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Production Manager - Ankleshwar, India - Miracle Hub
Description
Required PharmaceuticalProduction FormulationSpecialist
Location:
Ankleshwar GujaratIndia
IndustryPharmaFormulation
Musthave 35 Years of Experience (Must be from FormulationIndustry)
JobDescription:
Asa Pharmaceutical Production Formulation Specialist you will play apivotal role in the development and production of pharmaceuticalformulations.
Your responsibilities will encompass a range of tasksessential to the formulation process ensuring the quality safetyand efficacy of pharmaceutical products.
This position requires adeep understanding of pharmaceutical sciences formulationtechniques and regulatoryrequirements.KeyResponsibilities:
FormulationDevelopment: Lead the formulation developmentprocess for pharmaceutical products including solid dosage forms(tablets capsules) liquid dosage forms (syrups suspensions)semisolid dosage forms (creams ointments) and sterile formulations(injectables). Collaborate with crossfunctional teams to design andoptimize formulations that meet target productprofiles.
ProcessOptimization: Optimize formulation processes toimprove efficiency scalability and product quality. Implement bestpractices and innovative technologies to enhance manufacturingprocesses and reduce productioncosts.
QualityAssurance:
Ensure compliance with regulatorystandards and quality control requirements throughout theformulation process. Conduct thorough quality assessments andperform inprocess checks to maintain product consistency andadherence tospecifications.
Documentationand Reporting: Maintain accurate documentation offormulation development activities including formulation recordsbatch records and technical reports. Prepare comprehensive reportssummarizing formulation development activities results andrecommendations for furtheraction.
Troubleshootingand Problem Solving: Identify and resolveformulationrelated issues that arise during production ensuringminimal impact on manufacturing timelines and product quality.
Implement corrective and preventive actions to address root causesof deviations andnonconformances.
RegulatoryCompliance: Stay abreast of regulatory guidelinesand requirements governing pharmaceutical formulation developmentand production. Ensure all formulation activities comply withcurrent Good Manufacturing Practices (cGMP) InternationalConference on Harmonisation (ICH) guidelines and other relevantregulatorystandards.
Collaborationand Communication: Collaborate effectively withcrossfunctional teams including R&D regulatory affairsquality assurance and production to align formulation activitieswith overall business objectives. Communicate effectively withstakeholders to provide updates on formulation development progresschallenges andsolutions.
Qualifications:
Bachelors or Master s degree in Pharmacy Pharmaceutical Sciences Chemistryor related field.
Proven experience inpharmaceutical formulation development preferably in amanufacturing environment.
Strongunderstanding of pharmaceutical formulation principles techniquesandtechnologies.
Knowledgeof
cGMP regulations ICH guidelines and otherregulatory requirements applicable to pharmaceuticalformulation.
Excellent problemsolving skillsand attention to detail.
Effectivecommunication and interpersonal skills with the ability tocollaborate across functional teams.
Abilityto work independently and manage multiple projectssimultaneously.
Proficiency in data analysisdocumentation and reportwriting.
formulation,pharmaceuticalsciences,productquality,manufacturing,communication