214 Api Production Jobs - Page 3

Key Responsibilities: Operate and monitor production equipment such as reactors, centrifuges, dryers, and filters for API manufacturing. Ensure adherence to cGMP, safety, and regulatory guidelines during production operations.

Preferred candidate profile Diploma In Chemical Engineering 2024/25 passed out candidates are preferred Recruiter Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy

Preferred candidate profile B.Tech In Chemical Engineering 2024/2025 passed out candidates are preferred Recruiter Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy

Preferred candidate profile Diploma in Chemical Engineering / B. Sc Chemistry with minimum 1 year of experience in API Production Recruiter Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy

Position: Executive TSD (Technology Support / Technology Transfer) Department: TSD Location: Ahmedabad Reports to: TSD Manager / Head of Department Experience: 510 Years Education: B.E / M.E Chemical / Chemical Engineering Key Responsibilities: Execute technology transfer from R&D to pilot and commercial production. Support process scale-up and optimization for cost, yield, and safety. Prepare and review tech transfer protocols, BMR/BPR, SOPs, and risk assessments . Troubleshoot and resolve issues during pilot and commercial batch production . Ensure compliance with cGMP, GLP, QbD, and regulatory guidelines . Liaise with R&D, QA, AR&D, Production, and Regulatory Affairs teams. Support audits...

Roles and Responsibilities * Manage production processes, ensuring compliance with GMP and batch planning. * Handle manpower effectively, including training and development of team members. * Oversee API manufacturing, reactors, centrifuges, BMRs, batch planning, hydrogenation, chlorination, distillation, centrifuges, GLRs, API production, pharma production, bulk drugs, and batch manufacturing. * Ensure solvent recovery and maintain a clean and safe working environment.

Maintaining Good housekeeping in workplace as per cGMP Equipment Operation and cleaning should be followed as per SOP Receipt and storage of raw material in day stock area for the batch as per Material Requisition slip Carry out the process as per manufacturing & packing record instruction All safety rules/precaution to be followed strictly in manufacturing area In process checks and documentation should be followed as per procedure Maintaining cGMP standards, ISO 9001, ISO 14001 & HACCP standards in the plan Make sure that the production facilities are clean and when appropriate disinfected Ensure that the premises and equipment are maintained and records kept in respective area Responsibil...

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...

Role & responsibilities 1.To prepare a monthly production plan based on customer orders and minimum stock level decided by the company. 2. To requisition raw and packing materials required for achieving the monthly production plan. 3. To ensure that production activity is undertaken after properly ensuring the equipment and surrounding area are clean. 4. To carry out production activity as per the standard batch procedure. 5. To monitor the manufacturing activity as per the standard batch procedure. 6. To transfer material which is approved by the quality assurance department to store department 7. To transfer raw and packing materials issued by stores. 8. To report any deviation in producti...

Responsibilities: * Prepare SOPs, adhere to GMP guidelines. * Collaborate with R&D on new product development. * Ensure API quality through batch planning & execution. Annual bonus Provident fund

Roles and Responsibilities * Develop and implement research and development and production processes for bulk drugs, APIs, and other pharmaceutical products.

Roles and Responsibilities To be handle all API pharma equipment w.r.t. manufacturing. Perform operation related activities. Ensure compliance with regulatory requirements. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Maintain accurate records, reports, and documentation. Desired Candidate Profile having experience in API pharma industries. Strong understanding of Good Manufacturing Practices (GMP) regulations. Experience with Cleaning Validation & Equipment Qualification procedures.

Interaction with R&D department for New Product development Study of New Product in R&D and plan batch in Pilot scale Planning and resource management for continuous Pilot Plant operation Knowledge of Hazardous material handling and MSDS

Responsibilities: Ensure compliance with regulatory standards Collaborate with R&D team on new product development Develop and optimize production processes for APIs Monitor quality control procedures Annual bonus Provident fund

Job Summary We are looking for an individual who is competent in the ONCO operations and has the ability to handle the critical operations without compromise on the safety & quality of the operations. Additionally, competency is expected in understanding the basic troubleshooting of equipment's & ensuring any time audit readiness of the production block. Roles & Responsibilities You will be responsible for ensuring safe work area practices in compliant with all the best safety practices. • You will be responsible for manufacturing of products for ONCOLOGY in accordance with the batch production records and standard operating procedures. • You will be responsible for execution and review of D...

Post - API Pharma Production Engineer Location - SUPA Ahmed Nagar Experience - 02-04 yrs Email - punemechanical@gmail.com Contact - 9356395439 Skills - API , Pharma Production , PPC Education - BSC / MSC Chemistry / Bio technology

Hiring Chemical Plant Operator for API Plant. Handling and Monitoring of production batches. Should be able to handle Glas lined Reactors, SS Reactors, Centrifuge, Drying, Scrubbing, Vacuum system, worker management,handling manpower Required Candidate profile Handling of manpower under his duty. Ensure safety and compliance Reporting of production data and co-ordinating as well as assisting QA. Should have 3 to 5 years of relevant experience

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

Manufacturer chemist Shift - 9 am to 6 pm Package - 25 k to 40 k(3 year experience) location- patiala Skills- tablet and capsules(alopathy and pharma) Wtsapp me resume at 8295842337- MR. Bansal

Alembic Limited is seeking enthusiastic and detail-oriented B.Sc. Chemistry freshers to join our team in the Production Department within our API manufacturing facility. The selected candidates will contribute to production operations, ensuring adherence to quality standards and operational efficiency. Key Responsibilities: Assist in executing daily production tasks in the API manufacturing unit. Monitor and document manufacturing processes to ensure consistency and compliance. Conduct chemical reactions and related activities as per standard operating procedures (SOPs). Follow quality assurance protocols and maintain strict adherence to safety guidelines. Troubleshoot production issues and ...

The ideal candidate should have at least 3 years of experience of working in Pharmaceutical Production floor where the person is responsible for shift operations. The incumbent would typically be responsible for: Ensuring the targets are met keeping in mind safety and quality guidelines. Management and upkeep of facility, materials and manpower. Troubleshooting in operations, validations and equipment qualification Coordination with other functions like QC, QA, Warehouse among others. Knowledge and Adherence to SOPs , regulatory requirement Preparing Batch Manufacturing Records, Protocols, Reports, Investigation Reports, and Qualification Reports. Work on Continuous improvement Plans (like C...

Responsibilities: Responsible for creating, maintaining, managing accurate & compliant production-related documentation. This role ensures that all documentation adheres to internal standards and external regulatory requirements.

Maintaining good housekeeping and cGMP in shop floor Preparation of New documents like BPCR and SOP Deviation , change control, OOS, activity and is compliance Plant keeps ready for audit Overall responsibility of cGMP Production should be achieved as per target. Equipment cleaning Log book and Solvent log Book to be maintained. BPCR arrangements for running batches. Review and completion of all documents like BPCR, Equipment logbook, and format as per SOP

1. Plan and execute production schedules, 2. Supervise granulation, blending, compression, and coating operations, 3. Strong knowledge of pharmaceutical manufacturing processes (API, DC granules, FDF), regulatory standards (GMP, WHO, USFDA)

Greetings! I am Priyanka. We are hiring QA Trainee / Officer Off roll for A leading API Manufacturing Company. Designation: 1. QA Officer/ trainee Off Roll Salary : Take way home [no benefits. no deduction] Location: Mysore Looking forward to hear from you. Note: No Charges Thanks & Regards Priyanka [ 9518220852 || priyanka@avaniconsulting.com ]