963 Osd Jobs - Page 2

Role & responsibilities Preferred candidate profile -Hands on Experience in SCCM infra, Installation of SCCM, Upgrade of SCCM- Develop, standardize, and implement Microsoft SCCM solutions- Designing and Deploying medium to large scale SCCM environments (Single to multi-tier sites) - handle test and release of applications and Patches using SCCM - knowledge of SCCM Client management Suit all Levels.- able to resolve the tasks escalated by l2 teams.- able to create custom scripts for gathering the inventory from clients- Excellent working knowledge of the following within SCCM 2016 - Create\import applications and packages within SCCM - Create application task sequences - Troubleshoot applicat...

Job Description Role**SCCM and Intune Required Technical Skill Set**SCCM, Intune Desired Experience Range**7-12 Years Location of Requirement :Hyderabad Desired Competencies (Technical/Behavioral Competency) Must-Have** Designing, Planning, and Implementing System Center Configuration Manager, such as: - Planning System Center Configuration Manager hierarchy and site system roles. - Creating and managing Boundary Groups across one or more Distribution Points. - Management of site communications. (Bandwidth, Senders, Secondary Sites, etc.) - Planning and securing SCCM using security certificates. - General monitoring of site health via SSRS, log files, and the SCCM console. - Planning, config...

**Job Description:** As a Technical and Development professional, your role will involve working on the layout development and general process requirements of pharmaceutical and Life Science production facilities. This includes a deep understanding of the requirements for API, Sterile Products, OSD, Bio-Pharma, Gene Therapy products, and related R&D labs. You should be prepared to learn new types of facilities as per client specifications. **Key Responsibilities:** - Possessing a Degree in Architecture from an institute recognized by the Council of Architecture. - Demonstrating in-depth knowledge in layout development and process requirements of pharmaceutical production facilities. - Being ...

Roles and Responsibilities Ensure smooth operation of production activities, including formulation, and OSD (Oral Solid Dose) manufacturing processes. Monitor and control process parameters to ensure compliance with quality standards. Conduct regular inspections to identify areas for improvement and implement corrective actions. Collaborate with cross-functional teams to resolve issues related to production planning, scheduling, and inventory management. Maintain accurate records of production data, batch records, and equipment maintenance schedules.

Opening for Pharma Lifescience. Role & responsibilities : Candidate is having knowledge of OSD Formulation Plant. Depth knowledge of In Process Quality Assurance . Third Party Manufacturing Knowledge. Candidate is Ready for Within City Travelling for who are Manufacturing our Medicine. Qualification:-M-Pharma-QA or B-Pharma. Interested candidates shared resume on snehal@topgearconsultants.com

Role & responsibilities Responsible for overall Quality control function of General block and Hormone block. To ensure the monitoring of RM, PM, In-process (Compression, Blend, Coating, and Filled Capsule), Bulk product, Finished Product, Stability, Micro and Process Validation samples analysis plan for their timely sampling, analysis and release. To ensure proper destruction of the left over sample. To ensure cGLP/ cGMP/ 21 CFR part 11 compliance in the laboratory. Co-ordination with R&D/outside labs from where product is transferred at site. Co-ordination with the customers for easy transfer of the projects. To approve the job description and assign the job to all QC team. To ensure that a...

Should have current experience in OSD / Formulation (Non Sterile) Experience - 5 - 10 Years Education - B.Pharm/ M.Pharm/ M.Sc Role & responsibilities 1. Handling of market complaints. 2. To acknowledge the complaints to the reporter 3. conducting complaint Investigations 4. Co-ordinate with functional investigators (Cross Functional Team/Subject Matter Experts) for timely completion of complaint investigations. 5. Follow up for complaints closure letter from the Reporter and close the complaint in complaints closure form. 6. Involve in root cause analysis, Failure Investigations and Risk assessment activities. 7. Initiate, review of Corrective action & preventive action and To prepare trend...

"• Operation, & Maintenance, of all packaging equipment & Parenteral of following block: Main Pharma Block. Cephalosporin Block, Rifampicin Block • Operation & Maintenance of associated systems • To develop Total Quality Maintenance system on all manufacturing equipment • To develop workable history card system. • To create a PPM team to ensure thorough overhauling. • To ensure Preventive maintenance of all manufacturing equipment. • To co-ordinate with various contractors & consultants in matters related to Engineering works. • Follow up for periodical Scheduled maintenance of all utility equipment. • Placement of PPM schedule near the concerned equipment. • To develop a workable History ca...

"• To ensure smooth and efficient functioning of plant machineries at main Pharma block. • To attend routine breakdown maintenance of production machinery of main pharma block. • To attend the modification and development work in machinery as per guidance of engineer. • To ensure proper shift handover charge to next shift technician. • To ensure area readiness for audit point of view."

Candidate from Ahmedabad Only Assist in the production for tablets, capsules, & liquids, ensuring compliance with cGMP guidelines, SOPs, and regulatory requirements. Batch Manufacturing In-Process Quality Control Documentation and Record-Keeping

Job Description: (Walk-in Drive Production Department): Coating Operator Production (OSD Formulations) We are hiring Coating Operators for tablet production. Responsible for operating tablet coating machines , monitoring process parameters, ensuring uniform coating , following GMP & SOPs , and maintaining equipment cleanliness. Experience in OSD formulations is preferred.

Role & responsibilities Formulation development (solid, semisolid, liquid oral) Tech transfer & scale-up Troubleshooting & problem-solving QbD, DoE, FMEA Strong documentation skills Knowledge of regulatory requirements Project management & cross-functional coordination

Roles and Responsibilities Conduct analytical testing of finished products, including dissolution, UV-Vis, KF, FTIR, and GLP compliance. Develop and validate analytical methods for solid oral OSD products using techniques such as GC, HPLC, and UV spectroscopy. Perform method transfer and validation activities to ensure accuracy and reliability of test results. Collaborate with cross-functional teams to resolve OOS/OOT issues and implement corrective actions. Maintain accurate records of laboratory data, reports, and documentation in accordance with cGMP guidelines.

Job Responsibilities: 1. To ensure continuous improvement in achievement of productivity, manufacturing yields & quality norms; Launch of new products 100% in time. 2. Quality: Demonstrate compliance to established Manufacturing Operations and Quality Standards. To ensure that products are produced and stored according to the appropriate documentation in order to obtain the required quality. 3. Strive for reduction in Out of Specification, Deviations, reduce Market complaints. 4. Document Integrity: To support compliance of practices to established procedures and Good Manufacturing Practice standards. 5. To approve the SOPs & format, batch records relating to production operations and to ens...

Hiring experienced IPQA professionals (48 years) for OSD formulation unit. Job Responsibilities: Line clearance, in-process checks, documentation (BPRs / Logbooks), Empower-3, Analytical Data Review, and QMS activities. Perform in-process checks during granulation, blending, compression, encapsulation & coating. Monitor IPC parameters: LOD, bulk density, blend uniformity, we Provide line clearance for manufacturing & packing operations Review BMR/BPR and ensure real-time documentation as per GMP/GDP . Verify equipment cleaning and ensure absence of cross-contamination . Conduct online sampling and coordinate with QC for testing. Support process validation & cleaning validation for OSD equipm...

Responsibilities: * Collaborate with R&D team on formulations & solid oral products. * Operate compression, granulation, coating machines & raw material handling equipment. * Ensure OSD compliance during blending process. Office cab/shuttle Food allowance Health insurance Annual bonus Provident fund

Role Overview: As a member of the Batch File Review Team at PCI, you will be responsible for compiling and reviewing batch documents related to various process types such as OSD, Sterile, Biologics, Cell Therapy, and Gene Therapy. Your role will involve close collaboration with internal and external stakeholders to ensure documentation accuracy and compliance with regulatory standards. This position offers a diverse range of responsibilities and serves as an ideal foundation for individuals aspiring to pursue a career as a Quality Person (QP). Key Responsibilities: - Compile and review batch documents to ensure accuracy and completeness before QP review. - Collaborate with site personnel to ...

cross-functionalRole & responsibilities Should have in-depth knowledge of US Hatch-Waxman law & practice; should be knowledgeable in US patent litigation aspects and applicable case laws, Expected to have required knowledge of patent opposition and litigation procedure in ex-US countries e.g. Europe, Australia etc. Should be aware of IP system and litigation process in countries such as South Africa, Latin America & GCC. Expected to have in-depth knowledge about data and market exclusivities, patent term extensions, supplementary protection certificates in various countries, Project selection acumen: IP diligence to assist the US and Ex-US portfolio/business team in project selection process...

Job Description Relevant Experience : 1 To perform Operation activity of equipment and instruments as per SOP. 2. To affix the status label to equipments, instruments and IPC at each and every processing stage 3. To operate the equipment in safe and effective manner for production processing. 4. To follow and adhere to GDP and cGMP practices. 5.Inspect equipment to identify any replacement, and repairs. 6. Ensure that the equipment is maintained in good and safe working condition. 7. To Perform regular equipment maintenance to ensure production capacity and quality. 8. Identify and report unsafe operations and near misses to supervisor immediately. 9. Perform the activity as per SOP and inst...

Job Description Relevant Experience : Should have experience of Production for Formulation Plant of Oral Solids (Tablets, granules, powder) & Allied in PHARMACEUTICAL COMPANY / FACTORY. FDA Approval in Tablet Section Pharma Formulation plant would be preferred. 1. Batch Manufacturing Manufacture production batches as per Batch Manufacturing Record (BMR) and Batch Production Record (BPR). 2. BMR/BPR Documentation Complete the online BMR and BPR as per the respective activities. 3. Coordination with QA Coordinate with the Quality Assurance (QA) department for the issuance of monthly formats. 4. Manufacturing Parameters Review Review parameters during manufacturing stages such as compression, f...

Walk In Drive For Production OSD In Formulation Division @ Jadcherla Department:- Production OSD Qualification :-BA | Diploma |B Com | BSC | B Pharmacy Experience :- 2 To 8 Years Division :- Formulation Interview Date:- 07-12-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- MSNF-II, Kothur | MSNF-VI, Burgul| MSNF-IV, Mekaguda Venue Location:- ELITE HOTELS & RESORTSNH44,Bangalore Hyderabad Hwy Jadcherla, Telangana 509301 Contact No:- 040-304338701 | 8954 Skills :- Operator: Compression | Coating | Granulation | Capsule Filling Manufacturing: Supervisor | Shift IN charge Packing operators: Cartonator | Auto Cartonator | Packing Supervisor | Blister Packing | Bottle Packing | Primary & S...

Walk In Drive Quality Assurance Department In Formulation Division @ Elite Hotel ( MANJEERA HOTELS AND RESORTS) Department :- Quality Assurance OSD Qualification :- B Pharmacy | M Pharmacy | MSC Chemistry Experience :- 2 to 8 Years Division :- Formulation Interview Date:- 07-12-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location:- Elite Hotel ( MANJEERA HOTELS AND RESORTS) NH 44, Hyderabad - Bangalore Highway, Jadcherla, Macharam, Telangana 509301 Contact No:- 040-30438701 | 070970 92829 | Note:- Candidate should bring Update Resume ,Increment Letter,Payslips, Bank Statement, Certificates,Aadhar Card & Pan Card We are looking for candidates those who have expe...

Walk In Drive Quality Assurance Sterile Department In Formulation Division @ Elite Hotel ( MANJEERA HOTELS AND RESORTS) Department :- Quality Assurance Sterile Qualification :- B Pharmacy | M Pharmacy | MSC Chemistry Experience :- 2 to 8 Years Division :- Formulation Interview Date:- 07-12-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location:- Elite Hotel ( MANJEERA HOTELS AND RESORTS) NH 44, Hyderabad - Bangalore Highway, Jadcherla, Macharam, Telangana 509301 Contact No:- 040-30438701 | 070970 92829 | Note:- Candidate should bring Update Resume ,Increment Letter,Payslips, Bank Statement, Certificates,Aadhar Card & Pan Card We are looking for candidates those w...

About The Role Project Role : Application Tech Support Practitioner Project Role Description : Act as the ongoing interface between the client and the system or application. Dedicated to quality, using exceptional communication skills to keep our world class systems running. Can accurately define a client issue and can interpret and design a resolution based on deep product knowledge. Must have skills : Microsoft Intune Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Tech Support Practitioner, you will act as the ongoing interface between the client and the system or application. Dedicate...

Hiring: Engineering Packing Maintenance (OSD Manufacturing Unit) Experience: 2 to 7 Years Location: Jadcherla / (Add your unit/location) Industry: Pharmaceutical OSD Manufacturing Job Description: We are looking for skilled Engineering – Packing Maintenance professionals with hands-on experience in OSD manufacturing . The ideal candidate should have strong technical knowledge of packing machinery and an ability to ensure smooth, efficient, and compliant operations. Key Responsibilities: Perform preventive and breakdown maintenance of OSD packing machinery Handle equipment like blister packing, bottle filling, carbonators, labeling, and serialization systems Troubleshoot mechanical/electrical...