241 Bulk Drugs Jobs - Page 4

ONLY FOR MALE CANDIDATES ROLES: Executives and chemists SALARY: 2 lpa to 6.5 lpa Please carry last 3 months pay slips,6 months bank statements,CTC details and updated CV. Desired Candidate Profile * Conduct quality control tests on bulk drugs using HPLC, GC, and other relevant methods. * Develop and implement quality assurance procedures for API manufacturing processes. * 2-7 years of experience in API production or related field. * Proficiency in HPLC, GC, and other analytical techniques for testing bulk drugs. * Experience with QA management systems and implementation of quality control procedures.

Job Title: API Marketing (West India) Location: Mumbai / Ahmedabad / Bangalore (as per candidate preference) Experience: Minimum 3 years in API Bulk Drug Sales & Marketing Job Description: We are looking for a passionate and result-oriented professional to join our API Marketing team for the West India region (Mumbai & Ahmedabad markets) . Key Responsibilities: Drive sales of APIs (bulk drugs) in the West India market. Identify, develop, and manage new and existing customer relationships. Achieve sales targets through effective market penetration and business development. Handle negotiations, contracts, and pricing discussions with clients. Coordinate with internal teams (R&D, Production, QA...

Tall Storeys Collaborative is looking for Architects (Junior - Intermediate) to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

Hiring for Process Safety Executive for the leading Pharma API mfg. company at Navi Mumbai location Designation: Process Safety Executive Experience: 2+ Years Education: B.E. Chemical Location: Navi Mumbai Division: API Process safety, HAZOP Interested candidate can share their CV on hr3@sarthee.com or call on 9033033650

1. Plan and execute production schedules, 2. Supervise granulation, blending, compression, and coating operations, 3. Strong knowledge of pharmaceutical manufacturing processes (API, DC granules, FDF), regulatory standards (GMP, WHO, USFDA)

We are looking for passionate and dedicated Quality Control (QC) professionals with experience in the API / Pharmaceutical industry to join our team at Dahej. 1 to 8 years experience in QC

We are hiring experienced professionals for the API Production Department. The ideal candidate will be responsible for overseeing and executing all production-related activities in compliance with cGMP guidelines and regulatory requirements Role & responsibilities Last 3 Months' Payslips Last 6 Months' Bank Statement Current CTC Details Updated CV / Resume 10,000 for immediate joiners Preferred candidate profile API Production Department Preferred candidate profile

Area Of Responsibility - To review quality and manufacturing end data for various in-house developed APIs for regulatory adequacy for compilation of Drug Master Files/Registration Dossiers, Amendments/Variations, Technical Data Package/Open Parts of DMFs for In-House developed APIs and their updation to meet current regulatory requirements. - To review outsourced intermediates and APIs for regulatory adequacy to support Procurement Team in vendor selection and DF-Regulatory for ANDA/MA submission. - To coordinate & support Chemical Research Department, Analytical Department and Manufacturing locations in generating data as per the requirements of regulatory agencies for regulatory submission...

We are looking for an exp. and detail-oriented Procurement Manager –Raw Material (API) to optimize the procurement of Active Pharmaceutical Ingredient (APIs) for our contract manufacturing operation. Candidate must have deep Pharma industry knowledge

Role & responsibilities Provide Support to routine analysis of API Synthesis R&D and Stability samples. Documentation of Daily analysis in corresponding product LNB. Development of analytical methods for drug substances, raw materials and intermediates. Perform AMV, AMDR, AMT activities. Preparation of Analytical method validation / AMT protocol & report. Preparation of Tentative STP/MOA during Development. Trouble shooting at the time instrument operation and analytical method related problem. Preparation of COA, MOA and provide to LIMS. HPLC and GC Calibration and Documentation and provide GLP for the same. Prepare method development report. Analytical method transfers and Documentary Meth...

Junior Executive/ Executive - Production (API) Job Criteria: B.E-B.Tech (Chemical Engg.) / M.Sc./B.Sc. 1 to 5 years of experience Job Role: Ensure that the products are manufactured as per the cGMP and handle critical equipment like reactor, centrifuge, blender, sifter, multi-mill, etc. Maintain documentation as per regulatory requirement like change control, deviations. Highlight technical problems and take corrective actions, and maintain safety practices. Technical Officer/ Junior Executive/ Executive-Production+Packing (OSD) Production Job Criteria: M. Pharm/B. Pharm/DME/ITI 2 to 7 years of experience Job Role: Manage granulation, compression, coating, pelletization and capsule filling a...

Location:-Dahej (Bharuch) Industry:- Agro chemical Qualification:-Bsc /Msc chemistry/ Dip chemical *Experience:- Fresher * *Post :-Plant operator * Job time:- 8 hrs shift duty Salary:- 17400 ctc Facility:- travel + canteen Job type:- Permanent Required Candidate profile Perform In-Process Quality Control (IPQC) during tablet MFG. compliance with cGMP,coordinate with QA, QC, and Maintenance.

We are hiring experienced professionals for the API Production Department . The ideal candidate will be responsible for overseeing and executing all production-related activities in compliance with cGMP guidelines and regulatory requirements Role & responsibilities Last 3 Months' Payslips Last 6 Months' Bank Statement Current CTC Details Updated CV / Resume 10,000 for immediate joiners Preferred candidate profile API Production Department .

2-4 years in API. Exp. in GMP & Safety in handling production equipment Operate the various equipment under supervision Knowledge of DCS & ERP Exp. of Hydrogenation Exp. of Distillation Column share your cv on careers@nglfinechem.com Required Candidate profile should have Experience in Hydrogenation or in Distillation Column

Role & responsibilities To Follow Safety Instruction & Norms During Manufacturing. Batches Processing as Per SOP and prepare BMR . In Process Sampling For Reaction Monitoring/In Process Drying. Cleaning Manufacturing Area As Per Respective SOP. Movement, Labelling & Proper Segregation Of Materials As Per SOP & BMR. Recording Filter Differential Pressure Record Of Area, Balance Verification & Calibration Record & Other All Related Document To Production. Report To Shift Manager If Any Kind Of Deviation/Unsafe Working Condition Is Observed. Log Book Updated as per all Equipment operating Procedure. Document like BPR, Equipment Log Book, ECR, Calibration of weight balance. Working on a product ...

Responsible for nutrition addition, harvesting, washing, homogenization, spray drying, packing. Shall check the maintenance of the department, premises, and equipment as per SOP and GMP norms.

Roles and Responsibilities Conduct analytical research, including method development, validation, and sample analysis to support regulatory submissions. Collaborate with cross-functional teams to ensure compliance with cGMP guidelines during API manufacturing process development.

Develop and execute comprehensive marketing plans and strategies. Manage the marketing budget and allocate resources effectively. Conduct market research to identify new growth opportunities. Analyze consumer behavior and market trends to inform.

ONLY FOR MALE CANDIDATES Immediate requriment for QC AND EHS departments with 2 to 5 yrs Roles and Responsibilities Conduct analytical method validation, stability analysis, and sample testing for bulk drugs and APIs. Ensure compliance with GLP guidelines and maintain accurate records of test results. Develop and execute experimental protocols for new product launches or changes in existing products. Provide technical support to production departments on quality-related matters.

Oversee and manage daily production activities Ensure adherence to cGMP and EHS guidelines Coordinate with cross-functional teams for smooth operations Optimize processes for efficiency and quality

Should have experience into API Purchase that to into RM & PM

Execute and monitor production activities as per SOPs and cGMP guidelines. Ensure compliance with safety, health, and environmental regulations during production operations. Handle day-to-day production activities for API and intermediate products. Required Candidate profile B.Sc. / M.Sc. (Chemistry) / B.E / B.Tech. (Chemical Engineering) with 2 to 7 years in API or Intermediates Manufacturing Strong knowledge of API / Intermediates manufacturing processes.

Oversee and manage daily production activities Ensure adherence to cGMP and EHS guidelines Coordinate with cross-functional teams for smooth operations Optimize processes for efficiency and quality

Academic Background and Experience: Academics - M.Sc. in Chemistry Experience 13 to 25 years Key Skills Regulatory Guidelines Knowledge, Documentation, Problem-solving, Strong Communication, Collaboration, Organization Skills Role & responsibilities Review documents from various departments to compile regulatory submissions. Oversee Drug Master Files (DMFs) for submission to regulatory authorities, including updates, amendments, and revisions as required. Draft both the applicant and restricted parts of DMFs to ensure regulatory compliance. Coordinate with cross-functional teams (CFT) to address deficiencies and feedback from regulatory authorities and customers. Conduct CFT meetings to ensu...

To implement cGMP QC labo. pharma regulatory standards.• FDA of small molecule & analytical methods/equipment: GC, LC, ICP-MS, KF, LOD, ROI, optical rotation, RI, stability analysis, light obscuration, potentiometric titrations, spectroscopy