266 Tablets Jobs - Page 2

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.

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

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

Sr Production Officer -3-10Years in Effervecscent Tablets-Granulation, Compression and Coating plan,CGMP etc with salary pack of upto 7LPA and Dahej Location.

Preferred candidate profile Having IPQA experience in manufacturing & Packing Min 2 yrs of experience in Tablet/Capsule(OSD) Interested candidates may share profile at hr.plant@zuventus.com

As a Senior Executive Technology Transfer at Bluefish Pharmaceuticals, you will contribute to the Technology Transfer Department function objectives. Reporting to the Senior Manager-Formulation Development, your responsibilities will include executing technology transfer, site transfer, alternate vendor development, and troubleshooting activities for tablets, capsules, and pellets. You will evaluate technical queries, address issues faced during commercial batches, and ensure regulatory compliance. Key Responsibilities: - Execute technology transfer, site transfer, alternate vendor development, life cycle management, and troubleshooting activities for tablets, capsules, and pellets. - Evalua...

Role & responsibilities A Packing Head in the nutraceutical industry oversees all packaging operations, ensuring that products are packed efficiently and in compliance with strict quality and regulatory standards . The role involves strategic planning, team leadership, and process optimization to meet production targets and maintain product integrity. Core responsibilities Operational management: Lead and supervise the packaging department's daily activities, including planning and executing packing schedules to meet production demands. Quality and compliance: Enforce and uphold Good Manufacturing Practices (cGMP), FDA, and other relevant regulatory requirements. Review and approve batch pac...

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 / ...

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 Complete Analysis of various raw materials, In-process, Drug substance and finished Products in line with Pharmacopeia method and in-house Specification and test procedures. Change Control, Deviation, Root Cause investigation, CAPA, OOS, OOT, Incidence Calibration of Instruments HPLC , UV-Visible Spectrophotometer, pH Meter,KF Titrator, weight balance. Working standard preparation as per SOP. Ensure the timely analysis of samples GLP, GMP, GDocP (With respect to Regulatory Guidelines) Function in details of various Section of QC/QA(Eg.Raw Material, Finished Product,Stability Study etc. Data Integrity 21 CFR Part 11 Qualification, Calibration, Validation. Maintaining t...

Role & responsibilities: 1) VIP support engineer will own the reported incident, work with respective IT or outside IT teams to resolve the issue on topmost priority. 2) VIP support engineer should be thorough technical expert who can resolve most of the issues by him/herself, specially on MAC books, Smart phone, Tablets, iPhone devices and related software. 3) Should know WAN & Wifi technology for end user configuration and direct coordination with client backend team 4) Should address issues with permanent solution. Not >5% VIP issue should go to PM or anyone else in a month. VIP engineer must resolve it by himself / herself. 5) For VIP & VVIP user, no tolerance for ticket reopening and sh...

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 (...

Role & responsibilities : 1 To perform Operation activity of equipment and instruments as per SOP. 2. To affix the status label to equipments, instruments and IPC at each and every processing stage 3. To operate the equipment in safe and effective manner for production processing. 4. To follow and adhere to GDP and cGMP practices. 5.Inspect equipment to identify any replacement, and repairs. 6. Ensure that the equipment are maintained in good and safe working condition. 7. To Perform regular equipment maintenance to ensure production capacity and quality. 8. Identify and report unsafe operations and near misses to supervisor immediately. 9. Perform the activity as per SOP and instruction giv...

Job Description Line clearance in dispensing and production area. To perform in-process sampling, testing and document the observations. To handle IPQA activity in warehouse and production area. Review of BMR, process documents etc. APR Preparation. To ensure timely validation of production equipment w.r.t. process, cleaning and to collect samples for cleaning validation etc. To follow GMP and ensuring timely documentation of dispensing, manufacturing and packing activity. To identify problem areas in manufacturing and report to Head QA.

We are looking for a highly competent and experienced Senior Formulation & Development (F&D) Chemist with extensive hands-on exposure in the development of solid oral dosage forms, specifically tablets and pellets. Experience on Pellets is Must!! Office cab/shuttle Health insurance Leave encashment Gratuity Provident fund Job/soft skill training Annual bonus

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...

We are looking for Lead in Production (OSD plant), who can take care of all the activities in production includes Packing. Must have exp in OSD Must have exp in ROW Preferable Locals

For the position of Sr. Product Manager-Identification Management and Mobility We are looking for a dynamic Product Manager to lead the strategy, development, and execution of Identification Management and mobility products. You will be responsible for driving innovation across biometric authentication devices, secure identity systems, access control solutions ecosystems. The ideal candidate has a deep understanding of identity technologies, embedded systems, and enterprise security requirements. Location: Bangalore,Mumbai Key responsibilities include: Strategic responsibilities : Conduct primary and secondary research; generate and qualify market analytics/research & drive the execution of ...

Role Overview: As a Field Executive at Kadence International, your main responsibility will be to collect accurate data from respondents through face-to-face or telephonic interviews. You will need to ensure timely and quality fieldwork execution as per project requirements. Key Responsibilities: - Conduct primary data collection through surveys, interviews, and observations in the field (door-to-door, retail, public places, etc.). - Ensure proper sampling and adherence to research protocols and guidelines. - Maintain accurate and complete records of interviews and respondent information. - Liaise with the field supervisor and project manager for updates and instructions. - Handle survey too...

B.Pharm / M.Pharm with 2 to 6 years of experience in Regulatory Affairs. To Review dossier prepared by executives & trainees & submit to client along with artworks for countries like ASIA, LATAM & ROW Market. Follow up with FRD & Microbiology Dept. Required Candidate profile Ensure that a company's products comply as per current ICH & Country Guidelines. To work on Renewals of Registration Certificate for countries. Courier of Legalized Documents such as COPP, FSC, POA. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Dear Candidate, Greetings from Intas Pharmaceuticals Ltd.! We are pleased to invite you to a walk-in interview for positions in our Manufacturing/Production (Solid ) department at our SEZ facility in Ahmedabad. If you are looking for a rewarding career with one of India's leading pharmaceutical companies, we welcome you to be part of our journey of growth, innovation, and excellence. Vacant Position: Senio Officer/ officer /Technician/ associate - Solid Oral Production Experience: 3 to 10years Qualification: B. Pharmacy/ M. Pharmacy/ITI / Diploma Job Description: handling manufacturing operations Equipment handling and maintenance GMP & Documentation Operate and ensure proper maintenance of ...

microbiology responsibilities include performing microbiological testing on raw materials, in-process components, and finished products to detect and control contamination. Required Candidate profile Conducting environmental monitoring of manufacturing areas, and ensuring product sterility and purity

ITI Fresher - Coating Operator RA - 4 to 6 Years ECTD Experience Compulsory R&D - Pharma Factory - 5 TO 10 YR - Male / Female Send CV on sdpbharuch@gmail.com with Subject: Formulation Panvel Share with Friends No Job Charges Required Candidate profile Interview Venue: SDP HR SOLUTION 611, Golden Square Beside DMART Near ABC Circle Bholav, Bharuch - 392001 No Interview & Joining Charges Share with your Friends Bring Your Friends along with You Perks and benefits Transportation, Canteen, Medical, ESIC