225 Capsules Jobs

shall be responsible for maintaining and improving all QMS activity, GMP and GLP across the company Handling QMS activities like change control, validations, stability, qualifications, APQR and Risk assessment etc Label artwork review and management Required Candidate profile Assisting HOD in customer complaint analysis and preparation of customer complaint report. Investigation of incidents, deviations, OOS and ensure corrective actions in place.

Job Responsibilities: Development of oral solid dosage forms (tablets, capsules) including IR, MR, and coated products. Handling product development, optimization, and scale-up activities.

Key responsibilities: Executes online Batch Packing Records, online in process as per the parameters mentioned in the BPR, logbook, documents and other formats. take line clearance of area / machine as per respective SOPs. maintain / fill all area / machine related documents like Sequential, area cleaning, daily cleaning log books and other formats of machine & area as per SOP. verify and receiving of dispensed packing material. indent / receive / handle / verification / uses & destruction of stereo as per respective SOP. verify the Leak test of blister / strip as per frequency. If result not satisfactory, rectify the problems. maintain, handle / storage / labelling of machine spares /change...

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

Medicamen Biotech - SRL Pharma R&D Centre Required Formulations Profile Designation: Executive/ Scientist Qualifications: M. Pharma - Pharmaceutics Vacant Post: 6 Nos. Experience: 4 to 8 Years Please share profile on uday@shivalikrasayan.com Required Candidate profile Pharma R&D experience must in Formulation USFDA exposer prefer Preparation of Pharmaceutical Development Report Ready to relocate Bhiwadi, Rajasthan Ready to join Immediately Prefer Team Player Perks and benefits Best of Industries Salary based on Experience

Purpose/Objective Shift Manager - LT Operations is responsible for overseeing the entire product operation cycle, from berthing to the dispatch of products at the Liquid Terminal. Oversees managing daily shift operations, planning vessel activities, coordinating manpower, liaising with stakeholders, updating SOPs, accounting for stock, and maintaining cleanliness within the terminal. Key Responsibilities of Role Liquid Terminal Operations Management: Direct and manage daily shift operations at the Liquid Terminal, ensuring efficient and safe execution of all activities. . Resource Management: Evaluate operational needs and allocate the necessary manpower for effective Jetty and Tank Farm ope...

Purpose/Objective Shift Manager - LT Operations is responsible for overseeing the entire product operation cycle, from berthing to the dispatch of products at the Liquid Terminal. Oversees managing daily shift operations, planning vessel activities, coordinating manpower, liaising with stakeholders, updating SOPs, accounting for stock, and maintaining cleanliness within the terminal. Key Responsibilities of Role Liquid Terminal Operations Management: Direct and manage daily shift operations at the Liquid Terminal, ensuring efficient and safe execution of all activities. . Resource Management: Evaluate operational needs and allocate the necessary manpower for effective Jetty and Tank Farm ope...

Purpose/Objective Engineer - Automation and Instrumentation (Liquid Terminal) is responsible for the effective management and maintenance of automation and control systems specific to liquid terminal operations. This role is crucial for ensuring accurate and efficient handling of liquid cargo, maintaining safety standards, and optimizing the performance of liquid terminal facilities. Key Responsibilities of Role System Maintenance and Optimization: Conduct regular maintenance, troubleshooting, and optimization of automation and instrumentation systems to ensure uninterrupted liquid terminal operations. Technical Support: Provide expert support for automation systems, including programmable l...

Roles and Responsibilities Plan, organize, and control production activities to meet quality standards. Ensure compliance with regulatory requirements (GMP) and company policies. Develop and implement process improvements to increase efficiency and reduce costs. Collaborate with cross-functional teams to resolve issues related to raw materials, equipment maintenance, and personnel management. Conduct regular audits to ensure adherence to SOPs and identify areas for improvement. Desired Candidate Profile 8-13 years of experience in pharmaceutical manufacturing or nutraceutical industry. Strong knowledge of capsule filling processes, drug development life cycle, medicine formulation techniques...

Role & responsibilities JOB RESPONSIBILITY Your job responsibilities are listed below for your understanding and acceptance. In case of any system up-gradation in future, you will be simultaneously re-trained to understand the new implementation. 1. Responsible Manufacturing of Oral Solid Dosage Tablets and Capsule and for Production planning as per order or availability of material. 2. Responsible for Preparation of BMR for new product. 3. Responsible for verifying the filled BMR and yield reconciliation of each stage. 4. Responsible for preparation of Standard Operating Procedure (SOPs). 5. Responsible for Preparation MFR for new product development. 6. Responsible for coordinating with En...

Job Description Strong expertise in formulation development of sterile liquid injectable dosage forms, including end-to-end development and troubleshooting. Hands-on experience in drug device combination product development, with good understanding of device compatibility, functionality, and regulatory expectations. Proven experience in developing and handling lyophilized drug products (peptides, proteins, and small molecules), including cycle development and optimization.

Roles and Responsibilities Plan production activities to meet customer requirements, ensuring compliance with GMP guidelines. Coordinate with various departments (QA, QC, Packing) for smooth plant operations. Ensure timely availability of raw materials and packaging materials through effective planning and coordination. Monitor daily production planning, shift planning, and manpower handling to achieve productivity targets. Oversee blister packing, granulation, compression machine operation, WHO inspections, and tablet/capsule filling processes. Desired Candidate Profile 10-12 years of experience in pharmaceutical production management or related field. Bachelor's degree in Pharmacy (B.Pharm...

Opening for Pharma Lifescience. Role & responsibilities : Candidate is having knowledge of OSD Formulation Plant. Depth knowledge of In Process Quality Assurance . Third Party Manufacturing Knowledge. Candidate is Ready for Within City Travelling for who are Manufacturing our Medicine. Qualification:-M-Pharma-QA or B-Pharma. Interested candidates shared resume on snehal@topgearconsultants.com

Job Title: SGO Validation Lead Job Grade: G9B/A Function: Global Information Technology Sub-function: Manufacturing & Quality IT Manager’s Job Title: Head SGO IT India Skip Level Manager’s Title: Global Head Manufacturing & Quality IT Function Head Title: Global Chief Information Officer Location: Halol Areas Of Responsibility At Sun Pharma, we commit to helping you “ Create your own sunshine ”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as...

Role & responsibilities Formulation development (solid, semisolid, liquid oral) Tech transfer & scale-up Troubleshooting & problem-solving QbD, DoE, FMEA Strong documentation skills Knowledge of regulatory requirements Project management & cross-functional coordination

Department: Production Position Title: Officer/Sr. Officer Section :- Compression, Capsule, Packing Number of Positions: 12 Experience Required: 03 to 08 Years Qualification: B. Pharm/M. Pharm Job Description: Responsible for compression, Coating, and capsule sections activities in a pharmaceutical manufacturing plant. Hands-on experience in pharmaceutical packing lines for OSD. (Primary & Secondary). Good knowledge of SOPs and electronic logbooks (eLogs). Familiarity with GMP documentation. Should have experience in following section: Compression, Coating Capsule Blister and Strip packing machines Powder and bulk packing lines

Walk In Drive For Production OSD In Formulation Division @ Jadcherla Department:- Production OSD Qualification :-BA | Diploma |B Com | BSC | B Pharmacy Experience :- 2 To 8 Years Division :- Formulation Interview Date:- 07-12-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- MSNF-II, Kothur | MSNF-VI, Burgul| MSNF-IV, Mekaguda Venue Location:- ELITE HOTELS & RESORTSNH44,Bangalore Hyderabad Hwy Jadcherla, Telangana 509301 Contact No:- 040-304338701 | 8954 Skills :- Operator: Compression | Coating | Granulation | Capsule Filling Manufacturing: Supervisor | Shift IN charge Packing operators: Cartonator | Auto Cartonator | Packing Supervisor | Blister Packing | Bottle Packing | Primary & S...

Responsibilities: *1. Ensure quality control during granulation and compression processes. 2. Collaborate with formulation team on OSD, RMG, FBD, blending, FBP, tablet production. 3. Machine Operation & Setup, Maintenance & Troubleshooting

Role & responsibilities Graduate/Post Graduate in Chemistry with 3 to 5 years of experience in QC, familiar with HPLC/GC/FTIR/UV Preferred candidate profile Graduate/Post Graduate in Chemistry with 3 to 5 years of experience in QC, familiar with HPLC/GC/FTIR/UV Job Location : Sikkim Interested candidates may apply at hr.plant@zuventus.com

Quality Head required at panipat for a genric pharmaceutical company Qualification- B. pharma Exp- min 10 yrs Salary- upto 18 lacs Note:- candidate must have generic, ethical both time of exposure Wtsapp me resume at 8295842337- Mr. Bansal Required Candidate profile Ensure GMP compliance, lead QA/QC teams, oversee audit & documentation, drive quality systems, manage regulatory requirements, reduce deviations, and ensure product quality for generic & ethical lines

quality executive required at baddi, himachal and roorki, Uttarakhand for a genric pharmaceutical company Qualification- B. pharma Exp- min 3yrs Salary- upto 30k Note:- required local candidates Wtsapp me resume at 8295842337- Mr. Bansal Required Candidate profile candidate must have to visit at 3party manufacturer for inspection of production at baddi, himachal and roorki, Uttarakhand. required local candidates from baddi, himachal and roorki, Uttarakhand. Perks and benefits travelling allowances

Job Title: Officer Business Unit: Sun Global Operation Job Grade G12C Location : Gangtok At Sun Pharma, we commit to helping you “Create your own sunshine” — by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Key responsibilities: o Ensure completion of all SOP as Training need matrix...

Role & responsibilities 1. Knowledge of calibration and operation of HPLC with empower software. 2. Sound knowledge of analytical method development and Analytical method validation of OVI, purity, and assay method by HPLC as per pharma guidelines. 3. Knowledge of caliberation and operations of all equipments like balance, ph meter, in analytical opeartion. 4. good knowledge of sample preperation as per GLP. 5. Knowledge of retreival and storage working standards and columns. 6. Handling of final compilation of raw data, chromatographic data complying with GLP requirements. 7. Recording all analytical activities, approximately in respective raw data forms. 8. knowledge of preperation of gene...

Preferred candidate profile - Male Role & responsibilities - 1 .Knowledge in various dosage forms especially Solid- Oral dosage form- tablets, capsule and pellets as both immediate release and modified release. 2 .Familiar with Pharmacokinetic Principles, ICH guidelines and regulatory requirement (US/EU/ROW). - Formulation development for Regulated Market like US,EU and ROW countries - Preformulation, prototype development, lab scale stability studies. - Knowledge on QbD development. - DOE knowledge preferred. - Technology transfer document preparation like SAP code, MFC, PVP, HTP and SSP. - Technology Transfer at plant level.

Responsibilities: Conduct routine and non-routine chemical and instrumental analysis of raw materials, in-process samples, and finished products. Ensure compliance with cGMP, GLP, and regulatory guidelines. Review and approve analytical documents, test reports, and batch manufacturing records. Maintain accurate laboratory documentation and ensure timely reporting. Oversee calibration, validation, and proper functioning of lab instruments (HPLC, UV, FTIR, etc.). Coordinate with the Quality Assurance and Production teams for smooth operations. Participate in audits and inspections conducted by regulatory authorities. Provide technical guidance and training to junior chemists and lab staff. Ens...