Pharmaceutical Production Jobs

We are looking B.Sc(Chemistry) freshers in Vijayawada Location.Skiil set:Pharmaceutical Production,Pharma,Life Sciences.Knowledge of GMP, GLP, and regulatory requirementsStrong attention to detailGood documentation practices (GDP)Problem-solving and analytical skillsTeamwork and communication skillsBasic knowledge of production equipmentImmediate Joiner Preferred.

Jr Officer Production - 1 Post - Bsc / B Pharm - Fresh or 1 to 2 Year Experience - Urgent OpeningJunior Officer-ProductionEducation: B Sc, B PharmaExperience: Fresher to 2 YearsImmediate JoiningJob Location: Palghar East PalgharSalary: 1.5 LPA to 2.5 LPAMost Urgent Opening

We are seeking dedicated API Plant Operators for our facility in Nandesari GIDC, Vadodara. The ideal candidates will support manufacturing operations, ensuring strict adherence to GMP and SOP guidelines. This full-time position involves operating various equipment, monitoring process parameters, and maintaining accurate documentation. It's an excellent opportunity for junior and trainee operators, as well as freshers with relevant qualifications. Join our team to kickstart a rewarding career in the API and pharmaceutical industry

We Arew Hiring On Urgent Base for Our Client Base Pharma Company At Ankleshwar Gidcpost : Production Executiveeducation: Bpharm, Mpharm, Bsc Mscexperience : 5-7 Year in Pharmalocation : Ankleshwar Gidc Ankleshwar Gujaratsalary : 7-10 Lpa Depend On Interview

WE ARE HIRING PRODUCTION OFFICER FOR PHARMA COMPANY POST : PRODUCTION OFFICEREDUCATION : BPHARM, MPHARMEXPERIENCE : 1-3 YEARLOCATION : MANJUSAR GIDC VADODARASALARY : 20-30 K DEPEND ON INTERVIEWAPPLY : tpo.vp2017@gmail.comCALL : 8306133342

WE ARE HIRING ON URGENT BASE IN PHARMA COMPANYMAINTANANCE PRODUCTION MANAGERRELEVANT EDUCATION AND EXPERIENCE MUST REQUIREDLOCATION : RANIYA MANJUSAR VADODARASALARY : NO BAR FOR RIGHT CANDIDATEFULL TIME LONG TERM POSITION REQUIREDAPPLY : tpo.vp2017@gmail.comCALL : 8306133342

Required Research Scientist Formulation & development In R&D For reputed Pharma Company At Ankleshwar .Please. your resume which must have your Cell number. All resumes and employment-related correspondence will remain confidential.

JOB Profile - ADL (Analytical & Development Officer)Our Client . is looking for profiles to fill the position of Chemist (Analytical Development), contributing to the accomplishment of the Analytical development function objectives. The position will report to Quality Control and Analytical Development Manager. The role would be involved not limited to below mentioned areas:1. Execute Analytical Method Development activities of drug products.2. Execution of Analytical Method validation activities for drug products as per the regulatory requirements.3. Trouble shooting related to Testing methods, Stability studies, test results and designing of additional experimentations as necessary.4. Preparation and review of Specifications, Method of analysis procedures and Analytical development reports.5. To identify, develop and qualify/validate methodology suitable for the product. 6. Preparation of analytical technical documents for dossier / Technology transfer executions / Regulatory submissions of projects.7. Assessment & coordination on regulatory deficiencies. 8. Assisting with analytical requirements in finalization of project costings.9. Any other specific functional activities defined on case to case basis

Urgent requirementProduction ChemistPharmaceutical CompanyEducation: B.Sc, M.Sc, B Pharma, M PharmaSalary: Starting: Rs. 11,000/- PMLocation: Hamrapur WADA-PalgharImmediate Joining shall be preferred

Urgent RequirementProduction OfficerAPI Pharmaceutical CompanyJob Location: Boisar, Palghar MHSalary Rs. 3 LPA to 3.5 LPAEducation: B.Sc, M.Sc,

Urgent RequirementProduction OfficerAPI-Pharmaceutical companyJob Location Boisar (Palghar)Salary Rs 2.5 LPA to 3.50 LPAExperience: 3 to 4 Years

Job Title: Production Shift In-charge Location: Nandesari, VadodaraPositions: 2 Education: B.Sc. / M.Sc. / Diploma in Chemical Engineering.Experience: 5-10 years of working experience in an API (Active Pharmaceutical Ingredient) and intermediate plant, with a strong understanding and practical application of GMP (Good Manufacturing Practices)Job Summary:We are seeking a highly motivated and experienced Production Shift In-charge to join our team for Pharmaceutical Company. The successful candidate will be responsible for overseeing and managing all production activities during their assigned shift, ensuring efficient operation, adherence to quality standards, and compliance with all safety and regulatory requirements. This role requires a strong leader with proven experience in pharmaceutical manufacturing, specifically in API and intermediate production.Key Responsibilities:Shift Management: Lead and supervise a team of production operators and technicians during the assigned shift. Plan and organize daily production activities to meet targets and schedules. Allocate tasks and responsibilities to team members effectively. Monitor production processes and troubleshoot any issues that arise. Ensure smooth shift transitions and effective communication with incoming/outgoing shifts.Production Operations: Oversee the manufacturing of APIs and intermediates, ensuring processes are followed according to batch production records and standard operating procedures (SOPs). Monitor raw material consumption, in-process parameters, and finished product quality. Optimize production efficiency and minimize waste. Coordinate with other departments such as Quality Control, Quality Assurance, Maintenance, and Stores to ensure seamless operations.Quality and Compliance (GMP): Ensure strict adherence to Good Manufacturing Practices (GMP) and other relevant regulatory guidelines. Oversee the accurate and timely completion of all production documentation, including batch records, logbooks, and deviation reports. Identify and report any deviations, non-conformances, or quality incidents, and participate in investigations. Implement corrective and preventive actions (CAPA) as required. Ensure equipment and facility are maintained in a state of readiness and compliance.Safety and Environment: Promote and enforce a strong safety culture within the production area. Ensure all team members follow safety procedures and use appropriate personal protective equipment (PPE). Report any safety hazards or incidents promptly. Ensure compliance with environmental regulations.Team Development: Provide training and guidance to production operators and technicians. Foster a positive and productive working environment. Conduct performance evaluations and provide feedback to team members.Reporting: Prepare daily, weekly, and monthly production reports. Communicate production status, challenges, and achievements to management.Skills and Qualifications: Proven leadership and supervisory skills in a manufacturing environment. In-depth knowledge of API and intermediate manufacturing processes. Strong understanding and practical application of GMP, GLP, and other relevant pharmaceutical regulations. Excellent problem-solving and decision-making abilities. Strong communication (verbal and written) and interpersonal skills. Ability to work effectively in a fast-paced, dynamic environment. Proficiency in using relevant computer software for data entry and reporting. Ability to work flexible shifts, including nights, weekends, and holidays, as required.