759 Osd Jobs - Page 23

To ensure that all raw materials (API & excipients) are sampled, tested, and released. Key Responsibilities: 1. Sampling & Receipt 2. Testing & Analysis 3. Documentation & Release 4. Compliance & Audit Readiness 5. Instrument Handling Required Candidate profile Candidate must have experience in handling team of minimum 10 members. Candidate must have experience into routine analysis of raw material and QMS knowledge.

Greetings From Immacule Lifesciences Pvt Ltd! We are conducting Mega Walk-In Drive for both OSD & Sterile Injectable Manufacturing on Sunday (22/06/25). Requirements: Positions : Officer to Assistant Manager Experience : 2 - 10 Years in Pharma Industry Job Location : Nalagarh, Baddi Departments: Production & Packaging OSD : ( Granulation, Compression, Coating, Capsule, Blister, Alu - Alu, Strip, AutoCartonator) Sterile : Manufacturing, Filling & Sealing, Autoclave, CNC, Vial Washing, Tunnel, Lyophilization Quality Control OSD & Sterile : Instrumental and chemical analysis i.e RM/PM/FG/ Validation/ Micro/ Stability and having competency on instruments like HPLC, GC. Quality Assurance OSD &Ste...

Roles and Responsibilities Collaborate with cross-functional teams to identify market trends, competitor analysis, and customer needs to inform sales strategies. Provide backend support to the sales team by managing data entry, documentation, and reporting tasks efficiently. Ensure timely delivery of high-quality products to customers while maintaining excellent communication skills throughout the process. Identify areas for improvement in existing processes and implement changes to increase productivity and efficiency. Desired Candidate Profile 2-4 years of experience in pharmaceutical or nutraceutical industry with a focus on domestic marketing or CDMO services. Strong understanding of for...

Role & responsibilities: To receive instructions from AM / Manager / GM. To plan the work as per instructions from department head. To track the daily exhibit / site shift product's trail, engineering, Exhibit & Validation (not limited to) batches manufacturing and monitor it's progress constantly. To organize, supervise and control the activities of Technology Transfer department. To co-ordinate and co-operate with various departments like Raw material store, Engineering, Quality Assurance, Administration, Information Technology, Operational Project, Quality Control, Production etc. for smooth functioning of Technology Transfer department. To check and update various documents and records, ...

Aurobindo Pharma Ltd. Unit IV (Oral Solid Dosage) Work Location: Naidupeta, Tirupati District, Andhra Pradesh WERE HIRING | Aurobindo Pharma Ltd. Unit IV (Oral Solid Dosage) Work Location: Naidupeta, Tirupati District, Andhra Pradesh Tablet/Pellet Coating Operators (2-7 yrs) | Key Responsibilities • Run tablet / pellet coating machines (Glatt, Gansons, ACG, etc.). • Mix coating solution and load materials as per the batch sheet. • Set and watch basic machine settingspan speed, temperature, spray rate. • Do simple in-process checks (weight gain, colour, appearance) and note results. • Fix small issues like blocked spray guns or wrong settings; call maintenance if bigger problems arise. • Keep...

Responsible for the development and dossier deliverable of genreic application for projects assigned with in the team for Europe ,Canada Australia. Preparation ,review and approval of test licenses Import license applications. Planning and procurement of RMPMs/ RLDs and inventory control at R&D for development. Preparation and review of RMPMs/Justification of Specifications/Cleaning validation report/Risk assessment report/ stability protocol/CDRs/Technology Transfer dossiers. Review of MFRs/BMRs/BPRs/PVPs/HTS, product specific questionnaire, Protocol; and report etc. for scale up and registration batches Timely and Appropriate Reponses for CMC and Bio deficiencies from regulatory agencies f...

Walk-in Drive @ Bangalore on 22nd June 2025 (Sunday) Strides Pharma is hosting a Walk-In Drive for multiple roles. Venue: Strides Pharma Science Ltd. (R&D office): 165/2, 3rd Main Road, Oppo. Kalyani Magnum Tech Park, JP Nagar 4th Phase, Bengaluru-560076 Open Positions Department: Production Experience: 2-7 years Qualification: B.Pharm/M.Pharm Job Location: Chennai Key Skills: Granulation, Compression, Coating, Capsule Filling, OSD Production Department: Packing Experience: 2-7 years Qualification: B.Pharm/M.Pharm Job Location: Bangalore Key Skills: OSD Packing, Bottle Packing, Blister Packing, BQS, CVC, BPR Department: Quality Control Experience: 2-7 years Qualification: B.Pharm/M.Pharm/M.S...

Role & responsibilities Sampling and Analysis of water, Raw materials, Packing materials. Sampling of swab samples. Analysis of In process, Finished product, Swab and Stability samples. Responsible for calibration of Balance, conductivity meter and pH meter. Responsible for preparation and pasting of approved labels. Responsible for In process and Finished product sample receipt and analysis. Responsible to perform the analysis by UV-Visible spectrophotometer, KF Autotitrator, Polari meter, HPLC, GC, FTIR, Dissolution, Disintegration, Friability and Hardness tester, Tap density, Melting point apparatus. Responsible for the preparation of Specifications, STP, Analytical Raw data sheets for Ra...

Role & responsibilities Lead and manage the Quality Control team to ensure timely and accurate analysis of finished products (OSD & Injectables). Review and approve analytical reports, ensure compliance with GLP and cGMP standards. Oversee operations involving HPLC, GC, UV, IR , and other sophisticated instruments. Ensure proper implementation of MPCL and maintain all microbiological standards in compliance with regulatory guidelines. Handle all regulatory audits (USFDA, MHRA, WHO, etc.) and prepare necessary documentation. Manage OOS/OOT investigations and ensure CAPA implementation. Coordinate with cross-functional teams (QA, production, regulatory affairs) to ensure product quality. Train...

Roles & Responsibilities: Develop and execute regulatory strategies for the registration and lifecycle management of pharmaceutical products in ROW markets. Compile, review, and submit high-quality regulatory dossiers (CTD/eCTD format) in compliance with regional authority requirements. Interact with local affiliates, regulatory agencies, and distributors to ensure timely approvals and resolve queries or deficiencies. Maintain regulatory documentation and product information to ensure compliance with health authority regulations. Monitor and analyze changing regulatory landscapes in ROW regions and update stakeholders on impact. Support cross-functional teams including R&D, QA, Supply Chain,...

We are seeking a skilled professional for the role of Formulation Development (FRD) in Quality Assurance (QA) to join our team in Hyderabad. The ideal candidate will have hands-on experience in QA within the production department, specifically related to formulations in the Oral Solid Dosage (OSD) segment. Role & responsibilities Ensure compliance with quality standards in the production department related to formulations Oversee and support QA activities in manufacturing processes Prepare and review documentation including Master Formula Records and other QA-related documents Collaborate with cross-functional teams to maintain and improve product quality Participate in audits and implement ...

Dear Respected All, Greeting from Biophore India pharmaceutical Pvt Ltd. (oral solution exp) We have opening for Formulation R&D Department. Position : Executive or Sr Executive 1)Candidate must have knowledge Prototype & Product Development. 2) Must have Literature Search. 3) Scale-up Batches, Exhibit Batches, DOE Experiments. 4) PDR Preparation & Development related documentation. 5) Experience in US ,EU Markets. 6) Preparation of documents form development stage to Technology Transfer Stage. Preparation and Review of SOP,S related to formulation R&D. Good Communication Skills Ref to Friends or colleagues Please share update resume: careers@biophore.com Total Exp : Current CTC: Exp CTC: No...

Job Title : Capsule Filling Operator OSD (2-8 Yrs) Company : Aurobindo Pharma Ltd – Unit IV Location : Naidupeta, Tirupati (AP) Key Skills : Capsule Filling, Bosch/ACG Pam/IMA, BMR, cGMP, Hard-Gelatin Education : ITI / Diploma / B.Sc / B.Pharm Apply To : ganesh.janne@aurobindo.com | WhatsApp 8096888868

Great 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 Scientist - Technology Transfer - EU market at...

Qualification: Bsc Chemistry/Bpharma Experience : 0 to 5 Years CTC: Up to 4.5 LPA Work Location : Ankleshwar Experince in Pharma Company Prefer Like OSD, Tables, API send cv on sdpbharuch@gmail.com with Sub : Production Ankleshwar Required Candidate profile Interview Venue: SDP HR SOLUTION 610, GOLDEN SQUARE BESIDE DMART ABC CIRCLE BHARUCH Share CV on sdpbharuch@gmail.com with Subject: Production Ankleshwar No Charges Share with Friends & Colleagues

Title: Business Development Head - (Contract Manufacturing/CMO / CDMO) - Pharmaceutical Human Health Industry (DOMESTIC MARKETING & BUSINESS DEVELOPMENT ONLY) Summary: We are currently seeking a dynamic and experienced Business Development Head (FOR DOMESTIC MARKETING) to spearhead our business development initiatives in the pharmaceutical human health sector. This pivotal role requires a focus on B2B marketing and contract manufacturing, particularly in oral liquids and nutraceuticals. The ideal candidate will bring a strong background in multinational corporate environments, with a demonstrated track record of success in generating new B2B orders and selling developed products within the h...

Roles and Responsibilities Ensure compliance with BPR review, batch manufacturing, and batch planning processes. Conduct granulation activities according to OSD requirements. Perform formulation tasks as per BMR guidelines. Collaborate with cross-functional teams for smooth production operations. Desired Candidate Profile 2-6 years of experience in pharmaceutical industry with expertise in Production Manufacturing (OSD). Bachelor's degree in Pharmacy (B.Pharma) from a recognized institution. Strong understanding of Batch Manufacturing Record (BMR), Batch Processing, and Tablets processing.

Roles and Responsibilities Operate compression machines to produce tablets in OSD manufacturing process. Ensure accurate weight control during compression operations. Monitor machine performance and troubleshoot issues as needed. Maintain cleanliness and organization of production area. Collaborate with team members to achieve production targets. Desired Candidate Profile 1-4 years of experience in pharmaceutical production, preferably in compression operations. Strong understanding of formulation, compression, and manufacturing processes. Ability to work accurately with precision instruments and equipment. Basic knowledge of tablet coating techniques would be an added advantage.

Greetings!!!! We are looking for Global Project Lead _ for a Global Pharma Company _ Bangalore. Job Summary: Responsible for the establishment, development and execution of detailed project plans for the Site Transfer projects and Portfolio management Program which includes: Technical Operations Support Services, Manufacturing Technical Support, and Commercial Product Site Technology Transfer Teams. The Manufacturing Technical Services (MTS) Program focuses on managing Product Lifecycle Management projects across the GTA sites, and technology transfer of Commercial products between internal sites as well as to External Suppliers in alignment with commercial strategies and the product portfol...

Experience with IMA-PG TR 100LT Primary & 1C-150C Secondary Packing Responsibilities: Operate blister packing machines to package pharmaceutical products in blisters. Ensure accurate and efficient packaging of tablets, capsules & solid dosage forms.

operation of Granulation, Coating, Compression and Filling machines. Prepare tablet & capsules as per BMR Maintain GMP documentation Ensuring daily cleaning activity, machine preventive maintenance as per schedule. Knowledge of GMP, SOPs Ability to work in shifts

•Experience in pharmaceutical Formulation company •Handling of instrumentation and calibration processes and hands on experience in trouble shooting of instrumentation breakdowns, •Well versed experience of PLC & IPC Validation

Company is Big and Reputed name in Pharma Manufacturing. Only Candidate having 1 Yr+ experience in Granulation or Tablet Machine Operator, can only apply. Job Location - Moraiya, Ahmedabad For any Query, call 8000044060 Required Candidate profile Company is Big and Reputed name in Pharma Manufacturing. Only Candidate having 1 Yr+ experience in Granulation or Tablet Machine Operator, can only apply. For any Query, call 8000044060

The reputed pharmaceutical company engaged in development, manufacturing and marketing of oral solid dosages forms in regulated market. We are looking for competent, growth-oriented professional in Quality Assurance and Quality Control profiles for our USFDA & EU-GMP approved OSD manufacturing facility at N-32, Additional Patalganga MIDC, Tal.- Panvel, Dist.- Raigad.Roles and Responsibilities Ensure compliance with cGMP guidelines during formulation development, solid oral manufacturing, and OSD production. Conduct analytical method validation, stability studies, and quality control activities to ensure product quality. Develop and maintain documentation for batch records, test results, and ...

The reputed pharmaceutical company engaged in development, manufacturing and marketing of oral solid dosages forms in regulated market. We are looking for competent, growth-oriented professional in Quality Assurance and Quality Control profiles for our USFDA & EU-GMP approved OSD manufacturing facility at Patalganga MIDC, Tal.- Panvel, Dist.- Raigad.Roles and Responsibilities Ensure compliance with cGMP guidelines during formulation development, solid oral manufacturing, and OSD production. Conduct analytical method validation, stability studies, and quality control activities to ensure product quality. Develop and maintain documentation for batch records, test results, and equipment calibra...