225 Capsules Jobs - Page 4

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.

Exciting Career Opportunities at Natco Pharma Limited for the following requirements Open Positions: Operators & Supervisors OSD Production & Packing (Onco & Non-Onco) Experience: 0 to 8 Years (Freshers graduated in 2024/25 are eligible) Qualifications: I.T.I / Diploma / B. Pharmacy Key Responsibilities: Operate equipment's in Granulation (RMG, FBD, ACG, GEA), Compression (GEA, Sejong), Coating (NEOCOTA), Capsule Filling (Bosch, MG02), Blister Packing (CAM NMX, HV1, BQS, IMA/ACG), and Bottle Packing (CVC, Optel) lines. Supervise production lines, including Granulation, Compression, Coating, and Packing (Blister/Bottle). Good verbal and written English communication skills 2. Operators & Supe...

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...

Job Title: Validation Specialist Job Grade: G11A/ G10 Function: Global Information Technology Sub-function: Manufacturing & Quality IT Manager’s Job Title: Validation Lead Skip Level Manager’s Title: Head SGO IT India Function Head Title: Global Chief Information Officer Location: Mohali 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 you ‘Take charg...

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...

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

ITI AOCP / DIPLOMA/ BE CHEMICAL / LACP / BSC / MSC CHEMISTRY Plant: PHARMACEUTICAL / CHEMICAL Location: SURAT / ANKLESHWAR Qualification: AOCP / LACP / CHEMISTRY / CHEMICAL Experience: 0 to 2 Years Required Candidate profile Job Time: 9 AM –6 PM Salary: – 15 K TO 45 K

Job Title : Infrastructure Lead Job Grade: G11A Function: Global Information Technology Sub-function: Manufacturing & Quality IT Manager’s Job Title: Manager-2 Skip Level Manager’s Title: SGO India Cluster 2 IT Lead Function Head Title: Global Chief Information Officer Location: Baska No. of Direct Reports (if any) 0 Date of Joining: 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 ...

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...

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 ...

Topical Powder Manufacturing, Filling & Sec.Packing Activities oral Powder Manufacturing, Filling and Sec. Packing Activities Batch Initiation Manufacturing Secondary packing & tertiary Packing Share resume to hrd@stedmanpharma.com, Call - 7904827192 Required Candidate profile B.pharm Looking for candidate with Pharma formulation experience

Stedman Pharmaceuticals is looking for a dynamic and experienced candidate for the Quality Control (QC) department with hands-on experience in Analytical Method Validation for various dosage forms. Share your Resume to hrd@stedmanpharma.com

Job Title: AQA Quality Assurance (LCMS, GCMS, ICPMS) Company: Energon Labs Location: Hyderabad Experience Required: 2 - 6 years Employment Type: Full Time, Permanent Role Overview We are seeking experienced professionals in Analytical Quality Assurance (AQA) to review and ensure compliance in analytical data generated through LCMS, GCMS, and ICPMS techniques. The role requires a keen eye for detail, strong knowledge of analytical methods, and the ability to uphold the highest quality standards. Key Responsibilities Review analytical data for LCMS, GCMS, and ICPMS techniques. Conduct electronic audit trail reviews for analytical instruments and ensure compliance. Review Analytical Method Vali...

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.

Role & responsibilities To ensure GMP practices are followed during various stages of production activities of finished drug product. To perform in process checks in Tablets/Capsule/Ointment/ Liquid/Dry powder To ensure various operations are complying as per SOP. Daily & Monthly calibration of IPQC instruments. Sampling of Control and Stability samples. To ensure that the facility is maintained in a clean and sanitary conditions. In-process checks during dispensing & secondary packing activities. To ensure timely sampling of finished products, control samples, validation samples & stability samples. To monitor Dispensing of raw material and packing material required for the manufacturing of...

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...

Urgent Hiring QC Executive (OSD / Formulations) | Immediate Joiners / 1 Month NP Preferred Location: Karkapatla, Hyderabad Industry: Pharmaceuticals (Tablets & Capsules OSD) Shift & Timings: Day Shift | 6 Days Working | only MALES Role Overview: We are looking for a QC Executive with hands-on experience in OSD/Formulations (Tablets & Capsules). The role involves ensuring quality compliance in production processes and maintaining strict adherence to industry standards. Key Responsibilities: Conduct quality control tests for OSD formulations (tablets & capsules). Review and analyze in-process and finished product samples. Ensure compliance with regulatory standards and SOPs. Maintain accurate ...