963 Osd Jobs - Page 12

About The Role Project Role : Application Developer Project Role Description : Design, build and configure applications to meet business process and application requirements. Must have skills : SAP Document and Reporting Compliance Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Developer, you will be responsible for designing, building, and configuring applications to meet business process and application requirements. You will collaborate with teams to ensure successful project delivery and implementation. Roles & Responsibilities:- Expected to be an SME- Collaborate and manage the team...

About The Role Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : SAP Document and Reporting Compliance Good to have skills : NA Minimum 7.5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your day will involve overseeing the application development process and ensuring seamless communication within the team and stakeholders. Roles & Responsibilities:- Expected to be an SME- Collabo...

Walk-in at Matoda 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 requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Engineering - (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech QUALITY ASSURANCE IPQA (injectable) / IPQA (OSD) / Documentation (Officer / Senior Officer / Executive/Senior Executive) Experience - 02 to 09 Years Qualification - B. Pharmacy/ M Pharmacy / M.Sc. / B.Sc. MICROBIOLOGY (Officer / ...

Job Overview: The Product Development Leader (PDL) for Oral Solid Dosage (OSD) will play a pivotal role in leading the development of oral solid dosage forms such as tablets and capsules from early formulation stages through to commercialization. This position requires strong leadership skills in overseeing product development strategies, managing cross-functional teams, ensuring timely project execution, and maintaining compliance with regulatory standards. The PDL will work closely with formulation development, analytical services, regulatory affairs, and manufacturing departments to deliver high-quality pharmaceutical products. Roles & Responsibilities: Formulation Development and Optimiz...

Roles and Responsibilities Manage warehouse operations, including inventory management, storage, and dispatch. Coordinate with production team to ensure timely delivery of raw materials (RM) and packaging materials. Ensure accurate recording of stock levels, orders, and deliveries using ERP systems. Desired Candidate Profile Experience: 2-5 years Qualification: B.A/ B.Sc./ B. Com Must have experience in OSD Formulation Warehouse operations Should be willing to work in shift operations Interested candidates can share their updated CV to jahnavi.kodali@granulesindia.com

Review of daily coordination activities related to Quality Compliance for products recalls and change control. Investigation of Market Complaints. Interaction with R&D for technology transfer and Analytical Method Development. Release and Rejection of Raw Materials, Packaging Material, Intermediates and Finished Goods. Identification of the training needs of all the individuals and referring if to personnel Department. Validation of Analytical Method, Process and Cleaning Preparation of Protocol & Specification for Finished Product, Raw Materials Packing Material & Stability samples. Maintenance of quality control instruments Ensure systems are in place including appropriate documentation an...

Role & responsibilities Complete Analysis of various raw materials, In-process, Drug substance and finished Products in line with Pharmacopeia method and in-house Specification and test procedures. Change Control, Deviation, Root Cause investigation, CAPA, OOS, OOT, Incidence Calibration of Instruments HPLC , UV-Visible Spectrophotometer, pH Meter,KF Titrator, weight balance. Working standard preparation as per SOP. Ensure the timely analysis of samples GLP, GMP, GDocP (With respect to Regulatory Guidelines) Function in details of various Section of QC/QA(Eg.Raw Material, Finished Product,Stability Study etc. Data Integrity 21 CFR Part 11 Qualification, Calibration, Validation. Maintaining t...

Role & responsibilities Handling of compression machine and inprocess checks like as Friability test, Hardness test, Thickness test, Disintegration test, weight variation test, and appearance of tablets. To Monitor and control yield of batches. Completion of batch BMR. Checking and Filling of Equipment Logbooks , Environment Logbooks , Balance Calibration Logbooks, Daily Verification Logbooks To distribute available manpower in different section of department. Handling Sop's. Labelling of all products correctly and ensure proper labelling system. Co-ordination with QA, QC, Engineering and R&D department of works. Maintaining correct process parameters & ensure the process operations correctl...

Role & responsibilities Responsible for Leading Manufacturing OSD, QMS & COMPLIENCE. Change over time reduction of Manufacturing and Packing lines. Improvement of yield at compression and Packing stage Leading production activity Execution of Monthly Manufacturing plan for OSD. Efficiency improvement project in manufacturing for reduction of shift with 100% targeted delivery. Capacity, efficiency, improvement, cost saving initiative and compliance initiative. Coordinate with production manufacturing dept. & other related depts. Concerning operation/ planning /packing activity To execute planned production/ packing in stipulated time limit. Ensuring on-time delivery of products as per specifi...

As discussed, please find herewith the brief Job Description for the vacant position: Position: Group Leader FD Reg. Mkt. (Asst. General Manager) Education: Ph.D./ M. Pharm. in Pharmaceutics/Pharmaceutical Technology. Experience: 15+ years of experience in formulation development, with proven leadership track record. Expectations: Expertise in OSD - Immediate Release (IR), Extended Release (ER), Powder for Suspension (PFOS) and Oral Liquid dosage forms (Solutions and Suspensions) for US, EU and Canada. Lead and manage a team of formulation scientists for Product Development, Technology Transfer and Trouble Shooting Self-Motivated and ability to drive things The role involves providing techni...

Roles & Responsibilities 1. Responsible for monitoring of basic norms of cGMP, ALCOA+ Principle, data integrity, GDP & to maintain his personal health hygiene. 2. To review and approve the analytical reports for raw materials, packing material, In-process, Finished product and release or reject raw materials, packing materials, In-process and finished product in the Supply Chain Management system. 3. To review and approve/reject the Certificate of Analysis of RM, PM & finished product. 4. To perform audit trial review for QC & Microbiology instrument CDS and non CDS. 5. To handle different types of activity in SCM, New LIMS, HRMS, Mysetu, Newtronics ICDS 3.1, DMS, EDMS, LMS, Empower , AMS So...

Preferred candidate profile Expert in independently handling HPLC along-with experience in handling other instruments Interested candidates can share their CV/Resumes on - noor.m.judge@zyduslife.com

About The Role Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : Dassault Systemes ENOVIA V5 Good to have skills : NA Minimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your typical day will involve collaborating with various stakeholders to gather requirements, overseeing the development process, and ensuring that the applications meet the specified needs. You will also be ...

Role & responsibilities Prepare, review and submit regulatory documents for new drug applications, product registrations, amendments and renewals to the US, Brazil, EU, India and State Level authorities. Regulatory Submissions : Prepare and submit regulatory documents, including INDs (Investigational New Drug Applications) and NDAs (New Drug Applications) to regulatory authorities. Compliance and Licensing: Ensure compliance with regulatory requirements of US, Brazil, EU & India. Liaise with regulatory authorities for drug licensing, including product registrations, renewals and manufacturing licenses for local and international markets. Ensure timely submission of import licenses and NOcs (...

Hiring Alert Join a Leading MNC Pharma Company! Division: OSD (Oral Solid Dosage) Department: Engineering Designation: Sr. Manager / AGM Experience: 18 to 22 Years Qualification: B.Tech Mechanical / Electrical Work Location: Hyderabad / Jadcherla Key Responsibilities: Lead the Engineering Department at the second level, ensuring smooth operations across functions. Strong exposure to Electrical Engineering and related systems Oversee process engineering, utilities, and mechanical maintenance for OSD operations. Handle regulatory and statutory requirements related to licensing and compliance. Drive operational excellence, energy efficiency, and equipment reliability. Ideal Candidate: Proven le...

Hiring Alert Join a Leading MNC Pharma Company! Position: Sr. Manager Division: OSD (Oral Solid Dosage) Department: General Engineering Location: Hyderabad Experience: 16 to 20 Years Qualification: B.Tech Key Responsibilities & Skills: Strong expertise in pharmaceutical engineering systems, particularly for OSD plants Thorough knowledge of cGMP, GEP (Good Engineering Practices), and regulatory compliance Skilled in troubleshooting and problem-solving Preventive Maintenance Vendor and contractor management Excellent communication and documentation skills Contact for Application: Pragati: 7032376834 Mansi: 7032376838

About The Role Project Role : Tech Delivery Subject Matter Expert Project Role Description : Drive innovative practices into delivery, bring depth of expertise to a delivery engagement. Sought out as experts, enhance Accentures marketplace reputation. Bring emerging ideas to life by shaping Accenture and client strategy. Use deep technical expertise, business acumen and fluid communication skills, work directly with a client in a trusted advisor relationship to gather requirements to analyze, design and/or implement technology best practice business changes. Must have skills : SAP Document and Reporting Compliance Good to have skills : NA Minimum 12 year(s) of experience is required Educatio...

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 6 Years Skills :- Operators :- Blister Packing | Primary Packing | Secondary Packing | Autocartonator Operators :- Granulation | Compression | Coating Division :- Formulation Interview Date:- 11-10-2025 Interview Time :- 9.00AM TO 4.00PM 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 who have exp...

OPEN POSITIONS Production Technical Assistant • Granulation, Compression, Coating, Capsule Filling • Liquid & Nasal Spray manufacturing Packing Technical Assistant • Bulk / Bottle packing, Labelling machine operation Quality Assurance Executive • QMS, IPQA, Market complaints, Training coordination Quality Control Executive • Nasal spray product analysis using LC-MS, HPLC, GC, UV, GC-MS, etc. EXPERIENCE RANGE 2 8 years (pharma formulation plants only) EDUCATIONAL QUALIFICATION • Production / Packing : ITI / Diploma / B.Sc. • Quality Control : M.Sc. (Chemistry) / B. Pharm • Quality Assurance : B. Pharm / M. Pharm WORK LOCATION APL Healthcare Ltd. Unit IV, Naidupeta, Tirupati District, Andhra P...

WALK IN Interview - OSD PACKING- Saturday, 11th Oct 2025 @ Unison Pharmaceuticals Pvt Ltd, Moraiya, Ahmedabad 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. Packing Operator: Experience: 2-8 years Location : Moraiya, Ahmedabad Education Qual...

Key Responsibilities: Prepare and administer radiopharmaceuticals to patients under the supervision of a Nuclear Medicine Physician. Operate and maintain gamma cameras, PET-CT scanners, and SPECT systems for diagnostic imaging. Conduct imaging procedures, process images, and ensure data quality and patient safety. Follow strict protocols for radiation safety, waste disposal, and contamination control . Calibrate and perform routine maintenance on imaging equipment. Maintain accurate patient records, dosage logs, and equipment usage reports. Educate patients on the procedures and ensure comfort during tests. Collaborate with physicians, radiologists, and other healthcare professionals for acc...

Role & responsibilities : 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 are 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 instruction giv...

Job Description Line clearance in dispensing and production area. To perform in-process sampling, testing and document the observations. To handle IPQA activity in warehouse and production area. Review of BMR, process documents etc. APR Preparation. To ensure timely validation of production equipment w.r.t. process, cleaning and to collect samples for cleaning validation etc. To follow GMP and ensuring timely documentation of dispensing, manufacturing and packing activity. To identify problem areas in manufacturing and report to Head QA.

The ideal candidate brings 5 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Own production execution and shift supervision; ensure line clea...

Job Summary We are looking for an individual to ensure strict adherence to safety protocols, SOPs, and quality standards, overseeing batch manufacturing activities, and coordinating with various departments to maintain operational efficiency. The role involves planning and executing production activities, coordinating with cross-functional teams, and ensuring compliance with regulatory requirements, critical for maintaining product quality and meeting production targets. Roles & Responsibilities • You will be responsible for adherence to company safety norms, policies, and SOPs (Standard Operating Procedures). • You will oversee batch manufacturing activities according to e-BMR instructions ...