Responsibilities The Intensive Care Nurse will provide specialized care to critically ill patients, including monitoring vital signs, administering medication, and collaborating with a multidisciplinary medical team. Additional responsibilities include responding to emergencies, supporting patient recovery, and ensuring adherence to healthcare standards and hospital procedures.  Qualification & ExpeirenceProficiency in general Nursing practices and patient care Specialized expertise in Emergency Nursing and Critical Care Nursing Knowledge of Critical Care Medicine and emergency medical procedures Strong medical assessment and decision-making skills Compassionate communication skills and ability to work collaboratively in a team Relevant nursing certification or degree, with a specialization in critical care preferred Current professional nursing licensure Previous experience in a critical care or intensive care setting is highly advantageous

ResponsibilitiesAs a Neonatal Intensive Care Nurse, you will be responsible for monitoring and caring for critically ill newborns, administering medications, maintaining medical equipment, and assisting with medical procedures. You will collaborate closely with physicians, healthcare providers, and parents to ensure the best possible care for neonatal patients. This is an on-site role that requires providing compassionate, round-the-clock support to premature and critically ill infants in the Neonatal Intensive Care Unit (NICU). Qualification & ExpeirenceProficiency in Neonatal Intensive Care and Nursing practices to provide specialized care for critically ill newborns Strong foundation in Critical Care Medicine and Critical Care Nursing for managing acute medical situations effectively Knowledge and experience in general Medicine for a comprehensive approach to neonatal health Exceptional organizational, communication, and teamwork skills critical for collaborating with multidisciplinary teams Relevant certifications in Neonatal Intensive Care Nursing or Critical Care Nursing are highly desirable Bachelor's or Master's degree in Nursing or a related field required Experience in a busy NICU or similar setting will be an advantage

ResponsibilitiesManager - Quality AssuranceJob Description Candidate should have good communication skill Must have Regulatory Knowledge and audit handling exposure Must have working exposure of Cleaning Validation and respective work area's Must have sound knowledge of Non-sterile dosage forms Having work experience of preparation of Risk Management, Cross-contamination control strategy etc. Handling of Change Management system Qualification B. Pharmacy / M. Pharmacy / MSc.

Responsibilities Design the scheme of experiments  Plant trouble shooting, investigation and root cause analysis.  IUT support for vendor qualification and plant batches.  Carry out experiments during the feasibility and optimization stage  Visualize the development needs of the product.  Understand the safety and environmental aspect  Solve the problems and queries related to the development of the product and discuss them with the Group Leader / HOD.  Familiarize with the problems faced during scale-up and identifying all critical process parameters for a seamless scale-up.  Knowledge on IUT, VQ, LFR / PDR reports documentation  Understand the scalability of the chosen process, in coordination with TSD and Production.  Amicable relationship with PRD and ARD and work planning accordingly  Keep the Group Leader well informed about the experiments and their results by maintaining the lab journal/ documents well  Technology Transfer for new project to Production plant.  Document project progress regularly with all relevant information.  Document all the relevant data in systematic manner and regularly discuss with group leader for way forward.  Required literature survey knowledge on project progress timely and discuss with group leader.  Mentor and guide the junior chemists in the lab on process development. Responsible for his/her training needs and appraisal along with the Group leader.  Keep the work area clean and the laboratory auditable all the time.  Responsible for department related administrative activities identified by the group leader / HOD from time to time.  Flexible for working on project requirement.  Voluntarily involve in additional responsibilities., Safety related, ESI, and corporate social responsible programs based on requirement  Ready, responsible and accountable for changes as per internal and customer requirements for successful execution of project on time as and when required.

Responsibilities Capable to handle the projects independently.  Analytical testing supports to PDG synthetic group.  Coordinate with QA regarding method transfer, CCF and investigation reports.  Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments..  API Stability knowledge.  Should aware about GLP practices and 21 CFR part-11.  Keep the work area clean and the laboratory under controlled temperature.  Calibrate the instruments according to the master calibration schedule and follow GLP and SOPs.  Understand the safety and environmental aspect.  Maintain the reagents and standardize the volumetric solutions as per schedule.  Maintain the laboratory journals and instrument log books online.  Ensure compliance to Hazardous waste and chemical management

ResponsibilitiesAnalysis and approvalSupporting in-process control sample testing by online analysis to support production activitiesSampling, analysis and ascertaining quality of intermediates, In-process samples and API for ChemistryTesting of the method validation samples and process validation samples and cleaning validation. Perform analysis and documentation of API finished product stability study as per stability study protocol.Coordinating with Production, CWH and QA for Approval / Rejection of raw materials/finished product.Validation and verification of analytical procedures as per requirement.Reporting OOS / OOT results and deviationsMaintaining retained samples as per standard procedure.Assisting in investigation of customer complaint.Testing of new samples (Vendor approval).Qualification & ExperienceEducation / Experience M.Sc. Analytical/Organic Chemistry/Inorganic Chemistry Min. 1-5 years’ Experience in a Quality Control/Analysis laboratory in a cGMP/ISO environment

ResponsibilitiesPerform prior art search to assess the novelty and/or obviousness of the patent for supporting patent invalidation which includes searches using various databases, identifying the prior arts, analysing the relevant prior art and preparing report. Prepare summary reports or patent landscape reports for the new molecules and to timely update the PLR (Patent and Literature Review) reports of existing molecules Coordinate the filing of patent applications for R&D in a timely manner, meeting all required deadlines, and correspondences with Patent Offices/Law firms and agents regarding the same. Ensure on-going record maintenance and renewal of patents. Prepare report for in-licensing products which includes searches using various databases in the countries of interest, identifying the prior arts, analysing the relevant prior for the specific country/market of interest and preparing the risk assessment summary in support to due diligence within stipulated timeline to support on-time product launch. Provide clearance report for Finished dosage form / Biosimilar or peptide molecules prepared in-house or procured from a third party with in-depth analysis on process, KSM, intermediates, polymorph, impurities, composition or formulation and involve in active interaction with the R&D scientists. Work as a member of a team to achieve all outcomes. Perform all work in support of our Corporate Values of Pride, Accountability, Integrity and Diligence; Demonstrate strong and visible support of our values. All other duties as assignedQualification & ExperienceM.Pharm. or M.Sc. Biotechnology, preferably with a PG Diploma in Patent Law is beneficial. Knowledge, Skills and Abilities Preferably, a Registered Patent agent with the Indian Patent office and familiar with patent laws of US, EP and India. Familiarity with patent and literature search related to Formulation & Biosimilar products and knowledge of databases such as Questel Orbit, SciFinder, STN and other regional databases. Experience 2-3 years of experience in intellectual Property related procedures are critical. At Apotex, we are committed to fostering a welcoming andaccessible work environment, where all everyone feels valued, respected, and supported to succeed.

ResponsibilitiesImplementing a monthly production schedule with consistent quality, adhering to Regulatory, GQS, and HSE guidelines, with proper utilization of resources and optimum cycle time. Performing the production activities in assigned areas to achieve 100 % customer service. Performing the SAP-related activities Able to handle a team consisting of Contractual persons, FTC & Operators in the allocated shift Able to do troubleshooting in the allocated area ISO 14001 and SAP Adhering to ISO 14001 activities and objectives in Pharma Mfg. Performing all the SAP-related activities as and when needed. Compliance Implementing and ensuring compliance with GQS, HSE, and ISO guidelines/standards and maintaining documentation for the same, including process validation and qualification. Coordination Coordinating with Engineering department for preventive and breakdown maintenance, modifications etc. The purchase department for procuring and controlling auxiliaries. Quality department for all quality-related matters. Packaging department for bulk availability.Qualification & ExperienceM. Pharm / B. Pharm from a reputed university, having 8 to 10 years in the pharmaceutical Primary and secondary packing section, and also exposure in manufacturing in Granulation, compression, and Coating.

Responsibilities Responsible for development and design of formulations for multiple products selected for development & conducting meeting with multidisciplinary teams. Conducts relevant patent searches on formulations. Reviews scientific literature and makes recommendations for formulation development strategies. Responsible to carryout Preformulation studies, manufacturing prototype batches and do formulation development based on QbD approach. Attends appropriate trainings, seminars, and presentations to maintain expertise in formulations and related areas. Communicates with buyers and peers to ensure that APIs, excipients, tooling etc. are available for the project in required quantities, as and when needed. Liaises with the plant operation supervisors and scheduler to ensure that experimental trials / registration batches are planned and executed in a timely manner. Liaises with the documentation groups to ensure that early development trial documents, process evaluation and process optimization documents required for execution. Coordinates with lab for sample requirement and provides timelines for testing of samples. Reviews and evaluates data analytical/ technical data on trials, and makes recommendations for bio/stability study batches, and communicates recommendations with management / peers to get necessary clearance to proceed further. Applies Quality-by-design (QbD) principles to product development and tests the ruggedness of the formula by conducting suitable trials to study the impact of variations in the excipients within SUPAC guidelines / variations in manufacturing process parameters to recommend control strategy for CMAs and CPPs. Liaises with the documentation group to ensure that all scale up master manufacturing and packaging documentation and other related documents required for submission to regulatory agencies are made available as and when required. To prepare Pharmaceutical Development Reports and other documents required for regulatory submissions and technology transfer. Responsible for responding to deficiency queries from regulatory agencies in timely manner. Provides scientific and technical expertise and performs consultations on issues regarding formulation to other members of Formulation Development and other departments. Works as a member of a team to achieve all outcomes. Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Integrity – We do the right thing, every time. Teamwork – We achieve more together. Courage – We face challenges head on. Innovation – We power progress with bold ideas. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned.Qualification & ExperienceMaster’s degree or Ph.D. in Pharmaceutics or Pharmaceutical Technology or related science. Knowledge, Skills and Abilities Excellent working and theoretical knowledge of different pharmaceutical solid oral dosage forms such as immediate release, controlled release & delayed release dosage forms Detailed understanding of the theoretical principles for major manufacturing processes and equipment. Excellent knowledge of excipient properties and their use in formulation development.10-15 years of working experience in a pharmaceutical development environment with related experience in formulation development of solid oral dosage forms for regulated market, scale up and/or technology transfer.

Responsibilities Initiate Master Manufacturing Records (MMaRs) & Master Packaging Record (MPaRs) Initiate Placebo and Optimization batch record for trails. Initiate Change Controls in QMS Track Wise for New Launch / Site Transfer / Submission batch / SOPs / Formats and commercial batch documents. Ensure QMS Change control closure within the stipulated timeline. Ensure support for timely completion of Investigations for document related deviations and document revision based on CAPA. Initiation of batch documents , SOPs and Formats in Content server. Check Monthly Schedule to ensure document readiness. Ensure all changes are aligned with cGMP regulations and corporate SODs. Perform all work in accordance with established regulatory, compliance and safety requirements. Coordinate with NPL and RA regarding Deficencies from Regulatory Agencies and Clarifix. Develop and maintain effective working relationships with internal and external customers. Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies and HR policies. All other relevant duties as assigned.Qualification & ExperienceMinimum Bachelor of Pharmacy / Science or any equivalent degree. Experience Minimum 1 year of experience in GMP regulated pharmaceutical industry.  Knowledge, Skills and Abilities Adequate knowledge in handling QMS Trackwise tool, Content server tool. People management skillset Adherence to cGMP Exhibit Perseverance in all the tasks performed Problem solving skills