183 Pharmaceutical Production Jobs - Page 2

Role Overview: As a Deputy Manager Production with more than 10 years of experience in Pharmaceutical Production, you will be responsible for overseeing various aspects of production to ensure the efficient manufacturing of specially liquid and ointment products. Key Responsibilities: - Production Planning & Scheduling: Develop and implement production plans, schedules, and workflows to optimize resource allocation and minimize downtime in manufacturing processes. - Equipment Management: Oversee the operation, maintenance, and troubleshooting of production equipment such as mixers and filling machines to ensure smooth production operations. - Material Management: Ensure proper sourcing, stor...

About The Role 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 : NA Minimum 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 w...

Seeking Senior Executive – Quality Control at Bhilgaon, Nagpur. 5–8 yrs experience in QC (RM/PM/FG testing, GMP/GLP compliance, documentation, audits). Qualification: B.Sc/M.Sc/B.Pharm/M.Pharm.

Assist in daily production activities related to polymer additives and chemical formulations. Monitor process parameters and ensure adherence to standard operating procedures (SOPs). Maintain proper documentation and production records. Required Candidate profile 0–1 year of experience in a chemical or polymer manufacturing unit (freshers may apply). Basic understanding of production processes, material handling, and lab practices.

1Responsible for Receipt of Raw, Packing & Miscellaneous Materials as per cGMP norms. 2Responsible for all time readiness for inspections by continuous monitoring of cGMP & regulatory norms. 3Responsible & ensure online documentation related to warehouse. 4To co-ordinate with production for PO & BMR arrangement. 5Responsible for arrangement of materials & cleaned accessories for dispensing. 6Responsible & ensure for area cleanliness & area monitoring of dispensing area as per SOP. 7Responsible for Raw materials releases from QC as per requirement. 8Responsible for retest due materials releases from QC as per requirement. 9Responsible for dispensing of Raw and Packing materials as per SOP. 10...

Role & responsibilities Handling of compression machine and inprocess checks like as Friability test, Hardness test, Thickness test, Disintegration test, weight variation test, and appearance of tablets. To Monitor and control yield of batches. Completion of batch BMR. Checking and Filling of Equipment Logbooks , Environment Logbooks , Balance Calibration Logbooks, Daily Verification Logbooks To distribute available manpower in different section of department. Handling Sop's. Labelling of all products correctly and ensure proper labelling system. Co-ordination with QA, QC, Engineering and R&D department of works. Maintaining correct process parameters & ensure the process operations correctl...

Role & responsibilities Responsible for Leading Manufacturing OSD, QMS & COMPLIENCE. Change over time reduction of Manufacturing and Packing lines. Leading production activity Execution of Monthly Manufacturing plan for OSD. Efficiency improvement project in manufacturing for reduction of shift with 100% targeted delivery. Capacity, efficiency, improvement, cost saving initiative and compliance initiative. Coordinate with production manufacturing dept. & other related depts. Concerning operation/ planning /packing activity To execute planned production/ packing in stipulated time limit. Ensuring on-time delivery of products as per specifications. Monthly production planning and weekly schedu...

Role & responsibilities Responsible for Leading Manufacturing OSD, QMS & COMPLIENCE. Change over time reduction of Manufacturing and Packing lines. Improvement of yield at compression and Packing stage Leading production activity Execution of Monthly Manufacturing plan for OSD. Efficiency improvement project in manufacturing for reduction of shift with 100% targeted delivery. Capacity, efficiency, improvement, cost saving initiative and compliance initiative. Coordinate with production manufacturing dept. & other related depts. Concerning operation/ planning /packing activity To execute planned production/ packing in stipulated time limit. Ensuring on-time delivery of products as per specifi...

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 collaborat...

Roles and Responsibilities Perform electrical maintenance, repairs, and installations of equipment to ensure optimal functioning. Conduct routine checks on electrical systems and identify potential issues before they become major problems. Troubleshoot and resolve electrical faults in a timely manner to minimize downtime. Collaborate with other teams to complete projects efficiently and effectively. Ensure compliance with safety protocols and regulations when working with electricity. Desired Candidate Profile 1-4 years of experience in electrical installation, maintenance, or related field. Diploma/ITI Electrical qualification required; relevant certifications an asset. Strong knowledge of ...

Roles and Responsibilities Assist in API production activities, including cleaning equipment, operating reactors, dryers, centrifuges, filters, and other manufacturing machinery. Ensure adherence to safety protocols and maintain a clean working environment. Perform routine maintenance tasks on equipment and facilities to prevent downtime. Collaborate with team members to troubleshoot issues and optimize production workflows. Requirement- Qualification: B.Sc. Chemistry / Diploma in Chemical Engineering / B.Tech in Chemical Engineering Experience: 02 Years (Freshers ,Apprentices and Interns are welcome to apply) Interested candidate share your resume at preeti.thakur2@cipla.com

Qualification: B.Sc / M.Sc / B.Pharma Experience: 2 – 4 Years in Pharma Production Location: G.I.D.C., Kabilpore, Navsari Shift Timings: 8 Hours Duty Salary: Up to 3,00,000 CTC Gender: Male Industry: Pharmaceuticals – Manufacturing 9081799800 Required Candidate profile Experience in pharmaceutical manufacturing operations Strong understanding of GMP and regulatory expectations Only candidates from Navsari/South Gujarat region will be considered

The GSSS will report to the GSSS Team Leader (India) and interact with the Clinical Supply Chain stakeholders. Main responsibilities include: Common: Clinical Trial & Supply Knowledge Understandingof clinical trial design, protocols, regulatory requirements (GxP) Understandingof clinical endpoints, patient randomization processes, study arms, dosing regimens, cohort management, stratification factors Understandingof investigational product management in clinical trial including kit types, shelf life, IMP production plan, depot management, IMP distribution, IMP reconciliation, returns/destruction. Level 1 responsibilities: Create and manage transfers to depot in IRT, customize them in Sanofi ...

Role Overview: You will be responsible for supervising factory operations at a facility in Gurgaon, IMT Manesar. Your role will involve overseeing daily production, dispatch, and quality control processes to ensure smooth workflow and timely completion of production schedules. Additionally, you will manage factory-related documentation, handle billing and dispatch coordination, oversee sales and purchase activities, and lead a team of factory staff. Key Responsibilities: - Supervise daily factory operations, including production, dispatch, and quality control. - Manage and maintain all factory-related documents, such as production reports, inventory logs, dispatch records, and quality contro...

We are looking for ambitious and detail-oriented Production professionals for our Oral Solid Dosage (OSD) and Injectable formulation plants located at Kathua & Jammu to execute day-to-day production activities as per cGMP and regulatory requirements. Required Candidate profile Experience in Pharma Production (OSD / Injectable). Strong knowledge of cGMP and regulatory guidelines. Good communication and documentation skills. Ability to handle shop-floor operations.

Responsibilities: *Look after Production of Pharma Products,BMR Reviewing, * Ensure compliance with pharmaceutical production standards. * Manage XEPNT system for quality control.

Topical Powder Manufacturing, Filling & Sec.Packing Activities oral Powder Manufacturing, Filling and Sec. Packing Activities Batch Initiation Manufacturing Secondary packing & tertiary Packing Share resume to hrd@stedmanpharma.com, Call - 7904827192 Required Candidate profile B.pharm Looking for candidate with Pharma formulation experience

Oversee the formulation, blending, and packaging processes in compliance with GMP and industry regulations Ensure adherence to quality control standards, safety norms, and environmental regulations Optimize resource utilization Required Candidate profile Coordinate with R&D, QA/QC, and supply chain teams for smooth product flow. Liaise with management on production planning, reporting, and audits. Maintain documentation as per regulatory guidelines.

Experience in a chemical industry with batch processing plant Must have knowledge of solid handling and should be aware of process such as grinding milling ,extraction filtration and drying. Should work in DCS operated plant Required Candidate profile Must have knowledge of IMS,IATF,RC. Should be aware of safety norms of a chemical industry.

Production Supervisor Pharma & Chemical Manufacturing (Hiring for a Leading Chemical/Pharma Manufacturer) Location: Vasai (1 Vacancy) & Tarapur – Boisar (2 Vacancies), Dist. Palghar, Maharashtra Experience: 2 – 8 Years Qualification: Diploma / B.E. in Chemical Engineering / Industrial Chemistry or related field Salary: As per Interview & Company Norms Gender Preference: Male Candidates Working Hours: Standard Shift Timings (No OT) 9 AM TO 6 PM Roles & Responsibilities: Plan, organize, and monitor daily production activities to achieve targets. Ensure compliance with SOPs, GMP, ISO, and statutory regulations . Supervise operators, technicians, and contract workers on the shop floor. Conduct s...

Oversee the formulation, blending, and packaging processes in compliance with GMP and industry regulations Ensure adherence to quality control standards, safety norms, and environmental regulations Optimize resource utilization Required Candidate profile Coordinate with R&D, QA/QC, and supply chain teams for smooth product flow. Liaise with management on production planning, reporting, and audits. Maintain documentation as per regulatory guidelines.

Develop & execute marketing strategies for APIs & Excipients (domestic + international). Identify and engage new clients, distributors, and channel partners. Achieve sales targets through lead generation, client retention & market expansion. Required Candidate profile Min 5 years in API & Excipient market Strong knowledge of pharma excipients, APIs & international regulation Good communication, presentation & negotiation client engagement & achieving sales growth

As an ideal candidate for this role, you should hold an M Pharm / B Pharm qualification with 1-10 years of experience in pharmaceutical production. Your experience should be from reputed organizations engaged in manufacturing Oral Liquids, Oral Solids, and Topical formulations. It is essential for you to have updated knowledge in pharmaceutical manufacturing technologies, along with experience in production planning, exposure to WHO-GMP norms, documentation skills, and people management skills. Key Responsibilities: - Manufacturing Oral Liquids, Oral Solids, and Topical formulations - Production planning - Ensuring compliance with WHO-GMP norms - Documentation management - Managing a team of...

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

Job Openings for Machine Operator / Production Supervisor in Perundurai Location Machine Operator: Responsibilities: Assist in operating and monitoring Moringa processing machines (grinding, drying, packing, etc.). Follow supervisor instructions for machine setup and daily operations. Check product quality during each production stage. Maintain cleanliness, hygiene, and safety on the shop floor. Requirements: Fresher candidates can apply (training will be provided). Basic reading and writing skills. Physically fit and willing to work in shifts. Qualification: Any Degree / ITI / Diploma Production Supervisor : Responsibilities: Supervise daily production (grinding, drying, packing). Ensure fo...