Responsibilities Analysis of Raw material samples as per method of Analysis by adhering to the Regulatory Procedures, Trending of Raw materials. To be responsible for all activities in the Quality Control Laboratory, including cGLP, documentation and implementation of departmental Quality systems. Performing Timely Analysis of Raw material Samples on Priority Basis. To provide technical support to Apotex group of companies during activities like technology transfer. Performs all work in accordance with all established regulatory and compliance and safety requirements. 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 & ExperienceMinimumMSc/BPharm or any equivalent degree. Knowledge, Skills and Abilities Effective command over verbal and written communication with good interpersonal skills. Command on Microsoft-Office (Word, Excel). Able to prioritize the tasks. Best in effective planning of work activities to meet the time lines. Experience Fresher

ResponsibilitiesInitiate 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

ResponsibilitiesPerforms all work in compliance with Code of Conduct, Business Ethics, related policies with the legal and regulatory requirements that apply to our job activities; Works as a member of a team to achieve the goal; Operates in accordance with Code of Conduct, Business Ethics, all established regulatory compliance and safety requirements;Performs all work in support of our Values: Collaboration, Courage, Perseverance, and Passion. To carry out the work as per the instructions given by the immediate Reporting Officer. To follow good manufacturing practices and Good documentation practices. To execute the operations / Process as per the written procedures in BPCR. To perform the cleaning activities as per the GCR’s. To ensure and execute that the SAP transactions are done as per work instructions. To stage the Raw materials and packing material to the respective areas. To report and record the deviations observed during the activity. To follow the safety procedures during working. To maintain a good housekeeping of the plant and surroundings. To co-ordinate with Engineering with respect to Breakdowns, preventive maintenance and day to day activities. To carry out safe disposal of spent and solid waste as per EHS norms. To undergo training and active participation in the following areas. Unit operations. Good Manufacturing Practices. Safety. Report abnormalities in the areas of GMP, Safety, Operations etc., to the immediate reporting officer / supervisor. All other relevant duties as assigned.Qualification & ExperienceMinimum Diploma / Degree in science / Pharmacy / Engineering. Knowledge, Skills and Abilities Self motivational skills allowing you to fuction independently. Communication style and interpersonal skills with the ability to work effectively in a APIPL environment.

Responsibilities Driving sales in the assigned territory as per organization's objectives. Potential mapping of doctors and institutions. Identify opportunities at marketplace, develop and maintain good relations with customers, hospital pharmacies, hospital authorities, distributors etc. Organize scientific meetings to enhance company's image, awareness about therapy area, products. Effective record keeping, maintain the data and timely submission of the data. Active participation in cycle meetings, NSM to ensure sales skills, in-clinic effectiveness, product knowledge and competitor's knowledge is maintained. Manage the process of hospital formulary inclusion to allow usage of product in that hospital. Ensure BMS values and ethics are followed while conducting business.Qualification & Experience Qualifications Pharmacy graduate or Science graduate, MBA preferred.  Languages English & Hindi  Experience and Knowledge Pharma sales experience of at least 5 years in Delhi NCR & Other states in Northern India. Knowledge of local market is an advantage and Oncology Experience is preferred.

ResponsibilitiesDevelop and maintain interactions with Thought Leaders, appropriate HCPs, and access stakeholders, within a given geography to answer scientific, unsolicited product and HEOR related questions. MSLs will use various channels for interactions (1 1, group presentation; remote, etc). Develop and execute a medical interaction plan with Key accounts (Army, Railways, CGHS etc.) as per the needs of the stakeholders and the overall medical strategy. Effectively present information to HCPs and be able to respond to questions, ensuring medical accuracy and compliance with local procedures, ethical and legal guidelines and directives. Actively assess the medical landscape by meeting with Thought Leaders to understand their needs and expertise. Continuously update their own knowledge in treatment strategies, products, unmet medical needs, clinical trials and scientific activities. Understand the competitive landscape and actively prepare to address informational needs of customers. Collect and provide meaningful medical insights back to the medical and commercial organizations to be actioned in support of the strategy development. Report safety information, including adverse events, in accordance with BMS Standard Operating Procedures. Qualification & ExpeirenceMBBS, MD 1-2 years of Field Medical experience in medical affairs is preferred. Candidates with experience in the Oncology and Haematology therapy area will be preferred.

ResponsibilitiesResponsible for accurate & timely Quality Assurance review, evaluation and approval of RS-CR qualification documents in a fast-paced, high-volume environment within established turnaround expectations (typically 3 days) while managing multiple concurrent assignments. Responsible to maintain high level knowledge and understanding of applicable procedures appropriate for the qualification of RS-CR used in clinical and commercial GMP testing across the BMS network. Ensure that critical thinking and risk-appropriate timelines are applied to assigned tasks, managing with due urgency. Use risk & time appropriate communication means to engage proactively, collaboratively, and timely with RSCR and AQC colleagues and senior management as appropriate to address quality and compliance issues associated with qualification activities (MS TEAMS preferred over email for time sensitive issues, as some critical qualification activities may require completion in 3 days or less). Collaborate with RS-CR and AQ&C colleagues to understand near term book of work, and qualification documentation assigned to you, and the expected date of completion. As required by management Receive feedback from RS CR and AQ&C colleagues to assign AQ&C standards of Quality Assurance of RS CR qualification is maintained, and align collaboratively on improvements and/or process changes to support timely right first time qualification document approval Participate in AQ&C team meetings as required to assure common level of quality and compliance of RS CR qualification activities. Prompt and participate in ad-hoc meetings with RSCR colleagues as necessary to triage resolution to Quality Assurance concerns related to assigned qualification documentation work packages.Qualification & ExperienceDegree/Certification/Licensure Bachelor of Science (Life Sciences, Pharmacy, Nursing, Chemical or Bio-Engineering or related field) Required Competencies Fluent in English, with proven professional working proficiency in English for reading, writing and speaking Excellent communication with management, peers, and other functional areas Excellent understanding of GMP analytical testing. Ability to apply critical thinking in a high-volume, fast-paced environment Ability to prioritize while balancing multiple tasks with urgent completion dates Highly organized, detail oriented, efficient operator in a fast-paced environment Customer and partner focus, including the ability to listen to and incorporate feedback from key stakeholders Ability to build and maintain collaborative relationships with stakeholders in multiple geographic locations by engaging transparently, performing reliably, and delivering on commitments Excellent proficiency in use of electronic systems & databases to support daily use in a fast-paced environment (VEEVA Infinity, BMS Docs, LIMS, Sharepoint, Outlook, TEAMs, Word, Excel, SuccessFactors)

Responsibilities Lead and supervise a team of production operators and technicians, fostering a collaborative and productive work environment.  Plan, organize, and monitor daily API production schedules to meet targets and deadlines, ensuring optimal utilization of resources.  Implement and enforce Good Manufacturing Practices (GMP) and other relevant regulatory guidelines throughout the production process.  Troubleshoot production issues, identify root causes, and implement effective corrective and preventive actions.  Monitor and analyze production data to identify areas for process improvement, efficiency gains, and cost reduction.  Participate in the development and revision of Standard Operating Procedures (SOPs) and batch records.  Ensure all production activities comply with environmental, health, and safety (EHS) regulations.  Collaborate with Quality Assurance, Maintenance, and Supply Chain departments to ensure seamless operations.  Conduct performance reviews, provide training, and support the professional development of team members.  Prepare and present production reports to management, highlighting key metrics and achievements. Qualification & Experience Bachelor's degree in Pharmacy, Chemical Engineering, or a related scientific discipline.  5-8 years of experience in API manufacturing, with at least 2-3 years in a supervisory or leadership role.  In-depth knowledge of cGMP, EHS regulations, and other relevant pharmaceutical industry standards.  Proven experience in managing production processes, including batch manufacturing, purification, and drying.  Strong analytical and problem-solving skills with a keen eye for detail.  Excellent leadership, communication, and interpersonal skills.

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 systemQualification & ExperienceB. Pharmacy / M. Pharmacy / MSc

ResponsibilitiesIndependently lead end-to-end formulation development and process design for personal care products across formats (creams, lotions, gels, deodorants, body oils, cleansing) Drive fast-track NPD ensuring OTIF timelines and First-Time-Right (FTR) commercialization Translate marketing concepts and consumer insights into technically feasible, cost-effective, and scalable formulations Manage multiple projects simultaneously, ensuring timely delivery and stakeholder alignment Perform technical scoping including literature review, benchmarking, ingredient selection, and formulation strategy Apply DoE and scientific approaches to optimize formulations for performance, stability, manufacturability, and cost efficiency Conduct trend mapping and competitive intelligence to drive innovation and differentiation Identify opportunities and drive innovation, cost optimization, and sustainability initiatives Execute formulation trials, stability studies, and product evaluations considering performance, cost, packaging, regulatory, and safety requirements Lead pilot batches, scale-up, and technology transfer in collaboration with manufacturing and supply chain teams Collaborate with cross-functional teams (Marketing, QA, Analytical, Regulatory, Procurement, Supply Chain) and manage external stakeholders (vendors, third-party manufacturers, labs) 

Responsibilities Participate in KOM, project planning/strategy making meeting.  Ensuring the aggregate reports and RMP documents are medically relevant, complete, consistent and accurate.  Providing inputs/insights from review of aggregated and RMP data aligned to client’s processes(s) and SOPs.  Addresses all previous Health authority comments and adhoc requests received from Health authority.  Review and provide any noteworthy cases & published studies including pregnancy registries.  Discuss and provide medical analysis for all relevant sections of AR and RMP  To provide the conclusion regarding the current safety profile of the product.  Address all medical queries/comments raised by the Client.  Perform QC of all the assigned aggregate reports and RMP documents.  Complete all trainings, assigned by internally or client on respective LMS within due date.  Responsible for knowledge sharing, coaching, review and providing feedback of reports medically analyzed by the mentees.  Notify critical and major deviations (referred, as Quality Issues) within one business days, and minor deviations within three business days to Accenture Quality Management team. Ensure to meet all SLAs and KPIs.  Incorporate comments from Client (or external) stakeholders into the draft RMP/ associated documents and seek clarification where applicable.Qualification & ExperienceQualifications:MBBS/MD Years of Experience:3 to 14 years