailed 2D drawings for manufacturing, ensuring compliance with cGMP standards, and coordinating closely with production, QC, and project teams.Key Responsibilities<ul><li>Prepare detailed 2D manufacturing drawings using AutoCAD for pharma machines such as:</li><li>ANFD, FBD, RMG, Sparkler Filter, RCVD, PNF, Vibro Sifter, Multimill, VTD, Reactors, Ointment Mfg Plant etc.</li><li>Develop GA drawings, fabrication drawings, assembly drawings, and BOMs.</li><li>Modify and update drawings based on:</li><li>Customer specifications</li><li>FAT observations</li><li>Production and QC feedback</li><li>Ensure designs comply with cGMP, FDA, and pharmaceutical industry standards.</li><li>Coordinate with production, purchase, store, QC, and service teams for design clarifications and execution.</li><li>Support the sales team with technical drawings and layout drawings when required.</li><li>Maintain proper drawing revision control and documentation.</li><li>Assist in standardization and improvement of existing designs.</li><li>Ensure timely release of drawings to meet project delivery schedules.</li></ul>Required Skills &amp; Competencies<ul><li>Strong proficiency in AutoCAD 2D (mandatory).</li><li>Good understanding of:</li><li>Fabrication drawings</li><li>Knowledge of pharma equipment design and manufacturing practices.</li><li>Familiarity with BOM preparation.</li><li>Basic knowledge of materials (SS 304 / 316 / 316L) used in pharma machines.</li><li>Ability to interpret P&amp;ID and process requirements.</li><li>Good coordination and communication skills.</li><li>Attention to detail and ability to work under timelines.</li></ul>Educational Qualification<ul><li>Diploma / BE / BTech in Mechanical Engineering or relevant field.</li></ul>Experience<ul><li>2 years of relevant experience in:</li><li>Pharma machinery</li><li>Process equipment</li><li>Industrial equipment manufacturing</li></ul>(Experience in pharma equipment design will be preferred.)Job Type: PermanentPay: ₹25,000.00 - ₹30,000.00 per monthBenefits:<ul><li>Leave encashment</li><li>Provident Fund</li></ul>Experience:<ul><li>Pharmaceutical machine: 1 year (Preferred)</li></ul>Location:<ul><li>Vasai, Maharashtra (Preferred)</li></ul>Work Location: In person

Mechanical Design Engineer - 2D

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