759 Osd Jobs - Page 18

Overview We Have following Job Opportunities 1. OSD Officer / Executive (Tablets, Capsules) 4Nos (0 to 3 years Experience with B,Pharma) 2. Liquid Orals Officer / Executive (Tablets, Capsules) 2Nos (0 to 3 years Experience B,Pharma) 3. Granulation and Blending Operator / Technicians 02 ( 2 to 5 years Experience with 12th Pass / ITI/ Diploma) 4. Tablet Press Operator (Cadmech ) 04 ( 2 to 5 years Experience with 12th Pass / ITI/ Diploma) 5. Coating Operator / Technicians -01 ( 2 to 5 years Experience with 12th Pass / ITI/ Diploma) 6. Blister Machine (PVC & ALU-ALU) Operator / Technicians -04 ( 2 to 5 years Experience with 12th Pass / ITI/ Diploma) 7. Liquid Filling Machine Operator / Technicia...

Interview on 26 July, Saturday for BSC Chemistry Fresher for Production Department for Large Formulation Pharma Company in Ankleshwar Call / WhatsApp on 7600033423 for More Details Send CV on sdpbharuch@gmail.com with Subject: Production Ankleshwar Required Candidate profile Join My LinkedIN: https://www.linkedin.com/in/urvisdp INTERVIEW VENUE: SDP HR SOLUTION, 610, GOLDEN SQUARE, OPPOSITE HOTEL REGENTA, NEAR ABC CIRCLE, BHOLAV, BHARUCH We Provide Best Jobs in Gujarat

Interview on 26 July, Saturday for BSC Chemistry Fresher for Production Department for Large Formulation Pharma Company in Ankleshwar Call / WhatsApp on 7600033423 for More Details Send CV on sdpbharuch@gmail.com with Subject: Production Ankleshwar Required Candidate profile Join My LinkedIN: https://www.linkedin.com/in/urvisdp INTERVIEW VENUE: SDP HR SOLUTION, 610, GOLDEN SQUARE, OPPOSITE HOTEL REGENTA, NEAR ABC CIRCLE, BHOLAV, BHARUCH We Provide Best Jobs in Gujarat

Walk-in interview For Sun Pharmaceutical Industries Limited, Dadra Date: 20th July 25 (Sunday) We are recruiting for our OSD manufacturing facility located at Dadra Time: 10 AM to 4 PM Interview Venue: Sun Pharmaceutical Industries Ltd, Survey No. 694, Dadra - 396193, (U.T. of D & N. H.), India, Following are the requirements for our manufacturing facility at Dadra Location. 1) Designation: Officer / Sr. Officer / Executive Granulation & Packing Education: B. Pharm / M. Pharm Department: OSD Manufacturing & Packing Experience: 2- 6 years of experience in OSD manufacturing handling Granulation, Compression, Tablet Coating, Tablet Inspection, and Bottle Packing activities in an OSD manufacturi...

Dear All, We are conducting Walk-in Interview at Indore for our OSD manufacturing Facility based out of our Ahmedabad (SEZ-II), please find the below details. Date : 13th May 2025 (Sunday) Interview Location: Indore Timings: 9:00 am 5:00 pm Interview Venue: Enrise By Sayaji Rau, Survey No. 27/1 27/2, Village Pigdambar Rau Tehsil Mhow Ab Road Job Location: Ahmedabad Education Qualification: ITI/Diploma/BSC/ B.E/B.Tech/B.Pharma Departments are as follows : Production- OSD : Plant Operator/ Technical Assistant : ITI / Diploma having 3 - 8 years of experience in operating machines like Granulation (ACG, Glatt, Tapasya, GEA), Fitzpatrick Roll Compactor, Compression machines (Fette), Wurster Coate...

Position Title: Team Member Formulation & Development – Tech Transfer ( Officer / Executive ) - OSD Department: Formulation & Development - Tech Transfer Location: Vadodara Reports To: Manager – Formulation & Development – Tech Transfer Job Overview: The Team Member will support the successful transfer of products from development to manufacturing by ensuring process accuracy, documentation integrity, and adherence to quality standards. This role involves close collaboration with cross-functional teams, participation in validation processes, and troubleshooting to optimize manufacturing efficiency. Key Responsibilities: Process & Documentation: Prepare Technology Transfer Dossiers (TTD) and ...

Looking candidates for PDR (Formulation & Development ) Dept. 5-10 years of relevant experience in solid oral dosage (Regulated Market US & Europe) Roles and Responsibilities 1.Candidate should perform literature search 2.Pre formulation development Required Candidate profile 1.knowledge of documents – Master formula card, Bill of Material, stability protocol 2.Preparation of various documents like PDR, stability protocol, development report writing FDR/PDR

Roles and Responsibilities Operate granulation equipment such as roller compactor, fluid bed dryer, etc. to produce high-quality granules. Monitor and control process parameters to ensure product quality and consistency. Perform routine maintenance tasks on equipment to prevent breakdowns and optimize performance. Collaborate with other departments (e.g., formulation, packaging) to ensure smooth production operations. Ensure compliance with cGMP regulations and company policies. Desired Candidate Profile 2-7 years of experience in OSD (Oral Solid Dose) manufacturing or related field. B.Pharma degree from a recognized institution. Strong understanding of FBD (Formulation & Bulk Drugs), USFDA ...

Walk-in @ Indore We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned, If any of the requirement is matching your current job profile, kindly walk-in with your latest resume. *Job Location: Matoda, Ahmedabad, Gujarat. Engineering (Instrumentation / QMS / Process Equipment maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech with relevant functional experience in Calibration / Instrumentation / QMS activities QUALITY ASSURANCE QMS / Documentation / Validation and Qualification / IPQA (OSD) (Officer / Senior Officer / Execut...

SCCM L2 Job Title: Software Distribution Engineer Proposed Grade: Band B3 & B2 Primary Skill: Software Distribution & Patch Management, Windows, MECM, Intune Location: Bengaluru / Chenna Experince - 7- 10 years Rates including mark up - 130K/M - 140 K/M Experience: Proven experience in software distribution and patch management, particularly in Oracle JRE to Microsoft SDK migration. Strong knowledge of Windows operating systems and related technologies. Responsibilities: Perform software distribution and patch management tasks for Oracle JRE to Microsoft SDK migration. Ensure compatibility and functionality of distributed software on target systems. Collaborate with cross-functional teams to...

Role & responsibilities Prepare document as when required like SOP, BMR/BPR/Process validation Protocol/Report in Production Department Handling of QMSs (Change control, Deviation and CAPA) Maintain cGMP requirements. Execution of batches and maintain BMRs. Perform SAP related activities Execute trainings Regulatory audit exposure

Regulatory Affairs Executive ( for Cosmetic Industry ) Kheda, Gujarat 3–5 Years Experience CTC up to 6 LPA Strong knowledge of global cosmetic regulations (EU/USA/ASEAN/Gulf) Expertise in labeling, claims review, and documentation

Walk In Drive For Production OSD In Formulation Division @ Burgula Department:- Production OSD Qualification :-ITI | Diploma | BSC | B Pharmacy | M Sc | M Pharmacy Experience :- 2 To 10 Years Skills :- Supervisor :- Granulation | Compression | Coating | Cartornator| Packing Operators :- Granulation | Compression | Coating | Cartornator| Packing Division :- Formulation Interview Date:- 10-07-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- Venue Location:- MSNF Unit-VI Burgula X5R8+CXH, Mothighanapur, Burgul, Telangana 509202 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidate those...

Opportunity to work with one of the fastest growing Pharmaceuticals in India!! About us: Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and affordable medicines across the nation. With more than 4 decades of medical service to society, Unison is today one of the fastest-growing companies in Gujarat State. In addition to this, the company is ranked 82 among the top companies of India (Rupee wise sales) MAT March 2020. This makes Unison a distinguished company across the pharma industry. We are expanding our team!! Looking for passionate Formulation Scientists for DOM/EMB market at our dedicated R&D c...

Role & responsibilities We are seeking a diligent and experienced QA & QC & production. The successful candidate will Ensure that our products meet specified quality standards. This role involves managing both Quality Assurance ( QA ) and Quality Control (QC) processes, conducting inspections, and implementing improvements to maintain and enhance product quality. Expanding role in building a team of QA/QC executives. Salary Range: 15,000 to 25,000 (negotiable based on experience & skills) Experience: Minimum 2 years in QA/QC department of Tablet & Capsule or pharma manufacturing unit Preferred candidate profile Quality control analyst Responsible for testing and analyzing pharmaceutical prod...

Project Role : Business and Integration Architect Project Role Description : Designs the integration strategy endpoints and data flow to align technology with business strategy and goals. Understands the entire project life-cycle, including requirements analysis, coding, testing, deployment, and operations to ensure successful integration. Must have skills : Oil and Gas Upstream Good to have skills : NAMinimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Business and Integration Architect, you will design the integration strategy endpoints and data flow to align technology with business strategy and goals. You will understand the ...

Scicore Nutra Private Limited is a state-of-the-art facility, located in Sanand Gujarat, is dedicated to producing high-quality nutrition products that are safe, effective, and meet the highest standards of quality. Our team of experts is committed to ensuring that every product we manufacture is produced with the utmost care and attention to detail. At our manufacturing unit, we use only the best raw materials and employ advanced manufacturing processes to ensure that our products are of the highest quality. We also adhere to strict quality control measures to ensure that every product meets our rigorous standards. This starts with doing a rigorous vendor qualification as well as testing of...

Role & responsibilities :- Hands on experience for BMR, Process validation report, Stability Protocol, Sampling Plan, Knowledge about GDP initiation and closure of Change control, deviation in GMP. Having good knowledge of guidelines SUPAC, cGMP, Compliance, ICH Q1A,Q2,Q7, Q8,Q9, A10, Q13. Knowledge about GAP assessment between sending unit and receiving unit equipment / instrument / documents. Hands on experience with Advanced Microsoft Word, Power point and excel Effective communication and Co-ordination with CFT. Sound Scale up/down knowledge Calculation, forecasting, Risk assessment etc. Plan Lab scale experiments and perform. Preferred candidate profile :- Must Have Experience in Tech T...

Roles and Responsibilities ONLY FOR MALE CANDIDATES. Conduct quality control tests on OSD products to ensure compliance with regulatory requirements. Perform IPQA activities such as inspection, sampling, and testing of raw materials, intermediates, and finished goods. Ensure adherence to cGMP guidelines during formulation development and manufacturing processes.

Role & responsibilities Candidate should be handling plant maintenance & Process Maintenance with OSD machines(Granulation, compression, packing and so on.) Preferred candidate profile

Job Summary We are seeking an associate for the Quality Control team responsible for conducting investigations in case of any failure, incidents, market complaint, OOS & OOT. The role involves ensuring accuracy in investigation, technical report writing/documentation, adherence to safety procedures and reporting discrepancies. Roles & Responsibilities • You will be responsible for conducting investigations in case of any failure, incidents, market complaint, OOS & OOT. The role involves ensuring accuracy in investigation, technical report writing/documentation, adherence to safety procedures and reporting discrepancies. • You will ensure accuracy of the documentation before submitting it for...

Responsible for formulation and process development of oral immediate-release dosage forms, including oral film and tablet formulations. Troubleshoot and problem-solve unresolved or new formula issue

Studies, and process optimization as per regulatory guidelines (USFDA, EU, WHO). Prepare and review development reports, PDRs, BMRs, MFCs, and technology transfer documents. Collaborate with cross-functional teams (QA, QC, RA, Production).

" Job Title: Head Procurement - Raw Materials (DGM/ GM) Location: Mumbai Reporting to: Commercial Head About the client: PSS has been mandated to hire the Head of Procurement - Raw Materials for a well-established and highly reputed Indian pharma company manufacturing formulations OSD and Injectables. Key Responsibilities: Department: Procurement Raw Materials Location: Mumbai HO Reporting to: Commercial Head Job Responsibilities: Overseeing the sourcing and procurement of Raw Materials for the manufacturing plants. Identifying, evaluating, and developing new vendors by inviting quotations, negotiating, and pricing. Preparing comparison statements, obtaining the necessary approvals, and proc...

Job Description Experience: 7 to 13 years Qualification: B. Pharm / M. Pharm / M. Sc Budget: 12 to 16 LPA Designation: Sr. Executive Required Key Skills: Supply & Planning, Product Management, Should have worked on Kinaxis software, Should be well versed with system, Should have process knowledge of Tablet, Capsule & Injectables. Candidate from OSD/Inject unit is preferred. Should have good interpersonal and communication skills. Job Description: Should co-ordinate with PDL, R&D and quality for integrated plan for exhibit/ Pre-validation batches for next 3M , 12M. Should co-ordinate with Prod for planning execution and updating daily status. Should maintain R Vs C Vs A metrics with actuals a...