88 Pharmaceutical Production Jobs

URGENT HIRING !!! For more information call or whatsapp +91 9650733400 location's : Canada , Australia , New Zealand , UK, Germany , Singapore ( Not In India ) Benefits : Medical Insurances , Travel allowances , Flight Tickets , Meals , etc Review and execute physicians prescriptions checking their appropriateness and legality Organize the pharmacy in an efficient manner to make the identification of products easier and faster Maintain full control over delivering, stocking and labeling medicine and other products and monitor their condition to prevent expiring or deterioration Listen carefully to customers to interpret their needs and issues and offer information and advice Provide assistance other medical services such as injections, blood pressure/ temperature measurements etc. Prepare medicine when appropriate using correct dosages and material for each individual patient Keep records of patient history and of all activities regarding heavy medication Keep abreast of advancements in medicine by attending conferences and seminars and collaborating with other healthcare professionals Comply with all applicable legal rules, regulations and procedures

Production Manager (Tablets, Capsule, Liquid and Ointment) Job description Approval Tablets, Capsule, Liquid and Ointment Experience 15 Yrs and Above Role & responsibilities : Thorough Knowledge of formulation manufacturing. The role involves managing production teams Optimizing processes, and ensuring efficient and safe production workflows Manage day-to-day production operations, ensuring timely and efficient manufacturing. Ensure compliance with GMP, safety, and environmental regulations. Timely getting work done as per planning Troub le shooting and managing all aspect of production. Reporting to Plant Head. Interested send their updated resume to Email Id hrd.recruitmentconsultants@gmail dot com & WhatsApp or Call - 9.2.1.1.6.1.8.4.4.8 / 9.7.1.7.2.2.1.3.8.9

Dispensing Medication: Accurately and safely preparing and dispensing prescription medications as prescribed by physicians and other healthcare providers. This includes verifying the prescription for correct dosage, patient information, and drug appropriateness. Patient Counseling and Education: Providing patients with clear and concise information about their medications, including proper use, potential side effects, drug interactions, and storage instructions. They also answer patient questions and provide advice on over-the-counter remedies and general health topics. Drug Therapy Management: Reviewing patient medication histories to identify and prevent potential drug interactions, allergies, or other safety concerns. They may also work with physicians to adjust dosages or recommend alternative medications to optimize patient health. Collaboration with Healthcare Professionals: Acting as a medication expert on the healthcare team. Pharmacists communicate with doctors, nurses, and other professionals to clarify prescriptions, provide drug information, and ensure coordinated patient care. Inventory and Operations Management: Maintaining and organizing the pharmacy's inventory of medications and supplies. This includes ordering stock, controlling controlled substances, and ensuring the secure and safe storage of all pharmaceuticals. Compliance and Safety: Adhering to all state and federal laws, regulations, and ethical guidelines governing pharmaceutical practice. They are responsible for ensuring a clean and safe working environment and maintaining accurate patient and medication records. Vaccinations and Health Screenings: In many settings, pharmacists are authorized to administer immunizations (e.g., flu shots) and provide health screenings for conditions like blood pressure or diabetes. Continuous Learning: Staying up-to-date with new drugs, treatments, and medical advancements by attending professional conferences, seminars, and training sessions.

Role & responsibilities Lead formulation and development projects from concept through commercialization Design and optimize formulations to meet product specifications and regulatory requirements Manage and mentor a team of formulation scientists and technicians Collaborate with cross-functional teams including QA, QC, regulatory, and manufacturing Ensure timely completion of project milestones and deliverables Prepare technical reports, presentations, and documentation Stay updated on industry trends, regulatory changes, and best practices Qualifications Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or related field Minimum of 2-3 years of experience in formulation and development Proven track record of successful product formulations Strong understanding of regulatory requirements and guidelines Excellent project management and leadership skills Strong analytical and problem-solving abilities Fluent English International Travelling - Targeted Country - Ghana, Africa, Nigeria, Ethiopia, Uganda, Kenya, Myanmar, Thailand etc. Skills Formulation development Project management Analytical techniques Regulatory compliance Team leadership Technical writing Problem-solving Benefits Yearly Bonus Provide PF, ESIC, PT Benefits Medical Insurance Travelling Allowances Yearly Increment

Responsibilities: * Manage team performance & results * Lead sales strategy in assigned area * Achieve revenue targets through doctor activities * Oversee distribution network development Provident fund

As an ideal candidate for this role, you should possess an M Pharm / B Pharm qualification with 1-10 years of experience in pharmaceutical production. Your experience should be gained from reputed organizations engaged in manufacturing Oral Liquids, Oral Solids, and Topical formulations. It is crucial to have updated knowledge in pharmaceutical manufacturing technologies, including production planning, exposure to WHO-GMP norms, documentation skills, and people management skills. Your expertise in these areas will be essential for the successful execution of your responsibilities in this role.,

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.

Roles: 1.Production Planning & Operations 2. Quality & Investigations 3. Engineering Store & Waste Management Minimum 5–8 years in a similar role within the Excipient/MCC industry. Strong understanding of GMP and FDA requirements. CTC: upto-10 LPA Required Candidate profile Education Required: B.Sc / B.Tech / B.Pharm / B.E. (mandatory) M.Sc / M.Pharm (preferred)

Role & responsibilities 1. Drive product robustness for all products in area of responsibility and lead the third party operation team. 2. Lead and manage all TPO Process activities and process validation for products developed and manufactured at outside contract facilities. 3. This includes, providing product stewardship by ensuring the performance of all products are monitored and maintained in a validated state, supporting root cause investigations by providing Technical intelligence to deviations, technical complaints, OOS & CAPAs. 4. Identifying and executing continuous improvement opportunities, leading New Product Launch third party teams and leading technical activities related to transfers of Drug Product Manufacture and Packaging. 5. Be familiar with statistical tools to analyze data. 6. Provide third party and techno-commercial leadership in the areas of production and packaging process and process optimization using pharmaceutical processes. 7. Knowledge of all pertinent technical information related to an assigned product. Detailed knowledge of the operation, maintenance, and utility of all manufacturing and/or packaging equipment for assigned projects. Thorough familiarity with cGMPs, SOP's, relevant government regulations, and current industry standards. 8. Responsible for Techno-commercial activities for all dosage form. 9. Responsible for Sourcing / coordinate with LL/TP manufacturers for product related documents. 10. Supplier Identification: • Identifying potential suppliers capable of meeting the quality, regulatory, and supply requirements for markets. 11. Supplier Qualification and Onboarding: • Developing and implementing a robust supplier qualification process to ensure that selected suppliers meet the necessary standards and regulations in coordination with quality team. Preferred candidate profile PHARMA THANKS YOU REGARDS MILAP RATHOD (7486829377) call or whtup HR DEPARTMENT OPES HEALTHCARE PRIVATE LIMITED

HIRING FOR OSD - PRODUCTION & QC PRODUCTION(OSD) Experience: (01-07Years) Compression, Granulation, Coating, Capsule filling, Inspection QC Experience: (02-09Years) HPLC, GC, RM,PM, Stability, IP/FP, Method Development, Method Transfer QUALIFICATION : ITI/DIPLOMA/BSC/MSC/B PHARM/M PHARM With relevant Experience ITI/DIPLOMA/BSC/MSC/B PHARM Freshers can Apply DESIGNATIONS: Operator/Sr Operator/Jr Officer/Officer/Jr Executive/Executive INTERVIEW VENUE: SK Consultancy Services, H.No-1-77, 3rd Floor, Bachupally X Road, Opposite Sri Swastik Multi Specialty Hospital, Towards Nizampet Road DATE &TIME: 26th July 2025 ( Saturday); From 09.00 A.M. to 03.00 P.M NEED TO CARRY: Resume 3 Month Pay slips Increment letter Previous company relieving letters Education Documents and ID Proofs Help Us Spread the Word (Refer): Circulate it in your Social Networking sites and groups for better reach and Refer your friends and colleagues, it could be a great opportunity for someone in need! WORK LOCATION: Hetero Labs Limited, UNIT V Polleypally, Jadcherla, Mahabubnagar CONTACT INFO: E-mail: Ashok.ch@hetero.com & Contact:8555912639 for further info.

Work with management and key decision makers to generate leads and convert the same to firm orders Providing product demonstrations to potential customers Support after sales requirements Seek service opportunities and convert to orders

Role & responsibilities Chemist Production Preferred candidate profile MSC Salary 20k gross( candidate able to travel monthly 2-3 times) Bsc.Diploma 18k gross Travel : Monthly 2 to 3 times Qualification : Diploma-Chemical Engg, B.Pharm, MSc-Chemistry Experience : Freshers to Min 3y Interested candidates pls share your resume to mail id : rakyam.bhavana@adecco.com WhatsApp link : https://wa.me/91918147381052 Refer to Friends & Colleagues Thanks & Regards Adecco India Private Limited

Responsible for day-to-day activities of Quality Control, prepare and maintain documentation as per cGMP norms. Working Experience on HPLC is must Coordinate with other depart for smooth running of plant Capable of handling external Audits Required Candidate profile Min Exp 2 to 10 years in Quality department of a reputed pharmaceutical Company Knowledge of working in GMP Co. MS Office (MS Word & MS Excel) / ERP software. and good time management skills Perks and benefits Performance linked incentive & annual bonus extra

Responsible for day-to-day activities of Quality assurance, prepare and maintain documentation, BMR, BPR, SOPs as per cGMP norms. Line clearance, IPQA Coordinate with other depart for smooth running of plant Capable of handling external Audits Required Candidate profile Min Exp 2 to 10 years in Quality department of a reputed pharmaceutical Company Knowledge of working in GMP Co. MS Office (MS Word & MS Excel) / ERP software. and good time management skills Perks and benefits Performance linked incentive & annual bonus extra

Responsible for day-to-day activities of Pharma manufacturing , prepare documentation as per cGMP norms. Working Experience on External preparations Coordinate with other depart for smooth running of plant Capable of handling external Audits Required Candidate profile Min Exp 2 to 10 years in Quality department of a reputed pharmaceutical Company Knowledge of working in GMP Co. MS Office (MS Word & MS Excel) / ERP software. and good time management skills Perks and benefits Performance linked incentive & annual bonus extra

Immediately required for reputed Pharma Industry @Pardi, Valsad Post: Chemist Trainee Qual: BSc/MSc Exp: Fresher or 01 Yrs Salary: As per candidates Ms Palak 9157895300 & Whatsapp

You are competent in two engineering disciplines and possess thorough site knowledge. Your responsibilities include diagnosing and correcting equipment problems, maintaining facilities, and production equipment. You will also be involved in installation, testing, inspecting, and commissioning new electrical equipment, calibration of instrumentation, and rectification of regulatory deviations. Accountability is key as you will be responsible for maintaining and documenting maintenance work, improving maintenance procedures in compliance with GMP, and communicating effectively any issues during handover. Feedback on completed engineering tasks, including root causes and outstanding issues, is essential. You will be expected to use various systems such as WORKMATE, EDMS, BEAMEX, DRAWING DATABASE, MYPIRAMAL, and MICROSOFT OFFICE for different tasks. Additionally, following site systems for change control, safety, risk assessment, and waste handling is crucial in day-to-day activities. As part of your critical tasks, you must work safely, follow isolation procedures, participate in ESH tours and risk assessments, and attend mandatory training. Planning and scheduling tasks with customer departments, working autonomously, and supervising contractors are also part of your responsibilities. Essential qualifications for this role include BS:7671 18th Edition Wiring regulations, Compex certification, apprenticeship in electrical maintenance, and HNC qualification. Relevant experience in maintaining and installing electrical items, reading engineering drawings, and fault finding is required, along with pharmaceutical or chemical production experience. Piramal Group, where this job is situated, has a history of pursuing organic and inorganic growth strategies while upholding core values and inclusive practices. The organization values equal employment opportunities, making decisions based on merit and providing equal opportunities for all applicants and employees. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering a wide range of services across the drug life cycle. With a global network of facilities, PPS provides solutions in drug discovery, pharmaceutical development, clinical trial supplies, APIs, finished dosage forms, and specialized services like highly potent APIs, biologics, and more. As an integral part of the engineering team at Piramal Pharma Solutions, you will play a vital role in ensuring the efficiency, safety, and compliance of the operation. Your expertise and experience will contribute to the success of the organization's goals and objectives. This full-time engineering position is located at Whalton Road, Morpeth, United Kingdom, with the job identification number 6610.,

Job * Engineering & Maintenance Management pharma machine installation,qualifiaction as per cGMP * Ensure compliance with regulatory standards during production, * Oversee CAD drawing creation using AutoCAD software .c ompliance & Validation Office cab/shuttle Maternity benefits in mediclaim policy Health insurance Employee state insurance Maternity policy Military leave policy Annual bonus

Feed tank operator- Capsules Organization Context Position Title: Feed tank operator Capsules Employee Name: Grade : Department: Mucilage preparation Location: Aurangabad Reports to: Chemist and Shift supervisor Reported by: Job Objective Execute feed tank preparation process, timely filling of Feed Tank BMR with online documentation to meet first time right Feed Tank preparation for production requirements. Primary responsibilities Strategic Planning Activities: Core: GMP and over gown adherence to shop floor. Ensure safety by using appropriate PPE and safe practices. Execute the FT preparation as per Production requirement in a shift as per SOP. Ensure shift handover/takeover on the shop floor and hold accountability for any failures/challenges in the previous shift. Ensure compliance to the daily dipping schedule for FT preparation, color change, ZMICs for specific requirements for all upcoming batches. Prepare all feed tank as per procedure mentioned in SOP. Ensure shade compliance of prepared feed tank on Mac bath to ensure zero productivity loss in account of color shade variation. Cross checking feed tank viscosity whenever required. Ensure zero cross contamination and subsequent productivity loss due to wrong colourant and additive addition. Ensure minimum losses of Colourant and additive. Ensure 100% online documentation for FT BMR to meet the GMP requirements. Generate and affix in-process status label to FT to meet GDP requirements and for the ease of identifications/to avoid cross contamination Preparation of new shades to achieve FTR wrt to capsule shade and inform recipe correction to chemist if required. A) Key Result Areas First time right feed tank preparation by complying all relevant SOP as per schedule B) Key Interfaces Internal InterfacesExternal Interfaces Gel room, Quality and production Auditor, Customer and Visitor C) Competency Technical Competency T CompassLeadership Competency L CompassCompetencyLevelCompetency Level GMP Communication GDP Team working Measurement system Auto viscosity unit and Y stirrer Mac beth, Y stirrer Prepared By Date Signature

Job Location Wada, Palghar Approval Tablets, Capsule, Liquid and Ointment Experience 10 Yrs and Above Role & responsibilities : Thorough Knowledge of formulation manufacturing. The role involves managing production teams Optimizing processes, and ensuring efficient and safe production workflows Manage day-to-day production operations, ensuring timely and efficient manufacturing. Ensure compliance with GMP, safety, and environmental regulations. Timely getting work done as per planning Troub le shooting and managing all aspect of production. Reporting to Plant Head.

Urgent requirement of a Production Executive for a pharmaceutical company located in Kurali 1. Tablet section 2. Liquid section (approved)3. Stripping alu alu section 4. Capsule section Interested candidate may call@7888488054

Position Overview: We are looking for a Sr. Manager will be responsible for leading and managing end-to-end multiple API production blocks. The role requires ensuring optimal productivity, quality, cost control and regulatory compliance in alignment with cGMP standards. This position plays a critical role in driving continuous improvement, cross-functional coordination, and operational excellence within the production unit.. Key Responsibilities: Oversee daily production activities to ensure efficiency, quality, and cost-effective management of resources. Develop and implement production schedules based on inventory / market requirements / capacity constraints and provide feedback accordingly. Deployment of manpower & supervisor as per production requirement. Monitor and adjust production processes as necessary to meet production targets and quality standards. Ensure all production batch records are completed and signed off on time. Responsible or keeping production facilities clean and appropriately disinfected. Responsible for the validation protocols and reports are completed and signed. Responsible for qualification of new and modied facilities, when appropriate and equipment. Responsible for maintaining and updating the documents related to the Production activities. Ensure smooth production under EHS & cGMP compliance. Ensure for reporting of all production deviations and evaluation of the same. Ensure process problems /deviations are solved and rectified within a set of time frame, co-ordination/follow up with all the departments like R&D, MSTG, QC, QA, Engineering & Stores. Institute operational controls, monitor the key characteristics, carry out root cause analysis for the non-conformity and take CAPA. Responsible for self-inspection of the area w.r.t EHS and production systems. Responsible for training all the employees of production. Responsible for preventive maintenance is executed as per the planned schedule. Responsible for analyzing the time cycle of each batch and taking corrective actions if any deviations are observed. Responsible for any optimization initiative across the production blocks. Ensure that the yield, % solvent recovery and quality of APIs and Intermediate products are as per the standard norms. Analyze production costs and recommend strategies to reduce costs and improve Profitability. Responsible for monthly RM requirement and weekly RM schedule. Responsible for performing of Internal audit. Responsible for water consumption, effluent generation as per the set norms. Responsible for controlling hazardous waste generation. Identification of Risks & Hazards, Environmental aspects & evaluation and review the same. Responsible for any other work assigned by senior management in the absence of Site Head/ Unit Head. Qualifications and Experience: Analytical Skills and Communication Basic understanding of pharmaceutical or chemical industry Strong organizational, multitasking abilities, time management skills Company Website :- www.scllifesciences.com

Kalol Institute & Research Center is looking for QA & Pharma. Chemist to join our dynamic team and embark on a rewarding career journey. Dispense prescription medications and other health - related products to customers. Maintain accurate and complete records of customer transactions and medications dispensed. Ensure that medications are stored and dispensed in compliance with all applicable laws and regulations. Excellent customer service skills. Good organizational and communication skills.

Supervising Production Teams & Production Planning Monitoring and controlling production parameters Ensuring GMP Compliance Collaborating with other departments Operating, cleaning, and maintaining manufacturing equipment & Documents BMR

Role & responsibilities : An experienced Production Manager with a strong background in the pharmaceutical manufacturing industry with a track record of effectively managing production processes, ensuring compliance with GMP standards, and optimizing productivity and quality. Who has leadership qualities, long-term vision, and a desire for growth within the Organization. Production Planning & Scheduling : Develop and implement production plans, schedules, and workflows for Specially liquid and ointment manufacturing, optimizing resource allocation and minimizing downtime Equipment Management: Oversee the operation, maintenance, and troubleshooting of production equipment, including mixers, filling machines, and other relevant machinery. Material Management: Ensure the proper sourcing, storage, and handling of raw materials, including liquids, ointments, and packaging materials, adhering to inventory control procedures. Safety & Compliance: Enforce safety protocols, maintain a safe working environment, and ensure compliance with all relevant health, safety, and environmental regulations. Team Management: Supervise and motivate production staff, providing training, guidance, and performance feedback. Cost Management: Monitor production costs, identify areas for improvement, and implement strategies to optimize efficiency and minimize waste Process Improvement: Identify opportunities to enhance production processes, improve efficiency, and reduce costs, implementing changes as needed. Documentation & Reporting: Maintain accurate production records, batch records, QMS, and other required documentation, and prepare reports on production performance. Preferred candidate profile : In-depth knowledge of GMP guidelines and regulatory requirements in the pharmaceutical industry. Strong understanding of production processes, Quality control, Quality assurance and supply chain management. Proven experience in especially liquid and ointment manufacturing processes. Strong understanding of production planning, scheduling, and control. Proficiency in operating and maintaining production equipment. Knowledge of regulatory requirements. Fluent Knowledge of Word and Excel. Excellent leadership, communication, and interpersonal skills. Ability to manage and motivate a team. Strong problem-solving and decision-making abilities. Familiarity with relevant safety regulations and procedures. Proficient in MS Office (Word, Excel, PowerPoint) Follow the rules and regulations of company with respect to Health, Hygiene, safety and quality of product & personnel Perks and benefits : Salary : CTC package will be suitable and negotiable based on the present package and industry norms for the right candidate Interested & eligible candidates may send their profile in - piyali.basu@mendine.com, atrayee.mandal@mendine.com