3773 Pharma Jobs - Page 48

Job Description Planning /Analysis (Routine and stability and QBD analysis) of ongoing projects by performing analysis of various tests (e.g. Dissolution, assay, Related substances test, or as per requirement) within given Time. Analytical Method development as per current SOP/guideline wherever required. Regulatory query/Plant Query related analysis for different products. To follow Good Laboratories practice while working. Documentation and compliance and review of data generated on all analytical activities as per the GLP/GMP norms and to keep working place neat and clean. Method transfer at plant. Method equivalency, method verification, pharmaceutical equivalency analysis of Pharmacopeial method. Preparation/review of various documents like method transfer waiver, method equivalency report, cleaning validation report SOP, T-STP/FP STP etc. Coordination with team members, superiors and subordinates within the group and across all relevant groups (customers) to achieve target timelines. Procuring of columns, reagents and miscellaneous items for analytical product development/support. Whenever required give training to subordinates/colleagues to upgrade their knowledge and current requirements. Work Experience 3 to 5 years of experience Education Masters in Analytical Chemistry or Analytical Chemistry Post Graduation in Pharmacy or Analytical Chemistry Competencies

ORGANISATIONAL OVERVIEW Lambda Therapeutic Research is a Global full-service Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK) and Warsaw (Poland), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries. JOB DETAILS Department: Bioanalytical Operations Designation: Research Associate Job Location: Ahmedabad (Gujarat) Education: M.Pharm/B.Pharm Experience: 5 to 7 years CTC Range: 5 to 7 Lacs Job Description: Ensure project coordination and conduct the study as per protocol and SOPs requirements. Work in close coordination with the Principal Investigator and Study team. Review of study protocol, ICF, CRF and other appendices (applicable in case of Special studies). Handling study related IMPs and its relevant documents (IP retrieval, verification, accountability, dispensing etc.). Communicate with sponsors, other departments and team on appropriate aspects of the clinical studies. Compile and complete raw data in TMF and resolve all QA/QC queries in timely manner. COMPETENCIES Accountability Communication Work Ethic Presentation / Communication skills Organizational Culture fit

A Day in the Life Responsibilities may include the following and other duties may be assigned. Promotes and sells Medtronics products and services within an assigned geographic area and /or specific customer accounts to meet or exceed sales targets. Responsible for developing, building, and strengthening long-term relationships with stakeholders including distributors and healthcare professionals. Responsible for pursuing leads, assessing needs and providing product services to maximize the benefits derived from Medtronics products and/or services. Promotes and establishes education of the companys products and/or services. Conducts market research including customers and competitors activities. Implements market development plans/strategies and changes as needed. Communicates customer feedback on new products and/or modifications to existing products or applications to internal stakeholders including R&D, Operations and Marketing. SALES PROFESSIONAL CAREER STREAM: Typically sales professional individual contributors with direct sales responsibilities. May direct the work of other lower level sales professionals or manage sales processes and / or accounts involving multiple team members. The majority of time is spent establishing and maintaining customer relationships, developing new customer relationships, implementing sales strategies and closing sales. DIFFERENTIATING FACTORS Autonomy: Established and productive sales professional managing multiple small to mid-size accounts. Sells products and/or services to a group of clients and identifies new and potential customers. Works independently with general supervision . Builds relationships. Organizational Impact: Works to achieve individual sales targets within product area and/or account by selling products/ services, developing new accounts and/or expanding existing accounts. Has a direct impact on achieving department s sales results. May help to set objectives or goals for individual or team accounts . Works on larger, moderately complex accounts or have a small or medium-sized quota/territory. Understands market landscape, marketing and pricing structure, more influence on pricing structures. Works with sales, marketing and finance to structure complex contracts. Innovation and Complexity: Makes adjustments or recommends enhancements in sales processes to solve problems or improve effectiveness of job area. Recommends changes in account tactics to achieve sales goals . Exercises judgment within defined procedures and practices to determine appropriate action. Communication and Influence: May influence parties within own job function at an operational level. Obtains or provides information requiring some explanation or interpretation . Communicates with external customers and / or vendors, involving negotiation and / or presentations in order to manage relationships and close sales. Leadership and Talent Management: Normally receives general instructions on routine work, detailed instructions on new projects or assignments. May provide guidance and assistance to entry level sales professionals and / or support employees. Required Knowledge and Experience: Requires practical knowledge gained through experience of sales techniques and job area typically obtained through education combined with sales experience. Developing professional expertise, applies company policies and procedures to resolve a variety of issues . Graduate (B.tech/B.E/BCA/B.Pharma) AND a minimum of 3-7 years of relevant work experience in the healthcare field.

A Day in the Life Chandigarh HQ, Coverage, Ambala, Yamuna Nagar, Himachal, PGI - Chandigarh, Fortis Mohali. AOP- 450L Responsibilities may include the following and other duties may be assigned. Promotes and sells Medtronics products and services within an assigned geographic area and /or specific customer accounts to meet or exceed sales targets. Responsible for developing, building, and strengthening long-term relationships with stakeholders including distributors and healthcare professionals. Responsible for pursuing leads, assessing needs and providing product services to maximize the benefits derived from Medtronics products and/or services. Promotes and establishes education of the companys products and/or services. Conducts market research including customers and competitors activities. Implements market development plans/strategies and changes as needed. Communicates customer feedback on new products and/or modifications to existing products or applications to internal stakeholders including R&D, Operations and Marketing. SALES PROFESSIONAL CAREER STREAM: Typically sales professional individual contributors with direct sales responsibilities. May direct the work of other lower level sales professionals or manage sales processes and / or accounts involving multiple team members. The majority of time is spent establishing and maintaining customer relationships, developing new customer relationships, implementing sales strategies and closing sales. DIFFERENTIATING FACTORS Autonomy: Entry-level sales professional on one or more individual or team accounts . Sells products and/or services to a group of clients and identifies new and potential customers. Work is closely supervised . Maintains relationships. Organizational Impact: Works to achieve individual sales targets within product area and/or account by selling lower complexity products / services, developing new accounts and/or expanding existing accounts. Has some impact on the overall achievement of sales results for the team. Work typically on smaller, less complex accounts, small quota or territory. Innovation and Complexity: Follows standard sales and business development practices and procedures in analyzing situations or data from which answers can be readily obtained. May recommend changes in account tactics to achieve sales goals . Implements improvements and changes to work processes and procedures. Communication and Influence: Communicates with external customers and / or vendors, involving basic negotiation and / or presentations in order to close sales. Obtains or provides information requiring some explanation or interpretation . Leadership and Talent Management: N / A - Job at this level are focused on self-development. Required Knowledge and Experience: Requires broad knowledge of sales techniques typically gained through education and / or on the job learning. Learns to use professional concepts Applies company policies and procedures to resolve routine issues. Requires a Bachelor degree-B.tech / B.E / B.SC / BCA / B.pharma with 1-5 years of experience

Title: Project Coordinator Date: 7 Jul 2025 Location: Bangalore, KA, IN Job Description We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out www.careers.indegene.com Looking to jump-start your career We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most brilliant minds in the industry. We are offering a global fast-track career where you can grow along with Indegene s high-speed growth. We are purpose-driven. We enable healthcare organizations to be future ready and our customer obsession is our driving force. We ensure that our customers achieve what they truly want. We are bold in our actions, nimble in our decision-making, and industrious in the way we work. Must Have Project coordinator Job Summary: Assist in coordinating project activities to ensure project is well organized and runs smoothly. Communicate and work closely with various departments to ensure everyone is on the same page. Manage administrative tasks such as documentation, report collation, and communication support. Job Description Explore, analyze and utilize platform from an end user perspective Record feedback on tools and processes, resolve internal and external query related to usage of customer engagement platform Keen learner who can quickly grasp business domain knowledge and explore the platform Ensure product manuals, documents etc. are kept up to date and are uploaded in the required location Should be able to analyze operational issues and enhancement requirements Ensure adherence to laws and policy requirements Liaise with internal team members through calls to document objectives Organize, document and follow up on important actions and decisions from meetings Providing administrative support as needed Ensure resources and equipment are always available Desired Profile (Education, Experience, Key Skills) Bachelors in Science, Technology or Business. 1-2 years of experience in a business support role. Ability to use MS Excel, and MS Power point with intermediate level skills Must have excellent communication skills both Verbal and Written High Potential to learn and deliver Experience in pharma domain Good to have EQUAL OPPORTUNITY

Maintain, upkeep and execute processes of stores with regard to direct/indirect material, area of work, material handling equipment and storage etc. as per safety compliance, cGMP norms and QMS to support, execute and coordinate in functioning of stores processes. Key Accountabilities (1/6) Execute the store operations like receipt, dispensing and dispatch etc. materials as per cGMP procedure to avoid any cross contamination & to achieve manufacturing targets Execute the dispensing activities as per the plan Weigh, count and verify materials as per purchase order and receipt documents and store materials in designated area Manage the dispensing activity to ensure compliance to cGMP Dispense the materials required for manufacturing, stock transfer and exports as per cGMP norms Ensure cross contamination of material is prevented while handling by following all procedure strictly Key Accountabilities (2/6) Maintain the online documentation & area as per cGMP guidelines and regulatory requirements to avoid any deviation Review the status labelling of materials to ensure correct labelling is performed by quality Perform status labelling for equipment and accessories Monitor logs and area on day-to-day basis to avoid any deviation during internal and external inspection Update data entries in online documentation to avoid data integrity Key Accountabilities (3/6) Dispose the scrap generated periodically in stores to remove blockage and ensure smooth store operations Ensure segregation and removal of scrap material by coordinating with housekeeping Minimise scrap related hazards through the risk management processes Key Accountabilities (4/6) Maintain safety in the store operations by complying to safety norms to reduce the incidences and accidents Monitor the store assistants to use proper safety appliances while handling materials during receipt and dispensing Identify and report possible hazards and handle (storage, receipt , issuance) hazardous materials safely Key Accountabilities (5/6) Prepare receipts and issue materials on time by coordinating with purchase and user department to ensure required material is positioned in scheduled time Indent of materials as per correct quantity & delivery schedule from purchase department Manage material receipts while adhering to relevant SOP & store the goods as per the required storage condition Account the receipts of materials by making GRN Issue materials to user department by following SOP as per given schedule Key Accountabilities (6/6) Review stock of materials and store goods in appropriate conditions to reduce materials damage due to improper storage and for smooth production activity, and update in the system Monitor and record the environmental conditions of area and equipment Store the goods in designated places as per required storage conditions Carry out the reconciliation of reviewed physical stocks and update the effect of reconciled stocks in system Major Challenges Delay in delivery time due to frequent changes in the production plans and shifting priorities. Erratic delivery time by production. Overcome by conducting status meetings, escalation and continuous follow ups Delay in routine work due to system failure and issue of slips. Overcome by training from SMEs and manually working to reduce idle time Key Interactions (1/2) Manufacturing for dispensing planning (Weekly) Packing for prioritization of production (Weekly) Quality Control for release and sampling (Daily) Quality Assurance for discrepancies and non-conformances (Daily) Purchase for receipts (Daily) Accounts for invoice submission (Daily) Planning prioritize production (Daily) Customs for re-warehousing (Daily) Safety for safety norms and approval of destruction material (Daily) Engineering for maintenance issues (Daily) Housekeeping for sanitization (Daily) Key Interactions (2/2) Equipment Supplier for dispatch related (Need Basis) Transporters for deliveries (Need Basis) Courier for tracking of materials monthly Government authorities for stamping of weights (yearly) Pest Control Services for pest related issues (Daily) Dimensions (1/2) Average number of GRN for raw material / packing material : 300 per month Average number of materials removed (expired/rejection) : 50 per month Average number of dispatches : 30 per month Achieve internal OTIF more than 90% Achieve Zero reportable accidents / incidences during manufacturing Achieve 0% errors in online documentation Meet 100% compliance to SOP and safety regulations Maintaining proper storage condition (100%) 100% Clearance/disposal of non-moving/rejected materials Dimensions (2/2) Key Decisions (1/2) Bin Allocation Handling of material at designated place Set priority for dispensing of a particular material as per manufacturing requirements Set priority for unloading of vehicle of a particular consignment Key Decisions (2/2) Improvements in store operations, facility and documents to Section Head - Stores Education Qualification Graduate or D. Pharm Relevant Work Experience 0-2 years of experience with exposure to stores operations, preferably in a pharma company with regulatory approvals

Designation: Research Scientist - Document Reviewer Job Location: Bangalore Department: Clinical Development About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R& productivity, speed up time to market and lower the cost of innovation. Job Purpose: The position holder is responsible for document review related to Bioanalysis, including Pharmacokinetics and Immunogenicity. Key Responsibilities: Review technical documentation and record review in a report Provide assistance/participate for the preparation of SOPs etc. Execution of review documents in accordance with planned timelines Technical data reviews for studies utilizing analytical skills, technical knowledge and utilizing excellent regulatory guidelines requirements Capable to focus attention to detail review and identify critical observations Routine review of laboratory log books, equipment calibration and validation status etc. Handle multiple studies data review simultaneously in an efficient and effective manner. Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety. Attend training on environment, health, and safety (EHS) measures imparted company Educational Qualification: Master s degree in Biological Sciences (Preferably Biochemistry background) or a related field. Technical/functional Skills: Good knowledge of MS Office applications is necessary Handling audits and participation in audits is preferable Knowledge and experience with regulatory requirements e.g. Organization for Economic Co-operation and Development (OECD), GXP, 21 CFR Part 11, European Medicines Agency (EMA) and Food and Drug Administration (FDA) guidelines. Experience: 12-15 years of total experience in Document review. Behavioral Skills: Should be independent. Excellent communication skills - written and oral in English Should have good interpersonal skills Large degree of flexibility and ability to work under strong time pressure Equal Opportunity Employer: .

JOB DESCRIPTION Designation: Associate Scientist / Senior Associate Scientist Job Location: Bangalore Department: TM-TDDT About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation . Job Purpose (1-2 Lines) We are seeking motivated master s level scientists (MS, MTech, MSc, etc) to join the Translational Medicine team at the Biocon Bristol Myers Squibb Research Center in Bangalore, India. Key responsibilities of this role are to serve as an execution arm for the preclinical support of asset programs through mechanism of action-based studies, differentiation from standard of care and competitive therapeutics, combination rationale, new indications (life cycle management), and patient selection strategies. S/He will work directly with translational scientists, disease leaders within translational medicine, and will also interact with thematic research centers in early development within the company. Key Responsibilities: Conduct preclinical/laboratory experiments on late stage BMS portfolio compounds to support annual goals and objectives for Translational Medicine (for internal /external, collaborations, compound specific plans etc). Responsible for delivering data in support of translational strategies including biomarkers, patient selection hypotheses, dose and schedule, combination strategies, resistance mechanisms and differentiation. Interfaces with TM scientists across departments to ensure seamless flow of information for assets which are entering the remit of translational medicine. Assists in designing experiments and delivering data for collaborative projects along with TM scientists. Maintains comprehensive records, communicates regularly and makes presentations within the department, as required. Reports experimental finding in written nonclinical pharmacology study reports, to support regulatory filings. Educational Qualification: Masters with at least 2 years of relevant work experience across immunology, oncology, heme-oncology focus areas. Industry experience is a plus. Multiple positions can range upto 6 years of experience. Technical/functional Skills: Cell culture, primary cell isolation, cell transfection and single cell cloning; including siRNA / CRISPR / TALEN or HDR workflows Gene expression methods including qRT-PCR and/or familiarity with RNA sequencing, epigenomic methods including methylation analysis, ChIP etc Protein analyses and immunoassays, and cell phenotyping analysis (e.g. ELISA, MSD, Luminex, TSA, CBA, flow cytometry). Design, setup and execution of autoimmune, solid tumor oncology or heme-oncology in vivo pharmacology models. Excellent verbal and written communication skills, familiarity with standard or relevant software platforms, and scientific qualities are expected. Competence in analysis and solving of problems, keeping track of overall goals. Maintain a good understanding of the methodological basis and biological significance of assays performed. Forecast potential issues regarding support of assays for current and long term projects. Devise strategic solutions to identified and potential hurdles/issues and efficiently and proactively troubleshoot technical and experimental problems. Experience: 2-6 years Behavioral Skills: A self-starter, who is/can become technically proficient in a diverse set of techniques and assays with a focus on quality and speed, and will meticulously follow internal SOPs Good basic lab skills required (pipetting, balances, etc.) Highly detailed and meticulous, high standards of data entering and QC Must be highly adaptive to changing timelines and goals Must be comfortable taking on complex tasks with minimal direct supervision An excellent multitasker with an ability to be level-headed in a fast-paced lab setting Team-oriented and comfortable working in a highly dynamic matrix environment across multiple locations Prior experience working with patient samples (i.e. FFPE tissue, Fresh Frozen tissue, blood) or working in a CLIA/GCLP/clinical environment is a plus Must be comfortable and able to work with animal (rodent) or human derived samples Equal Opportunity Employer: .

Project Manager Noida This role is for a Project Manager within the Professional Services (PS) Team. Our peoples passion and expertise are our greatest strengths. The S&S Team in India is an important execution group that provides end-to-end solutions to end-users. You will oversee project activities to ensure the delivery of high-quality results within defined timeframes and budget constraints. You will report to the Application centre Manager and have a hybrid schedule working in Noida, India. Your Responsibilities: Be an Single Point of Contact (SPOC) for the project, establishing relationships with relevant client stakeholders. Lead projects from requirements gathering through deployment. Define schedules, scopes, budgets, and implementation plans, including risk mitigation strategies. Communicate and manage partners, engaging clients, executives, and team members. Coordinate internal and external resources to ensure projects follow scope, schedule, and budget. Monitor project metrics; conduct regular project reviews. Mitigate project risks. Lead issue resolution during the project lifecycle. Prepare Monthly Progress Reports (MPR) for customers and develop action plans. Provide regular project updates to all partners. Provide and achieve revenue and shipment targets by driving projects to ensure profitability Ensure strict adherence to Project Management processes throughout the project lifecycle. Set quality and performance standards, assessing risks. Develop partnerships with vendors and third-party resources. Collaborate with Technical Leads to improve project efficiency and quality. Report project outcomes and risks, escalating issues. Manage end-to-end delivery of one or more medium to large/complex projects or milestones. Prepare and lead the project schedule; coordinate daily activities, issue resolution, and communication to ensure, within-budget delivery. Attend Kick-Off Meetings (KOM), liaise with the project and customer teams, and coordinate with manufacturing, supply chain, and logistics teams. Establish annual objectives for team members as applicable. Coordinate billing schedules with the sales team. Track Project status, issues, risks, and plans to all stakeholders. Build and develop the project/engineering team for future growth. Oversee Factory Acceptance Tests (FAT) and site dispatches; coordinate with field services for commissioning. Manage payments and receivables in collaboration with the sales team. Drive contract closure with high customer satisfaction. The Essentials - You Will Have: Bachelors degree in Instrumentation, Electrical Engineering, or E&C PMP certification. 15+ years of experience in automation industry project management, with hands-on project execution knowledge. Experience in PLC, DCS, VFD, SCADA, and automation design & engineering Experience with project management methodologies, risk management, and budgeting. Demonstrated leadership and stakeholder management skills. Domain expertise in Power, Metals, Aluminium, Cement, mining, infraConsumer, and Pharma industries. The Preferred - You Might Also Have: Knowledge of PLC/VFD/DCS programming and communication protocols (GE, Emerson, Schneider, Siemens, Rockwell, Honeywell). Experience managing global projects. Ability to promote a quality-driven culture within teams. Mentoring capabilities for project engineers and team leaders. Provide guidance and mentorship to a team of Project Engineers and Team Leaders to ensure project execution What We Offer: Our benefits package includes Comprehensive mindfulness programs with a premium membership to Calm Volunteer Paid Time off available after 6 months of employment for eligible employees Company volunteer and donation matching program - Your volunteer hours or personal cash donations to an eligible charity can be matched with a charitable donation. Employee Assistance Program Personalized wellbeing programs through our OnTrack program On-demand digital course library for professional development ... and other local benefits! At Rockwell Automation we are dedicated to building a diverse, inclusive and authentic workplace, so if youre excited about this role but your experience doesnt align perfectly with every qualification in the job description, we encourage you to apply anyway. You may be just the right person for this or other roles. #LI-Hybrid #LI-NB1

Manipal Hospitals is searching for an experienced and highly skilled Senior Pharmacist to lead our hospital pharmacy team. This critical role requires a professional with deep expertise in pharmaceutics and a strong foundation in clinical pharmacy practices. The ideal candidate will be responsible for overseeing efficient and accurate medication dispensing , ensuring optimal patient outcomes, and contributing to the continuous improvement of our pharmacy services. If you are a seasoned pharmacist looking to take on a leadership role in a dynamic hospital environment, we encourage you to apply. Medication Dispensing & Management: Oversee and ensure the accurate and safe dispensing of medications to inpatients and outpatients in accordance with physician orders, hospital policies, and regulatory requirements. Manage the inventory of pharmaceuticals, including ordering, receiving, storage, and proper rotation, to minimize waste and ensure availability. Supervise the preparation of sterile and non-sterile compounded medications, adhering to strict quality and safety standards. Clinical Pharmacy Practice: Apply advanced clinical pharmacy knowledge to review patient medication profiles for drug interactions, allergies, contraindications, and appropriate dosing. Collaborate with physicians and other healthcare professionals to optimize drug therapy and provide drug information and recommendations. Participate in ward rounds or multidisciplinary team meetings to contribute to patient care planning and medication management. Provide patient counseling on medication use, side effects, and adherence. Quality Assurance & Compliance: Ensure strict adherence to all hospital policies, national and local pharmaceutical regulations, and best practices in pharmaceutics . Implement and monitor quality control procedures for all pharmacy operations, including dispensing and compounding. Lead or participate in internal audits and accreditation processes for the hospital pharmacy . Team Leadership & Training: Provide guidance, mentorship, and training to junior pharmacists, pharmacy technicians, and other pharmacy staff. Oversee daily operations of the pharmacy department, ensuring smooth workflow and efficient service delivery. Participate in staff scheduling, performance evaluations, and conflict resolution within the team. Report Generation & Process Improvement: Maintain accurate records and generate reports related to medication usage, adverse drug reactions, and pharmacy performance. Identify areas for process improvement within the hospital pharmacy to enhance efficiency, safety, and patient care . Implement new programs or services that align with the goals of the hospital and advances in clinical pharmacy .

We are seeking a detail-oriented and technically adept QC Email Analyst - SFMC to join our Marketing Automation team. This role is responsible for ensuring quality assurance of email campaigns and journeys executed through Salesforce Marketing Cloud. You will work closely with campaign managers, developers, and compliance teams to validate that marketing assets are accurate, on-brand, and compliant before launch. Key Responsibilities: Quality Control & Testing Perform detailed QA checks on emails, templates, data extensions, dynamic content, and journeys within SFMC before launch. Validate rendering across various devices, email clients, and browsers using tools like Litmus or Email on Acid. Ensure links, tracking parameters, subject lines, from names, images, and personalization tokens are working as expected. Verify compliance with CAN-SPAM, GDPR, and other regional regulations (e.g., inclusion of unsubscribe, privacy policy links). Data & Segmentation Checks Ensure correct use of audience segmentation and filters. Validate test sends using test data extensions or live preview. Process & Documentation Maintain checklists, QC logs, and documentation for all reviewed campaigns. Support the development of QA best practices, SOPs, and templates for campaign QC. Collaborate with internal teams to triage and resolve issues quickly before deployment. Identify root causes of QA failures and propose process improvements. Required Skills & Qualifications: Bachelor s degree in Marketing, Communications, Computer Science, or related field. 2-4 years of experience in email marketing or digital QA, ideally in healthcare, consumer, or tech sectors. Strong knowledge of Salesforce Marketing Cloud components: Email Studio, Content Builder, Journey Builder, Data Extensions. Hands-on experience with email rendering tools (Litmus, Email on Acid). Understanding of email compliance standards and privacy laws. High attention to detail and a proactive approach to problem-solving. Preferred Qualifications: Experience in regulated industries (e.g., pharma, finance). Knowledge of multi-language or multi-region campaign QC. SFMC certifications (e.g., Email Specialist) are a plus.

" Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research & Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively. The manufacturing location at Mysore is spread over 69 acres and it s a USFDA approved site engaged in manufacturing of APIs, and caters to the sales worldwide. API portfolio focusses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules. The company is the market leader in four APIs and is amongst the top three players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand is state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focusses on B2B model for EU, Canada and emerging markets. Both manufacturing units are backward- integrated and are supported by around 500 research and development professionals based at Noida and Mysore. R&D works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids. All BA/BE studies are done In house at our 80 Bed facility which is inspected and having approvals /certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services. JGL s full-fledged Regulatory Affairs & IPR professionals ensures unique portfolio of patents and product filings in regulatory and non-regulatory market. Revenue of Jubilant Pharma is constantly increasing and during the Financial Year 2018 -19 it was INR 53,240 Million as compared to INR 39,950 Million during the Financial Year 2017-18. Kindly refer www.jubilantpharma.com for more information about organization. Scope of the role Scope - This role is responsible for Responsibilities Achievement of set targets. Maintaining set call Average/coverage. Complete use of allotted resources. Increasing prescriber base Focus on target customers. Maintaining call average and customer coverage Increasing PCPM. Timely reporting. Ensuring ROI Relationships around the role Reporting to (Business) Regional Sales Manager / Sr. Regional Sales Manager Reporting to (Matrix) NA No of Reportees Direct NA Indirect NA Key External Stakeholder(s) Doctors, Stockiest, Retailers, CFA staff, Fellow professionals, institutional administrators Key Internal Stakeholder(s) RSM, ZSM, BDM, NSM / SM, PMT, HR & Sales Admin Competencies critical for the role Scientific/ Technical Competencies Proficiency level Convincing ability Presentation Selling Communication Behavioral Analytical ability PR Skills Academic qualifications and experience required for the role Required Educational Qualification & Relevant experience Desirable - B.Pharm / D.Pharm / BSc. + MBA Essential - Graduates in any discipline Experience: 6 Months. to 2 years as a Medical Rep in a reputed organization. Age should be around 28 years ",

Maier Vidorno Altios is the leading service company for international market expansion for SMEs and medium-sized companies that want to expand both within India and worldwide. Over 50 years of shared experience in international trade and investments 750+ professionals in 32 offices worldwide -Presence in 22 countries: USA, Canada, Mexico, Brazil, Colombia, Great Britain, France, Italy, Spain, Germany, Poland / Eastern Europe, Russia, UAE, India, Bangladesh, China, Hong Kong, Singapore / Southeast Asia, Vietnam, Malaysia, New Zealand and Australia Maier Vidorno Altios offers pragmatic services for every phase of internationalization. From strategic advice and market analysis to local sales and business development to cross border M&A and location searches for greenfield projects. In addition, Maier Vidorno Altios provides worldwide services such as bookkeeping, payroll accounting, tax advice and a wide range of personnel solutions Personnel leasing, recruiting and HR services. We are looking for a APPLICATION ENGINEER for one of our client in India. Our client is the leading supplier of customized, highly productive machining systems for the manufacturing of complex high-precision components made of metal such as turbocharger Job Reference No: # 26965 Industry: Manufacturing Location: Pune Desired profile Qualifications Diploma/ Bachelor s Degree in Engineering Experience 3+ Years working experience Language Fluent in English & Hindi Desired Skills: Degree or Diploma Degree in Engineering, Minimum of 3 years experience in Technical Sales and Application Engineering Possess strong knowledge in factory automation, preferably in automotive, electronics, and/or medical/pharmaceutical equipment manufacturing Skilled user of AutoCAD and Inventor CAD Systems Ability to provide accurate cost calculation Job Description: Create 3D and 2D layouts based on operation sequence defined by application engineer Prepare 3D concepts of pallet and station to illustrate operation sequence Source and communicate with critical suppliers to obtain accurate cost and specifications (Bowl feeder, Vision, Sub-system, etc.) Support application engineer in updating existing proposal text and costing Responsible for maintaining Application 3D and 2D library as well as technical information Act as a coordinator for projects between Sales and ECP (Standardization, Bowl feeder classification, etc.) Support ECP team in design engineering during high workload (to be agreed by Application Engineering Manager) Adhere to company standards in terms of work procedures and use of standard documents and understanding of standard products.

Senior Associate/Associate - Field Force Operations (FFO) Location: Hyderabad Department: Insights & Analytics - FFO Industry: Pharma / Healthcare About Us: Chryselys is a Pharma Analytics & Business consulting company that delivers data-driven insights leveraging AI-powered, cloud-native platforms to achieve high-impact transformations. We specialize in digital technologies and advanced data science techniques that provide strategic and operational insights. Who we are: People - Our team of industry veterans, advisors and senior strategists have diverse backgrounds and have worked at top tier companies. Quality - Our goal is to deliver the value of a big five consulting company without the big five cost. Technology - Our solutions are Business centric built on cloud native technologies. Role Summary: As a Senior Associate/Associate - Field Force Operations (FFO) at Chryselys, you will support pharmaceutical clients with analytics-based solutions to optimize field team performance and improve commercial effectiveness. Your focus will be on delivering segmentation and targeting, sales force sizing, and call plan support using US-based datasets and claims information. You will work with internal analytics teams and client stakeholders to convert business questions into actionable field force strategies. The role involves applying both traditional and advanced segmentation techniques using machine learning models to enhance targeting precision and HCP engagement strategies. Key Responsibilities: Execute projects using US commercial and claims datasets to support field force planning Build and apply segmentation and targeting models, including machine learning-driven approaches, to optimize HCP engagement Perform sales force sizing analysis based on reach, frequency, and promotional goals Develop and refine call plans aligned with customer segmentation Design balanced Territories using the S&T and Sizing data Analyze claims data, CRM activity, and sales performance to assess rep impact Translate analytics into clear, business-friendly recommendations and reports Ensure accuracy, timeliness, and consistency in deliverables across projects What You Bring: Education: Bachelor s or Master s degree in Data Science, Statistics, Computer Science, Engineering, or a related field Experience: 2+ years of experience in Field Force Operations, preferably in the pharmaceutical or healthcare industry Technical Skills: Proficiency in SQL for querying and transforming large datasets Experience working with claims data, CRM systems, and sales activity data Strong knowledge of Advanced Excel for reporting Domain Knowledge: Understanding of segmentation and targeting, sales force sizing, and call plan development Experience in applying ML techniques (e.g., clustering, decision trees) for advanced HCP segmentation Familiarity with commercial data used in US pharma markets Strong problem-solving, communication, and teamwork skills Ability to manage deadlines in a collaborative, client-focused environment How to Apply: Ready to make an impact? Apply now by clicking [here] or visit our careers page at https: / / chryselys.com / chryselys-career / Please include your resume and a cover letter detailing why you re the perfect fit for this role. Equal Employment Opportunity: Chryselys is proud to be an Equal Employment Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Connect with Us: Follow us for updates and more opportunities: https: / / www.linkedin.com / company / chryselys / mycompany / Discover more about our team and culture: www.chryselys.com

Division Finance Department Commercial Finance Sub Department 1 NA Finance Job Purpose Enable North America BU team in timely Management Reporting & effectively partner with B2B Business, additionally handle competition benchmarking, CMO contracts for North America, provide various cuts for revenue and board requirements, Invagen opex analysis as Invagen controllership is re-assigned to India. Key Accountabilities (1/4) 1) Support in Month end closing activities & preparation of Consolidated BU P&L Consolidate Sales across entities to present overview of Revenue & Margins for North America Business Liaise with cross functional & corporate teams to reconcile Sales numbers Undertake Price Volume Variance Analysis & identify exceptional performance products Undertake Quarterly Cost Analysis of Standard Costing files to identify outliers Update Masters in Power BI & support in automation activities Undertake Analysis & Calculation of B2B spends, Freight & Inventory for timely closure of P&L Submission of Profit Share Payout & Other Expense Provisions Analysing Invagen opex and analysis of spends, its variance vs budget Key Accountabilities (2/4) 2) Prepare annual budget plant exercise for North America BU Prepare template for Budgeting exercise to share with Business teams Variance analysis vs previous years to understand the outliers and investments Analysis of revenue and EBITDA for budgeting, building bridges for different management views Competition benchmark data for various companies Key Accountabilities (3/4) 3) Active business partnering to achieve performance targets Roll out Sales Flash for B2B & Pvt Label Business Undertake Ageing Analysis of receivables outstanding to ensure compliance as per DOA Prepare DSO Quarterly Comparative statements for Corporate Prepare Pvt Label deck monthly to discuss with Marketing Head Monthly compute FTS & Other Penalties in Pvt Label Review CMO contracts for North America finance under development and post development projects Key Accountabilities (4/4) 4) Support North America team in complying with internal and external controls to ensure smooth and transparent operations Ensure monthly tracking of Debit Note & Credit Notes Monitor Profit Share Receivable statements from partners are received timely & Validate the same Support in payment mechanism of foreign payments, checking such DN/ CNs are in adherence to contractual terms Identifying negative, low GM / profit product, initiating conversation with business Preparation of product P&L for key products to see end to end profitability Ensure compliance of Payment Terms & Prices as per Agreement Tracker Major Challenges High Dependency on SAP requires IT support for resolving data & access queries. Co-ordination with cross functional- Corporate, FSS, BU. Ensuring establishment of a single communication base with different teams helps alignment of information Key Interactions Internal : B2B team - BD team, SCM team, NA Finance teams Corporate teams - FP&A Dimensions Support $900mn of North America business for margin improvement and cost controls Ensure proper accounting of revenue & expenses as per specified timelines. Ensure the DSO for B2B stays within guidance limits Key Decisions Decisions : Time Management to ensure closure of month end activities accurately & timely. Recommendations : Automation Initiatives Profit Share Receivable/ Payable Statements Comments: The incumbent would be actively interacting with cross functional teams to provide inputs on Queries raised & in timely closure of P&L, month end activities. Listed above are just a few activities, the incumbent would be expected to work on many adhoc projects and provide necessary inputs to enable leadership in efficient decision making Education Qualification Qualified Chartered Accountant / MBA - Finance Relevant Work Experience 4 - 8 years of work experience in business/ corporate finance in Pharma/FMCG companies. Prior experience in a cross-functional (multi-geographic) environment will be added advantage

Provide expert skills as part of a Medical Data Review team to provide efficient, quality Medical Data Review products that meet customer needs; Provide Project management to the team in the area of clinical data review and viewed as an expert in data management; Drive the delivery of end-to-end study data quality and integrity; Provide medical, clinical, and scientific advisory expertise. Essential Functions Conduct in-stream data trend analysis in support of data quality and integrity (includes protocol compliance and targeted review of patient data) Ensure data quality focus to audit readiness with Clinical Compliance and Systems Validation Compliance. . Define data capture requirements in line with protocol and reporting needs. Represent clinical data scientist at multi-disciplinary team meetings and external meetings. Maintain strong customer relationships With guidance, track service performance and provide leadership to identify root causes of issues and implement remedial actions Ensure timely follow-up and resolution of compliance issues Serve as Subject Matter Expert (SME) Continuously look for opportunities to improve efficiency of tasks and quality of deliverables Provide therapeutic area/indication training for the project clinical team. Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested. Manage staff in accordance with organization s policies and applicable regulations. appraising performance and guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems. Approve actions on human resources matters. Qualifications Other Medic with 5 year college degree or MBBS Req Bachelors Degree Clinical, biological, mathematical sciences, or related field, or nursing qualification, with 7 years of relevant work experience Req Equivalent combination of education, training and experience in lieu of degree Req Experience in clinical data sciences at a CRO, pharmaceutical company or other medical environment with demonstrated leadership experience Req Good understanding of clinical/medical data Proven expertise in the proactive identification of issues Demonstrated ability to plan, organize and manage resources to bring to successful completion specific study or project goals and objectives in accordance with defined quality and time based metrics Proven ability to work within a matrix team environment requiring minimum level of supervision Attention to detail Interpersonal and analytical skills, Ability to represent clinical data scientist at multi-disciplinary team meetings and external meetings Knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology Must have Medical but also an operational focus towards metrics and status information to take the appropriate actions to resolve Excellent communication, interpersonal, customer service, and teamwork skills Excellent organizational and problem-solving skills Excellent project management skills and coaching skills Ability to work with minimal supervision, using available resources Ability to work on multiple projects and manage competing priorities Strong customer focus skills Ability to establish and maintain effective working relationships with coworkers, managers and clients

About HCP Wellness At HCP Wellness Private Limited , we are committed to delivering safe, effective, and high-quality skin care, cosmetic, and oral care products. Our culture thrives on scientific excellence, GMP compliance, and sustainable innovation. We believe in empowering our team to lead quality-focused solutions that help build trusted personal care brands. Job Overview We are looking for a Microbiologist to join our Quality & R&D division in Ahmedabad. The ideal candidate will be responsible for ensuring microbiological safety and compliance of all raw materials, bulk, and finished goods used in cosmetic and personal care product manufacturing. Your insights will directly impact product integrity, consumer safety, and regulatory compliance. Key Responsibilities Perform microbiological testing of raw materials, in-process samples, water systems, packaging, and finished goods. Conduct environmental monitoring of cleanrooms and production areas (air, surface, and personnel hygiene). Validate disinfectants, preservative efficacy, and microbial limits as per pharmacopeial standards (IP/BP/USP). Maintain and calibrate laboratory equipment and ensure proper documentation (SOPs, logbooks, test records). Support product stability studies, contamination investigations, and root cause analysis. Coordinate with QA and R&D for batch release, deviation handling, and process improvements. Ensure adherence to GMP, ISO, and regulatory compliance for cosmetic and oral care formulations. Qualifications & Skills Education / Certifications: B.Sc / M.Sc in Microbiology, Biotechnology, or Life Sciences Hard Skills: Expertise in microbial testing techniques (TPC, Yeast & Mold, Pathogens) Hands-on experience with colony counters, autoclaves, incubators, and laminar airflow Familiarity with preservative efficacy testing (PET), D-value & Z-value analysis Knowledge of regulatory guidelines BIS, FDA, ISO, and cosmetic-specific standards Soft Skills: Detail-oriented and accurate in documentation and reporting Strong analytical and problem-solving skills Team player with good communication across departments Ability to handle audits and provide scientific justifications Preferred Experience: 3+ years of hands-on experience in microbiology testing within a cosmetics, pharma, or personal care manufacturing setup Why Join Us? Be part of a growing and future-focused company where your scientific contributions directly shape the quality and safety of consumer products. We offer a collaborative and innovation-driven work culture, aligned with global best practices in personal care manufacturing. Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: HCP HR Talent Acquisition +91 7600217962 +91 9998962424 Email hr@hcpwellness.in career@hcpwellness.in info@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

About HCP Wellness Private Limited: HCP Wellness is a GMP-certified, innovation-led contract manufacturer specializing in skin care, cosmetic, and oral care products. We believe in quality, consistency, and customer satisfaction fueled by science, safety, and sustainability. Join a growing team where quality meets innovation. Job Overview: We are seeking an experienced QC Microbiologist to support our quality control operations by performing microbiological testing on raw materials, bulk, and finished goods. The ideal candidate will ensure that all products meet regulatory, safety, and quality standards. Key Responsibilities: Conduct routine microbiological testing (TPC, yeast & mold, pathogens) on raw materials, in-process, and finished products. Perform environmental monitoring and maintain hygiene compliance across production areas. Validate sterilization methods and efficacy of preservatives in formulations. Calibrate and maintain laboratory instruments and microbial media as per SOPs. Document and report results accurately in line with cGMP and regulatory requirements. Coordinate with QA, production, and R&D teams for troubleshooting and investigations. Participate in internal audits and assist in regulatory inspections as needed. Required Qualifications: Education: B.Sc./M.Sc. in Microbiology or Biotechnology Hard Skills: Microbial limit testing, preservative efficacy testing, and identification techniques Use of laboratory instruments like autoclaves, incubators, laminar airflow cabinets Knowledge of pharmacopeial methods (IP, USP, BP) Proficient in documentation as per cGMP and SOP protocols Soft Skills: Detail-oriented with strong analytical and observational skills Team collaboration and good communication across departments Ability to manage lab timelines and troubleshoot independently Strong organizational and reporting ability Preferred Experience: Minimum 3 years of hands-on experience in a microbiology laboratory, preferably within a cosmetic, personal care, or pharmaceutical manufacturing setup. Why Join Us? Be part of an R&D-driven, future-focused manufacturing company Collaborative culture that values quality, innovation, and personal growth Competitive compensation, learning opportunities, and a cleanroom-grade work environment Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: HCP HR Talent Acquisition +91 7600217962 +91 9998962424 Email hr@hcpwellness.in career@hcpwellness.in info@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

Brief team/department description: We are seeking a strategic and experienced Global Director of Compliance Operations to lead and oversee the operational execution of the global compliance program across all regions. This role ensures the company adheres to global laws and requirements, internal policies, and industry standards. The Director will collaborate with cross-functional teams to implement and sustain a culture of compliance, mitigate risk, and support business objectives in a highly regulated environment. Principle Responsibilities: Operational Leadership: Lead the day-to-day operational activities of the global compliance function, including program management, resource allocation, and cross-regional coordination. Compliance Program Execution: Oversee the implementation of compliance policies, procedures, training, monitoring, and reporting frameworks in alignment with applicable laws (e.g., FDA, UK Bribery Act, GDPR and ABAC (anti-bribery laws like FCPA/UKBA). Global Governance & Risk Management: Identify and assess compliance risks across markets; implement risk mitigation strategies and conduct regular operational reviews. Cross-Functional Collaboration: Partner with Legal, Regulatory Affairs, Quality, Finance, Commercial, and Medical Affairs to ensure compliance standards are embedded into business processes. Training & Communication: Drive the global compliance training strategy, ensuring consistent communication and employee understanding of relevant policies, SOPs, and regulatory requirements worldwide. Audit & Monitoring: Manage operational aspects of internal and external audits; develop and maintain monitoring tools to ensure continuous improvement. Metrics & Reporting: Develop and maintain KPIs and dashboards to monitor compliance performance and report to Compliance leadership and the Executive Leadership Team, as needed. Team Management: Lead and develop a global team of compliance professionals, fostering a high-performance and integrity-driven culture. Qualifications and Education Requirements Bachelor s degree required; advanced certifications (CHC, CCEP), degree in Pharmacy, Life Sciences, Business, Analytics or related field strongly preferred. 10+ years of experience in pharmaceutical or biotechnology compliance, with at least 5 years in a leadership or operations role. Deep understanding of global regulatory requirements and industry codes (e.g., IMC, FDA, EMA, EFPIA, PhRMA). Proven experience managing global teams and complex, matrixed organizations. Strong strategic thinking, project management, and problem-solving skills. Excellent interpersonal and communication skills with the ability to influence stakeholders at all levels. High ethical standards and sound judgment in navigating compliance challenges. Proficiency in compliance systems and tools, data analytics, and reporting platforms. Experience with digital health technologies, AI/ML compliance frameworks By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.

About HCP Wellness Private Limited At HCP Wellness , we are committed to delivering high-quality, innovative, and safe cosmetic and personal care products. Rooted in scientific excellence and a customer-first approach, we combine tradition and technology to craft skincare, oral care, and cosmetic solutions that people trust. Our culture is built on integrity, continuous learning, and a passion for wellness. Job Overview We are seeking a detail-oriented and quality-focused Microbiologist to join our dynamic Quality Assurance & R&D team. The ideal candidate will play a vital role in ensuring microbiological safety and compliance of our cosmetic and oral care products, supporting regulatory requirements and brand integrity. Key Responsibilities Perform microbiological testing on raw materials, in-process samples, and finished goods (TPC, Yeast & Mold, Pathogens etc.) Maintain and calibrate microbiology lab instruments and ensure timely documentation. Prepare and standardize culture media as per ISO, BIS, and GMP standards. Conduct environmental monitoring (air sampling, surface swabs, personnel hygiene monitoring). Investigate microbial contamination and implement corrective & preventive actions (CAPA). Work collaboratively with QA/QC, production, and R&D teams to ensure product safety and compliance. Stay up to date with relevant cosmetic microbiology standards and regulatory guidelines (e.g., IS 14648, ISO 22716, FDA, BIS). Qualifications & Skills Hard Skills Strong knowledge of microbiological testing methods and GMP/GLP practices. Proficiency in working with microbiological instruments (Incubators, Autoclaves, Laminar Flow, etc.). Understanding of regulatory requirements specific to cosmetics and personal care manufacturing. Ability to handle and interpret microbial limit tests (MLT), preservative efficacy test (PET), etc. Soft Skills High attention to detail and accuracy. Strong analytical and problem-solving skills. Excellent communication and documentation skills. Team-oriented, self-motivated, and adaptable to a fast-paced environment. Education & Certifications B.Sc. / M.Sc. in Microbiology or related Life Sciences field. Preferred Experience 3+ years of hands-on experience in a microbiology role within a cosmetic, pharmaceutical, or personal care manufacturing environment. Why Join HCP Wellness? Be part of an innovative and ethical company committed to wellness and sustainability. Work in a GMP & ISO-certified facility with a strong quality-centric culture. Grow with a team that values integrity, scientific rigor, and continuous improvement. Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: HCP HR Talent Acquisition +91 7600217962 +91 9998962424 Email hr@hcpwellness.in career@hcpwellness.in info@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

About Us: HCP Wellness Private Limited is a leading name in the manufacturing of high-quality skincare, cosmetics, and oral care products. As a GMP-certified and innovation-driven company, we are committed to product safety, quality, and excellence. Our work culture promotes integrity, collaboration, and continuous improvement. Position Overview: We are seeking a detail-oriented and quality-focused Microbiologist to support our Quality Control and R&D teams. The ideal candidate will ensure all cosmetic and personal care products meet microbiological safety and compliance standards in line with national and international regulatory guidelines. Key Responsibilities: Perform microbiological testing of raw materials, bulk, and finished cosmetic products. Conduct environmental monitoring of production and packaging areas. Validate and monitor water systems (RO/DM/Water for Injection) for microbial contamination. Prepare and maintain microbiological documentation, reports, and SOPs. Carry out microbial limit tests (MLT), preservative efficacy testing (PET), and pathogen identification. Ensure adherence to GMP, ISO, and cosmetic regulatory norms. Support QA/QC investigations in case of non-compliance or contamination. Coordinate with the R&D and production teams for product formulation safety. Required Qualifications: Education: B.Sc./M.Sc. in Microbiology, Biotechnology, or related life sciences field. Experience: Minimum 3 to 4 years in microbiological testing within cosmetics, personal care, or pharmaceutical manufacturing. Hard Skills: Strong knowledge of microbial limit tests, preservative efficacy testing, and aseptic techniques. Proficient in operating microbiology lab equipment (incubators, autoclaves, laminar flow, etc.). Familiar with regulatory standards (GMP, ISO 22716, BIS, FDA guidelines). Technical writing and documentation skills for lab reports and audits. Soft Skills: Attention to detail with strong analytical thinking. Good communication and team collaboration abilities. Problem-solving mindset with a focus on root cause analysis. Ability to work under pressure and meet tight deadlines. Why Join HCP Wellness? Opportunity to work with a leading third-party cosmetic manufacturer. Culture of innovation, integrity, and continuous learning. Safe and compliant work environment with career growth opportunities. Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: HCP HR Talent Acquisition +91 7600217962 +91 9998962424 Email hr@hcpwellness.in career@hcpwellness.in info@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

Walk in interview for various jobs in the below industry BPO IT Education Manufacturing Pharma Fresher or experienced can come to office with resumes RSV HR Services 7/307, Raji Nagammal Complex, Ottiyambakkam, Sithalapakkam, Chennai Ph-9042673696

Career Category Engineering Job Description Join Amgen s Mission of Serving Patients At Amgen, if you feel like you re part of something bigger, it s because you are. Our shared mission to serve patients living with serious illnesses drives all that we do. Since 1980, we ve helped pioneer the world of biotech in our fight against the world s toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. What you will do Let s do this. Let s change the world. The Manager of Business Performance will lead a team focused on leveraging data and analytics to drive strategic decision-making and operational excellence. This role is responsible for overseeing performance measurement frameworks, developing advanced analytics capabilities, and ensuring alignment between business goals and data-driven insights. The ideal candidate will combine strong leadership skills with deep analytical expertise and a solid understanding of data technologies. The Manager of Business Performance offers a unique opportunity to join a fun, innovative engineering team within the Enterprise Data Strategy and Engineering (EDSE) organization. You ll work on building next-generation capabilities and services in Data and AI using innovative open-source software, frameworks, tools, and cloud computing services. The role also emphasizes demonstrating these capabilities to support critical business operations and initiatives, ensuring alignment with organizational priorities. The Manager of Business Performance will lead a team focused on leveraging data and analytics to drive strategic decision-making and operational excellence. This role is responsible for overseeing performance measurement frameworks, developing advanced analytics capabilities, and ensuring alignment between business goals and data-driven insights. The ideal candidate will combine strong communication skills with deep analytical expertise and a solid understanding of insights generation from data. Develop and implement business performance strategies, KPIs, and reporting frameworks. Manage a team of analysts to deliver high-impact insights and performance dashboards. Collaborate with cross-functional teams to identify performance gaps and provide recommendations. Design and delivery of executive-level reports and presentations. Ensure data compliance across performance reporting systems. Drive continuous improvements in reporting. Partner with different teams to get the data and produce insights for the leaders out of it. What we expect of you Minimum 8 to 11 years of Experience business performance Basic Qualifications: Lead a team of analyst to provide business insights about the ongoing projects and of overall departmental work to the leaders. Understanding of different KPIs/metrics (operational, projects and financials) and ability to track, monitor and report those. Know the frameworks and visualization methods to present the business progress to the leaders. Good analytical skills. Proficiency with data tools (e. g. excel, power bi, Tableau etc) Experience in communication and presentation to leadership. Excellent stakeholder management skills. Excellent communication and social skills, with the ability to work collaboratively with different teams. Preferred Qualifications: Ability to work effectively across matrixed organizations and lead in collaboration. Passion for technology and customer success, particularly in driving innovative AI and data solutions. Familiarity with biotech/pharma is beneficial. Soft Skills: Excellent analytical and solving skills. Ability to work effectively with global, virtual teams High degree of initiative and self-motivation. Ability to handle multiple priorities successfully. Team-oriented, with a focus on achieving team goals Strong presentation and public speaking skills. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers. amgen. com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. .

Rockwell Automation is a global technology leader focused on helping the world s manufacturers be more productive, sustainable, and agile. With more than 28, 000 employees who make the world better every day, we know we have something special. Behind our customers - amazing companies that help feed the world, provide life-saving medicine on a global scale, and focus on clean water and green mobility - our people are energized problem solvers that take pride in how the work we do changes the world for the better. We welcome all makers, forward thinkers, and problem solvers who are looking for a place to do their best work. And if that s you we would love to have you join us! Job Description Project Manager Noida This role is for a Project Manager within the Professional Services (PS) Team. Our peoples passion and expertise are our greatest strengths. The S&S Team in India is an important execution group that provides end-to-end solutions to end-users. You will oversee project activities to ensure the delivery of high-quality results within defined timeframes and budget constraints. You will report to the Application centre Manager and have a hybrid schedule working in Noida, India. Your Responsibilities: Be an Single Point of Contact (SPOC) for the project, establishing relationships with relevant client stakeholders. Lead projects from requirements gathering through deployment. Define schedules, scopes, budgets, and implementation plans, including risk mitigation strategies. Communicate and manage partners, engaging clients, executives, and team members. Coordinate internal and external resources to ensure projects follow scope, schedule, and budget. Monitor project metrics; conduct regular project reviews. Mitigate project risks. Lead issue resolution during the project lifecycle. Prepare Monthly Progress Reports (MPR) for customers and develop action plans. Provide regular project updates to all partners. Provide and achieve revenue and shipment targets by driving projects to ensure profitability Ensure strict adherence to Project Management processes throughout the project lifecycle. Set quality and performance standards, assessing risks. Develop partnerships with vendors and third-party resources. Collaborate with Technical Leads to improve project efficiency and quality. Report project outcomes and risks, escalating issues. Manage end-to-end delivery of one or more medium to large/complex projects or milestones. Prepare and lead the project schedule; coordinate daily activities, issue resolution, and communication to ensure, within-budget delivery. Attend Kick-Off Meetings (KOM), liaise with the project and customer teams, and coordinate with manufacturing, supply chain, and logistics teams. Establish annual objectives for team members as applicable. Coordinate billing schedules with the sales team. Track Project status, issues, risks, and plans to all stakeholders. Build and develop the project/engineering team for future growth. Oversee Factory Acceptance Tests (FAT) and site dispatches; coordinate with field services for commissioning. Manage payments and receivables in collaboration with the sales team. Drive contract closure with high customer satisfaction. The Essentials - You Will Have: Bachelors degree in Instrumentation, Electrical Engineering, or E&C PMP certification. 15+ years of experience in automation industry project management, with hands-on project execution knowledge. Experience in PLC, DCS, VFD, SCADA, and automation design & engineering Experience with project management methodologies, risk management, and budgeting. Demonstrated leadership and stakeholder management skills. Domain expertise in Power, Metals, Aluminium, Cement, mining, infraConsumer, and Pharma industries. The Preferred - You Might Also Have: Knowledge of PLC/VFD/DCS programming and communication protocols (GE, Emerson, Schneider, Siemens, Rockwell, Honeywell). Experience managing global projects. Ability to promote a quality-driven culture within teams. Mentoring capabilities for project engineers and team leaders. Provide guidance and mentorship to a team of Project Engineers and Team Leaders to ensure project execution What We Offer: Our benefits package includes Comprehensive mindfulness programs with a premium membership to Calm Volunteer Paid Time off available after 6 months of employment for eligible employees Company volunteer and donation matching program Your volunteer hours or personal cash donations to an eligible charity can be matched with a charitable donation. Employee Assistance Program Personalized wellbeing programs through our OnTrack program On-demand digital course library for professional development . . . and other local benefits! At Rockwell Automation we are dedicated to building a diverse, inclusive and authentic workplace, so if youre excited about this role but your experience doesnt align perfectly with every qualification in the job description, we encourage you to apply anyway. You may be just the right person for this or other roles. #LI-Hybrid #LI-NB1

JOB DESCRIPTION Designation: Associate Scientist / Senior Associate Scientist Job Location: Bangalore Department: TM-TDDT About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation . Job Purpose (1-2 Lines) We are seeking motivated master s level scientists (MS, MTech, MSc, etc) to join the Translational Medicine team at the Biocon Bristol Myers Squibb Research Center in Bangalore, India. Key responsibilities of this role are to serve as an execution arm for the preclinical support of asset programs through mechanism of action-based studies, differentiation from standard of care and competitive therapeutics, combination rationale, new indications (life cycle management), and patient selection strategies. S/He will work directly with translational scientists, disease leaders within translational medicine, and will also interact with thematic research centers in early development within the company. Key Responsibilities: Conduct preclinical/laboratory experiments on late stage BMS portfolio compounds to support annual goals and objectives for Translational Medicine (for internal /external, collaborations, compound specific plans etc). Responsible for delivering data in support of translational strategies including biomarkers, patient selection hypotheses, dose and schedule, combination strategies, resistance mechanisms and differentiation. Interfaces with TM scientists across departments to ensure seamless flow of information for assets which are entering the remit of translational medicine. Assists in designing experiments and delivering data for collaborative projects along with TM scientists. Maintains comprehensive records, communicates regularly and makes presentations within the department, as required. Reports experimental finding in written nonclinical pharmacology study reports, to support regulatory filings. Educational Qualification: Masters with at least 2 years of relevant work experience across immunology, oncology, heme-oncology focus areas. Industry experience is a plus. Multiple positions can range upto 6 years of experience. Technical/functional Skills: Cell culture, primary cell isolation, cell transfection and single cell cloning; including siRNA / CRISPR / TALEN or HDR workflows Gene expression methods including qRT-PCR and/or familiarity with RNA sequencing, epigenomic methods including methylation analysis, ChIP etc Protein analyses and immunoassays, and cell phenotyping analysis (e. g. ELISA, MSD, Luminex, TSA, CBA, flow cytometry). Design, setup and execution of autoimmune, solid tumor oncology or heme-oncology in vivo pharmacology models. Excellent verbal and written communication skills, familiarity with standard or relevant software platforms, and scientific qualities are expected. Competence in analysis and solving of problems, keeping track of overall goals. Maintain a good understanding of the methodological basis and biological significance of assays performed. Forecast potential issues regarding support of assays for current and long term projects. Devise strategic solutions to identified and potential hurdles/issues and efficiently and proactively troubleshoot technical and experimental problems. Experience: 2-6 years Behavioral Skills: A self-starter, who is/can become technically proficient in a diverse set of techniques and assays with a focus on quality and speed, and will meticulously follow internal SOPs Good basic lab skills required (pipetting, balances, etc. ) Highly detailed and meticulous, high standards of data entering and QC Must be highly adaptive to changing timelines and goals Must be comfortable taking on complex tasks with minimal direct supervision An excellent multitasker with an ability to be level-headed in a fast-paced lab setting Team-oriented and comfortable working in a highly dynamic matrix environment across multiple locations Prior experience working with patient samples (i. e. FFPE tissue, Fresh Frozen tissue, blood) or working in a CLIA/GCLP/clinical environment is a plus Must be comfortable and able to work with animal (rodent) or human derived samples Equal Opportunity Employer: .