4097 Gmp Jobs - Page 50

Job Title: Sr. Executive/Executive Department: DQA Job Summary, Duties/Responsibilities: Ensure proper guidance on quality issues to the Product Development Teams Review the documents received from R&D, AR&D, etc. so that the same can be shared with authorities and customers . coordination communication and to respond customer complaint/query and regulatory authority. Review the process change proposals and help the team members provide guidance on change proposals Review the in-house expert reports/Quality overall summary (QOS) prepared by the team members Ensure proper stage gate compliance at various stages of product development Ensure that internal audits are conducted properly Review t...

Role & responsibilities : Partner with business leadership to understand the business requirement and try to fulfil or suggest improvement plan. Responsible for meeting production schedules with efficient and optimized use of resources and machine time. Managing multiple priorities in a fast paced manufacturing environment. Budget preparation and adherence with approved budget. Interfaces with supply chain to develop mid-and long range master production schedules. Plan, organize, and control the production process to ensure the efficient and timely manufacturing of products. Monitor production schedules and adjust as necessary to meet demand and maintain inventory levels. Ensure adherence to...

Responsible for maintaining compliance and to ensure GLP in lab Responsible for preparation of AMV protocols and reports Responsible to provide request to section head for issuance of AWR and to record analysis related activities Responsible for execution of Analytical Method Validation/Verification activities in lab Responsible to carry out AMV activities as per planning Responsible to participate in investigation generated during AMV activities Responsible to participate in investigation of OOS/OOT to find out the root cause like verification of force degradation data. Responsible for preparation calibration and preventive maintenance planner. Responsible for daily temperature monitoring o...

Role & responsibilities : Review of all QMS documents related to regulatory submissions Prepare status of all documents related to submission Co-ordinate with all stakeholders of plant for collection of documents Provide all regulatory documents to HO-RA for submission. Evaluation of change control, deviations and out of specifications. Review of specifications, BMRs, BPRs, COA, Method transfer report, Method verification/validation report, Analytical chromatograms, Sterility assurance data package. General Review of plant equipment qualifications, filter validation documents and layouts for its adequacy to support regulatory submission. To facilitate LoA, Debarment certificate, GMP certific...

Strong skills in Core Java, J2EE, , JavaScript, JSP, and DHTML/Web Page development. Experience in Labvantage LIMS development Strong relational database knowledge and experience using either Oracle and/or SQL Server.

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.

Position: IA Computer System Validation (CSV) Engineer (CE25SF RM 3581) Job Summary: The Computer System Validation (CSV) Engineer is responsible for ensuring that computerized systems used in regulated environments (e.g., GMP, GCP, GLP) are validated in compliance with applicable regulatory requirements such as 21 CFR Part 11, Annex 11, GAMP 5. This role involves planning, authoring, reviewing, and executing validation deliverables, and supporting cross-functional teams. Key Responsibilities: Develop and execute validation strategies and plans for new and existing computerized systems. Create and maintain validation documents including: User Requirements Specifications (URS) Functional Spec...

Job Title: Engineering & Projects - Electrical Business Unit: Sun Global Operations Job Grade (G10 - Manager 1) Location : New green field site (Pithampur - Indore) Overall In charge of HT, LT, LV Electrical systems installation at site. Handling of DG sets, Chillers, UPS, Rotary UPS system. Based on received drawings, assign work and timelines and ensures the implementation of the same. Ensure collection of data; analyze to achieve relevant construction quality and safety. Help overcome constraints, work out alternatives to the design in case of difficulties Retention of records in respective area. Preparation & completeness of documentation for qualification of electrical system. Prepare s...

Job Title: Executive/Sr Executive Process Engineering OSD Business Unit: Sun Global Operations Job Grade G12A/G11B Location : Guwahati At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine As you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other s journeys. Key responsibilities: Diagnose malfunction...

Accountabilities Scope of work Reduce Filler downtime 5% in comparison to last year. To ensure all responsibility for maintenance activities of all line & utility equipment’s, in the plant. All responsibility for availability, issue of spares, raw & packaging material specifications. To Ensure completion of all types of maintenance activities in timely. Timely maintenance of equipment’s- 90%. To ensure effective implementation of Food Safety Management System. No LTA To ensure all monitoring, maintaining and improvement of the plant QM rating results, All responsibility for implementation of GMP, HK & pest-control activities in plant, To upgrade and any change in the verification of PRP's, O...

Roles and Responsibilities Conduct IPQA activities during production runs to ensure compliance with GMP guidelines. Monitor line clearance processes to prevent defects and deviations. Perform BMR reviews, BPR reviews, and BPRF review to maintain quality standards. Ensure raw material procurement meets regulatory requirements through documentation checks. Collaborate with cross-functional teams to resolve issues related to packaging materials.

Your Responsibilities: Reporting to the Senior Quality Manager - Global Supply Chain Programme Manager, the primary scope of the role: Ensure records of suppliers and contractors are fully compliant with regulatory and Reckitt guidelines to minimize risk to consumers, the company, and the brand. Generate supplier evaluation packs to support supplier approval and ongoing supplier maintenance. Ensure quality technical agreements (QTAs) and all other supplier compliance documents are in place and within the required date. Manage supplier documentation, including QTAs and templates. Support the maintenance of the Raw and Packaging material supplier risk matrix and updates to the approved vendor ...

Your Responsibilities: Reporting to the Senior Quality Manager - Global Supply Chain Programme Manager, the primary scope of the role: Ensure records of suppliers and contractors are fully compliant with regulatory and Reckitt guidelines to minimize risk to consumers, the company, and the brand. Generate supplier evaluation packs to support supplier approval and ongoing supplier maintenance. Ensure quality technical agreements (QTAs) and all other supplier compliance documents are in place and within the required date. Manage supplier documentation, including QTAs and templates. Support the maintenance of the Raw and Packaging material supplier risk matrix and updates to the approved vendor ...

As a Head Quality Assurance (QA) at Instrumentation & Control Solutions in Indore, your role will involve leading and managing Quality Assurance activities in the pharmaceutical unit. Your primary focus will be to ensure compliance with cGMP, regulatory standards such as WHO-GMP, USFDA, EU, and internal QMS protocols. Key Responsibilities: - Lead QA operations, including documentation, audits, and compliance. - Handle deviations, CAPA, OOS investigations, and regulatory audits effectively. - Oversee the development and maintenance of SOPs, validations, and training programs. - Ensure the robust implementation of Quality Management Systems to maintain high-quality standards. Qualifications Re...

Job Description: As a Quality & Assurance Executive at the snacks and confectionery manufacturing company, you will play a crucial role in ensuring the production processes meet the required quality standards. Your responsibilities will include: - Monitoring production processes to uphold quality standards - Conducting in-process checks and maintaining records in compliance with export and regulatory standards - Collaborating with the production team to address quality issues and implement corrective measures - Ensuring strict adherence to hygiene, GMP (Good Manufacturing Practices), and food safety protocols - Assisting in managing traceability and recall procedures Qualifications Required:...

Role Overview: You will be responsible for evaluating and executing new products and site transfer products, focusing on process safety, environment, plant availability, and infrastructure mapping. Additionally, you will support commercial products by identifying opportunities for capacity improvement, cost reduction, troubleshooting process-related issues, and ensuring safety data compliance. Your role will involve coordinating with various teams and preparing equipment equivalency for any required changes. Key Responsibilities: - Evaluate and execute new products and site transfer products - Analyze process with focus on process safety and environment - Map process in available plant and e...

As an Analytical Development Scientist at our company, your role involves conducting departmental operations efficiently, maintaining laboratory areas to meet quality and safety requirements, providing training and support to production and QC groups, engaging in compliance projects, and identifying opportunities for cost reduction and waste minimization. You will also be responsible for ensuring timely completion of project deliverables, leading aspects of projects, planning and carrying out work in line with customer requirements, and providing project support for method development and validation activities. Key Responsibilities: - Perform assigned work as agreed with the project lead and...

As a candidate for the position at Surmount Laboratories Pvt. Ltd., you will be responsible for managing day-to-day production activities in the field of Pharmaceutical formulation. Your key responsibilities will include: - Demonstrating a minimum of 3 to 4 years of experience in Pharmaceutical formulation - Possessing knowledge of Good Manufacturing Practices (GMP) - Managing day-to-day production operations - Providing regular reporting with online documents to meet regulatory requirements Qualifications required for this role include: - B.Pharm / M.Sc. / B.Sc. degree - Minimum of 3 to 4 years of experience in the field of Pharmaceutical formulation - Knowledge of Good Manufacturing Practi...

As a Raw Honey Quality Inspector, your role involves inspecting and testing incoming raw honey to ensure high quality standards are met. You will be responsible for conducting various tests including: - Checking moisture content (which should be below 20%) - Monitoring HMF (Hydroxymethylfurfural) levels - Analyzing sugar profile for fructose/glucose ratio - Assessing color and aroma - Verifying pollen content for origin identification - Detecting presence of contaminants or residues such as antibiotics or pesticides In addition to the quality inspection, your key responsibilities will include: - Performing regular lab tests like moisture test using refractometer, HMF test, and diastase activ...

You will be responsible for supervising and managing day-to-day production activities during the shift. Your key responsibilities will include: - Ensuring adherence to cGMP, safety, and quality standards in all production processes. - Managing manpower and allocating tasks effectively to meet production targets. - Monitoring batch processing, documentation, and timely reporting. - Coordinating with Quality Assurance, Quality Control, and Maintenance teams for smooth operations. - Handling equipment operations, troubleshooting, and ensuring preventive maintenance schedules are followed. - Maintaining production records as per regulatory requirements and internal SOPs. - Ensuring compliance wi...

As an Analytical Scientist C at BacAlt, you will play a crucial role in the Research and Development Department. Your primary responsibility will be to develop and validate analytical methods for various instruments such as HPLC, GC, GC-MS, IR, UV-Visible Spectroscopy, Particle Size Analyser, and more. Additionally, you will be responsible for conducting wet analysis in the lab, planning stability studies, and performing testing according to established protocols for formulations, APIs, and excipients. Key Responsibilities: - Develop and validate analytical methods for various instruments including HPLC, GC, GC-MS, IR, UV-Visible Spectroscopy, and more. - Conduct wet analysis in the lab and ...

Roles and Responsibility Provide exceptional customer service to airline passengers, ensuring their comfort and safety. Manage passenger complaints and concerns professionally and courteously. Coordinate with airlines, airports, and other stakeholders to ensure smooth operations. Develop and implement effective strategies to enhance passenger satisfaction. Collaborate with teams to achieve operational goals and objectives. Maintain accurate records and reports of passenger interactions and transactions. Job Requirements Minimum 5 years of experience in a related field, preferably in the aviation industry. Strong communication and interpersonal skills are essential. Ability to work well under...

We are looking for QC Chemist to join our QC. The role involves analysis of raw materials, in-process samples, and finished products in compliance with regulatory standards.Freshers candidates can apply.

Hi, Greetings from Avani Consulting!! We have job opportunities with API Manufacturing Company for the Sr. Executive/Executive- Electrical position, Mysore Location. Position- Sr. Executive/Executive- Electrical & Instrumentation Work Experience +8 in API / Pharmaceutical / Chemical / FMCG / Continuous Process Industry Location Mysore Qualification- B.E. / B.Tech / Diploma in Electrical Engineering. Knowledge of SAP. Must Have Electrical Supervisor License Must have experience in 66KV Job Summary: To lead and manage all electrical maintenance activities and ensure optimal performance, reliability, and safety of electrical systems in an API manufacturing facility. The role also includes effic...

We are looking for a skilled Process Validation Engineer to join our team in Pune. The ideal candidate will have 3-10 years of experience in process validation and quality systems, with a strong background in regulatory compliance and hands-on experience in manufacturing activities. Roles and Responsibility Perform gap assessments and conduct remediation of documents with stakeholder inputs. Develop and maintain Manufacturing/Service Work Instructions and related documents. Create/modify process flows within the Manufacturing/Service Departments. Support the development and introduction of new products, processes, and technologies, focusing on quality systems. Monitor and drive corrective ac...