331 Solid Orals Jobs - Page 4

Note: Walk In Interview at Vadodara. Date: - 28.09.2025 (Sunday) Job Location: Daman & Dahej Qualification:- M.Sc. (Chemistry)/ B. Pharma/ M. Pharma Experience:- 2-6 Years in (API or Solid Oral) Required Candidate profile * 2-6 years of experience into LCMS, HPLC, GC & Wet Chemical sections, Analytical Validation, Finished Goods, Raw Material, Stability & GLP

Role & responsibilities Responsible for finding opportunity for cost reduction. Evaluation of low cost API/RM, taking lab trials and documentation thereof for solid oral products. The candidate is responsible for the scale up and technology transfer at plant scale for identified cost reduction products. Should prepare technology transfer documents and support the filing of the product. Should handle the regulatory queries and support the product launching.

Roles and Responsibilities Develop formulations for solid oral dosage forms (tablets) and liquid orals. Conduct literature search to support product development decisions. Perform formulation development activities, including scaling up processes from lab to commercial scale. Ensure compliance with regulatory requirements during all stages of product development. Collaborate with cross-functional teams to resolve formulation-related issues.

Job Title : Executive / Sr. Executive Formulation Development Entity : Evonik India (Evonik India Research Hub) Work Location : Thane PRINCIPLE ACCOUNTABILITIES: Conduct formulations experiments, coordinate for analysis of samples and carry out the required stability studies. Troubleshoot technical problems related to the manufacturing processes and formulations independently, in order to meet the project goals. Guide fellow scientists and trainees on technical matters. Manage a Quick run innovation project independently. Communicate with the project manager(s) and other stakeholders. Presentations with due connect to the overall technical and business goals. Coordinate with analytical depar...

Job Title:- Assistant / Deputy Manager – Regulatory Affairs (US Market) We are hiring Regulatory Affairs professional for the US Market. The candidate will be responsible for preparing, reviewing, and submitting ANDA

Roles and Responsibilities Ensure compliance with cGMP guidelines during all stages of product development. Design and optimize formulations that meet regulatory requirements and customer needs. Collaborate with cross-functional teams to ensure successful technology transfer from R&D to manufacturing scale-up. Conduct research on solid oral, liquid oral, injectable, OSD, and other dosage forms to improve existing products or develop new ones. Develop new products from concept to launch, ensuring timely delivery of high-quality formulations.

Greetings!!!! We are seeking experienced professionals in Regulatory Affairs US Market (CMC, Module 3) with expertise in Formulation, for our Hyderabad-based R&D Centre. Regulatory Affairs US Market (CMC) with strong exposure to ANDA/NDA submissions and post-approval changes. Key Responsibilities: Hands-on experience in US Regulatory Affairs for ANDA & NDA (Approved and Tentative) submissions. Responsible for filing supplements : CBE, CBE-30, PAS, Controlled Correspondence, Annual Reports/Updates. Planning, reviewing, and timely submission of assigned projects in compliance with FDA guidelines . Strong interpretation of FDA queries and drafting of high-quality responses. Review and preparati...

Study feasibility and planning inputs Provide inputs in PK/PD/IM based study porotocol and plans Operational expertise in use of Phoenix WinNonlin, NLME and IVIVC tools Regualtory query response and techincal consultation with study team Scientific support in pre-clinical, clinical and in-vitro study planning & execution PK/Stats data analysis and reveiw of study reports EXPERIENCE Pharma industry / CRO experience with > 5 yrs - core invlovement in PK/PD/IM - BABE study planning & data analysis Involved in regualtory query resposness, investigaiton and reporing EDUCATIONAL QUALIFICATION M.Pharma (Pharmacology) or Pharm.D. (Pharmacology) or Ph.D. (Pharmacology)

Walk In Drive For Production OSD In Formulation Division @ Kothur Department:- Production OSD Qualification :-ITI | BA | Diploma | BSC | B Pharmacy | M Sc | M Pharmacy Experience :- 2 To 8 Years Skills :- Operator: Compression | Coating Manufacturing: Supervisor | QMS Packing operators: Cartonator | Auto Cartonator | Packing Supervisor Division :- Formulation Interview Date:- 20-09-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- MSNF-II , Kothur Venue Location:- Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Ca...

Position : 2 Position Education: Be- Mechanical Preferred candidate profile Plant Maintenance Process Equipment - Injectable Process Equipment - OSD

Job Title: Inspection - Sensum Operator Work Location: Gagillapur, Hyderabad Department: Production - Manufacturing Experience: 2 to 7 Years Qualification: ITI / Diploma (Mechanical/Electrical) or B.Sc. (Chemistry or related field) Key Responsibilities: Operate Sensum Inspection Machines for tablets and capsules as per batch manufacturing instructions. Monitor machine performance, identify visual defects, and take timely corrective actions. Ensure compliance with SOPs, cGMP, and safety guidelines at all times. Maintain proper documentation of inspection activities, deviations, and quality checks. Perform cleaning and line clearance of equipment and surrounding work areas. Coordinate with cro...

Company: Strides Pharma Science Ltd Department: Quality Control (QC) Position: Senior Executive Job Location: Alathur, Chennai Qualification: M.Sc. (Chemistry), B-Pharm, M-Pharm Experience: 4.5 to 8 Years Skills required: Experience on Raw material, In-process, Finished product, Stability and Microbiological testing. Work experience on FDA regulatory plants Flexible to work in shifts Job responsibility: Handling of Sophisticated instruments such as HPLC, GC, UPLC, UV, AAS & Dissolution Tester Analysis in LIMS e-RDS Experience on Microbiological testing Instrument Qualification knowledge on IQ, OQ, PQ. Regards, Srinidhi S HR Talent Acquisition

Execution of Production Process, Documentation Process, Conducting Process operations and maintaining BMR records. Utilization of Manpower and equipment capacity. GMP compliance in Manufacturing Department.

Main Accountabilities Routine analysis & Stability Analysis (assay, RS, dissolution, water content etc.) of R&D formulation projects (solid & liquid orals, injectables) Daily calibration of pH meters, balances etc. Stability sample management (loading & withdrawal as per stability plan) Preparation of Stability Reports & other protocol based study reports for assigned projects, as applicable Hands-on experience of analytical instrumental techniques (HPLC with chromatographic software etc.) Assisting analytical method development/validation/method transfer activities, as per need Supporting other assigned lab responsibilities for GLP compliance Performance Indicators: Timely execution of assi...

Walk-In Interview for Manufacturing OSD Supervisors/ Officers on 17-Sep-2025(Wednesday) for SEZ MATODA, Ahmedabad Job Location : SEZ MATODA, Ahmedabad Date : 17-Sep-2025 (Wednesday) Time : 9.30 am to 12:00 pm Venue for Interview : Amneal Pharmaceuticals Plot No 15,16,17 Pharmez, Sarkhej Bavla Highway, Village Matoda, Ahmedabad - 382213 (Oral Solid - OSD Requirement) 1.Manufacturing & Packing (Tablet/Capsule) Requirement For Officers & Executives Designation: Officer/ Sr. Officer /Executive Qualification: B. Pharm, B.sc Total Experience: 02 to 06 years Area: Coating, Granulation, Compression, Packing (Bottle Packing only) Machine Exposure along with 21 CFR compliance: RMG, FBE, Fette compress...

Effective operation and maintenance of equipment like autoclave, Garment cubicle, sealing machine, vessels CIP and SIP SKIDS To practice the c GMP activities and to follow the clean room discipline Cleaning and sterilization of the vessels and transfer lines using CIP & SIP equipment Preparation and filtration of disinfectant and cleaning of the area Monitoring of LAFU, AHU, Dynamic pass box, Garment cubicles and cold rooms Maintaining of all cGMP activities and housekeeping activities in the critical operations Maintenance and updating of equipment log books and GCRs Manual recording of the temperature and positive pressures Cleaning of equipment Blending of vaccines Preparation, Sanitizati...

Hands-on experience in monitoring manufacturing and packaging processes, line clearance, and in-process checks. Proficiency in DOC-MS systems, SOP preparation, deviation handling, and change control. Involvement in TT activities including protocol review, execution, and coordination between RCD and manufacturing. Familiarity with validated software systems that meet FDA electronic records and signatures requirements. Strong understanding of equipment qualification (D, I, O, P), process validation, and cleaning validation. E-BMR G E-Log: Experience with electronic Batch Manufacturing Records and Logbooks for real-time documentation and traceability. uality Management Systems (MS): Implementat...

Were looking for a skilled Shopify Developer to create and maintain e-commerce solutions on the Shopify platform. Key Responsibilities: Develop and maintain Shopify stores with focus on front-end features Customize Shopify themes to meet client requirements Collaborate with designers and project managers Implement responsive designs for mobile and desktop Requirements: Minimum 1 year of Shopify development experience Strong knowledge of Liquid, HTML, CSS, and JavaScript Understanding of e-commerce best practices and SEO Excellent problem-solving skills and attention to detail

Walk In drive for Formulation Research & Development - Department FR&D - MSN R&D Center Pashamylaram on 20.09.2025 (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...

Walk-In Drive for Development Quality Assurance - Formulation Department @ MSN R&D Center Pashamylaram on 20.09.2025 (Saturday ) Roles & Responsibilities 1. Issuing of Batch Manufacturing Records, Analytical Raw datas and maintaining the respective log books. 2. Issuing of registers and formats for all departments and maintaining of records for issuance and reconciliation. 3. Issuance approval, Issuance and Retrieval of the documents in eDMS. 4. Receiving, Issuing and reviewing the bio batches related executed Batch Manufacturing Records, Analytical raw datas and archiving. 5. Responsible for review of product development documents and analytical documents related to technology transfer. 6. ...

Your Day-to-Day Tasks Include: 1. Initiating first level contact with Inbound and Outreach leads. 2. Creating and executing an outreach strategy in collaboration with the PDR Managers and PDR team leads.

R&D (Synthesis) -Agrochemical Industry-Saykha,Gujarat. Capital Placement Services Industry IT Software - Application Programming / Maintenance Qualification M.Sc Key Skills Green Field Projects UPLC Gujarat R&D (Synthesis) PDR R&D Develo

Officer Sr. Officer - Engineering: Qualification - B. E (Mechanical/ Electrical) Experience - 03-06 years experience in pharmaceutical manufacturing machine maintenance Job Responsibility - 1. E xperience in maintenanceof semisolids (Ointment/ cream / gel manufacturing machines, Metal andlaminated tube filling machines) oral liquid manufacturing (mfg. Tanks withbottom entry agitators, volumetric filling machine, ROPP Cap sealing machine). 2. Should be able to draw & edit 2 D drawings with AutoCAD. 3. Mechanicalseal handling, assembly, dismantling and troubleshooting 4. Should haveknowledge about CLIT 5S and Kaizen 5. Maintaindocumentation related to ISO - EMS and OHS standards 6. GMPdocument...

We are seeking an experienced in Production Manager to lead the end-to-end lifecycle of pharmaceutical / Nutraceutical .The candidate should possess hands-on experience in the manufacturing of Tablets, Capsules, Softgels, Sachets & Protein Powders. Required Candidate profile 1. Production Planning & Management , Quality Assurance & Compliance, Process Improvement & Cost Control, Equipment & Facility Management, Team Leadership, Compliance with Health & Safety Regulations

Job profile Qualification : Bachelors Degree / Master Degree Industry Type : FM Services, Hotels, Projects, Overall Experience : 12 -14 years Industry Experience : 10-12 years of relevant / equivalent experience Technical Skills : Building Services Generic Skills : Leadership, Communication, Vendor/people management, Strategies Behaviors : Team work, Learning attitude, Innovation mindset Job Aim: To take complete ownership for all client deliverables for all the facilities in the city. The person will be responsible to provide comprehensive facility management services, as per the contractual terms with a focus on continuous improvement for the respective facilities. Will also be responsible...