ResponsibilitiesAssess and ensure compliance to QC regulatory requirements and track quality metrics and drive them down for API Panoli site . Effectively manage the site Quality Control activities and resources necessary to smoothly run the QC operation includingrelease of raw materials, intermediates, in?process samples, APIs, and monitoring API stability as per regulatory commitments.Ensure analytical methods (for intermediates and APIs) are validated/transferred as per ICH Q2 and API regulatory requirements.Monitor and review investigations and QMS with adequate CAPA to minimize errors. Qualification & ExperienceB.Pharm / M.Pharm Experience Tenure : 18+ Yrs

ResponsibilitiesFormulation development of NCE projects, generic projects and line extension projects Preparation/review of literature summary and development report to the assigned product. Involve in execution and/or supervision of formulation development, process development and manufacturing of GMP batches of assigned product. Preparation/review of technical documents, which includes but not limited to MFC, BMR, BPR and Stability protocol following GDP. Representation in departmental audit Follow GxP (GMP, GDP etc.) for all processes and train the subordinates to follow the same. Execution and/or supervision of scale up/pilot scale batches in pilot plant under GMP condition. Preparation and/or review of technology transfer documents and technology transfer to manufacturing site, whenever required. Preparing/reviewing of QMS includes but not limited to change control, deviation, SOPs and OOS Communication with cross-functional team and client via mails, meetings and oral communication Provide training on but not limited to SOPs, technology, guidelines and project specific activitiesQualificationB.Pharma/M.Pharma/ B.Sc

Responsibilities Lead and manage a team, providing guidance, coaching, and performance feedback to foster a high-performing environment.  Develop and implement operational strategies and procedures to enhance efficiency and productivity.  Monitor and analyze key performance indicators (KPIs), identifying areas for improvement and implementing corrective actions.  Ensure compliance with all relevant regulatory requirements, company policies, and industry standards.  Collaborate cross-functionally with other departments to achieve organizational goals and streamline processes.  Manage project timelines, resources, and budgets, ensuring successful completion within defined parameters.  Prepare and present regular reports on team performance, operational status, and strategic initiatives to senior management..Qualification Bachelor's degree in a relevant field (e.g., Pharmacy, Chemistry, Business Administration, Engineering).  Minimum of 5-7 years of progressive experience in a similar role within the pharmaceutical industry.  Proven track record of successful team leadership and management.  Strong understanding of pharmaceutical manufacturing processes, quality systems, and regulatory requirements (e.g., GMP, FDA).

Responsibilities Helps in demonstrating the operation in case of a new machine or a new pack-profile is implemented Preparation of protocol for validation/qualification pertaining to Process, Cleaning, Equipment and area/HVACExecution of validation/qualification activities Coordination with different departments for performing validation/qualification activities Compilation of data and report preparation Maintaining documents as per Document control policy  Lessoning with FDA for manufacturing licenses and certificates.QualificationB.Pharma/M.Pharma/ B.Sc

Qualification & Experience        Qualification: M.Sc Nursing             Experience: Minimum 5+ years 

Qualification & Experience Qualification: MD., DM. (Neurology)        Experience: 3 years                 Gender: Male / Female                       

Qualification & Experience  Qualification: Any PG in relevant field  Experience: Minimum 5+ years       Gender: Male / Female                       

Qualification & ExpeirenceQualification: B.Sc / M.ScPreference: Candidates from Goa will be preferred

ResponsibilitiesSets up and operates hemodialysis machine to provide dialysis treatment for patients with kidney failure: Attaches dialyzer and tubing to machine to assemble for use. Mixes dialysate, according to formula. Primes dialyzer with saline or heparinized solution to prepare machine for use. Transports patient to dialysis room and positions patient on lounge chair at hemodialysis machine.  Takes and records patient's predialysis weight, temperature, blood pressure, pulse rate, and respiration rate. Explains dialysis procedure and operation of hemodialysis machine to patient before treatment to allay anxieties. Cleans area of access, using antiseptic solution. Connects hemodialysis machine to access in patient's forearm or catheter site to start blood circulating through dialyzer. Inspects equipment settings, including pressures, conductivity, and temperature to ensure conformance to safety standards.  Starts blood flow pump at prescribed rate. Inspects venous and arterial pressures as registered on equipment to ensure pressures are within established limits. Calculates fluid removal or replacement to be achieved during dialysis procedure. Monitors patient for adverse reaction and hemodialysis machine for malfunction. Takes and records patient's postdialysis weight, temperature, blood pressure, pulse rate, and respiration rate. May fabricate parts, such as cannulas, tubing, catheters, connectors, and fittings, using handtools. Qualification & ExperienceAble to work accurately and with minimal supervision. Ability to comprehend written instructions given by the related departmental personnel. Ability to plan & organize ones work schedule effectively. Speaking and listening are essential requirements to understand and carry out the instructions given by the supervisors and other related departmental personnel. Affinity to work in team.

ResponsibilitiesAssess the identity, strength and purity of medications. Review prescriptions to assure accuracy, to ascertain the needed ingredients, and to evaluate their suitability. Provide information and advice regarding drug interactions, side effects, dosage and proper medication storage. Analyze prescribing trends to monitor patient compliance and to prevent excessive usage or harmful interactions. Order and purchase pharmaceutical supplies, medical supplies, and drugs, maintaining stock and storing and handling it properly. Maintain records, such as pharmacy files, patient profiles, charge system files, inventories, control records for radioactive nuclei, and registries of poisons, narcotics, and controlled drugs. Advise customers on the selection of medication brands, medical equipment and health-care supplies. Collaborate with other health care professionals to plan, monitor, review, and evaluate the quality and effectiveness of drugs and drug regimens, providing advice on drug applications and characteristics. Compound and dispense medications as prescribed by doctors and dentists, by calculating, weighing, measuring, and mixing ingredients, or oversee these activities. Offer health promotion and prevention activities, for example, training people to use devices such as blood pressure or diabetes monitors. Prepare sterile solutions and infusions for use in surgical procedures, emergency rooms, or patients' homes. Plan, implement, and maintain procedures for mixing, packaging, and labeling pharmaceuticals, according to policy and legal requirements, to ensure quality, security, and proper disposal. Qualification & ExperienceQualification: D. Pharma/ B. PharmaExperience: preferably over 3 yearsAble to work accurately and with minimal supervision.Ability to comprehend written instructions given by the Doctors and the other related departmental personnel. Ability to plan & organize ones work schedule effectively. Speaking and listening are essential requirements to understand and carry out the instructions given by the supervisors and other related departmental personnel. Affinity to work in team. Enthusiasm. Open-mindedness.