Unison Pharmaceuticals is looking for Product Management - PMT profile, please refer to the job details below,Company: Unison PharmaceuticalsCompany URL: www.unisonpharmaceuticals.comPosition: Product Executive/ APM/ PMLocation: AhmedabadExperience: 3-8 yrsJob Description: Working upon Brand Building through Brand plansField work to understand the market & evaluate developed strategies in processDeveloping & finalizing innovative brand campaigns/strategies/activities under guidance of managerTo prepare proposal & plan for new product launches, market research survey of Dr s & study (as per ORG) before launching of new productsFormulating & implementing innovative strategies for launching new brands and increasing sales of the existing ones under guidance of managerTo analyze the market and competition in order to identify the opportunities, threats and key issuesDesigning of sales promotional inputs including visual-aids, LBL, sales & sample packsConducting sales promotion meetings.Interested candidates can share their profiles on maitrivakil@unisonpharmaceuticals.com

Unison Pharmaceuticals is urgently seeking talented Production Supervisors for our OSD Production team. Apply now to become a part of our team!!Experience: 2-6 years Job Role : 1) Compression Supervisor 2) Granulation SupervisorDesignation: Officer / Sr. Officer / Executive Qualification: B.Pharma/M.scLocation: Moraiya, Ahmedabad.No. of Openings : 3Perks & Benefits Dynamic work environment Career development opportunities Work-life balance Free transportation Free insurance coverage for self, spouse, and kids Range of learning opportunities to help employees grow and thriveIf you are passionate about continuing to work in the pharmaceutical industry and possess the required skills, we encourage you to apply for this position.Please submit your resume to career@unisonpharmaceuticals.com to be considered for this role. Join our team at Unison Pharmaceuticals and take the first step towards a rewarding career.RegardsHR department

Opportunities for Engineering & Projects_Unison Pharma_Moraiya AhmedabadWe are expanding!!You are invited to join one of the fastest growing pharma companies in India!!About us: Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and affordable medicines across the nation. With more than 4 decades of medical service to society, Unison is today one of the fastest-growing companies in Gujarat State. In addition to this, the company is ranked 82 among the top companies of India (Rupee wise sales) MAT March 2020. This makes Unison a distinguished company across the pharma industry. 1. EngineerDesignation: Officer / Sr. Officer / ExecutiveEducation Required: BE / B.Tech (Mechanical / Electrical/ Instrumentation)No of Openings (6):- OSD Plant Maintenance- Utility , HVAC , BMS Maintenance - Project Engineering- Engineering Store- Engineering Purchase2. Fitter / ElectricianDesignation: Technician Education Required: ITI (Fitter / Electrician) / Diploma (Mechanical / Electrical)Experience Required: 2-7 Years No of Openings (4):- OSD Plant Maintenance- Utility , Chiller, Water System operation & maintenanceIf you are passionate about continuing to work in the pharmaceutical industry and possess the required skills & experience, we encourage you to apply for this position.Kindly share your updated resume on career@unisonpharmaceuticals.com RegardsHR TeamUnison Pharmaceuticals Pvt Ltd

Greetings form Unison Family!We are under screening process for Supply Scheduling Professionals Company Name : Unison Pharmaceuticals Pvt Ltd.Position: Dy. Manager / Manager - Supply Scheduler Location: Moraiya Plant, Ahmedabad Department: Production Planning / SCMAbout Company :Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality & most affordable medicines across the nation. With 4 decades of medical service to the society, Unison is today one of the fastest growing company in Gujarat State. The base of operation being a single state, the company has very strong footing in the market. The company strictly believes in ethics and moral values throughout the operations of the business.Website : https://www.unisonpharmaceuticals.com Role Summary: The Supply Scheduler will oversee and optimize production schedules to ensure timely manufacturing of Oral Solid Dosage (OSD) products while maintaining cost efficiency, resource allocation, and customer service targets. The role requires a seasoned professional with 8+ years of experience in supply chain, production planning, or scheduling in a pharmaceutical manufacturing environment.Key Responsibilities:Production Scheduling:Develop and manage production schedules for OSD products based on sales forecasts, inventory levels, and production capacity.Ensure alignment of production schedules with demand planning and supply chain goals.Identify and address potential scheduling conflicts and delays to minimize production downtime.Capacity Planning & Optimization:Analyze production capacity and resource availability to optimize scheduling efficiency.Monitor utilization of equipment, manpower, and materials to ensure adherence to production plans.Collaborate with the production and engineering teams to improve OEE (Overall Equipment Efficiency).Material Availability & Coordination:Coordinate with procurement, warehouse, and production teams to ensure material availability as per production schedules.Maintain strong oversight of raw materials, APIs, excipients, and packaging materials inventory levels.Cross-Functional Collaboration:Work closely with departments such as Sales, Quality Assurance, Production, and Logistics to align schedules with business objectives.Communicate changes to schedules and resolve issues to ensure minimal disruption.Data Analysis & Reporting:Prepare and analyze production and supply metrics, including adherence to schedules, delays, and capacity utilization.Present reports to senior management highlighting key performance indicators (KPIs).Compliance and Documentation:Ensure scheduling activities comply with cGMP, regulatory requirements, and SOPs.Maintain accurate documentation of schedules, delays, and changes for audit and review purposes.Interested candidates can share your resume on krupagohil@unisonpharmaceuticals.com

Greetings from Unison!!!We are under screening process for IPR - API professionals Company Name : Unison Pharmaceuticals Pvt Ltd.Location : AhmedabadDesignation : IPR-APIAbout Company :Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality & most affordable medicines across the nation. With 4 decades of medical service to the society, Unison is today one of the fastest growing company in Gujarat State. The base of operation being a single state, the company has very strong footing in the market. The company strictly believes in ethics and moral values throughout the operations of the business.Website : https://www.unisonpharmaceuticals.com Job Responsibilities:Preparation of IP landscape report for API/Finished formulation and accordingly able to identify and provides opinion against critical granted patents/patent application for US marketInfringement/FTO analysis for API/Finished Formulation/Platform Technology Products for US market business Dealing with outside vendor/R&D team for guiding and implementing various IP approaches and handling customer queries for API/Formulation part for US marketInvalidity/prior art analysis of key patents for US markets business New product identification/505(b)(2) concept identification support Patent application drafting, filing and prosecution for various markets Knowledge in dealing with outside law firms (US, Europe and others) for patent prosecution/litigation matterTracking of key concern products litigation stages and patent applications and accordingly analyzing its business impactLaunch date analysis/generic entry for US market productsInterested candidates can share your resume on krupagohil@unisonpharmaceuticals.com

Greetings form Unison Family!We are under screening process for Income Tax professionalsCompany Name : Unison Pharmaceuticals Pvt Ltd.Location : AhmedabadDesignation : AM/DM Direct Taxation About Company :Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality & most affordable medicines across the nation. With 4 decades of medical service to the society, Unison is today one of the fastest growing company in Gujarat State. The base of operation being a single state, the company has very strong footing in the market. The company strictly believes in ethics and moral values throughout the operations of the business.Website : https://www.unisonpharmaceuticals.com Job Responsibilities:Preparation of quarterly TDS return for salary, foreign payments and all other taxable transactionsPreparation of quarterly TCS return.Facilitate filling of TDS return in consultation with tax consultant including resolution of queries and submission of information requiredArrange 15CA/15CB certification for foreign remittances through tax consultant, reviewing tax compliance documents of service provider, coordination with internal stake holders / tax consultants / banks Assist tax lead in data preparation and compilation for annual tax audit report and liasoning with tax auditorAssist tax lead in preparation of various information & data for annual income tax return in consultation with tax advisor for company/group companiesAssist account head and tax lead in day to day monitoring of income tax compliance for various transaction across the company / group companiesAssist tax lead for income tax assessment, departmental enquiry/audit including preparation of data in coordination with internal and external stakeholders and tax consultant Coordinating with international marketing team and overseas tax consultant for various tax compliances for the company, overseas branch and overseas subsidiary in consultation with tax lead and tax advisors.Maintaining tax & TDS compliance records for periodical returns, submission, assessment etc. Checking and validating PAN data of vendors, customers & employees and provide necessary guidance to all stakeholders for effective compliancePeriodical and annual reconciliation of income and TDS/TCS as per income tax records (26AS) and books of account Assist Tax lead in preparation of Advance tax working.Verify proofs submitted by various Employees in supporting to form 12BB to claim deduction. Proactive and continuous participation in maintenance & improvement of compliance oriented work environment and knowledge update initiatives for all stake holders.Interested candidates can share your resume on krupagohil@unisonpharmaceuticals.com

Experience : 3-6 YearsJob Role : Technology TransferLocation : Moraiya, AhmedabadRole & responsibilities Technology transfer for Domestic market, EMB market projectsExecution of Exhibit batches/commercial validation batches for Domestic/EMB marketAlternate vendor development trials/stability evaluation for Domestic market.Interested candidates can share their resume on career@unisonpharmaceuticals.com.

About Us: Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality & most affordable medicines across the nation. The company is having 1st Rank (Unit wise sales) in Gujarat state since more than 17 consecutive years as per ORG IMS. In addition to this, the company is ranked 82 among top companies of India (Rupee wise sales) MAT December 2021.Website : www.unisonpharmaceuticals.comWe are seeking specialists for multiple roles into Quality Assurance at our EU Approved OSD Manufacturing facility at Unit I Moraiya, Ahmedabad. Company : Unison Pharmaceuticals pvt ltd.Location : Unit I (Moraiya, Ahmedabad) - Transportation provided from Ahmedabad routes(1) Quality Assurance - ValidationDesignation: Sr. Executive /Assistant Manager /Dy. Manager Education Qualification: B.Pharm/M.Sc/M.Pharm Experience Required: 8 to 12 yearsJob Exposure required: Must Have: Process Validation, Cleaning ValidationPreferred to have: QMS, Risk Management, Qualification (2) Quality Assurance - Compliance & Training ManagementDesignation: Executive / Sr. Executive Education Qualification: B.Pharm/M.Sc/M.Pharm Experience Required: 6 to 10 yearsJob Exposure required: Must Have: Audit Compliance, Training Management (3) Quality Assurance - DocumentationDesignation: Officer / Sr. Officer / Executive Education Qualification: B.Pharm/M.Sc/M.Pharm/B.ScExperience Required: 4 to 7 YearsJob Exposure required: Must Have: APQR or IPQA & Batch Record Preparation (4) Quality Assurance - Process ValidationDesignation: Officer / Sr. Officer / Executive Education Qualification: B.Pharm/M.Sc/M.Pharm/B.ScExperience Required: 5 to 8 YearsJob Exposure required: Must Have: Process Validation, Hold Time Study (5) Quality Assurance - IPQA - PackingDesignation: Officer / Sr. Officer / Executive Education Qualification: B.Pharm/M.Sc/M.Pharm/B.ScExperience Required: 4 to 8 YearsJob Exposure required: Must Have: In process QA , Line clearance of Packing areaPerks & BenefitsDynamic work environmentCareer development opportunitiesWork-life balanceFree transportationFree insurance coverage for self, spouse, and kidsRange of learning opportunities to help employees grow and thriveIf you are passionate about continuing to work in the pharmaceutical industry and possess the required skills, we encourage you to apply for this position.Please submit your resume to career@unisonpharmaceuticals.com to be considered for this role. Join our team at Unison Pharmaceuticals and take the first step towards a rewarding career.

Unison Pharmaceuticals, one of the fastest growing organization is looking for Multiple positions in Regulatory Affairs - Emerging / ROW Market for pre-submission and post-submission. Role and responsibilities Responsible for preparing/reviewing various regulatory documents for Emerging markets (South East Asia, Africa, CIS, Latin America, Gulf Countries) such as,Dossiers in ACTD, CTD and in country specific format.Variation filling, renewal fillings, Query response, Site registration applications, Tender fillings.Legal Applications related to local FDA\CDSCO like FSC, COPP, Product permissions, WHO GMP inclusions. Responsible for coordinating with Cross functional teams for timely receipt of technical documents.To verify and approve all technical documents in line with current regulatory requirements.Regulatory assessment of CCN/Deviation for Impact assessment. Artwork development, amendments and maintenance without adversely affecting the business continuity to implement regulatory changes.Maintain various regulatory status.2. Monitoring of product lifecycle as per regulatory requirement.3. Literature search, data collection, evaluation to meet the requirement of above job responsibilities.Candidate should have detailed knowledge on:Regulatory requirements for submission of product dossiers.Registration samples submission in ROW countries.Candidate must have Good in written and verbal communications.Candidate must have basic knowledge of Microsoft Word, Excel & Power PointInterested candidates may also email their resume to maitrivakil@unisonpharmaceuticals.com

Unison Pharmaceuticals, one of the fastest growing organization is looking for Multiple positions in Regulatory Affairs - Europe/ regulated Market for pre-submission and post-submission.Roles and ResponsibilitiesEnsure timely authoring and submission of dossiers (Module 2-5) for regulated regions such as Europe, Australia, South Africa, New Zealand and Canada in the eCTD format including familiarity with publishing activities.Preparation and submission of documentation for post-approval applications (CMC and Administrative changes) such as Type IA/ IB/ II variations for Europe/UK, Level I/II/III changes for Health Canada, Renewals, and MAH Transfers.Work with submission teams and provide appropriate support for managing the lifecycle of product submissions, and authorizations.Assessment of change controls, defining the correct variation code and preparation of the variation packages as per the agreed timelines.Preparation of quality responses to the deficiency letters from various Clients/agencies within agreed time frame.Co-ordinate with various departments to obtain essential scientific data and documents required for dossier preparation and query responses.Evaluates proposed manufacturing and quality changes for impact to ongoing and existing filings and provides strategic regulatory support for optimal implementation of changes.Involve in review of source documents for in-house: product development report, specification (excipients, API and finished product), manufacturing batch record, analytical method, validation report, validation protocol etc.Actively participate in the evaluation of regulatory compliance of document/product/ process/test methods changes.Provide regulatory insights and support for contract manufacturing projects (CMO/CDMO).Preform gap analysis for extension of dossier to other territories as per country specific requirements.Identifies and communicates risks and issues impacting project progression.Assist in the development of Regulatory CMC strategies for assigned products and projects.Ensure product compliance with respect to approvals and regulatory requirements.Tracker Management: Update/Maintenance of database with regulatory submission and approval.Candidate(s) having previous exposure in EU dossier authoring, product life cycle management/variation and Health Canada filings are preferable.Core competencies:Strong technical understanding of ICH/EU/ANZ/Health Canada guidance's, time management skills, right first time approach, work with minimal supervision.Strong written and verbal communication skills.Interested candidates can share your resume on krupagohil@unisonpharmaceuticals.com

We, Unison Pharma - One of the fastest growing global pharma company are seeking candidates with rich experience to join our International Business (Asia/ Africa markets) role.Position: Executive / Sr. Executive / Assistant ManagerJob Location: Head Office, Ahmedabad (2nd & 4th Sat Off)Frequency of Travel - Need basedKey Accountabilities/ Responsibilities 1. BD, Marketing & SalesIdentifying and Finalizing potential partners followed by CDA & the main agreementFinalize products for registrationsPrepare business plan including target prices and yearly sales quantitiesPrepare annual sales & expense budget, territory wise & thus establish the profit / loss scenario. Managing sales by developing a business plan that covers sales, revenue, and expense controls.Overseeing the activities and performance of the agency & / or sales team.Promoting the organization and products; Expanding foot-print of the company in the territoryImpart training & / Or knowledge of the products to the targeted audience. 2. Backend activitiesEnsure timely preparation of product dossiers by RA, followed by in-time submission in the territory by partnerTimely update of products lying under registrations from the partnersCollecting purchase orders from the partners once the products are registeredPunching of purchase orders into the systemTimely receipt of paymentsEnsure timely dispatch of the products Interested candidates to apply here or email their updated profile on maitrivakil@unisonpharmaceuticals.com

Greetings form Unison Family!We are under screening process for Income Tax professionalsCompany Name : Unison Pharmaceuticals Pvt Ltd.Location : AhmedabadDesignation : AM/DM Direct TaxationAbout Company :Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality & most affordable medicines across the nation. With 4 decades of medical service to the society, Unison is today one of the fastest growing company in Gujarat State. The base of operation being a single state, the company has very strong footing in the market. The company strictly believes in ethics and moral values throughout the operations of the business.Website : https://www.unisonpharmaceuticals.comJob Responsibilities:Preparation of quarterly TDS return for salary, foreign payments and all other taxable transactionsPreparation of quarterly TCS return.Facilitate filling of TDS return in consultation with tax consultant including resolution of queries and submission of information requiredArrange 15CA/15CB certification for foreign remittances through tax consultant, reviewing tax compliance documents of service provider, coordination with internal stake holders / tax consultants / banksAssist tax lead in data preparation and compilation for annual tax audit report and liasoning with tax auditorAssist tax lead in preparation of various information & data for annual income tax return in consultation with tax advisor for company/group companiesAssist account head and tax lead in day to day monitoring of income tax compliance for various transaction across the company / group companiesAssist tax lead for income tax assessment, departmental enquiry/audit including preparation of data in coordination with internal and external stakeholders and tax consultantCoordinating with international marketing team and overseas tax consultant for various tax compliances for the company, overseas branch and overseas subsidiary in consultation with tax lead and tax advisors.Maintaining tax & TDS compliance records for periodical returns, submission, assessment etc.Checking and validating PAN data of vendors, customers & employees and provide necessary guidance to all stakeholders for effective compliancePeriodical and annual reconciliation of income and TDS/TCS as per income tax records (26AS) and books of accountAssist Tax lead in preparation of Advance tax working.Verify proofs submitted by various Employees in supporting to form 12BB to claim deduction.Proactive and continuous participation in maintenance & improvement of compliance oriented work environment and knowledge update initiatives for all stake holders.Interested candidates can share your resume on krupagohil@unisonpharmaceuticals.com