13 Dry Syrup Jobs

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...

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

Oversee complete Production & Manufacturing operations at the Pharmaceutical Formulation Unit Ensure smooth execution of batch manufacturing for OSD (Tablets, Capsules, Dry Syrups) Ensure compliance with FDA regulations and GMP guidelines Monitor production efficiency, process optimization & manpower management Coordinate with QA, QC, and Regulatory teams for smooth operations Handle regulatory audits, validation, and documentation processes OSD Manufacturing Tablets, Capsules, Dry Syrups FDA Approval & Regulatory Compliance (WHO-GMP, Schedule M preferred) Production Planning & Process Optimization Team Leadership & Manpower Management

Roles and Responsibilities Assist in production packing activities such as blister packing, bottle packing, capsule filling, compression, granulation, tablet coating, and tablet manufacturing.

Role & responsibilities Lead formulation and development projects from concept through commercialization Design and optimize formulations to meet product specifications and regulatory requirements Manage and mentor a team of formulation scientists and technicians Collaborate with cross-functional teams including QA, QC, regulatory, and manufacturing Ensure timely completion of project milestones and deliverables Prepare technical reports, presentations, and documentation Stay updated on industry trends, regulatory changes, and best practices Qualifications Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or related field Minimum of 2-3 years of experience in formulation a...

Role & responsibilities We are seeking a diligent and experienced QA & QC & production. The successful candidate will Ensure that our products meet specified quality standards. This role involves managing both Quality Assurance ( QA ) and Quality Control (QC) processes, conducting inspections, and implementing improvements to maintain and enhance product quality. Expanding role in building a team of QA/QC executives. Salary Range: 15,000 to 25,000 (negotiable based on experience & skills) Experience: Minimum 2 years in QA/QC department of Tablet & Capsule or pharma manufacturing unit Preferred candidate profile Quality control analyst Responsible for testing and analyzing pharmaceutical prod...

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. Resume to hrd@stedmanpharma.com / 9786920463

Process Mechanical, Process Electrical, HVAC, Water System with WFI Knowledge, Utility Electrical (Chiller, DG, Air compressor, Heat pump, Boiler)

Role & responsibilities : Candidate should have experience in Primary/Secondary packing Key Skills: Bottle Packing CVC/Dry Syrup Packing Must have skills on Primary/Secondary are equipment operation and cleaning operation Trouble Shooting in CVC Bottle packing (Secondary) Key Skills: Blister Packing BQS & Elmach CAM & IC150 Cartonator (Automatic Machine) Track & Trace Work Location : UNIT V Jadcherla (80 km far from the Hyderabad) Interested one share there resume to : sharadha.b@hetero.com Contact Number: 9100408534/8121003471

We have been hired by a highly reputed and fast growing Pharma company to hire a "DGM - Formulation & Development' to be based at their plant located at Aurangabad . Details of the position are mentioned below: Role & responsibilities: Literature search/study and to prepare development trials strategies. Pre formulation study execution. Market/Innovator/reference product characterization. Execution and documentation of trial batches for prototype formulation development. Execution and monitoring of development stability studies. Execution of process optimization/scale-up batches. Technology transfer activities at site. Preparation/review of documents like BOM, MFR, compatibility study protoc...

Role & responsibilities We are seeking a diligent and experienced QA & QC & production. The successful candidate will Ensure that our products meet specified quality standards. This role involves managing both Quality Assurance ( QA ) and Quality Control (QC) processes, conducting inspections, and implementing improvements to maintain and enhance product quality. Expanding role in building a team of QA/QC executives. Salary Range: 15,000 to 25,000 (negotiable based on experience & skills) Experience: Minimum 2 years in QA/QC department of Tablet & Capsule or pharma manufacturing unit Preferred candidate profile Quality control analyst Responsible for testing and analyzing pharmaceutical prod...

Job Title: Senior Manager Formulation Development (Generic Finished Formulations) Department: Research & Development (R&D) Formulation Development Reports To: Head – Formulation Development / Vice President – R&D Job Purpose: To lead and manage the development of generic pharmaceutical finished dosage forms (oral solids, liquids, injectables, topical, etc.) from concept through scale-up, technology transfer, and regulatory submission. Responsible for ensuring robust, cost-effective, and regulatory-compliant formulations aligned with company strategy and market requirements. Key Responsibilities: Formulation Development & Optimization Lead the design and development of generic formulations fo...

Roles and Responsibilities Develop new markets for pharmaceutical products through business development initiatives in ROW Market. Identify potential customers, build relationships, and negotiate deals to increase sales revenue. Conduct market research to stay updated on industry trends and competitor activity. Collaborate with cross-functional teams to launch new products in international markets. Manage export documentation and logistics for pharmaceuticals. Desired Candidate Profile 5-15 years of experience in International Business Development (IBD). Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma). Strong understanding of formulations, solid orals, tabl...