Qualification & ExperienceGraduated / post-graduate in Pharmacy/Medicine or Chemistry/Biotechnology 10 to 14 years minimum experience in Quality or Regulatory Affairs Experience obtained in pharmaceutical manufacturing sites (+8 years). Knowledge of stability regulations and its application to the industry Skilled in the usage of IT tools (for example: Quality Forward, Share/DrugTrack, eDMS), SAP. English speaker Good organizational skills, stress resistance, and flexibility Good Team player and good in decision-making Interpretation/Analytical data. Experience in the pharmaceutical/biotech industry with a good level of GxP know-how is a strong plus. Reactivity, autonomy with a sense of urgency and priorities.

Responsibilities Achieving assigned Area/TBM wise sales target.  Support team to achieve monthly/quarterly/yearly target.  Achieve brand & product wise target.  Conduct activities and programs as per division strategy.  Develop & mentor team for next level.  Ensuring areas stock availability of all products with all stockists of the area assigned.  Achieve division wise primary & secondary target for the area by guiding team members to achieve their territory wise targets.  Monitoring brand wise & value wise month on month sales progression.  Guide TBMs on critical doctor conversion and engagement.  Guide team to accurately forecast sales for all top stockist by analyzing trends from stockist statements of the area.  Driving team towards execution of business strategy by simplifying them in to tactical activities.  Prepares sales plan for the month; anticipate barriers and identify opportunities to overcome the deficit in target achievement.  Monitor team performance, identify gaps with divisions and help bridge the same; developing TBMs field effectiveness through.  Monitor teams effort parameter, execution of strategies and identifying correct mix of doctors and distributors.Qualification & ExperienceBSc/BPharma background. Post Graduate/Graduated from any other background with sound education and performance track record. Candidate with prior/current experience of 2 to 4 Years of First Line manager in same therapy. Candidate from MNC and top Indian Pharma companies will have added advantage.

ResponsibilitiesDeveloping the plan / strategy for the brand ( Operational and Strategic Plan) & gaining support from internal and external stakeholders Leading the innovation agenda from Ideation to Launch as per Brand StrategyEnsuring timely Implementation of brand plans for HCPs as per annual brand plan calendarIdentifying and drawing up any corrective action plan required based on opportunities and challengesConstantly tracking brand performance on various performance matrix of Internal & External data trendsBuild plan and equity for KOL / KBL ManagementHandle brand P&L and liaison with all the stakeholdersMeasure and report performance of all marketing campaigns and assess ROI and KPIsQualification & Experience10- 12 years of Brand management exposure along with 3-4 years of team handling experience Education Graduation in Pharmacy

ResponsibilitiesLead, coach, and manage Quality Control teams through goal setting, performance reviews, feedback, development planning, and succession readiness. Identify development needs, foster teamwork, inclusion, and a culture of accountability and continuous improvement. Manage workforce planning, leave management, and performance appraisal cycles. Actively share knowledge, encourage innovation, and support risk?based decision making. Quality Control & Laboratory Operations Plan, manage, and oversee analytical activities related to: In?process, finished product, stability, process validation, exhibit batch, market complaint, and retention sample testing Stability sample pulling, testing, protocol approval, compilation reports, and annual stability report submissions Visual inspection of retention samples per approved schedules Ensure timely review, approval, and completion of all QC activities in alignment with site KPIs. Review and approve, Laboratory investigations, QC documentation including raw data, protocols, reports, and SOPs in compliance with cGMP. Equipment Qualification, Calibration & Lifecycle ManagemenQualification & ExperienceEducation: B. Pharm / M. Pharm / M.Sc. Experience: Minimum 10+ years of pharmaceutical industry experience with a strong background in Quality Control. Extensive knowledge of cGMP compliance for Quality Control laboratories, including, testing, stability management, lab investigations, equipment qualification, and data integrity.

Qualification & Experience         Experience : 0              Place : CALICUT        Description : MBBS With TCMC 

ResponsibilitiesPatient Care Examine patients and take medical histories Diagnose illnesses and medical conditions Prescribe medications and treatment plans Monitor patient progress and response to treatment Manage admitted patients and coordinate care Emergency Management Handle emergency and trauma cases Provide first aid and life-saving interventions Stabilize critically ill patients before specialist referral Attend code blue/emergency calls Clinical Procedures Perform minor medical procedures such as: Suturing IV cannulation Catheterization Wound dressing Basic airway management Coordination with Specialists Refer patients to consultants/specialists when needed Discuss treatment plans with senior doctors Coordinate with nursing staff and allied health professionals

ResponsibilitiesMonitor patients’ health conditions (vital signs, symptoms) Administer medications and treatments as prescribed Assist doctors during examinations and procedures Assessment & Planning Assess patient needs and develop nursing care plans Update patient records accurately Observe and report changes in patient condition Communication Educate patients and families about health conditions and treatments Coordinate with doctors, therapists, and other healthcare staff Provide emotional support to patients and relatives

ResponsibilitiesExplain treatment plans to the patient and answer questions about treatment Follow safety procedures to protect the patient and themselves from overexposure to radiation Examine machines to make sure they are safe and working properly X ray the patient to determine the exact location of the area requiring treatment Check computer programs to make sure the machine will give the correct dose of radiation to the appropriate area of the patient's body Operate the machine to treat the patient with radiation Monitor the patient to check for unusual reactions to the treatment Keep detailed records of treatment

Qualification & Experience   Qualifications for Full-Time Consultants: . MD/MS with a minimum of 5 years of experience.Retiring HODs and Senior Registrars looking for full time roles are also encouraged to apply.Qualifications for Senior Registrars: . MD/MS with a minimum of 2 years of experience.

Qualification & Experience   Qualifications for Full-Time Consultants: . MD/MS with a minimum of 5 years of experience.Retiring HODs and Senior Registrars looking for full time roles are also encouraged to apply.Qualifications for Senior Registrars: . MD/MS with a minimum of 2 years of experience.