1455 Formulation Jobs - Page 16

Job description Job Title PHARMA PRODUCTION HEAD FOR EXTERNAL PREPARATION (FDA APPROVED) Overview Experienced FDA approved Production Head for external preparation (PHARMA/DRUG) who can handle external preparations like 1.Ointments : Calcipotriol ,tacrolimus ,mupirocin,Clobetasol. 2.Creams : Bifoconazole, Ivermectin, Eflornithine, Ciclopirox Olamine, Azealic Acid. 3.Gels : Itraconazole, Nadifloxacin, Adapalene,Clobetasol & Ammonium Lactate. 4. Lotions : Tacrolimus, Methoxsalen, Amorolfine, Fusidic acid, Trioxsalen. 5. Solutions : Minoxidil, Finasteride, Procapil 6. Soaps : Permetherin, Clindamycin, Coal tar,Luliconazole, Clotrimazole 7. Dusting Powders: Ketoconazole, Fluconazole , Sertaconaz...

Job description: Job Title COSMETIC F&D AND PRODUCTION HEAD / DRUG BASE COSMETIC Overview Experienced Cosmetic manufacturing chemist who can handle cosmetic preparations like - Creams (Azelaic acid, Tranexamic acid, Glutathione, Hydroquinone, Kojic acid) Face serums (Azelaic acid, Tranexamic acid, Glutathione serum, Castor oil serum, Niacinamide serum etc), Hair serums (Procapil, Minoxidil, Biotin, Keravis, Anagain, Castor oil etc) Lip serum,Lip balm, Under eye serum,Face wash, Sunscreen, Creams, Gels, Lotions, Soaps etc. Skills and Qualifications Required Should have worked as a Cosmetic Manufacturing Chemist for 7+ years Previous work experience in Cosmetic Preparations mandatory Should be...

Execution of Production Process, Documentation Process, Conducting Process operations and maintaining BMR records. Utilization of Manpower and equipment capacity. GMP compliance in Manufacturing Department.

Develop and validate robust analytical methods for various aspects of peptide and complex injectable formulations, including: Purity determination Identity confirmation Quantification of degradation products Stability assessment Demonstrate expertise in relevant analytical techniques, including: High-Performance Liquid Chromatography (HPLC) Liquid Chromatography-Mass Spectrometry (LC-MS) Ultraviolet-Visible (UV/Vis) Spectrophotometry Gas Chromatography (GC) Particle size analysis In vitro release testing Perform thorough data analysis and interpretation, prepare comprehensive analytical protocols and reports, and contribute to regulatory submissions. Proactively identify and resolve analytic...

Product Selection/Opportunity Identification Review of patent & non-patent product literature to support product selection, Preparing & analyzing IP landscape to come up with launch scenarios and IP strategies Evaluation of possible invalidation grounds of identified patents Product Development Support Formulation evaluations and IP clearances Suggesting IP driven formulation approaches to R&D team IP updates Monitoring new/pending patent families/grants and timely updating changes in IP situation Monitoring pending litigation/new litigations and updating their influence on product development or launch Business Development Support Provide possible launch dates based on IP situation for diff...

Alembic Pharmaceuticals Hiring Project Management (AM / DM/Manager) Professionals Alembic Pharmaceuticals, with a 118+ years legacy in pharmaceuticals, is looking for a driven professional to join our Project Management team at the Corporate Office, Vadodara. We have 2 openings for candidates with expertise in Solid Orals Formulations and Parenteral experience Key Responsibilities: Coordinate with F&D, ADL, DQA, and IPR on formulation development and technology transfer status. Ensure timely availability of TTD documents and follow up on deliverables. Work closely with PPIC, SCM, and API teams for API/RM/PM readiness for exhibit and submission batches. Conduct regular plant visits to monitor...

Research & Development Management : Manage R&D projects from concept to commercialization, including formulation development for new products (e.g. skincare, haircare, oralcare, shavegel, etc) using raw materials like emulsifiers, preservatives, and active ingredients. Collaborate with cross-functional teams (e.g., production, marketing, and suppliers) to scale up lab prototypes to manufacturing levels, optimizing processes for efficiency, stability, and cost-effectiveness. Stay abreast of industry trends, scientific literature, patents, and emerging technologies (e.g., sustainable ingredients or clean beauty formulations); conduct research on raw material properties and consumer testing to ...

Roles and Responsibilities Conduct stability analysis, method validation, and OOS investigations to ensure product quality. Ensure compliance with regulatory requirements by maintaining accurate records and documentation. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Perform HPLC, GC, FP, and OSD testing as per SOPs.

Exp 2 yrs Exp in canada market Exp in formulation for 2 years

• Undertake experimental work in accordance with R&D Manager/Management to develop new products & improve functioning of existing products. • Research Product formulations & Properties of raw materials. • Establish Product Specifications & Procedures as required • Obtain Process Technology & Equipment information for Production. • Testing and evaluation of Raw Materials. • Undertake Day to day batch manufacturing required during lab scale development of existing as well as new products. • Formulate Product prototypes & evaluate them for Chemical & Physical Properties, performance & stability. • Develop Reports & Documents detailing Projects processes, result & conclusions. • Calibration of e...

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

To drive & execute the coal sourcing function effectively with proper planning, Liassioning and analysis of various sources of coal with better quality and optimized cost. ORGANISATION CHART Head Coal Sourcing KEY ACCOUNTABILITIES Coal Annual Operating Plan Provide inputs for Preparation of AOP to Head coal sourcing and Logistics. Review and implement the Coal AOP plans prepared by the Head Coal Sourcing / Head Operations Coal GCV: Responsible for controlling GCV between Loading Coal, Receipt coal and fired coal Responsible for coordinating with third party at Loading, unloading end and follow up for the results MIS related to GCV deviations Review parity sheets to evaluate landed cost of al...

To drive & execute the coal sourcing function effectively with proper planning, Liassioning and analysis of various sources of coal with better quality and optimized cost. ORGANISATION CHART Head Coal Sourcing KEY ACCOUNTABILITIES Coal Annual Operating Plan Provide inputs for Preparation of AOP to Head coal sourcing and Logistics. Review and implement the Coal AOP plans prepared by the Head Coal Sourcing / Head Operations Coal GCV: Responsible for controlling GCV between Loading Coal, Receipt coal and fired coal Responsible for coordinating with third party at Loading, unloading end and follow up for the results MIS related to GCV deviations Review parity sheets to evaluate landed cost of al...

As a Research Associate in R&D at Vilvah, a dynamic Direct-to-Consumer Ecommerce brand specializing in sustainable, safe, and natural skincare and hair care products, your role will involve focusing on the research, formulation, and development of high-quality products aligned with the clean beauty philosophy. Your responsibilities will include: - Researching current and upcoming consumer trends, new actives, ingredients, product formats, and packaging innovations. - Conducting bench-scale experiments for new product development and demonstrating product performance through standard protocols. - Building a comprehensive database from scientific literature, patents, competitor benchmarks, and...

As a Principal Project Engineer at Wood, you will play a crucial role in leading and coordinating life sciences projects in the pharmaceutical sector. Your responsibilities will include: - Leading and coordinating life sciences projects (API/Biotech and Formulations) from initiation to closeout, ensuring adherence to timelines and budget constraints. - Implementing best practices in project delivery for successful project outcomes. - Monitoring progress of work for life science projects and coordinating between multidisciplinary teams to ensure high-quality solutions aligned with industry standards. - Collaborating with clients to identify project goals, objectives, and key performance indic...

Hiring for a Well-Established MNC Pharma 2nd Largest in the Industry! Division : FORMULATIONS Department : Regulatory Affairs Qualification : M.Pharma-Pharmaceutics/Pharmaceutical Analysis/Regulatory Affairs/Quality Assurance/Pharmaceutical Technologies) Experience : 2 to 10 Years Work Location : Hyderabad No of Positions Vacant : 5 Key Responsibilities : PRE and POST APPROVALS : 1. Component with EU-Filing requirements with respect to Module 2 & 3 ability to independently and correctly review technical documents related to Quality Module 2. Well versed with EU- Regulatory guidance and Processes (i.e., Ability to understand and interpret technical expectations as per applicable ICH & EMEA gu...

Set up bolus compression machines acc. to production specifications, Adjust machine settings, Identify & report mechanical issue, Load raw materials (powder/granules) into the machine hoppers, Maintain accurate production logs.

Job Description Job Objective: To strategize, lead & integrate the manufacturing system so as to anticipate & deliver market requirements, maintenance of operational efficiencies whilst simultaneously introducing contemporary manufacturing practices & systems in a climate of continuous improvement Job Responsibilities Job Responsibilities: Production To lead production planning from the unit’s objectives and ensure that production happens on time and as per plan To ensure that volume production targets during season and non season is as per plans To plan the resources for production in relation to costs and productivity norms To benchmark and introduce contemporary manufacturing practices an...

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Injectable Manufacturing (Executive/Senior Officer / Officer) Experience - 02 to 08 Years Qualification - B. Pharmacy/ M Pharmacy / Msc / Bsc / Engineering - (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech QUALITY ASSURANCE IPQA (injectable) / QMS / Documentation (Officer / Senior Officer /...

Job Summary Roles & Responsibilities Review and approval of all analytical test data of Quality control. Review and usage decision of analytical reports in LIMS, Empower and SAP. Electronic signatures level-2 for chromatography data station (CDS) and standalone instruments. Review the Analytical test report in LIMS. Review the reported results against specification and trends. Review the method validation and method transfer documents. Review the instrument calibrations and working standard qualification records. Handling the Incidents/ Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure. Monitoring of analytical a...

Handling of Change control,Review and assessment of Deviation,CAPA Market complaint, Recall Investigation and Vendor Qualification Dishman is a global, dynamic group of companies offering a continuum of services to the pharmaceutical industry. We are a global outsourcing partner for pharmaceutical companies, offering a portfolio of products and development, scale-up and manufacturing services.

Dishman Group is looking for Executive - Formulation QC to join our dynamic team and embark on a rewarding career journey. Develop and implement quality control procedures, standards, and specifications for products or services. Conduct regular inspections and tests of raw materials, in-process goods, and finished products to ensure compliance with quality standards. Identify and investigate quality issues, determine the root cause, and implement corrective actions. Ensure that production processes meet quality requirements and make recommendations for improvements. Collaborate with other departments such as R&D, production, and customer service to ensure a seamless quality control process. ...

Handling of Change control,Review and assessment of Deviation,CAPA Market complaint, Recall Investigation and Vendor Qualification Dishman is a global, dynamic group of companies offering a continuum of services to the pharmaceutical industry. We are a global outsourcing partner for pharmaceutical companies, offering a portfolio of products and development, scale-up and manufacturing services.

Handling of Change control,Review and assessment of Deviation,CAPA Market complaint, Recall Investigation and Vendor Qualification Dishman is a global, dynamic group of companies offering a continuum of services to the pharmaceutical industry. We are a global outsourcing partner for pharmaceutical companies, offering a portfolio of products and development, scale-up and manufacturing services.

Handling of Change control,Review and assessment of Deviation,CAPA Market complaint, Recall Investigation and Vendor Qualification Dishman is a global, dynamic group of companies offering a continuum of services to the pharmaceutical industry. We are a global outsourcing partner for pharmaceutical companies, offering a portfolio of products and development, scale-up and manufacturing services.