321 Injectables Jobs - Page 4

We are seeking to hire an innovative and highly motivated Formulation Scientist to join our Biologics RD team . The qualified individual will have at least 3-5 years of relevant industry working experience in developing parenteral formulation, solid and liquid oral dosage forms for use in first-in-human studies. The Formulation Scientist in the Large Molecule Drug Product Development will be a lab-based role, responsible for experimental studies in the pre-formulation, formulation, characterization, and analytical development of therapeutic proteins including monoclonal antibodies, virus-like particles, RNA therapeutics, and subunit-based vaccines. Since most of our clients are based out of USA and Europe, we expect candidates to have some exposure working on international projects. Major Duties and Responsibilities: Develop formulations for parenteral/ injectable and oral drug products. Develop parenteral formulations for biotherapeutic modalities such as monoclonal antibodies, antibody-drug conjugates, proteins, and vaccines. Perform rapid, comprehensive characterization of candidate molecules to determine the stability profile and apply this information to develop an appropriate dosage form to meet clinical needs. This will be achieved by applying various biophysical and biochemical techniques such as HPLC (SE-HPLC, IEX, RP-HPLC), SDS-PAGE, Capillary Gel electrophoresis (CGE), and imaged Capillary Electrophoresis (iCE). Evaluates feasibility of analytical methods to support product characterization, formulation stability, and compatibility testing. Rational formulation design/selection and characterization studies relevant to the stage of development. Development and optimization of liquid and lyophilized biologics formulations. Design and execute compatibility studies to support the administration of large molecules Design and manage stability studies on target and experimental formulations Perform her/his duties consistent with good laboratory practices Preferred qualifications: Knowledge of protein science, including biochemical, immunological, and biophysical characterization. Knowledge and experience in the development of large molecule formulation. Familiarity with biochemical, biophysical, and/or analytical methodologies for characterization of proteins and peptides. Hands-on experience and trouble-shooting proficiency with column chromatography (SEC, IEX, RP, HIC), biophysical characterization (DLS, DSC, DSF, fluorescence, EM), capillary electrophoresis (CE-SDS, cIEF, iCE), charge variant analysis, oxidation analysis, and peptide mapping for protein characterization are highly desirable. Required qualifications: Ph.D. + > 3 years experience, M.S. + > 5 years experience, or B.S. + > 8 years experience in an appropriate scientific discipline is required. Strong scientific understanding and extensive research experience is necessary. Experiences in the areas of formulation/drug product development, biophysical/biochemical characterization, analytical method development for mAb or recombinant protein-based biotherapeutics and pharmaceutical development are desirable Ability to interpret and analyze data from biophysical assays and design appropriate experiments. Demonstrated experience delivering high quality and timely data while adhering to compliance and data integrity requirements Self-motivated, attention to details, excellent teamwork, organization, oral/written communication skills are highly desirable

Job Summary: We are seeking a dynamic and experienced Regional Marketing Manager to lead and expand our pharmaceutical distribution network, with a focus on the Defence sector . The ideal candidate will have prior experience working in or with Defence healthcare logistics or procurement systems and a strong grasp of B2G (business-to-government) sales dynamics. Key Responsibilities: Develop and execute regional marketing strategies tailored to Defence institutions, armed forces hospitals (AFMS), and government healthcare establishments. Identify and pursue new business opportunities within Defence procurement channels (e.g., DGAFMS, ESIC, Army Hospitals, Base & R&R and Defence). Build and maintain strong relationships with key decision-makers in Defence medical procurement and logistics units. Liaise with Defence Medical Stores Depots (DMSDs), armed forces hospitals, and tendering authorities to ensure participation in bids and tenders. Monitor regional market trends, competitor activities, and Defence medical policy changes to inform marketing strategies. Coordinate with supply chain teams to ensure timely product availability and fulfilment. Ensure regulatory compliance and documentation for institutional and Defence sales. Conduct product training sessions and awareness programs for Defence medical staff and procurement officers in concern with corresponding manufacturing companies. Lead a team of field marketing and institutional sales representatives across the region. Qualifications & Skills: Graduate/Postgraduate in Pharmacy, Life Sciences, or Business Administration. MBA preferred. Minimum 12 years of pharma sales/marketing experience, with 12-18 years working in or with Defence healthcare institutions or supply chains. Strong knowledge of Defence procurement systems, tenders, and sales cycles. Proven leadership and regional team management experience. Excellent communication, negotiation, and stakeholder management skills. Willingness to travel extensively within the assigned region. Preferred Background: Retired Defence personnel with experience in medical/logistics corps or those who have worked in government healthcare procurement. Candidates with experience in dealing with AFMS, ECHS, DGAFMS, MES , and other Defence-related healthcare bodies. Role & responsibilities Preferred candidate profile

Role Description Position Title: Trainee - Hospital Sales Executive Reports To: Key Account Manager, Orchid Pharma Formulations Division Experience: Freshers are Welcome Role Highlights Represent our brand and promote innovative healthcare solutions to medical professionals. • Build and maintain strong relationships with doctors, hospitals, and other healthcare stakeholders. Stay updated on medical advancements and product knowledge. Meet sales targets and contribute to the mutual growth. What Were Looking For: B. Pharma graduates with good communication and interpersonal skills. Self-motivated individuals with a passion for sales and healthcare. Ability to learn and adapt in a fast-paced environment. Willingness to travel as part of the role. Why Join Us? Comprehensive training and development programs to ensure your success. Opportunities to grow within a dynamic and thriving industry. Competitive compensation and performance-based incentives. Be part of a team that's transforming healthcare delivery Profile & Education B. Pharma or relevant field in Pharmaceuticals

-Operation of Vial/Ampoule washing machine -BMR -Classified area monitoring -validation of the machine Interested candidates can share resume on dipika.parmar@milanlabs.com

-Operation of Vial/Ampoule filling machine -BMR -Classified area monitoring -validation of the machine Interested candidates can share resume on dipika.parmar@milanlabs.com

-Operation of Lyophilizer machine -BMR -Classified area monitoring -validation of the machine Interested candidates can share resume on dipika.parmar@milanlabs.com

Should have minimum 1-4 years of experience in Production Injectable (Small Volume Parentral). Immediate Joiners will be preffered. Interested candidates can share resume on dipika.parmar@milanlabs.com

Role & responsibilities Handling of pre and post approval regulatory activities of US/EU/CA submissions. Review of developmental documents for regulatory submission. Good knowledge of handling CMC documentation for Dossier submission Compilation and Submission of Annual reports and Supplements. Having the experience of solid orals and injectables. Preparation of Sterility Assurance Package for injectable Dossiers. Preparation of Pre-IND/scientific advice meeting packages Drafting, compiling & eCTD publishing of dossiers for regulatory filings. Review of specifications and test procedure as per pharmacopoeia requirements. Providing regulatory support for customer filings and customer queries. Evaluation of regulatory authority deficiencies and preparation of action plan accordingly. Also follow up of response documents with concern stake holders. Evaluation and approval of QMS documents, wherever applicable. To update cross functional teams for different regulatory compliance & requirements. Responsible for outlining requirements for labelling, storage and packaging. Review of product development report and QBD concepts. Updating product approval package to plant team. Preferred candidate profile Should Have Formulation Regulatory Affairs Relevant Experience in US/EU/Canada Perks and benefits

7Excellent scope for both (Fresher & Experienced Dermatologist) to offer client consultation, supervise and execute advanced skin & hair cosmetic procedures at the clinic. Responsibilities & Duties: Consult with and treat patients at the designated clinic, perform all dermatology-led medical procedures, and supervise non-dermatology-led procedures. Ensure the efficacy, safety, and adherence to high professional standards for all medical procedures performed under your supervision. Deliver treatments of the highest quality, following established SOPs and company guidelines. Strive for high client satisfaction in all consultations and treatments, as reflected by client feedback and evaluations from the Area Medical Head (AMH) and Area Operations Manager (AOM). Required Candidate profile: MBBS and Masters (MDDVL), Diploma (DDVL, DVD) or Doctorate (DNB) in Dermatology. Strong knowledge and experience in medicine and dermatology. Excellent communication skills and Energy Levels. Ability to connect well with clients. For more details contact 8886639172 or 951534300

Manager - Processing (Production) Role: We are seeking a dynamic and seasoned individual responsible for overseeing day-to-day processing operations in sterile manufacturing, ensuring alignment with production schedules and regulatory standards. The role focuses on identifying process inefficiencies, leading improvement and automation projects, and collaborating with cross-functional teams to drive productivity, reduce waste, and enhance product quality. This position demands strong technical knowledge of sterile processing equipment and a proactive approach to maintaining seamless production workflows and continuous operational improvements. Location: Umarsadi (Vapi, Gujarat) Main Tasks: Manage and oversee work orders for our product lines, ensuring efficient execution of production plans to maximize machine performance. Plan and implement batch production on a product-specific basis, optimizing throughput and minimizing downtime. Collaborate with cross-functional departments to ensure uninterrupted operations and timely execution of preventive maintenance schedules. Lead initiatives to reduce market complaints, aiming to maintain a production ratio of over 20 million units per justified complaint. Review BMR for new products to be processed on syringe lines. Review and approve BMRs for new products prior to processing and verify completed BMRs for submission to Quality Assurance. Develop, review, and implement SOPs for syringe processing operations, ensuring thorough training and compliance among line operators. Monitor and enhance line yield while working to minimize rejection rates through process improvements and quality control measures. Ensure timely preparation of customer samples as per specifications, with accurate documentation in BMRs and logbooks. Oversee SAP activities related to batch processing, including data entry, reconciliation, and return of unused materials to inventory.. Ensure optimal shift-wise performance of SPRC machines, maintaining complete and accurate documentation in SAP, BMRs, and logbooks. Prioritize and coordinate the ETO process of completed batches, ensuring all related entries are updated in both BMRs and SAP. Maintain audit readiness by ensuring no critical observations in the production area through strict compliance and monitoring. Ensure NVPC records are correctly attached to the respective BMRs and submitted to QA within the designated timeline. Lead training programs for staff and operators on cleanroom protocols and enforce adherence to cGMP standards. Ensure full compliance with the most recent EHS guidelines across all production activities. Drive continuous improvement of the EHS management system through effective implementation, monitoring, and periodic review. Requirement: M.Pharm /B.Pharm /B.Sc /M.sc / BE (Chemical, Electrical, Instrumentation, Mechanical) from an accredited institution. Experience: Proven record of 12+ years in Junior Management in any Pharmaceutical industry with relevant experience in the area of Process Engineering. Competencies: Strong organizational skills and attention to detail. In-depth knowledge of sterile processing equipment: Washing Systems, Depyrogenation Tunnels, Sterilizers, Siliconization Systems. Sound understanding of cGMP, GEP, FDA/ regulatory requirements, and cleanroom operations. Strong command over lean manufacturing, root cause analysis, CAPA, and risk assessment tools. Strong leadership with proven ability to motivate and guide cross-functional teams. Skills: Proficiency in local languages and English, both written and spoken, to facilitate effective communication with employees and stakeholders. Knowledge of SAP, MS Excel, PowerPoint, etc. Strong learning agility and continuous improvement mindset. Contact: careers.hr@schott-poonawalla.com

Role & responsibilities Develop, execute, and document qualification protocols (DQ/IQ/OQ/PQ) for equipment, utilities, and facilities. Collaborate with Engineering, Production, QA, Or other Cross functional teams to coordinate qualification activities. Maintain qualification documentation, including risk/impact assessments and change-control records. Ensure compliance with USFDA, MHRA, WHOGMP, and ICH Q9/Q10 standards. Support internal and external audits and inspections focused on qualification. Diagnose deviations in qualification processes and initiate CAPAs. Manage and update the Qualification Master Plan and requalification schedules. Specialize in injectable product qualification (media fill, aseptic simulation, smoke studies). Oversee qualification of systems such as water, steam, HVAC, filling/sealing machines, autoclaves, isolators, washing tunnels/DHS units, and more Preferred candidate profile Deep knowledge of qualification and validation best practices (equipment, utilities, facilities) and Hands-on experience with media fill/aseptic simulation, smoke studies, and utilities (water, steam, HVAC). Proficient in URS/DQ/IQ/OQ/PQ processes for various equipment (vial/ampoule washers, filling/sealing units, autoclaves, isolators). Strong understanding of equipment qualification, utility validation, and cleanroom classification. Familiarity with cGMP, data integrity (ALCOA+), and GxP documentation standards. Competent in creating/reviewing technical documentation and qualification protocols in line with regulatory requirements. Excellent analytical and problem-solving skills, with a methodical attention to detail. Proven ability to collaborate cross-functionally and interface confidently during audits and inspections.

Job Description: Regulatory Affairs Assistant Manager / Manager Injectable & OSD Facility Department: Regulatory Affairs Location: GIDC Ankleshwar Key Responsibilities: Prepare and submit dossiers (CTD/ACTD) for ROW & US markets. Ensure compliance with local regulatory guidelines and GMP standards. Liaise with regulatory agencies and respond to queries promptly. Manage product registrations, renewals, and variations. Monitor regulatory updates and ensure adherence to changes. Support quality audits and review labeling/artwork for compliance .

Position: Production Executive / Officer Injectables Location: Ankleshwar,Gujarat Experience: 2-4 years Key Responsibilities: Carry out production activities as per SOPs and schedule Ensure adherence to cGMP and regulatory guidelines Maintain accurate production documentation (BMRs, logbooks) Coordinate with QA/QC for line clearance and sampling Support equipment cleaning, operation, and minor troubleshooting Follow all safety and hygiene protocols Requirements: B.Pharm/M.Pharm/B.sc/ Msc or equivalent 2- 4years experience in parental production Good knowledge of GMP and pharma documentation Strong attention to detail and communication skills

Role & responsibilities Responsible for Pre-formulation studies for lab formulation development trials of solid orals, Oral Liquid, injectable, products, and Nutraceuticals product. To design strategy for projects through literature surveys. Respective API characterization, excipients characterization, drug and excipient study and its ratio. Worked on different manufacturing strategies for the development of products. To evaluate product for stability in manufacturing, monitor and review the stabilized batches. To study on existing formulations. Responsible for co-ordination, execution and monitoring of scale up activity, Responsible for Trial batches, Scale up batches, Optimization batches, Exhibit batches. Co- ordination with all cross-functional teams. TT sites and LL Sites To design/assist/support/ review for documents such as SOP, LNB, QQ, Risk assessment, PDR, MFR, Scale up BMR, stability protocol, qualification, validation documents, change controls, deviations, investigations and CAPAs etc. Preferred candidate profile

The CSSD Technician is responsible for the effective sterilization and disinfection of surgical instruments and medical equipment. This role involves preparing, sterilizing, and ensuring the safe handling of instruments to maintain the highest standards of hygiene and safety within the hospital environment. The technician will also be responsible for the quality control of sterilization processes and will work closely with various departments to support surgical procedures. Roles and Responsibilities - Clean, decontaminate, and sterilize instruments and medical equipment using appropriate methods and technologies. - Ensure the proper functioning of sterilization equipment and report any malfunctions. - Monitor and maintain sterilization logs and quality assurance records. - Prepare and package instruments for surgery, following established protocols. - Collaborate with surgical teams to meet instrument and equipment needs during procedures. - Follow infection control standards and safety protocols to prevent contamination. - Conduct routine checks and maintenance of CSSD supplies and inventory management. - Participate in ongoing training and professional development related to sterilization techniques and infection control practices. Skills Required: - Knowledge of sterilization techniques, principles of infection control, and safety standards. - Familiarity with surgical instruments and medical equipment. - Attention to detail and strong organizational skills. - Ability to work under pressure and manage time effectively. - Excellent communication and teamwork skills. - Analytical skills to monitor sterilization processes and troubleshoot issues. Tools and Equipment: - Autoclaves and sterilization equipment. - Decontamination tools and instruments. - Personal protective equipment (PPE). - Inventory management software. - Quality control systems and logging tools.

Role & responsibilities : Supervise sterile manufacturing processes such as compounding, filtration, filling, and sealing of injectable products. Ensure compliance with cGMP, FDA, and other regulatory requirements in all production activities. Monitor and control environmental conditions in aseptic areas, ensuring cleanroom discipline is maintained. Coordinate with quality control, quality assurance, and engineering departments for production-related activities. Review and maintain batch manufacturing records (BMR), logbooks, and other relevant documentation. Perform in-process checks and ensure timely reporting of deviations and non-conformances. Assist in validation activities including media fill, equipment qualification, and process validation. Train and guide production staff on aseptic techniques, gowning procedures, and SOP adherence. Ensure timely availability of materials, equipment, and manpower for smooth production operations. Participate in internal and external audits and support compliance initiatives. Preferred candidate profile Education: B.Pharmacy/ M.Sc. Experience: 1-7 years in injectable (sterile) production in a pharmaceutical company. Knowledge of aseptic processing and cleanroom protocols. Familiarity with equipment like autoclaves, vial washers, filling lines, lyophilizers, and isolators. Understanding of documentation and regulatory requirements (e.g., USFDA, EU GMP, WHO GMP).

Role & responsibilities For Production : Having Injectable Experience of Shop floor activities like Filling, Sealing, Stoppering, Garment Washing Machine, Vial Washing, Autoclave, Ophthalmic, Suspensions (Handling of Homogenizer, Netzsch Mill/Bead Mill and Single use Systems) filtration, Lyophilizes. Having Injectable Experience of Shop floor supervising activities like Filling, Sealing, Stoppering, Garment Washing Machine, Vial Washing, Autoclave, Ophthalmic, Suspensions (Handling of Homogenizer, Netzsch Mill/Bead Mill and Single use Systems) filtration, Lyophilizes. Operations and Training and QMS. For Quality Assurance : Having Injectable Experience of QMS, Audit & Compliance, IPQA, AQA (Microbiology), CSV Validations

Role & responsibilities • Have working knowledge of lyophilized product development and transfer to plant. • Have good knowledge on documentation practices with respect to preparation and review. • Timely development and delivery of allotted formulations and any other assigned project as per agreed timelines and budget. • Completion of document preparation and formulation activities to support pre-clinical, clinical supplies and technology transfer, exhibit batch manufacturing of developed product. • Development of non-infringing strategies for novel formulations in compliance to regulatory requirements for US, EU, and ROW market. • To write Lab note books, stability data compilation and tracking of project progress. • To prepare BOM for new UID activities with respect to costing of NPDs. • Preparation and request of spec for raw material, packaging material, in-process controls and finished product specification. • Preparation/review of documents for manufacture exhibit/ commercial batches like master formula card, product specifications, product development report and technology transfer docket and co-ordination with support functional team for timely delivery of projects. • Identification of product/Process specific equipments/ machinery and record keeping of usage and maintenance. • Ensure compliance of SOPs, GLP, and GDP in product development of group Ideal Candidates Preferred candidate profile : Only In F&D Injectable candidates preferred.

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:

Role & responsibilities 15 to 20 years of relevant industry experience. Must have experience working in organizations supplying to the USA and EU markets. Must have participated in at least 5 successful USFDA audits. Hands-on experience in sterile formulations, including vials, pre-filled syringes, and ophthalmic solutions. Exposure to working with isolators is essential. Comprehensive experience in managing Quality Management Systems, including Change Control, Deviations, CAPA, and Annual Product Quality Reviews (APQR). Overall responsibility for IPQA activities and batch release processes. Handling compliance-related activities, including internal audits and external regulatory inspections. Responsible for the training and development of the quality team.

Qualification : B.Pharma Experience : 3 to 10 yrs. Designation : Officer Salary Range : 6 to 7 Lacs PA. Unit : Injectable Kindly Find the JD. Management of Aseptic Process Simulation (Media Fill) Program. Review of quality systems such as Change Control, Deviations, CAPA, OOS, OOT, LIR, Market Complaint, FAR, Product Recall and other QAMS documents. Preparation and Review of APQR. Nitrosamine Risk Assessment of Drug Product Preparation and review of site QA SOP and review of cross-functional department SOP. Review of Batch Manufacturing Record and Batch Packing Record. Preparation, review and execution of hold time study of drug product. Preparation and review of thermal cycling and temperature excursion study If interested mail cv at :- neetij@selectsourceintl.com

Only from Pharmaceutical - Injectables candidate required Role & responsibilities Operation of filling machine, sealing machine , ALUS operation , storage vessel operation and cleaning Experience of operating Glass Vial filling machine / Autoclave / Sealing machine Interested candidates can apply on " hemin.darji@adecco.com" or call on 7567844566

Job Description Experience in institutional sales, particularly within the pharmaceutical, surgical, injectable, or rehab product industries. Slaney Healthcare (A group company of Shalby Limited) Designation : Territory Manager/ Senior Territory Manager Department : Sales & Marketing Employment Type : Full Time(Permanent) Experience : 4+ Location : Delhi Qualification : Any Objective To Highly motivated, results-driven with expertise in identifying new business opportunities while maximizing on existing relationships to increase revenue. Capable of developing and implementing marketing and sales plans. To promote the product specialties through branding, camps and events, corporate/TPA tie-ups with the aim to reach as much revenue as possible. Key Responsibilities - Independently manage and execute the sales strategy for the designated region, aiming to achieve or exceed sales targets for surgical, injectable, rehab and pharmaceutical products. - Ensure maximum coverage of the assigned area. - Meeting daily call plans & weekly / monthly targets. - Track new projects, tenders enquiries and its execution - Identify business opportunities and evaluate prospects in respective product lines. - Monitor upcoming equipment / consumables requirements in existing hospitals and understand the purchase process. - Establish and maintain strong, long-term relationships with key healthcare professionals, including doctors, distributors, institutional clients. - Prepares reports by collecting, analyzing, and summarizing funnel and sales forecasting with accuracy. - Monitor Competitor activities in the assigned area. - Maintains professional and technical knowledge by attending various training programs. - Work along with the product managers, therapy application specialists and ensure sales growth. - Attend commercial and technical meetings; submit offers and other desired documents. - Achieve the desired objectives. Regards, Tejaswini Sahu hr1.corp@shalby.in

Role & responsibilities To develop, execute, and monitor production planning and scheduling strategies for pharmaceutical manufacturing, ensuring smooth operations, material availability, and compliance with regulatory requirements. Reporting To Head-PPC Geographic Location Ahmedabad, Gujarat, India Education: B. Pharm / M. Pharm / B.Sc. / M.Sc. / MBA (Operations / Supply Chain) or equivalent. Experience & exposure Experience: 10-15 Years years in Production Planning & Control (PPC) in Injectable Pharmaceutical Manufacturing. Key Responsibilities 1.Production Planning & Execution Develop and oversee monthly, weekly, and daily production schedules based on Sales or Demand forecasts and inventory levels Monthly Production plan preparation based on pending export, tender orders and sales forecast. Create Plan order in SAP. Monitor Daily production plan VS Actual, incase of any deviation then discuss with production team Optimize batch planning to minimize changeovers and maximize equipment utilization. Track and monitor production performance, identifying and resolving issues. 2. Inventory & Material Management Inventory Monitoring and Product availability Ensure the availability of raw materials, excipients, and packaging materials by coordinating with procurement and warehouse teams. Maintain optimum inventory levels to avoid shortages or overstock situations. Collaborate with the procurement team to forecast material requirements based on production schedules. 3. Coordination & Cross-Functional Collaboration Coordinate with Cross Function teams like Quality Assurance (QA), Quality Control (QC), Warehouse, and Engineering teams to ensure seamless production flow. Communicate production status, changes, and challenges to stakeholders in a timely manner. Work closely with regulatory teams to ensure compliance with global standards. Coordinate with PDD team for New Product Development & review existing. 4. Compliance & Documentation Ensure adherence to GMP, WHO, and other regulatory requirements. Maintain accurate documentation for production schedules, material planning, and deviations. Assist in internal and external audits by providing necessary production planning data. Preferred candidate profile Exposure Strong background in sterile/injectable formulations is mandatory. Key Skills Required Expertise in production planning, scheduling, and capacity management. Strong knowledge of GMP, WHO and other pharmaceutical regulations. Proficiency in SAP Analytical skills for demand forecasting and production efficiency improvement. Strong leadership and team coordination skills. Ability to work under pressure and manage multiple priorities.

Role & responsibilities Responsible for In-process production related activities in DP manufacturing, filling, and packing sections Preparation of batch manufacturing records, process validation protocol/report of DP area and its associated records Responsible for calibration and qualification program of equipment of DP area Execution and review of IQ, OQ, PQ of equipment. Perform the Qualification/Verification of equipment's and compilation of PV documents of the DP Area