331 Solid Orals Jobs - Page 2

Understand and develop immediate release and modified release oral formulations for regulated markets (US and EU market). Troubleshoot. Knowledge of using Design Expert/Mini Tab QbD Software. 2) Handling equipment’s for solid oral dosage forms Required Candidate profile Preparing reports like PDR, specifications, stability protocols, DoE, Tech transfer & Reports. Patent analysis, develop non- infringing formulations. Troubleshoot existing products & optimize process

We have an urgent opening coming up with one of the leading Pharmaceutical organization at Mumbai (Kandivali West) for the role of Product Manager - PMT. Location: Mumbai (Kandivali West) Industry: Pharmaceutical Manufacturing Job description : We are looking for an experienced and proactive Pharma Product Manager to lead our Product Management Team (PMT), focusing on Domestic Sales. The successful candidate will play a pivotal role in shaping the strategic direction of our product portfolio, specifically in the areas of OSD (Oral Solid Dosage). This role requires a strong marketing leader with a proven track record in brand management and promotional strategy execution. Key Responsibilities...

Key Responsibilities: Operate and monitor packaging machines for blister, sachet, and cartoning lines of oral solid dosage forms. Ensure adherence to GMP and SOPs during packaging operations. Perform quality checks, documentation, and assist in machine maintenance. Maintain cleanliness and comply with safety protocols.

Walk In Drive for Production OSD Department In Formulation Division @ Mekaguda Qualification :- Diploma | B Tech | B Sc | B Pharmacy | M Sc | M Pharmacy Experience:- 2 to 8 Years Interview Date:- 18-10-2025 (Saturday) Interview Time:- 9.00AM TO 2.0PM Work Location :- MSNF- IV, Mekaguda Venue Location :- MSN Laboratories Pvt Ltd,. Formulation Unit-04-Mekaguda 37XJ+W82, Mekaguda, Telangana 509228 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidates those who have experience in Manufacturing:- Capsule Filling | Granulation | Liquid | Roll Compactor Packing:- ...

Trainee - Operator: Educational Qualification - Diploma in Engineering (Mechanical/Electrical/Electron ics) Experience - 0 - 3 years experience of operating pharmaceutical manufacturing machines in Ointment & Liquid section Job Responsibilities - To operate machines related to manufacturing andpacking activities of Semi Solid Dosage(Ointment), ExternalPreparations & Liquid oral. To adhere with cGMP & SOP Compliance in the department and ensure safety & quality ofproduct during manufacturing & packing operation To achieve desired production targets, control of wastage and yield improvement during process operations. To do online in process checks and donecessary entries in BPR at regular inte...

Line Clearance for Dispensing, Manufacturing & Packing activities Dispensing of RM/PM for batch Mfg Monitoring of IPQA activities (Granulation, Blending, Capsulation, Compression, Coating, Packing Sampling of IP and FP Samples Batch documents review

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com . Job Summary This role will develop experimental approaches and will be responsible for ana...

Walk In drive for Formulation Research & Development - Department FR&D - MSN R&D Center Pashamylaram on 18.10.2025 (Saturday ) Formulation R&D Department ( Formulations R&D) in Formulation Division - R&D Center. Key Responsibilities: Formulation Development : Lead the formulation development process for new pharmaceutical products, including solid oral dosage forms, liquids, and semisolids. Experimental Design : Plan and execute formulation experiments, optimizing product composition, excipients, and processes for efficacy and stability. Documentation : Maintain comprehensive records of experimental procedures, results, and regulatory documents, ensuring compliance with industry standards an...

Executive / Sr. Executive Level: • Assistant Manager & Above: Position: Export (International Business) Business Development Team Target Market: Rest of the World (ROW) candidates with strong experience in Oral Solid Dosage (OSD) products across the Middle East, Southeast Asia, LATAM, Africa, and CIS regions are preferred. Preferred Profile: • Science graduates with an MBA in International Business • Maximum age: 45 years • Energetic, proactive individuals who are open to traveling for business requirements What We’re Looking For: Expertise in Pharma ROW Markets & Global Expansion Strong business development & sales acumen Knowledge of regulatory processes & international client handling Exc...

Roles and Responsibilities (5 days working) Dossier (CTD, ACTD & Country Specific Format) review for Latam, ASEAN, CIS & African countries. Collaborate with various departments within the organization, such as Plant (QA, QC, Production, Packing & Purchase) and R&D, to gather the necessary inputs for regulatory submissions. Compilation and timely submission of Dossiers to the respective regulatory authorities in the assigned countries. Planning, monitoring, review, strategy & delegation of the below mentioned activities for Countries: New Product Registration, Re-Registration, Retention, Tender. Handling of queries from various regulatory authorities/consultants. Post Approval Changes GMP (Co...

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...

Authorize to prepare and review the following documents: a. Trial Batch /Development Batch Manufacturing Record. b. Trial Batch / Scale up batch protocol & report. c. All other documents (If any) from R&D and other locations 2. Responsible for monitoring of Trial / Development / Scale up / Exhibit batches to be executed in manufacturing area. 3. Responsible to coordinate with CFT members for preparation of production plan related to Trial/Development/Scale-Up/Exhibit batches. 4. Responsible to maintain the area with GMP compliance. 5. Responsible for handling of new products from R&D and other locations 6. Responsible for handling of technical issues/OOS/Deviation investigation related to on...

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 (...

Roles and Responsibilities (5 days working) Manage regulatory dossiers for solid oral products, including CTD and ACTD preparation and submission to global markets. Handle team responsibilities related to dossier compilation, review, and approval. Ensure compliance with GMP regulations and provide guidance on regulatory affairs matters within the organization. Collaborate with cross-functional teams to ensure timely completion of tasks and meet project deadlines. Provide expertise in ASEAN, LATAM markets Team Handling, and Dossier Preparation. Desired Candidate Profile M.Pharma degree from a recognized university with 10-12 years of experience in drug regulatory affairs. Strong understanding...

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...

On offer is the opportunity to develop in a young and rapidly growing pharmaceutical company, Key Pharmaceuticals. The organisation operates as a virtual generics company which holds its own marketing authorisations (primarily oral dosage forms) within the United Kingdom/ EU and United Arab Emirates. Key Pharmaceuticals is part of the Bestway Healthcare Group, a vertically integrated business. About the Role We are seeking a visionary and experienced Head of R&D to lead formulation development and regulatory strategy for oral solid and liquid generic dosage forms. This role is pivotal in driving innovation, ensuring regulatory compliance, and accelerating product development for highly regul...

QC planning; GLP/QMS; chemist schedule/qualification Plan/review validation, calibration -AMC/CMC; audits; SOP/STP prep/training; COAs; stability loading/protocols prep Compile batch analysis data Indent materials Internal/External Mail coordination Required Candidate profile QC lead(GMP pharma—oral solids). GLP/QMS docu; ICH method & process validation HPLC/GC/UV, dissolution stability; OOS & CAPA-change control; monthly SOP/STP prep/review-mentoring, working std dev,

QC planning; GLP/QMS; chemist schedule/qualification Plan/review validation, calibration -AMC/CMC; audits; SOP/STP prep/training; COAs; stability loading/protocols prep Compile batch analysis data Indent materials Internal/External Mail coordination Required Candidate profile QC lead(GMP pharma—oral solids). GLP/QMS docu; ICH method & process validation HPLC/GC/UV, dissolution stability; OOS & CAPA-change control; monthly SOP/STP prep/review-mentoring, working std dev,

Walk-in drive: Senior Chemist / Junior Research Associate - HPLC Analytical Method Validations Work Location: Hyderabad Eligibility: Must have 1 to 3 Years of experience in Analytical Method Validations by using HPLC for Formulation products. M.Sc. / M-Pharmacy or Equivalent Qualification. Job Description : Analytical method validations and method transfer as per cGMP requirements for drug products. Strong experience in handling various analytical instruments like HPLC, UPLC, UV and Dissolution USP type-I and II and type-IV. Dissolution, Assay and Related Substances method validationand method development of finished products like Tablets, Capsules, Pellets, oral suspensions and Injectables ...

Role & responsibilities Manufacturing area:- Line clearance before start of batch processing and after cleaning. In-process checks during manufacturing stages Verification of machines settings, process parameters and yield reconciliatoin Sampling of in-process materials for testing. Monitoring of environmental conditions and compliance during production Verification of online entries in BMR Packing area: Line clearance before start of packing and after product/pack change over. Monitoring batch coding, overprinting, labeling, and packaging operations Performaning in-process checks - correct packing components, label reconciliation, and proper sealing. Monitoring controlled area discipline, g...

Role & responsibilities APLHC Unit IV (Naidupeta, Tirupati Dist., Andhra Pradesh) Open Functions: Quality Control/Quality Assurance Experience Required: 1 - 6 years in USFDA Approved pharmaceutical manufacturing facility Quality Control and Quality Assurance Job Titles & Grades: Executive / Sr. Executive (based on experience) Job Description: QC Routine & stability testing of RM / IP / FP samples on HPLC, GC, LCMS, UV, etc. Prepare/standardize analytical methods, calibration & instrument qualification (IQ/OQ/PQ) Adhere to GDP, ALCOA+ and cGMP guidelines; ensure timely LIMS/SAP data entry Investigate OOS/OOT results and implement effective CAPA Support regulatory, customer and internal audits...

Dear All, We are seeking a highly motivated and talented Formulation R&D Scientists to join our innovative team. The ideal candidate will have a strong foundation in formulation development and you will play a crucial role in developing new and improved formulations, ensuring product quality, and meeting regulatory requirements. Location: Hyderabad(Dulapally) Required Experience: 2-7 Years Job Responsibilities: 1. Plan and execute Pre-formulation and formulation activities and ensure the timely execution of project related tasks in coordination with team members. 2. Actively participate in the literature search and preparation of formulation development strategy. 3. Coordinate with QA depart...

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...