331 Solid Orals Jobs - Page 6

Interview for SVP / Injectable & OSD Pharma Formulation Plant in Bharuch on Company / Permanent Payroll Exp: 0 to 13 Yrs CTC: As per Interview Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch & Call 9727755486 Free Job Required Candidate profile Qualification: BE / Diploma Mech / Elec / Inst Vacancies Instrument: 3 Mechanical: 3 Electrical: 3 Experience in SVP & OSD Plant in Must Share with Your Colleagues & Seniors Free Job Placement

Interview for SVP / Injectable & OSD Pharma Formulation Plant in Bharuch on Company / Permanent Payroll Exp: 0 to 13 Yrs CTC: As per Interview Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch & Call 9727755486 Free Job Required Candidate profile Qualification: BE / Diploma Mech / Elec / Inst Vacancies Instrument: 3 Mechanical: 3 Electrical: 3 Experience in SVP & OSD Plant in Must Share with Your Colleagues & Seniors Free Job Placement

Compilation and submission of eCTD dossier for new product (Finished) application & post approval submission Query response, PAS,CBE and annual report, drug listing Review of artwork and submission of labelling section Maintain product life cycle.

Name Of the Company - Zydus Life Sciences Industry - Pharmaceuticals Website of the company - https://www.zyduslife.com/zyduslife/ Location - Ahmedabad Based Plant Department Engineering Electrical Designation Sr. Executive /Deputy manager Experience Required - Between 7-12 Years Of Experience Job Summary: The Electrical Engineer will be responsible for the installation, maintenance, troubleshooting, and continuous improvement of electrical systems and equipment used in pharmaceutical manufacturing. This includes support for production machinery, cleanroom utilities, HVAC systems, and compliance with GMP and safety standards. Key Responsibilities: Ensure uninterrupted operation of electrical...

Responsibilities Global Pay Plus Testers. MT MX messaging , SWIFT payments Preferred Skills: Banking->GPP Financial Services Domain->Payments->GPP Generic Skills: Banking Roles and Responsibility Manage and process payments transactions efficiently. Collaborate with cross-functional teams to resolve payment-related issues. Develop and implement new payment systems and processes. Analyze payment trends and provide insights for improvement. Ensure compliance with regulatory requirements and industry standards. Provide excellent customer service and support to clients. Job Requirements Strong knowledge of payment processing and reconciliation. Experience with payment gateways and payment system...

Excellent job opportunity for QA - AQA Specialist in 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. You are invited to join one of India's fastest growing pharma companies in India!! Experie...

We are seeking a talented and motivated Shopify Developer with 2 to 3 years of hands-on experience to join our team. In this role, you will be responsible for building and maintaining e-commerce stores on the Shopify platform, developing custom themes and apps, and ensuring overall performance and optimization of our clients' online stores. Key Responsibilities: Design, develop, and maintain custom Shopify themes and templates. Work with the Shopify API to integrate third-party tools and custom features. Customize Shopify stores using HTML , CSS , JavaScript , and Liquid (Shopifys templating language). Troubleshoot, debug, and optimize store performance for speed and mobile responsiveness. I...

We are looking for a highly enthusiastic & passionate candidate for the post of R&D Associate to develop next-generation dental materials, including cements, 3D printing resins, sealers, and composites. You will be part of a high-energy team driving innovation from concept to commercial launch. 3-5 years of hands-on R&D experience for mid-level roles in polymer or biomaterial development, including formulation, characterization, and scaling from lab to production Relevant sector : Dental Materials & Products, Medical Device & Biomaterials, Polymer & Chemical manufacturing, Additive Manufacturing/ 3D printing, Advanced Materials Science & nanotechnology Role & responsibilities : Formulate and...

Experience in Solid Oral Dosage & Liquid Orals form in Formulation & Development Dept. for Regulated Market. Required Candidate profile Candidates should have 4-8 Years of relevant experience.

Dear All, We are conducting Walk-In Interview on 29th August 2025(Friday) for Quality Assurance and Quality Control( Formulations ) departments. Quality Assurance: Validations - 4-5 Years of experience in Process and Cleaning validations and equipment qualifications Quality Control: IPFP - 4-5 Years of experience in HPLC, GC, UV, Dissolution and RS. Stability - 4-6 Years of experience in Dissolution, GC, UV and Sample management Raw Materials - 2-3 Years of experience in sampling of Raw and Packing materials Analytical Method Validations - 3-5 Years of experience in Method validations, GC and Dissolution instruments GLP - 2-4 Years of experience in management of working and reference standar...

Walk In Drive For Production OSD In Formulation Division @ Kothur Department:- Production OSD Qualification :-ITI | Diploma | BSC | B Pharmacy | M Sc | M Pharmacy Experience :- 2 To 8 Years Skills :- Packing Operators :- Primary Packing:- Cam MNX | ACG|B Max|BQS|IMAPG||EL Mach|Pharma Pack|CVC Secondary Packing:- HI-Cart|IC-150|CAMHV1|CVC| IMA A 300 Cartonator & Pharma Pack| Labelling Packing Supervisors| Inchargers|Bottle Line Supervisors QMS Supervisors : Handling deviation|Change Controls|Market Complaint&Investigations|Audit Complaince&Intiations of Quality Intiatives Manufacturing:- Compression | Coating | Granulation | Capsule Filling| Executives | Operators| Supervisors Division :- For...

Role & responsibilities Plan, execute, and review Validation Protocols and Reports (Process, Cleaning, Analytical Method, and Computer System Validation). Execute and review Equipment Qualification activities (IQ/OQ/PQ, Re-qualification). Support preparation and maintenance of Validation Master Plan (VMP) . Ensure compliance with cGMP, FDA, MHRA, WHO, and other international regulatory guidelines. Coordinate with cross-functional teams (Production, Engineering, QC, R&D) for smooth execution of validation activities. Conduct risk assessments and gap analysis for equipment, utilities, and processes. Review and maintain SOPs, protocols, and technical documentation related to validation. Handle ...

Role & responsibilities Operate and monitor tablet compression machines (e.g., Cadmach, Fette, Korsch, or equivalent). Set and adjust machine parameters (RPM, compression force, weight, thickness, hardness, etc.) as per BMR. Ensure proper tooling installation, changeover, and maintenance of punches & dies. Perform in-process checks (IPC) like weight, thickness, hardness, friability, and appearance. Record all operational activities in BMR, logbooks, and other documents as per GDP. Ensure line clearance, cleaning, and preventive maintenance of machines. Report deviations, breakdowns, and abnormalities to supervisors/engineering. Adhere strictly to cGMP, GDP, EHS, and safety guidelines during ...

Role & responsibilities Operate and monitor tablet coating machines (Auto Coater/Conventional Pan) as per batch manufacturing records (BMR). Perform coating processes (aqueous/organic) ensuring uniformity and quality standards. Set and monitor machine parameters (spray rate, pan speed, inlet/outlet temperature, atomizing pressure, etc.). Carry out equipment cleaning, calibration, and preventive maintenance. Record all operational details in BMR, logbooks, and related documents. Coordinate with QA/QC for in-process checks and ensure compliance. Report deviations, breakdowns, and abnormalities immediately. Maintain proper stock of coating materials and consumables. Follow cGMP, GDP, safety, an...

Role & responsibilities Operate RMG, FBD, Multi Mill, and related granulation equipment as per BMR and SOP. Carry out wet granulation, drying, sizing, and blending processes. Set machine parameters and monitor process conditions (impeller/chopper speed, inlet/outlet temperature, drying time, etc.). Prepare and handle binder/solution as per production requirement. Ensure proper cleaning, line clearance, and preventive maintenance of equipment. Record production activities in BMR, logbooks, and other documents as per GDP. Coordinate with QA/QC for in-process checks (LOD, particle size, etc.) and implement corrective actions. Report any deviations, equipment breakdowns, or abnormalities promptl...

Excellent job opportunity for Production Supervisor @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. Experience : 2 to 6 years Job Role : Production Supervisor Designation : Officer / Sr. Off...

-Formulation of trials for solid, liquid and semisolid formulations -To perform literature search & preparation of literature survey report -Execution of formulated/ Design trials and sample order batches -Preparation of R&D Departmental SOPs Required Candidate profile -To maintain GLP and GMP in the laboratory -Preparation & review of Technology Transfer Document and other relevant documents -To involve in scale-up and initial commercial batches preparation

1.Experience in Regulated Market (US, Europe) 2.Candidate should perform literature search 3.Should have some basic understanding of patent and generic formulation development. 4.Characterization of marketed product wrt market requirements Required Candidate profile 5.Knowledge of ICH stability conditions and compilation of analytical data 6.Preparation of various documents like PDR, stability protocol, development report writing FDR/PDR

Walk -in drive at Hotel Parc Estique - Pune - Macleods Pharma Department : PDR Designation : Research Associate/ Sr. Research Associate Experience : 4 - 8 Years Location R&D Mumbai Qualification : M. Pharm/ PHD (Pharmaceutics) Job Responsibilities Candidates should have 4-8 Years of relevant experience in Solid Oral Dosage & Liquid Orals form in Formulation & Development Dept. for Regulated Market

Role & responsibilities Formulation Development (Solid Orals, Liquids, MUPS, Molten Mass, Roll Compaction) Technology Transfer & Scale Up. QbD & DoE Methodologies Regulatory Compliance (US, EU, Emerging Markets) Preferred candidate profile Leading Successful Technology Transfer of Multiple Site Transfer Products for US & EU Markets, Ensuring Zero Regulatory observations during Inspectoins.

Role & responsibilities Key Responsibilities: Perform routine and preventive maintenance of electrical panels, motors, MCCs, PLCs, and field instruments in formulation (Granulation, Compression, Coating, Capsule filling, Blister packing, etc.). Attend to electrical breakdowns in production equipment with minimum downtime. Assist in installation, commissioning, and qualification (IQ/OQ/PQ) of new formulation machines. Maintain logbooks, calibration records, and preventive maintenance schedules as per SOPs. Ensure adherence to GMP, safety, and electrical compliance standards. Support in audits (regulatory, safety, internal, and external). Monitor and maintain compliance of electrical safety st...

Role & responsibilities Formulation Development (Solid Orals, Liquids, MUPS, Molten Mass, Roll Compaction) Technology Transfer & Scale Up. QbD & DoE Methodologies Regulatory Compliance (US, EU, Emerging Markets) Preferred candidate profile Leading Successful Technology Transfer of Multiple Site Transfer Products for US & EU Markets, Ensuring Zero Regulatory observations during Inspectoins.

Role & responsibilities The Engineering Manager will direct and coordinate all engineering activities within the company's flagship pharmaceutical manufacturing facility, including equipment maintenance, project management, and process validations to ensure overall plant goals and objectives are accomplished. Being the Lead Manufacturing Engineer for the Engineering Department, ensuring best practice processes are developed. Providing Manufacturing Engineering support to both customers and suppliers Identifying and implementing improvements to equipment, processes and methods Identifying and driving improvement initiative to reduce costs and improve on time delivery Provide technical assista...

Responsibilities: * Manage manpower resources effectively * Oversee production processes from liquid & solid oral formulations adhering to GMP guidelines * Ensure timely delivery of products within quality standards

Job Title: QMS Manager Business Unit: Global Quality Compliance Job Grade G10 / Manager 1 Location : Mohali Educational Qualification: M.Sc / B.Pharm / M.Pharm Experience: 12+ yrs Quality Management System 1. Implement, operate, monitor and maintain Quality Systems which enable operations on site to occur in an efficient manner and in compliance with Global Quality Standards and cGMPs. 2. Review and Archival of Quality System documents. 3. Follow up for timely closure of Quality Management System documents. 4. Participating in the investigation analysis for Complaints and Audit finding, moreover responsible for providing batch disposition decision as per the outcome of PQC investigation. 5. ...