15 Pharmaceutical Formulation Jobs

We are looking for dynamic candidate for QA team.Expertised in pharmaceutical formulation unit catering to regulated markets.Cephalosporin formulations preferred.Oversee finished product quality systems in compliance with cGMP

Prepare And Process Requisitions - Purchase Order For Supplies Maintain Records Of Goods Ordered And Received Identify the Best Vendors for Materials Supply - Vendor Development And Management Compare Different Quotation for Quality And Price Required Candidate profile Purchase Manager Must be capable to handle department independently Executive - prepare reports on purchases, including cost analyses , Vendor Selection To Track Orders And Ensure Timely Delivery

As a member of Surmount Laboratories Pvt. Ltd., your role will involve handling inventory management tasks, such as issuing materials with online records and maintaining stock. Your expertise in Pharmaceutical formulation will be crucial in contributing effectively to the team. Key Responsibilities: - Handle inventory management, including issuance of materials with online records and stock maintenance. - Utilize your knowledge and experience in Pharmaceutical formulation to contribute effectively to the team. Qualifications Required: - B.Sc. or B.Com degree. - Minimum of 1 to 4 years of relevant experience. - Previous experience in Pharmaceutical formulation is preferred.,

You will be responsible for ensuring the quality of pharmaceutical formulations in the QA department. Your key responsibilities will include: - Minimum 3 to 5 years of experience in QA department of pharmaceutical formulation - Knowledge of In-Process Quality Assurance (IPQA) is required - Familiarity with Good Manufacturing Practices (GMP) - Preferable to have experience in Regulatory work No additional details of the company are mentioned in the job description.,

Role Overview: As an IPQA Officer/Trainee at Axilix Drugs & Pharma, you will have the opportunity to positively impact health around the world. If you are just beginning your career, you will find opportunities to broaden your skill base through learning and development programs. By joining us, you will become part of a leading sterile pharmaceutical formulation manufacturer. Key Responsibilities: - Ensure quality assurance in pharmaceutical manufacturing processes - Conduct in-process quality checks to ensure compliance with standards - Document and report any deviations or non-conformances - Assist in investigations and root cause analysis of quality issues - Support continuous improvement...

Role Overview: Sandoz is undergoing an exciting phase as a global leader in providing sustainable Biosimilar and Generic medicines. As the organization progresses on a new and ambitious path, you have the opportunity to lead the Large Molecules & Injectables platforms MS&T organization. Your role involves maintaining and enhancing scientific oversight of manufacturing processes, technical changes, and ensuring product stewardship across process units and functions at the platform. Key Responsibilities: - Act as the Single Point of Contact (SPOC) for Global MS&T head, Large Molecules & Injectables platform QA head, site heads, and site MS&T heads for all MS&T related topics. - Set objectives ...

As a candidate for the position at Surmount Laboratories Pvt. Ltd., you will be responsible for managing day-to-day production activities in the field of Pharmaceutical formulation. Your key responsibilities will include: - Demonstrating a minimum of 3 to 4 years of experience in Pharmaceutical formulation - Possessing knowledge of Good Manufacturing Practices (GMP) - Managing day-to-day production operations - Providing regular reporting with online documents to meet regulatory requirements Qualifications required for this role include: - B.Pharm / M.Sc. / B.Sc. degree - Minimum of 3 to 4 years of experience in the field of Pharmaceutical formulation - Knowledge of Good Manufacturing Practi...

You should have a minimum of 10 to 15 years of experience in the QA department of Pharmaceutical formulation. Your responsibilities will include having knowledge of regulatory requirements and documentation such as water validation, process validation, incident management, change control, CAPA, etc. It is essential for you to be capable of providing training to junior staff. Familiarity with WHO GMP/cGMP is a requirement. The ideal candidate will hold an M.Pharm/B.Pharm/M.Sc. degree.,

Detailed Job Role Lead research and development of new pharmaceutical formulations, conduct experiments and improve existing products. KRA (Key Responsibility Areas) Research planning, project execution, patent filings, collaboration KPI (Key Performance Indicators) Milestone achievement, patents filed, publication count, project timelines Job Summary: We are seeking an innovative R&D Scientist to lead the research and development of new pharmaceutical formulations, conduct experiments, and improve existing products. The ideal candidate will contribute to product innovation, scientific publications, and patent filings while ensuring timely project execution. Key Responsibilities: Design and ...

Detailed Job Role Lead research and development of new pharmaceutical formulations, conduct experiments and improve existing products. KRA (Key Responsibility Areas) Research planning, project execution, patent filings, collaboration KPI (Key Performance Indicators) Milestone achievement, patents filed, publication count, project timelines Job Summary: We are seeking an innovative R&D Scientist to lead the research and development of new pharmaceutical formulations, conduct experiments, and improve existing products. The ideal candidate will contribute to product innovation, scientific publications, and patent filings while ensuring timely project execution. Key Responsibilities: Design and ...

You should have a Bachelor's or Master's degree in Pharmacy or Science with a minimum of 3 to 4 years of experience in Pharmaceutical formulation. It is essential to have knowledge of Good Manufacturing Practices (GMP). As a candidate, you will be responsible for managing day-to-day production activities and providing regular reports with online documentation in compliance with regulatory standards.,

You should have a minimum of 10 to 15 years of experience in the QC department of Pharmaceutical formulation. Your responsibilities will include troubleshooting sophisticated instruments such as HPLC, IR, UV, etc. It is essential to have knowledge of calibration, validation of instruments, and system management. You will also be responsible for managing sample inventory, conducting analysis, and ensuring timely release of samples. A degree in M.Pharm, B.Pharm, or M.Sc. is required for this position at Surmount Laboratories Pvt. Ltd.,

You will be required to have a B.Sc. / B.Com degree along with a minimum of 1 to 4 years of experience. Your responsibilities will include managing inventory, issuing materials with online records, and maintaining stock. Prior work experience in Pharmaceutical formulation will be preferred.,

08 to 12 Years Experience of Pharmaceutical Formulation Industries We are seeking an experienced and proactive Maintenance Officer to join our Formulation manufacturing facility. The ideal candidate will be responsible for overseeing the maintenance and reliability of equipment, facilities, and utilities in the factory. The role involves developing and implementing preventive maintenance programs, troubleshooting issues, and ensuring the uninterrupted operation of production processes.

Expertise in API / Formulation regulatory compliance across EU/ROW regions Sound knowledge of Drug Substance control strategies Familiarity with global regulations: ICH, FDA, EMA, USFDA etc Skilled in responding to Ministry of Health (MoH) queries Required Candidate profile M. Pharma / B. Pharma / M.Sc / B.Sc with 7 to 15 Years Experience Deep Knowledge of Regulatory Affairs Compliance And Procedures Must be able to work independently And Head Team of junior Officers