Pharmaceutical Production Jobs in India

Job Duties & ResponsibilitiesSr. No. Job Duties & Responsibilities1 Perform testing of Raw Materials, Finished Goods, and In-Process Materials and report analytical results accurately.2 Handle and operate analytical instruments such as HPLC, UPLC, GC, ICP, DSC, XRD, and PSA.3 Carry out calibration of analytical instruments as per the master calibration schedule.4 Investigate analytical errors/deviations, identify root causes, and implement corrective and preventive actions (CAPA).5 Prepare laboratory SOPs, analytical study reports, and related technical documentation.6 Execute method validation activities and prepare validation protocols and reports.7 Review analytical chemistry testing records for raw materials, stability samples, and finished products for compliance and accuracy.8 Prepare and review specifications, methods of analysis, and analytical development reports.9 Ensure compliance with quality systems, laboratory procedures, and regulatory guidelines.10 Discuss daily work plans with supervisors/managers and mentor junior laboratory personnel.11 Participate in project meetings and prepare weekly and monthly progress reports for management review.12 Perform routine laboratory activities including equipment maintenance, chemical inventory management, and laboratory housekeeping.13 Maintain strict IP confidentiality and comply with all related data privacy and company policies.

As a MED Representative based in Azamgarh, you will play a key role in promoting and selling medical products to healthcare professionals and institutions. Your primary goal will be to ensure the availability and visibility of our products in the market while building strong relationships within the medical community.**Key Responsibilities:**- **Promote Products:** Actively engage with doctors, pharmacists, and hospital administrators to present and explain our medical products, highlighting their benefits and features. - **Sales Target Achievement:** Work towards achieving monthly sales targets by developing effective sales strategies and maintaining a strong sales pipeline.- **Market Research:** Conduct regular market surveys to understand customer needs, competitor activity, and market trends. Use this information to adapt your sales approach accordingly.- **Customer Relationship Management:** Build and maintain long-term relationships with healthcare professionals to ensure customer loyalty and repeat business.- **Product Training:** Provide necessary product training and demonstrations to potential clients, ensuring they are well-informed about the medical products.- **Reporting:** Prepare and submit regular reports on sales activities, customer feedback, and market conditions to the management team for strategic decision-making.**Required Skills and Expectations:**Candidates should have 1 to 3 years of experience in medical sales or a related field. Strong communication and interpersonal skills are essential for effectively engaging with clients. Candidates should also possess good organizational capabilities and be detail-oriented. A thorough understanding of the medical industry and a passion for healthcare will be an advantage. Ability to work independently and as part of a team is essential. Applicants should be proactive, motivated, and capable of adapting to changing market conditions. Knowledge of local healthcare regulations and practices is a plus.

Job Responsibilities: Manage daily Head Office administration operations efficiently. Oversee office infrastructure, housekeeping, pantry services, stationery, and overall facilities. Monitor maintenance activities, including repairs, AMC services, and facility upkeep. Liaise with internal departments to provide timely administrative support. Act as the single point of contact for all facility-related coordination and escalations at the Head Office. Coordinate with vendors and service providers for office maintenance, repairs, and service contracts. Maintain updated vendor records, agreements, invoices, and related documentation (physical & digital). Manage courier, dispatch, and inward/outward documentation, including sensitive and confidential pharma-related documents. Maintain administrative files including important documents, agreements, registers and office documentation systematically. Support the management in organizing internal meetings, reviews, training programs, festivals, and corporate events. Coordinate travel arrangements including car bookings, hotel reservations, and logistics for tours and travel. Prepare and maintain weekly, monthly, and quarterly administrative MIS reports. Track daily Xerox usage, stationery consumption, and other office consumables. Assist in maintaining legal records, agreements including premises leave and licenses and statutory compliance documents. Ensure timely renewal of contracts, licenses, and regulatory documents. Ensure adherence to company policies, administrative SOPs, and compliance guidelines.Candidate Requirements: Bachelors Degree Candidate should be a resident of Mumbai. Mini 5 years of experience in administration or office coordination preferably in pharmaceutical corporate HO. Good communication and interpersonal skills Basic knowledge of MS Office (Word, Excel, Email) Well-organized, proactive, and capable of handling confidential information

Responsible for day to day production operations in factory

As a QC Pharmacist, you will play a vital role in ensuring the quality and safety of pharmaceutical products. Your primary responsibilities will include:- **Quality Control Testing**: Conduct tests on incoming raw materials and finished products to ensure they meet the required specifications and standards for safety and effectiveness.- **Documentation and Reporting**: Maintain accurate records of all quality control processes, including test results and any deviations from expected outcomes. This ensures compliance with regulatory standards.- **Equipment Maintenance**: Regularly check and calibrate laboratory equipment to ensure they operate correctly, providing reliable and accurate results for quality testing.- **Collaboration**: Work closely with other departments, such as production and research and development, to address any quality issues that may arise during the manufacturing process.- **Regulatory Compliance**: Stay updated with industry regulations and guidelines to ensure that all quality control activities adhere to legal and safety standards.To succeed in this role, candidates should possess strong analytical skills and attention to detail to identify and resolve quality issues. Effective communication skills will be crucial for working with team members across various departments. A strong foundation in pharmaceutical sciences, gained through a B.Pharma or B.Sc degree, is necessary. While freshers are welcome to apply, candidates must be committed to maintaining high standards of quality and safety.

As a MED Representative in Patna, India, you will be responsible for promoting and selling medical equipment and devices to healthcare facilities. This role involves building relationships with potential clients, providing product demonstrations, and coordinating with the sales team to meet targets.Key responsibilities include visiting hospitals, clinics, and other healthcare institutions to showcase the features and benefits of our medical products. You will also be responsible for conducting product training sessions for medical staff and assisting with any troubleshooting or technical issues that may arise.To excel in this role, you must have excellent communication skills, be detail-oriented, and have a good understanding of medical terminology and equipment. A high school diploma is required, and previous sales experience in the medical field is preferred. Additionally, you should be organized, self-motivated, and able to work effectively both independently and as part of a team.

We are hiring a Documentation Executive for our pharmaceutical operations.Roles & Responsibilities:Prepare, review, and maintain pharmaceutical documentationHandle SOPs, batch records, and quality-related documentsEnsure compliance with regulatory and quality standardsCoordinate with R&D and QC teams for document updatesEligibility:Bachelors Degree in Pharmacy or ChemistryPost Graduates preferredFreshers or candidates with up to 2 years experience can applyJob Type: Full TimeLocation: IndiaInterested candidates can apply through PlacementIndia or send resume toupendarbakaram9@gmail.com

We are seeking dedicated API Plant Operators for our facility in Nandesari GIDC, Vadodara. The ideal candidates will support manufacturing operations, ensuring strict adherence to GMP and SOP guidelines. This full-time position involves operating various equipment, monitoring process parameters, and maintaining accurate documentation. It's an excellent opportunity for junior and trainee operators, as well as freshers with relevant qualifications. Join our team to kickstart a rewarding career in the API and pharmaceutical industry

Production Assistant (b Sc/b Pharma) Required for a Nutraceutical Manufacturing Unit At 311, Industrial Focal Point, Phase 9, Mohali

SALES PERSON REQUIRED FOR MEDICAL STORE

We are seeking a dedicated and experienced professional to operate and manage the functioning of a fully automatic capsule filling machine, preferably with hands-on knowledge of the PF-90 model.Key Responsibilities:Operate and oversee the performance of the fully automatic capsule filling machine (preferably PF-90).Ensure smooth and efficient production runs while maintaining high-quality standards.Maintain accurate and timely records of batch production, machine performance, and other relevant documentation as per regulatory and organizational requirements.Supervise, guide, and coordinate with helpers/labourers on the production floor to ensure operational efficiency and adherence to safety protocols.Conduct basic troubleshooting and coordinate with maintenance teams when necessary.Ensure compliance with GMP (Good Manufacturing Practices) and company SOPs.Requirements:Prior experience in operating fully automatic capsule filling machines (experience with PF-90 is an added advantage).Ability to handle production documentation and maintain regulatory compliance.Strong leadership skills with the ability to effectively manage and guide support staff.Attention to detail, reliability, and commitment to quality.

Prepare daily and weekly production schedules in coordination with production, QA/QC, and store departments. Monitor production progress and adjust plans as per actual output or delays. Coordinate with the stores and purchase team to ensure timely availability of raw materials and packaging materials. Track material consumption and prepare usage reports for RM and PM. Assist in maintaining inventory levels and raise requirements in advance to avoid line stoppage. Communicate with the quality department to plan batches as per sampling/testing timelines. Ensure proper documentation of batch planning, material requisitions, and issuance records. Actively participate in shop floor planning and line allocation based on machine availability. Support in capacity planning, equipment loading, and manpower forecasting. Work closely with ERP/MRP systems for production and inventory planning entries.

We have vacant of 4 Production Chemist Jobs in Hyderabad, Visakhapatnam, Experience Required : 1 - 6 years Educational Qualification : B.Sc, B.E, M.Sc Skill Pharmaceutical Production etc.

Promote and detail the companys pharmaceutical or healthcare products to doctors, pharmacists, and other healthcare professionals.Build and maintain strong relationships with healthcare professionals, including physicians, pharmacists, and hospital staff.Cover the assigned territory and plan regular visits to doctors, clinics, hospitals, and pharmacies to promote product awareness.Meet or exceed sales targets assigned by the company within the designated territory.Monitor product sales performance and report progress regularly to the manager.Educate healthcare professionals on the appropriate use of products and answer technical queries related to the product.Maintain accurate records of all sales activities, product orders, and client interactions.Provide daily, weekly, and monthly sales reports to management.

Responsible for the execution of Production plan and managing the use of man power for multiple shifts, coordination between various departments.Ensuring timely up keep and preventive maintenance compliance of all equipments.Monitor and manage staff to meet deadlines and commitments. Prioritize, direct and oversee work activities and schedules and communicates with cross functional teams to ensure adherence to objectives and goals.Ensures adherence to cGMP's, standard operating procedures, safety practices Ensures the safety of all through compliance with all company policies, procedures, safety rules, and regulations.Participates in external and internal audits and inspections. Appraise the management on departments performance and self-evaluate on key responsibility area. Proactively responds to audit observations and takes appropriate corrective actions.Responsible for ensuring that training and development systems of control are in place to meet future objectives of the business.Ensure quality standards and processes are used throughout manufacturing. Work constantly with Quality Assurance on continuous improvements and provide preventative and correction actions when problems occur.Supervise, regulate and manage operations of raw and packing material stores.Assist, and review Root Cause of general problems arising on day-to-day basis.Handling Visitors and Auditors, in coordination with QA for those coming to Manufacturing area.Monitoring all activities related to stores - Raw Material and Packing Material.Review Audit Reports and its compliance.

Having experience in tablet and capsule manufacturing company (OSD). He must have over all knowledge of compression, granulation and coating area of production.Interested candidates can apply on 7226019227/ hr@jambuwalapharma.com

Oversee the manufacturing processEnsure production targets are metCoordinate production schedulesTroubleshoot issues that arise during manufacturingComplete production plans by scheduling and assigning personnelMonitor progress and revise schedulesReport results of the processing flow

Job Title: Production Shift In-charge Location: Nandesari, VadodaraPositions: 2 Education: B.Sc. / M.Sc. / Diploma in Chemical Engineering.Experience: 5-10 years of working experience in an API (Active Pharmaceutical Ingredient) and intermediate plant, with a strong understanding and practical application of GMP (Good Manufacturing Practices)Job Summary:We are seeking a highly motivated and experienced Production Shift In-charge to join our team for Pharmaceutical Company. The successful candidate will be responsible for overseeing and managing all production activities during their assigned shift, ensuring efficient operation, adherence to quality standards, and compliance with all safety and regulatory requirements. This role requires a strong leader with proven experience in pharmaceutical manufacturing, specifically in API and intermediate production.Key Responsibilities:Shift Management: Lead and supervise a team of production operators and technicians during the assigned shift. Plan and organize daily production activities to meet targets and schedules. Allocate tasks and responsibilities to team members effectively. Monitor production processes and troubleshoot any issues that arise. Ensure smooth shift transitions and effective communication with incoming/outgoing shifts.Production Operations: Oversee the manufacturing of APIs and intermediates, ensuring processes are followed according to batch production records and standard operating procedures (SOPs). Monitor raw material consumption, in-process parameters, and finished product quality. Optimize production efficiency and minimize waste. Coordinate with other departments such as Quality Control, Quality Assurance, Maintenance, and Stores to ensure seamless operations.Quality and Compliance (GMP): Ensure strict adherence to Good Manufacturing Practices (GMP) and other relevant regulatory guidelines. Oversee the accurate and timely completion of all production documentation, including batch records, logbooks, and deviation reports. Identify and report any deviations, non-conformances, or quality incidents, and participate in investigations. Implement corrective and preventive actions (CAPA) as required. Ensure equipment and facility are maintained in a state of readiness and compliance.Safety and Environment: Promote and enforce a strong safety culture within the production area. Ensure all team members follow safety procedures and use appropriate personal protective equipment (PPE). Report any safety hazards or incidents promptly. Ensure compliance with environmental regulations.Team Development: Provide training and guidance to production operators and technicians. Foster a positive and productive working environment. Conduct performance evaluations and provide feedback to team members.Reporting: Prepare daily, weekly, and monthly production reports. Communicate production status, challenges, and achievements to management.Skills and Qualifications: Proven leadership and supervisory skills in a manufacturing environment. In-depth knowledge of API and intermediate manufacturing processes. Strong understanding and practical application of GMP, GLP, and other relevant pharmaceutical regulations. Excellent problem-solving and decision-making abilities. Strong communication (verbal and written) and interpersonal skills. Ability to work effectively in a fast-paced, dynamic environment. Proficiency in using relevant computer software for data entry and reporting. Ability to work flexible shifts, including nights, weekends, and holidays, as required.

Supervision of Factory Operations:Oversee daily factory operations, including production, dispatch, and quality control.Ensure smooth workflow and timely completion of production schedules.Supervise factory staff and maintain a productive work environment.2. Documentation Handling:Manage and maintain all factory-related documents, including production reports, inventory logs, dispatch records, and quality control documents.Handle MIS reporting and ensure data accuracy.Ensure all documentation is in compliance with company policies and regulatory guidelines.3. Billing & Dispatch CoordinationSupervise billing procedures and ensure accurate and timely invoicing.Coordinate with logistics for the dispatch of finished products.Track and manage the movement of goods within the factory and to clients.4. Sales & PurchaseOversee and monitor raw material procurement and maintain inventory records.Coordinate with the sales team for product delivery and ensure all purchase orders are fulfilled on time.5. Team Management-Lead and train factory staff to ensure they are performing their tasks efficiently.Resolve staff issues and maintain discipline on the factory floor.Monitor performance and ensure adherence to safety and quality protocols.Desired SkillsStrong experience in supervising factory operations in the pharmaceutical or chemical industry.Excellent documentation and organizational skills.Knowledge of MIS and billing systems.Ability to manage and lead a team effectively.Strong attention to detail and problem-solving abilities.