33 Cmo Jobs

Formulation - Research & Development - Pellets exp is must , Comply with GMP’s, SOP’s,regulatory documentation.,Develop Robust formulations & Evaluate patents and develop non-infringement strategiesScale up and optimization of manufacturing process.

Looking for CMO for one of the biggest Apparel Manufacturing Company @ Gurugram Exp: 27 - 32 yrs/open Salary: inr 100 - 120 L pa/ nego Mail at careermark@motujji.com & JOBSatCAREERMARK@gmail.com Required Candidate profile Strengths in handling all the products ( Tops, bottoms, Outerwear / formal wear & casual wear / knits, woven, denims, sportswear, activewear, etc ) and categories is a must

Job Location : Ghansoli, Navi Mumbai Job Type : FTE ( Fixed Term Employment ) - 2 years Job Accountabilities : Providing routine / emergency treatment for employees and family members Conduct medical monitoring as per schedule Manage liaising services Conduct OH programs # CASHe, OH Sub-committee, Awareness Programs Provide training to employees and contract workers Conduct internal audits Support CMO in preparing, executing & monitoring medical department budget Provide Industrial Hygiene services in the offices / sites as applicable Focus on continuous research & development Skills : Passion to Excel Entrepreneurial Mindset Knowledge of Statutory Requirements Emergency Management Training Delivery Customer Service Orientation Communication Education : Necessary : MBBS Desirable : OH Courses (AFIH, CIH, DIH) Experience : 3 to 6 years

MBBS Qualified Doctors are required in the multi-specialty hospitals and in a Factory as RMO for Ward & Emergency Services, offering Lucrative remuneration with min. 02 years of experience. Call/what's App: 9819454343 | e-mail: cv@sarajobs.com Required Candidate profile An MBBS, experienced Doctor, to manage... >Ward Management >Emergency & Trauma >Assist consultants *MBBS with MHA, MBA, AFIH may also applied. Perks and benefits Accommodation, subject to location

---------------------------------------------------------------------------------------------------- I.] FOR ONLINE / TELEPHONIC INTERVIEW, PLEASE CALL: MS. DHANASHREE ZETE MAM +9175582 07297 / +91 91455 00742 MR. CHETAN SAKHARE SIR +9195117 22359 WALK IN INTERVIEW: 9 AM - 6 PM II.] ONLY MBBS ARE ELIGIBLE. III.] POSTING IN WARDS / ICU / EMERGENCY / ---------------------------------------------------------------------------------------------------- 1. WE ARE THE LARGEST CHAIN OF CANCER HOSPITALS IN SOUTH EAST ASIA. 2. https://www.hcgoncology.com/ 3. https://www.hcgmanavatacancer.org/ 4. WE HAVE TIED UP WITH KIMS-THE LARGEST HEALTHCARE PROVIDER IN TELANGANA & ANDHRA PRADESH TO SET UP A 325 BEDS MULTI SUPERSPECIALITY HOSPITAL IN NASHIK. 5. https://www.kimshospitals.com/ 6. LOCATION: NASHIK 7. FINAL ROUND OF INTERVIEW IN PERSON AT NASHIK ONLY. 8. JOINING AT THE EARLIEST. 9. INCOMPLETE APPLICATIONS [NOT HAVING CV / RECENT PASSPORT SIZE PHOTOGRAPH / LATEST SALARY SLIP POST AUG 2024] WILL BE SUMMARILY REJECTED BY THE AUTOMATED SYSTEM AND WON'T BE INFORMED OF THE SAME. 10. careers@manavatacancercentre.com

We are looking for Medical Superintendent for Patna for a renowned hospital Must be a MBBS, 10+ Years of experience and working with Top Hospitals Budget 36-40 LPA Please share your CV at manoj@intendminds.com WhatsApp : wa.me/917349718665

Position Overview : We are seeking a skilled and strategic-minded General Manager to lead our External Manufacturing division. The successful candidate will play a pivotal role in coordinating and optimizing our external manufacturing operations, ensuring seamless collaboration with partners, and maintaining the highest standards of quality, compliance, and efficiency. Key Responsibilities: Coordinate and facilitate effective communication between third-party vendors and internal stakeholders to ensure the fulfillment of company requirements and timely query resolution. Review production plans and coordinate with demand planning, supply planning, and Contract Manufacturing Organizations (CMO). Circulate production plans to vendors and oversee their timely execution in alignment with export requirements. Monitor and proactively manage the quality of Ryvis Pharma products, implementing measures to prevent any quality issues that may arise. Explore alternate vendor development options for critical SKUs. Create purchase orders for materials and services needed for production. Lead efforts for packaging changes and product improvements in collaboration with relevant teams. Manage the end-to-end coordination of goods dispatch and QA release, addressing any associated queries and concerns. Take ownership of coordinating and resolving queries raised by the QA team. Facilitate CMO site audits and ensure compliance with standards. Manage market complaints by coordinating between CMO sites and our QA team, including investigating reports and implementing CAPA arrangements. Oversee the creation of product codes and vendor codes. Manage product shifts between CMO units, including evaluation, QA, and R&D approval, as well as site-to-site product transfers. Collaborate with internal stakeholders to prepare and release new artworks in response to changing regulations. Coordinate with vendors and arrange necessary documents for the company's tender business. Initiate change controls for CMO products and maintain vendor records. Coordinate supplier payments, resolving invoicing, taxation, and other discrepancies. Analyze cost sheets, validate prices, negotiate with third parties, and finalize rates. Ensure the timely delivery of committed products to support monthly sales closing. Generate monthly MIS reports for sales and purchase details of third-party products. Maintain and update the CMO Material Master Product List and Vendor Master List monthly. Identify opportunities for cost savings against the budget and implement necessary measures. Proactively manage product risks to ensure continuous alignment with business requirements and supply. Qualifications: Bachelor's degree in Pharmaceutical Sciences, or related field. An advanced degree (MBA, MSc, PhD) preferred. Proven experience (10+ years) in pharmaceutical manufacturing, with a focus on external manufacturing and/or loan license manufacturing. Strong understanding of cGMP regulations and global regulatory requirements for pharmaceutical manufacturing. Demonstrated experience in managing external partners and contract negotiations. Exceptional leadership skills with the ability to inspire and lead cross-functional teams. Excellent communication, interpersonal, and problem-solving skills. Strategic thinker with a track record of driving process improvements and operational excellence. Ability to thrive in a fast-paced, dynamic, and evolving pharmaceutical industry. Experience: Experience in managing supplies of more than 100 finished goods from multiple CMO sites. Experience in implementing multiple projects at CMO sites. Experience in managing production for export orders. Benefits: Competitive salary commensurate with experience. Opportunity to work in a senior management role within a rapidly growing pharmaceutical company. Collaborative and dynamic work environment. If you are a results-driven professional with a proven track record in pharma external manufacturing and are excited to take on a leadership role, we encourage you to apply. Please send your updated CV along with the requested details to hrdept@ryvispharma.com Age: Qualification: Current Company: Current Designation: Current CTC: Expected CTC: Years of Experience: Notice Period: Current location: Reason for Job Change:

JOB DESCRIPTION OF CASUALTY MEDICAL OFFICER ( CMO ) Qualification: M.B.B.S. Reporting to: Registrar / Medical Administrative Job Duties: To attend any new patient (admission) immediately. To take a proper history of the patient (If he is in a position to give it on his own) or from his relative. Examine the patient. Check any previous records, if available. Charts down all the details in the history sheet. Let the patient or his relative go through all the details and take his signature on the history sheet. Inform the respective consultant about the admission follow his orders. Instruct the nursing staff about the necessary orders to be carried out. If theres a transfer in-patient from the ICU. Read the transfer summary carefully. See the patient and examine him thoroughly. Inform the respective consultants and carry out their orders. Inform the nursing staff if any changes. To take rounds and examine individual patients. Inform the respective consultant/ Registrars if any new findings. Attend rounds with the respective consultants and carry out the necessary changes in the order. Enter them in the treatment sheet. Inform the nursing staff on duty about the same. To follow up with all the investigations to be seen and trace their results. Inform the Registrar/ consultant. Note down investigation results in the investigation sheet. To enter the treatment sheets . To enter pre-operative orders in the treatment sheet. To check whether the consent for the surgery has been taken from the patient. If not inform the respective person. To inform the Anesthetists on duty and instruct him / her about the patient. To carry out all the pre-operative orders. To attend patients complaints. To calm the patients if they are apprehensive. Inform the consultant if needed. To go for the health checkup. Maintain records of Medico Legal Case (MLC). Assisting Registrar in preparing Clinical SOP. Skill Sets: • Technical Skill: Should have undergone all the mandatory training programmes (BLS, ACLS, ATLS) • Analytical Skill Verbal Ability/Communication Skill. Problem Solving/Decision Making Others: Alert/Promptness Presence of mind Emotional maturity

Role & responsibilities To be well versed about coordination and collaboration with Quality functions of third party manufacturing (CMO) sites and CMO team for compliance of product, facility, systems, procedures. and for documents required from third party for various purpose; review, RA submission etc. Must have knowledge and know how on regulatory pathway for registration of product as per third party and or loan license norms/rules and requirement of documentation for regulatory submissions. Incumbent is expected a good reviewer and investigator To know the function of oversight of CMO sites for batch/lot releases as applicable form the manufacturing (Feed supplements and Pharma products facilities for update on compliance of system, procedure, systems) To be well versed with vendor qualification procedures and must be experienced in conducting audits/inspections at CMO sites for qualification and compliance To verify CoA for in line with product specifications and CoA. To verify and to confirm stability study of finished products and to coordinate for documents of stability, RM, PM, product specifications, CoA. To identify Govt. approved third party labs for testing of RM, PM (if any) and finished product and to support CMO-QA for Qualification of vendor (Third party lab/service provider) To review batch documents and test analysis reports of batches /lots executed in line with established batch formula and test method/product specification To be well versed and possessing know how of establishing Quality Function (QA & QC) for CMO Function To perform investigation related to product complaints, observations/notices and to collaborate and coordinate with CMO function and Quality function of third party manufacturing site for root cause analysis and CAPA actions To possess knowledge on quality management system such as change management, complaint handling, CAPA procedures, recall procedures, regulatory queries responding and handling of queries from customers and market. To be well versed with procedures of artwork (PPI & label etc.) preparation, review and approval To have very good operational knowledge of computer: Microsoft word, excel and any other software based task related to CMO-QA function To coordinate with sourced lab and third party manufacture for timely completion of testing of routine batch(s) and testing of samples as part of investigation and for timely responses on queries and product complaints To possess very good communication skills, willing to travel as part of job role Job Location: Kadi,Gujarat ( Bus facility available from Ahmedabad,Kalol & Kadi)

Medanta the Medicity Gurugram, Haryana We are Hiring Medical Officer Department of Cardiology, Endocrinology & Diabetes, Gastroentrology & Hepatology & Medical Administration. Experience- 1-4 years of relevant experience of healthcare industry. Salary- 6.60LPA - 10.0LPA Kindly share me your update resume on my email id- neha.bhatnagar@medanta.org Contact Person- Neha Bhatnagar (7310800356)

We're Hiring: Group Chief Marketing Officer (CMO) Location: South Mumbai | Industry: Hospital Experience: 15+ years of reputed hospital experience only Interested candidate can share resume to 9152064207 or mail at eminenthr786@gmail.com

Job description Dear Aspirants, Greetings from Pragnya Priya Foundation. We have 2 openings for Male(Kodad) / Female(Nellore) Junior Medical Officer in our Hospitals Job Location: Unit-1 , Ramapuram, Kodad,, Suryapet(Dist), Telangana - Male Job Location: Nellore Lakshmi Devamma Free Hospital, Kalayakagollu(V), Buchireddipalem (M), Nellore (D), Andhra Pradesh - Female Role & responsibilities Responsible for conducting pre-employment and periodical medical examination Provides acute and chronic illness-related health care to patients. Documents all patient health information, such as medical history, examination findings, and investigation results Play active role in community health care services. Conduct regular health checkup of employees working in the factory To conduct Awareness campaigns on various Health & First Aid etc. To conduct Occupational Health Surveys. Handling Medical cases ( First Aid & serious injury if any) Responsible for effective functioning of Medical centre and nurses. Responsible for readiness of Medical centre first Aid boxes and ambulance Preferred candidate profile MBBS Graduation is Required 03-05 years of hands-on experience in the Medical Feild Excellent organizational and managerial skills Strong people-management and interpersonal skills with ability to collaborate Attention to detail Ability to motivate and direct people from varied backgrounds towards achievement of organizational goals Fluency in Telugu and English. Perks and benefits Perks and benefits Emoluments will be at par with the best in Industry, including pleasant family accommodation and other convenient facilities in the company township. if you would like to explore the opportunity, please revert with your updated resume at the earliest to ramakrishna.hrd@priyacement.com if you have any questions or comments, please do not hesitate to reach us at 040-4040 1234/1284.required details in CV / Resume are as follows: current CTC expected CTC notice Period at your current job/organization relevant Experience

Position Overview: The Chief Marketing Officer (CMO) is a senior executive responsible for developing and executing comprehensive marketing strategies to drive brand growth, patient engagement, and market expansion. The CMO ensures the alignment of marketing initiatives with the organizations mission and goals, leveraging data-driven insights to optimize marketing performance and improve patient outreach. Key Responsibilities: 1. Marketing Strategy and Planning: o Develop and implement a strategic marketing plan that supports the organization's business objectives. o Identify market opportunities and threats through comprehensive market analysis and research. o Define brand positioning, messaging, and value proposition for the organization's services and products. 2. Brand Management: o Oversee the development and maintenance of the organization's brand identity. o Ensure consistent brand messaging across all marketing channels and materials. o Lead initiatives to enhance brand awareness and reputation. 3. Digital Marketing and Patient Engagement: o Develop and execute digital marketing strategies, including SEO, SEM, social media, email marketing, and content marketing. o Enhance patient engagement through personalized and targeted communication. o Implement and manage patient relationship management (PRM) systems. 4. Product Marketing: o Lead the marketing efforts for new product launches and service offerings. o Collaborate with product development teams to ensure market needs are met. o Develop marketing materials and sales tools to support product adoption. 5. Market Research and Analytics: o Conduct market research to understand patient needs, preferences, and behaviours. o Analyze marketing performance data to measure the effectiveness of campaigns and strategies. o Utilize insights to make data-driven decisions and optimize marketing efforts. 6. Team Leadership and Development: o Build and lead a high-performing marketing team. o Foster a culture of creativity, innovation, and continuous improvement. o Provide mentorship and professional development opportunities for team members. 7. Stakeholder Collaboration: o Collaborate with clinical, operational, and executive teams to align marketing efforts with organizational goals. o Work with external partners, agencies, and vendors to execute marketing initiatives. o Serve as the primary spokesperson for marketing-related activities. 8. Budget Management: o Develop and manage the marketing budget. o Ensure cost-effective allocation of resources to maximize ROI. o Monitor financial performance and adjust strategies as needed. 9. Regulatory Compliance: o Ensure all marketing activities comply with healthcare regulations and ethical standards. o Stay informed about industry trends, legal requirements, and best practices. Qualifications: Education: Bachelors degree in Marketing, Business Administration, or a related field; MBA or advanced degree preferred. Experience: Minimum of 10 years of marketing experience with at least 5 years in a senior leadership role, preferably in the healthcare or medical industry. Skills: o Strong strategic planning and analytical skills. o Excellent communication, presentation, and interpersonal abilities. o Proficiency in digital marketing tools and platforms. o In-depth knowledge of healthcare marketing regulations and practices. o Proven track record of driving marketing performance and achieving business objectives. Work Environment: Office-based with occasional travel to conferences, meetings, and healthcare facilities. Requires participation in executive meetings and collaboration with cross-functional teams. Reporting: Reports to the Chief Executive Officer (CEO) or equivalent top executive. Supervises the marketing team, including managers and specialists.

Job description Overview: The business development team is an integral part of our commercial setup. The purpose of this team is to create long-term value from clients, markets and relationships. They look to grow business with the existing business account and pave the way for new businesses in key markets/geographies. This is an excellent opportunity for someone who is driven, personable, and team-work oriented but also someone who will create, manage and grow the new business development activities. Role and Responsibilities: Business Development - Sourcing deals and managing relationship with companies/ organizations to enable successful partnerships - Exploring Strategic business opportunities for assigned products, globally - Identify key markets and stakeholders within those markets to facilitate brand expansion - Enable rapid and appropriate assessment of risks and opportunities in identified markets and stakeholders - Enable a structured approach to focus on scientific marketing and long term brand building in key global markets - Setting goals and developing plans for business and revenue growth - Researching, planning, and implementing new target market initiatives - Pursuing leads and moving them through the sales cycle - Developing quotes and proposals for prospective clients - Network and build trust based relationships throughout target accounts from technical personnel to the executive level. - Maintains strong technical and market knowledge to enable meaningful conversations with prospective customers - Market Research: Prepare investment analysis report to enable discussion on potential inclusion of product in pipeline; Conduct primary and secondary research, interpret data, formulate reports and prepare financial model for analysis CDMO/CMO : - Assist in proposals writing, RFI, RFP & RFQ handling, lead generation, contract negotiation, key account management and managing relationship with companies/ organizations to enable successful partnerships - Prospect, network, and make contacts to potential customers by visiting and or other marketing activities, attend industry conferences to expand BE reputation and seek out new leads from existing to new customers. - Design, plan and execute marketing and branding strategies including brochures, posters, conferences, biotech-related media, business shows, etc - Draft and present contract proposals to customers for their specific CDMO projects - Work closely with internal technical CMC team to meet client project requirements leading to the closing of contracts - Provide customer support, manage customer relationships, establish positive, long-term client relations through scheduling and conducting calls with clients. - Responsible for achieving quarterly, annual sales goals. - Market research for due diligence/ sales analysis reports Timely follow-up and co-ordination with stakeholders (external/internal) as and when needed Desired Skills and Experience - The candidate should have - 5- 7 years of work experience in in biological/Biopharmaceutical Industry Experience in handling CMO/CDMO business / B2B client proficiency in financial modelling, market research, demand forecasting, due diligence, client management and project management high level proficiency in Excel & other IT skills excellent communication skills; written and oral

Title: Business Development Head - (Contract Manufacturing/CMO / CDMO) - Pharmaceutical Human Health Industry (DOMESTIC MARKETING & BUSINESS DEVELOPMENT ONLY) Summary: We are currently seeking a dynamic and experienced Business Development Head (FOR DOMESTIC MARKETING) to spearhead our business development initiatives in the pharmaceutical human health sector. This pivotal role requires a focus on B2B marketing and contract manufacturing, particularly in oral liquids and nutraceuticals. The ideal candidate will bring a strong background in multinational corporate environments, with a demonstrated track record of success in generating new B2B orders and selling developed products within the human pharmaceutical industry. Qualifications: Masters degree in business, Marketing, Pharmaceutical Sciences, or a related field is mandatory. A minimum of 08 to 15 years of progressive experience in business development within the human pharmaceutical industry, specifically in multinational corporations. Demonstrated expertise in B2B marketing and contract manufacturing, with a focus on OSD formulations and nutraceuticals. Proven ability to develop and execute successful business development strategies in the pharmaceutical sector. Strong understanding of market dynamics, regulatory requirements, and product development in the pharmaceutical industry. Exceptional negotiation, communication, and interpersonal skills. Proven track record of meeting or exceeding business development targets. Ability to work collaboratively in a team environment and lead cross-functional initiatives. Core Responsibilities: Lead and strategize business development activities in the pharmaceutical human health sector with a specific focus on oral liquids and nutraceuticals. Identify and secure new business opportunities in the B2B market, ensuring they align with the company's strategic objectives. Secure and manage comprehensive contracts for CDMO and CMO services with multinational corporations, leveraging market insights and strategic partnerships. Maintain and enhance relationships with existing clients while actively pursuing new partnerships in the pharmaceutical industry. Collaborate with internal teams to develop and propose tailored solutions for clients, ensuring compliance with industry standards and customer satisfaction. Negotiate and finalize business deals, focusing on profitability and sustainable growth. Stay abreast of industry trends, competitor activities, and regulatory changes to inform and adapt business strategies. Provide leadership and mentorship to the business development team, setting clear goals and tracking performance. Regularly report on business development activities and progress to senior management, providing insights and recommendations for continuous improvement. (NOTE: CANDIDATES WHO ARE HAVING RELEVANT EXPERIENCE IN THE PHARMACEUTICAL INDUSTRY AS PER THE ABOVE JOB DESCRIPTION ONLY SHOULD APPLY FOR THIS POSITION)

KAILASH HOSPITAL, GREATER NOIDA is looking for CMO, PRO, YOGA-Teacher to join our dynamic team and embark on a rewarding career journey A Teacher is responsible for delivering lessons and facilitating learning in a classroom setting This includes planning and delivering lessons, assessing student progress, creating a positive and engaging learning environment, and communicating with students, parents, and other stakeholders The ideal candidate should have a strong understanding of the subject matter they are teaching and the ability to effectively communicate complex ideas to students Additionally, excellent interpersonal and organizational skills, a commitment to student learning and development, and a growth mindset are essential for this role

External Manufacturing & Supply Operations Quality Management System on regional (Asia Pacific) level : Develops, Implements, maintains and continuously improves quality processes and systems to ensure the quality oversight of commercial products manufactured, packaged, tested and released at Contract Manufacturing Organizations (CMOs) EMSO Quality Oversight about CMOs : Implements, monitors, and reinforces Corporate Quality and TGO Standards at the CMO sites or suppliers, consistent with the business objectives, to ensure the manufacture of high quality pharmaceutical products, in accordance with regulatory compliance, internal, local, and international requirements to protect Tevas global branding. Supplier Evaluation, Due Diligence and Qualification : Collaborates with EMSO and Global Quality on the identification and spearheads the selection process of CMOs for third party projects EMSO Proactive CMO / Supplier Management : Establishes a closer collaboration with strategic CMOs /suppliers by adopting the key account management approach. (Supplier Relationship Management) Auditing of CMO : Ensure establishment and approval of the annual EMSO EU and APAC supplier audit plan Compliance issue : Ensures the GMP and regulatory compliance for EMSO products manufactured in the APAC Region for all TEVA markets Launches : Ensures Compliance with Pharmaceutical Regulations and TEVA Standards Budget: Establishes an annual regional budget for EMSO Quality as part of the AOP process, taking into account variable influences like volume changes, projects, launches, acquisitions and divestments, strategic and compliance remediation work.

Role & responsibilities Identify and onboard new CMO clients for injectable manufacturing To work for tech transfer, out licensing, search CMO for developing company Developed Products for commercialization, and to find suitable marketing partner for selling company product into Regulated Markets partnering with potential and suitable Marketing Partners Manage and grow relationships with domestic & international partners Work cross-functionally with operations, QA, RA, and supply chain teams for smooth project execution Develop and execute a roadmap to achieve 100 crore business potential Serve as the key customer contact point and ensure complete client satisfaction and compliance Preferred candidate profile Education : B .Pharm / M.Pharm with strong academic credentials Experience : 8 to 10 years in the pharmaceutical industry, with proven track record in CMO/Third-Party Manufacturing Prior experience in handling injectables and CMO operations across India and Global Markets is essential Excellent business development , client relationship , and coordination skills Capable of leading customer interactions, technical evaluations, price & negotiations, and end-to-end support formalities Must possess solid communication , negotiation , & project execution skills

Urgent Opening for RMO (BAMS/BHMS) Location: Ratnagiri, Maharashtra Experience: 0 to 5 Years Free Accommodation Provided Great opportunity for freshers & experienced candidates! Contact: 7385087674 Apply now! Required Candidate profile * RMO (BAMS/BHMS) * Experience: 0 to 5 Years * Ready to relocate Perks and benefits Free Accommodation Provided

BHMS, BAMS, MBBS Medical Officer Experience 2- 5 years (ICU & Emergency) Salary- Negotiable interested candidates share their CV at info@trhrecruitment.com WhatsApp- 7078260333 Perks and benefits Free Residence

Role & responsibilities Physical examination , Assessment of patients. Collecting information related to patient and integration in clinical plans; Ensuring continuous medical cover for all patients admitted. Communication with patients relatives, referring hospital etc. Management of the airway Emergency cardioversion defibrillation, CPR Management &Catheterization Ventilatory management Appropriate documentation of medical history and progress in patients notes; Prescription and update of therapeutic plans; Ensuring plans are acted upon and specific diagnostic tests carried on diligently

Roles and Responsibilities Develop new business opportunities through strategic partnerships, alliances, and market research. Identify potential clients and develop targeted sales strategies to drive revenue growth. Build strong relationships with key decision-makers at client companies to understand their needs and preferences. Analyze market trends, competitor activity, and customer feedback to inform business development initiatives. Desired Candidate Profile Strong understanding of Contract Manufacturing (CDMO), Third Party Manufacturing (TPM), Domestic Marketing concepts. Proven track record of success in developing new business opportunities through effective relationship-building skills.

We have job opening of 10 Medical Officers (MBBS & BAMS) for well established Multispecialty Hospitals in various cities and town of Punjab and Haryana. The Doctors should be interested to relocate and willing to work as Resident Medical Officer. Required Candidate profile Candidate should be BAMS or MBBS BAMS must be 2+ years experience and Fresher MBBS can be considered Salary is Negotiable as per experience and job knowledge. If interested, please send us your CV

Job Overview: The Packaging development engineer will be responsible to work for various packaging projects. He/ She will work with cross functional teams to develop, test, validate, and commercialize package solutions / Medical devices for both new and existing products. He/she will support continuous improvements as well as problem resolution and redesign when required for marketed products. The candidate will work on new product development, preparation of technical documentation for regulatory files (i.e., FDA 510k and CE mark technical files), performance analysis, risk management, and design transfer to manufacturing. Key Stakeholders: Internal Supply Chain, CMO sites, QA, RA and Manufacturing site colleagues Reporting Structure: Role reports to: Chief Manager Packaging Technology Experience Bachelors degree with 8-12 years of professional experience in pharmaceutical (sterile product experience is preferred) or medical device industries Experience in developing primary container designs and specifications and supporting primary packaging related regulatory filings Project management skills with proven track record within Packaging and/or Engineering Experience in writing technical documentation for regulatory files (i.e., FDA 510k and CE mark technical files) Strong understanding of global regulations regarding packaging & medical device regulations. Key Roles/Responsibilities: Designing packaging systems for the anesthetic and sterile drug products (ampoule , vial and PFS) including primary, secondary, and tertiary packaging components as well as equipment automation for the packaging process. Handling of CMO sites for the Injectable vertical along with complete documentation support (eMPD , eSPEC). Development 3D CAD & SolidWorks models of parts and assemblies along with creation of engineering drawings for product, components, tooling, etc. Coordinate with manufacturing / SCM / Logistic team to understand the challenges / improvement scope. Leverage 3D printing & additive manufacturing processes for prototyping and low-volume production Strong experience in component development including and not limited to knowledge of stabilitystudies/machine feasibility study/packaging trials, Regulatory filing, shipping studies and validation. Selection of components and materials for use in product designs and development. Preparation of the protocols, testing procedures as per ASTM & ISO standards, analysis, and interpretation of test data. Preparation of technical documentation for regulatory files (i.e., FDA 510k and CE mark technical files) Create, improve, and maintain Design Control and Quality Management System procedures in collaboration with Quality and Regulatory. Perform root cause analysis, provide recommendations, write, implement corrective/preventive actions, verify effectiveness and train per requirement. Create product priority timeline and coordination with team members Developing, reviewing, and approving the following packaging documents: packaging component specifications, packaging component drawings, design history files (for combination products), project value stream mapping, and procedures for bulk and finished drug product. Supporting primary packaging related regulatory filings. Exposure on distribution testing, shipping studies, line trials, packaging material qualifications, child resistant requirements, human factor studies and patient centric designs. Identification and validation of secondary and tertiary package materials and suppliers. Project execution for harmonization/standardization, quality risk remediation/reduction, and continuous improvement projects. Developing, tracking, and maintaining project plans allied to budgets for packaging related projects. Originating and developing new packaging projects and initiatives that lead to process improvements & have a significant business impact. Supporting sustainability / green packaging initiatives as per organizational requirement. Responsibilities Qualifications BS, Mechanical Engineer / Graduate in Packaging Technology with experience in sterile packaging development along with exposure in Medical device development function.

Experienced in pharmaceutical RA labeling, cGMP/FDA/CFR compliance, SPL creation, proofreading, and DSCSA. Skilled in MS Office, Adobe, TrackWise, SharePoint, and graphic design. Knowledge of label lifecycle, drug listing, and patent carve-outs.