1756 Gmp Jobs - Page 27

To handle DCS as operator. Ensure batch charging other manufacturing operations should be strictly as per BMR/SOP in line with current GMP practices. To maintain manufacturing records online should comply data integrity practices. To take out sample of intermediate/in-process material and send to IPQC/QC lab. To ensure the production related inputs in SAP system. To be check and ensure the PISCADA reports generation review of DCS alarms. Transfer finished goods through Finished Goods Transfer Note. To Check and ensure minimum stock of consumables, Logbooks status labels. Ensuring preventive maintenance of all equipment as per schedule. Co-ordinate with service departments (QA, QC, stores, E M) for various production related activities. If any abnormality found in production area / activities, authorized to stop activity immediately inform to superiors/production Manager. Responsible to maintain housekeeping in plant take care the cleanliness of equipment. Follow safety instructions/procedures ensure use of safety outfit while on works. To attend GMP safety trainings implement the trainings outcome at work place. Should be aware of the location of firefighting equipment and should know the operation. He should not leave the work spot unattended and go away without prior permission from shift-in-charge/Manager Responsible for allotment of work to operators casuals. To involve in other initiatives such as AET CSR Qualifications Diloma in Chemcial / BE/B.TECH Chemcial Engineering

Job Overview Within the strategic framework and direction of Excom and the EVP of Global Operations, the VP of Supply Chain is responsible to oversee, lead and develop the Global Supply Chain for PCC. Specific responsibilities include External Supply Operations, end-to-end Global Planning, Logistics, Procurement, revenue forecasting, and Supply Chain Operations/ Management in each of our three regions. Key Stakeholders: Internal Regional Supply Chain heads, EVP Global Operations, all Excom Vice Presidents, all Sales General Managers, Alliance Management Head Key Stakeholders: External Customers, 3PLs, Suppliers; CMOs Reporting Structure Reports to: EVP, Global Operations Direct Reports: Director, Global Planning, Director, Supply Chain USA, Chief Manager, Supply Chain, Deputy General Manager, Supply Chain, General Manager, Packaging Technology, Sr. General Manager, Sales, Director, Supply Chain EU & ROW Essential Qualification Bachelors Degree in Business, Supply Chain, Engineering or related degree MBA or Graduate level Supply Chain degree or training preferred. Certifications such as CPM, CPIM, CSCP, and CPP are a plus. Experience Minimum twenty (20) years manufacturing or supply chain experience in a pharmaceutical, life sciences or medical device company Five (5) years experience leading global Supply Chain teams with a generic pharmaceuticals company preferred. Deep knowledge and experience with all aspects of SCM including demand planning, inventory planning, capacity planning and supply planning as well as procurement and P2P practices. Deep experience base in Global Supply Chain Management, External Supply and Material Management (supplier, planning, logistics), Management of Global Multiple Sites and operational teams Experience with global supply chain teams including policy and procedure development, strategy execution, regulatory compliance, quality systems and product life cycle planning Develop supply chain management best practices in areas such as systems integration and optimization. Knowledge and experience of USA, EU and India Logistics and warehousing practices and regulations including international trade compliance regulations Knowledge of pharma GDP and 3PL O2C operations Ability to lead and provide direction to large, complex, cross-functional projects Knowledge of SAP MM, SD, PP modules desirable Five (5) years of experience working with Supply Chain software General knowledge of MRP and inventory control systems Superior Microsoft Excel skills Deep and direct knowledge and experiencing managing and maintaining critical global supplier relationships to insure short- and long-term continuity and sustainability of supply through our external partners Knowledge of US healthcare Supply Chain and contracting for GPO, IDNs, 340b, VA and wholesalers Experience with USA wholesale distribution, contracting and sales operations Proven abilities as a collaborative, innovative and organizational thinker who is decisive and has a strong results-orientation; demonstrates high sense of urgency, bias for action, personal energy and stamina to handle multiple priorities and extensive time demands Organizational-mindset with strong oral and written communication skills including presentations and reports to executives, functional teams and other groups Be a hands-on team leader and player willing to work in an environment where initiative, responsiveness, accountability, and professional maturity are valued and required Experience managing and/or working with a staff of senior professionals Experience interacting with executives and senior leaders Excellent analytical skills including the ability to quickly identify trends, related competitive opportunities and market conditions Analytical and critical thinking skills and a proven track record of identifying and solving problems Working cross functional knowledge of business areas to quickly identify and reach resolution of issues Willing to travel internationally up to 20% Strong and working familiarity with GMP, GDP, FDA, ICH, EU, JP, OFAC, BIS, Trade Compliance and other applicable regulations, laws, guidelines, procedures and standards Roles & Responsibilities Lead and oversee cost efficient, sustainable supply chain operations all three regions including Planning, Sourcing, Order Fulfillment, Inventory Management, Logistics and Process/Data/System enablement Ensure continuity of supply for all PCC products. Develop and execute risk management and mitigation strategies to prevent supply disruption. Lead and oversee Global Planning and B2B order processing within PCC. Manage inventory working capital to budget targets. Serve as the de facto Kurla Site Administrative Head for PCC Provide leadership and problem resolution within the SCM group Develop team members, policies, and processes Lead the SCM team to help achieve the organization's overall strategic goals and financial goals Overseeing the complete operation of the PCC Supply Chain organization in accordance with the direction established in the strategic plans and EVP Global Operations. Ensure trade and business compliance with all regulations, rules, federal and international laws involving SCM and Business Operations. Ensure compliance with all narcotics regulations touching the PCC business Perform other responsibilities as assigned by the EVP of Global Operations Competencies Critical Thinking using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems. Excellent customer service skills and professional demeanor at all times to interface effectively with all internal and external customers. Excellent verbal and written communication skills Creative and able to present various solutions nergetic, enthusiastic and motivational disposition Negotiation skills Exhibit Piramal Success factors Coaching & Mentoring skills

B.Com | M.Com | B.Sc.| M.Sc. | B.Pham Department: Primari Packing & Secondary Packing Location: Santej Ahmedabad. * Transportation Facility Available (As Per Circumference Of Sunrise Remedies) Mediclaim and Food Facility provide By Company. Key Responsibilities: Supervise primary and secondary packing operations as per batch packing records (BPR). Ensure compliance with GMP, SOPs, and safety standards during packing. Monitor packing line efficiency, material usage, and yield. Coordinate with production, QA, and warehouse departments. Conduct line clearance and reconciliation of packing materials. Ensure proper labeling, coding, and packaging a s per product specifications. Maintain and update packing documentation and logbooks. Train packing staff on standard procedures and safety protocols. Troubleshoot minor equipment issues and escalate when needed. Area Maintenance: Ensures cleanliness and organization of the packaging line and work area.

We are looking for skilled Automation Engineers with experience in pharmaceutical projects and hands-on involvement in DCS and PLC-based industrial automation systems . The ideal candidate should be familiar with various communication platforms , automation technologies , and GAMP protocols . Key Responsibilities: Execute and manage automation projects in pharmaceutical environments. Design, configure, and implement DCS systems for process automation. Work with industrial communication protocols (e.g., Modbus, Profibus, Ethernet/IP). Ensure compliance with GAMP guidelines and validation processes. Collaborate with cross-functional teams for project execution and documentation. Participate in FAT/SAT and provide technical support during commissioning. Desired Candidate Profile: Bachelors degree in Instrumentation, Electronics, or related engineering field. 4+ years of experience in pharmaceutical automation projects. Hands-on experience with DCS/PLC systems (e.g., Siemens, Rockwell, ABB). Familiarity with SCADA/HMI systems and GAMP protocols. Strong analytical and troubleshooting skills. Good communication and team collaboration abilities.

Designation: (Junior manager 8 I) (Assistant manager 8 II) Job Location: Bangalore Reporting to: Department Head Job Grade: 8 (I/II) The Company Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development, and manufacturing solutions company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. Syngene s 4500+ scientists offer both the skills and capacity to deliver great science, robust data management and IP security, and quality manufacturing at speed, to improve time-to-market and lower the cost of innovation. With a combination of 1. 9 Mn sq ft of specialist discovery, development and manufacturing facilities, as well as dedicated research facilities for Amgen, Baxter, Bristol-Myers Squibb and Herbalife, Syngene works with biotech companies pursuing leading edge science as well as multinationals including GSK and Merck KGaA. Key Result Areas Role-specific: Following GMP and GDP and data integrity Responsible for DP manufacturing facility manufacturing activities (operation and cleaning of autoclaves, compounding vessels, filtration vessels, pass-boxes, filter integrity machines, leak testing machine, glove integrity tester, LAFs, bag sealing machine, weighing balances, O RABS, washing & tunnel with filling lines and packaging) for DP. Responsible for operation and cleaning of Automatic visual inspection machine and labelling machine for DP. Preparation, review and execution of Study protocol/SOPs/QRM/ Study report/QRM report in the drug product facility. Ensure QMS compliance in qualification and manufacturing related activities . Assist the validations/study and routine validations/study of equipment and facility. Identify and implement the manufacturing procedures with compliance to current GMP requirements and shop-floor area walkthrough on weekly basis. Coordinating with engineering and validation department for calibration, preventive maintenance and qualification. Assist the installation and commissioning activities like FAT, SAT etc. of DPM equipment s. Performing/Executing/Assisting the IQ, OQ and PQ related to equipment s in drug product facility. Preparation and review of SLIA, URS, CLIA, QRM, IQ and OQ documents and support for routine activities in DP manufacturing. Coordinating with cross functional departments to complete the QMS activities Preparation & review of all SOP s/protocols related to equipment and drug product facility. Making the facility ready for various customer audits and regulatory audits. To maintain and review the audit trail, user privileges and alarms trending of critical equipment s as and when required. Performing the FAT & SAT of drug product manufacturing equipment at vendor sites or at our facility. Preparation and execution of QMS documents in the department. Planning periodic training for operators and juniors related to SOP s. Preparation and execution of training modules on QMS and safety SOP s in the department. Supporting regulatory audits Education and Experience Education Master s degree/ bachelor s degree in pharmacy, Master s degree in Pharmaceutical Sciences. Industry Experience Minimum 7 - 8 years of relevant practical experience in sterile injectable for drug products etc. Other competencies required for the role Ensure QMS compliance in qualification and manufacturing related activities . Coordinating with cross functional departments to complete the QMS activities Completion of SAP related transactions (as applicable) related to functional work. Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities. Pls visit us at https://syngeneintl. com/ to know more about us and what we do.

Role & responsibilities :- Achievement of targets set as per the production plan for a single line to maintain production prorate. Knowledge of Manpower Handling Knowledge of S.A.P. in PP module. Responsible for compliance with all SAP related working in a single line (Production plan execution/ Production posting/ Breakdown) Knowledge of ISO / HACCP / FSMS / GMP / GHP and food safety management in Production section. Knowledge of 5S/Kaizen/ TQM etc Coordinate with Shift Engineer & Shift In-charge. Responsible to take product change over as per need of the time depending on the floor situation with respect to material availability. Training & Development of a team in a shift. Responsible for onsite verification of Process with respect to Food Safety Documentation. Responsible for reporting any incident of the shift to concerned shift in-charge with cc to Production Head. Responsible for preparing shift report/ daily production report/ wastage data and its circulation to all concerned. Responsible for managing shopfloor by utilizing all available resources with respect to man/material and process. Maintenance of stock register. Requisition of Packing Material & Final Product transferring in BSR. Final visual check of product. Responsible for maintaining cleanliness, sanitation and hygiene standards as per the company's SOP in storage and packaging section. Ensuring the availability of packing material in the Department by raising indent and follow up Ensure the safety in the department. To increase Awareness in the department w.r.t. to Environment/ Safety & Health. Preferred candidate profile :- Round the clock shift working in all 3 shifts including night shift. Candidates having experience in baking (Biscuit) industry will be preferred.

Rsponsible for managing the initial and periodic validation and qualification activities for various areas and facilities. This includes drug substance and drug product manufacturing equipment, cold storage equipment, utilities, media fill of aseptic areas, and smoke studies. The role requires a seasoned professional with experience in validation and qualification processes within the pharmaceutical or biotechnology industry, specifically on injectables. Key Responsibilities: Validation and Qualification Management : Manage the validation and qualification activities for manufacturing equipment such as Autoclaves, Tunnels, Lyophilizers, Bioreactors, and Dry-heat Sterilizers. Handle the validation and qualification of cold storage equipment including Cold Rooms, Deep Freezers, Refrigerators, Incubators, Blast Freezers, Freeze-Thaw units, and Warehouse storage areas. Ensure the validation and qualification of utilities such as Water systems, Compressed air, Nitrogen, Oxygen, and Carbon Dioxide systems. Aseptic Area Management : Manage media fill activities to ensure aseptic conditions are maintained. Conduct and oversee smoke studies to validate airflow and contamination control in aseptic areas. Documentation and Compliance : Develop and maintain comprehensive validation and qualification protocols and reports. Ensure all activities comply with regulatory requirements and internal SOPs. Maintain accurate and detailed records of all validation and qualification activities. Team Leadership : Lead a team of validation and qualification specialists, providing guidance, training, and performance management. Foster a culture of continuous improvement and ensure the team stays updated with the latest industry standards and practices. Project Management : Plan, coordinate, and execute validation and qualification projects within defined timelines and budgets. Collaborate with cross-functional teams including Quality Assurance, Manufacturing and Engineering. Risk Management : Identify potential risks in validation and qualification processes and develop mitigation strategies. Conduct risk assessments and ensure corrective and preventive actions are implemented effectively. Continuous Improvement : Drive continuous improvement initiatives to enhance validation and qualification processes. Stay abreast of industry trends, regulatory changes, and technological advancements. Qualification Education : Bachelor’s degree in Engineering, MSc or MPharm (Life Sciences), or a related field. Experience : 10-15 years of experience in validation and qualification within the pharmaceutical or biotechnology industry. Skills : Strong knowledge of validation and qualification principles and practices. Excellent leadership and team management skills. Proficiency in regulatory requirements and industry standards (e.g., FDA, EMA, GMP). Strong project management and organizational skills. Excellent communication and interpersonal skills. Ability to analyze complex data and make informed decisions. Additional Requirements: Ability to work in a fast-paced, dynamic environment. Strong problem-solving skills and attention to detail. Additional Information About the Department Biologics Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 10–15-year time horizon. With a robust portfolio of biosimilar products across key therapeutic areas, covering ~US$80+ Bn in innovator sales – future business pipeline covers a variety of product classes and therapy areas, and new modalities. Fully integrated organization with over two decades of experience in developing, manufacturing and commercializing multiple biosimilar products. With a Product Development engine that has end-to-end capabilities – in-house clone development, upstream and downstream process development, bioanalytical development and proprietary formulation. Supported by a Clinical and Regulatory team with experience in executing complex biosimilar programs with innovative global trial designs. We have a proven experience in commercial-scale manufacturing across a variety of technology platforms with global quality standards and a highly competitive cost structure Rich experience of commercializing high-quality biosimilars in multiple markets with over 900,000 patients having benefited from our products till date. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Key Tasks & Responsibilities: The IRT Project Manager assumes responsibility for operational execution of the IRT system used in clinical studies in development phases I to IV within clinical operations development operations The IRT is a critical system in ensuring safety of all patients taking investigational medicinal product (IMP,) and if not set-up correctly, could jeopardize the usability of data obtained within the clinical studies. As an expert in IRT, the Project Manager leads the set-up and testing of the system, ensuring it meets the requirements of the clinical study protocol and that all associated processes are fully compliant with GxP regulations. Revises / develops the clinical study protocol with particular focus on the attributes of study drugs including comparators, medical devices, randomization and blinding. Ensures appropriate supply of study medication for all patients in a clinical trial by implementing optimal IRT supply strategies. The Project Manager continues to assume accountability of the IRT during the systems life cycle, implementing all required amendments. Leads the IRT cross-functional sub-team and is accountable for the set-up and maintenance of the IRT System with special attention to the proper and correct supply of study sites with study medication, including the correct drug dispensation according to the study protocol. Responsible for providing guidance and training to study teams. Qualifications & Competencies: Bachelors Degree or equivalent. Pharmacist degree preferred 5 to 8 years of relevant healthcare clinical development experience Profound knowledge in drug development Profound knowledge in setting up Interactive Response (IRT) Systems Profound knowledge in GCP and knowledge of GMP Excellent project management skills Excellent communication skills (including fluent English)

Job Title : Sales & Marketing Manager Cleanroom Equipment & Filters Location: Faridabad Department: Sales & Marketing Reports To: Director Sales & Marketing / General Manager Job Summary: We are seeking a proactive and technically sound Sales & Marketing Manager to join our leadership team at the middle management level. The ideal candidate will have a strong background in marketing and sales within the cleanroom, HVAC, filtration, or life sciences equipment industry. This role is responsible for driving sales growth, executing marketing strategies, and managing customer relationships to expand the company’s market share in cleanroom equipment and air filtration products. Key Responsibilities: Marketing: - Plan and execute B2B marketing campaigns including trade exhibitions, digital marketing, product launches, brochures, and email campaigns. - Coordinate with the design and technical teams to develop product presentations, datasheets, case studies, and videos. - Analyze market trends, competitor offerings, and customer feedback to guide product positioning and messaging. - Manage digital presence including website updates, SEO, and LinkedIn campaigns to boost brand visibility. - Maintain marketing collateral in line with technical accuracy and compliance standards (e.g., ISO, GMP). Sales: - Develop and implement sales strategies to meet and exceed revenue targets across product lines including HEPA/ULPA filters, terminal housings, biosafety cabinets, air showers, and cleanroom products. - Identify and acquire new clients in key sectors such as pharmaceuticals, biotechnology, hospitals, electronics, and research labs. - Maintain and strengthen relationships with existing customers, consultants, and channel partners. - Conduct site visits, technical discussions, and product demonstrations to provide value-based solutions. - Prepare and present sales forecasts, pipelines, and performance reports to senior management. - Respond to RFQs, RFPs, and tender documents, ensuring accurate technical and commercial submissions. Team & Coordination: -Create, mentor and Lead a team of sales and marketing executives and coordinate cross functionally with production, design, and service departments. - Ensure timely customer follow-ups, order closures, and post-sales support coordination. - Work closely with the product development team to provide market insights and customer feedback for new products or improvements. - Monitor and manage departmental budgets and ensure efficient resource allocation. Qualifications: - Bachelor’s degree. MBA in Marketing is a plus. - 5–8 years of relevant experience in industrial product sales and marketing, preferably in cleanroom equipment, filtration, HVAC, or life sciences. - Strong technical understanding of cleanroom standards (ISO 14644), air filtration (EN 1822, ISO 16890), and HVAC systems is highly desirable. - Proven ability to handle high-value B2B technical sales and large-scale industrial clients. - Excellent communication, presentation, and negotiation skills. Preferred Skills: - Familiarity with industry-specific compliance standards: GMP, GLP, ISO, NABL, FDA. - Knowledge of CRM systems, digital marketing platforms, and ERP tools. -Proficient in MS office and computer. - Willingness to travel for client meetings, exhibitions, and technical support.

To Maintain production activities following cGMP. Responsible for online documentation. Responsible for issuance of Raw material /Packing material. Responsible to follow all cGMP requirements related production activity. Required Candidate profile Responsible to manpower handling & co-ordination with departments like QC, QA , Maintenance, Finished Product store etc.

his role is responsible for overseeing warehouse operations and ensuring seamless SAP transactions related to inventory management. The ideal candidate will have expertise in handling goods receipts, issues, and transfers while ensuring compliance with industry standards and safety regulations.

Role & responsibilities Preferred candidate profile ITI (Electrical / Fitter / Instrumentation or relevant trade) Completed Apprenticeship (mandatory) 1 to 3 years of relevant experience in Pharmaceutical or FMCG industry Freshers with apprenticeship in a regulated industry may also be considered Key Responsibilities: Assist in routine maintenance and operation of plant equipment Support preventive maintenance as per schedule Ensure timely reporting of equipment faults or abnormality Adhere to all GMP and safety procedures while working on machines Assist senior technicians in troubleshooting Maintain proper records of maintenance activities and equipment logs Follow SOPs and documentation protocols diligently Note: Only ITI holders with completed apprenticeship will be considered.

Oversee daily operations of QC lab Ensure all testing procedures & results meet standards Documentation of test results, equipment logs & QC records Equipment maintenance & calibration Train & guide people works under him Handling Customer Complaint Required Candidate profile Knowledge of Legal requirement & able to liaison with govt authorities QC Activity for Soap & fatty Acid Plant & other cosmetic products Knowledge of GMP & cGLP Msc/Bsc Chemistry with 7-10 yrs exp.

BDM - EXPORTS Client Acquisition: Actively prospect for potential new clients and convert leads into increased business opportunities. Client Relationship Management: Review and address objections in agreements, working through differences to achieve mutual benefits for both clients and the company Be the single point of contact for clients, addressing their needs and ensuring satisfaction. Product Presentation: Present new launch products to existing clients, stimulating new inquiries and fostering ongoing business relationships. Market Research and Analysis: Conduct thorough research to build relationships with new clients. Coordination and Project Management: Coordinate the submission of documents to clients, ensuring timely completion of projects. Collaborate with internal departments such as Purchase, F&D, QC, RA/QA/RA to deliver client projects within stipulated timeframes. Administrative Responsibilities: Create and maintain a monthly product list to stay updated with current developments. International Engagement: Plan and organize international client visits to the plant. Collaborate with management to identify and open new countries for GMP Target Approvals. Preferred Candidate should be Country Manager or Similar International Experience.in Semi-Regulated Market. This role requires a proactive individual with strong communication skills, a deep understanding of the pharmaceutical industry, and the ability to manage client relationships effectively. The candidate should be adept at coordinating internal departments and contributing to the overall growth and vision of the company . Candidate Profile: Presently working in similiar capacity i.e. as Export Executive/Manager with any leading Pharma Company. Candidate must be a Graduate/D.Pharm/B.Pharm or MBA. Experience: 2 - 5+ years Location: Andheri (E),Mumbai Local Resident of Mumbai preferred Salary: 50K 60K pm or depending on the domain experience Male / Female Candidate Only Only those candidates who have worked in Pharma Industry in this 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.

Division Department Sub Department 1 Job Purpose Monitor and execute the packing activities in a shift by maintaining cGMP and safety norms to achieve production targets Key Accountabilities (1/6) Execute shift packing activity by managing available resources and reduces micro stoppage of machine to achieve shift target Utilise shift resources optimally to get desired production output Regulate usage of consumables in the production process at optimum level to save cost Key Accountabilities (2/6) Review documentation related to packing activity and monitor standard packing parameters as per BPR to meet regulatory requirement Review and monitor critical in-process parameters like NFD, camera challenge, RH temperature etc. Review and perform all operations as per GMP and safety norms by reviewing all processes and documents for compliance Maintain system integrity by updating online documentation Perform qualification and calibration of equipment as per schedule and update output of all activities in the system Key Accountabilities (3/6) Prepare manufacturing records and update online documentation to meet production and cGMP requirement Maintain online documentation and timely entries in BPR and supporting documents by operating SAP and CipDox Prepare new documents and update existing documents as per GMP requirement Key Accountabilities (4/6) Monitor adherence to safety guidelines in the block during a shift for packing activities to create safe working environment Monitor safety systems and ensure procedures are followed in shift and near-miss cases are reported to HSE timely Ensure availability and usage of PPEs in the shift by coordinating with HSE department Ensure compliances to safety training targets by monthly reconciling attendance records Key Accountabilities (5/6) Provide training to staff & workmen for packing activity by regular interactions with them to get quality product Provide training to staff and daily workers for packing activities and safety procedures Conduct training related to equipment handling, cGMP, documentation and unit operations Key Accountabilities (6/6) Provide new ideas and simplify processes to reduce process cycle time and achieve new targets Provide new ideas during idea sessions for better productivity with minimum cost Identify the complexities and suggest process simplification areas to achieve new target with optimum utilization of resources Reduce and simplify documentation for better accuracy and to meet ALCOA (Attributable Legible Contemporaneous Original Accurate) Major Challenges Meeting shift target due to unavailability of adequate resources. Overcome by efficient work load distribution Maintaining cGMP requirements during system downtime. Overcome by coordinating with engineering and technical support team Key Interactions (1/2) Quality assurance and control for batches release as per packing plan (Daily) Engineering for preventive maintenance and help in modification (as per need) Safety for awareness training and near miss issue (Daily) Store for daily dispensing plan and availability of packing materials (Daily basis) Key Interactions (2/2) Maintenance contractor for any machine repairs (Need Based) Dimensions (1/2) Direct Reports : 3 Achieve average volume of 200 mn (FY2015-16) Average number of BPR s handled : 200 Average number of batches in packing : 200 Average number of sales order dispatched : 80 Achieve internal OTIF more than 90% Achieve Zero reportable accidents/ incidences during packing activities Achieve 0% errors in online documentation Meet 100% compliance to SOP and Safety regulation Dimensions (2/2) Key Decisions (1/2) Resources allocation and work distribution for each shift Key Decisions (2/2) Up-gradation in facility and documents to Section Head - Packing Modification in equipment to Section Head - Packing Deviation and implementation of CAPAs Section Head - Packing Education Qualification B. Pharm. / B. Sc. (Chemistry) Relevant Work Experience 1-5 years of experience in packing with knowledge of handling of QMS activity, qualification and other related documents

Job Summary: We re looking for an experienced and detail-oriented professional to manage and oversee all QC lab activities. This role demands strong leadership, in-depth technical knowledge, and a commitment to regulatory excellence. The selected candidate will support the HOD, lead lab teams, and drive compliance with GMP, ISO, and global quality standards. Key Responsibilities: Supervise daily QC lab operations and testing activities Act as HOD designee during their absence Ensure timely testing and release of RM, intermediates, and finished products Investigate and document deviations, OOS, OOT, and lab incidents Implement and maintain QMS in alignment with cGMP, ISO, FSSC, Halal & Kosher Review and update specifications and pharmacopeial methods Oversee validation and revalidation of analytical methods Train analysts on lab techniques, SOPs, GLP & GDP Monitor stability studies and ensure protocol adherence Manage instrument calibration, qualification, and maintenance Review analytical reports, calibration records, and lab documentation Lead/support internal and external audits Coordinate with Regulatory Affairs and QA teams Implement pharmacopeia updates and support regulatory readiness Contribute to continuous improvement and special quality initiatives Qualification : MSc Chemistry Experience : 4-8 Years

Business: Piramal Pharma Solutions Department: Engineering & Projects Location: Digwal, Hyderabad Travel: High Job Overview: Overall responsibility for end-to-end project management, including design, budgeting, vendor management, and timely execution at optimal costs. Ensures compliance with GMP, ISO 14001, OHSAS 18001, and other regulatory standards. Leads commissioning, validation, and operational readiness of facilities and equipment. Proactively manages safety, environmental risks, and implements robust SHE practices. Drives continual improvement through risk assessments, CAPA, and comprehensive training for teams and contractors. Reporting Structure: Directly reports to - Site Head Positions that report into this role - 6-8 Experience: 15+ years of experience in Manufacturing, GMP, Safety, resolving technical customer queries. Good communication skills Competencies: QMS handling Understanding of changing regulatory requirements Confident to face audits Team Management Quality Investigations Analytical knowledge Collaborating with CFTs SPOC for CDMO projects KEY ROLE & RESPONSIBILITIES: Overall responsible for identification, evaluation & implementation of projects in Time and optimum cost. Designing facilities including buildings, equipment and accessories. Identification of Vendors and Contractors for Projects in various fields. Inspection and testing of equipment and accessories. Inspection of project materials received in the factory. Issue of specifications and drawings for Project items. Approval and rejection of project materials. Project evaluation and review periodically. Preparation of budget and time schedule for all projects. Commissioning of projects. Validation of the facility as per the established procedure. Ensure compliance of legal and other requirements related to ISO14001:2004 and OHSAS 18001:1999. Identification of Risks & Hazards, Environmental aspects & evaluation and review the same. Develop objectives, targets and programmes under EMS & OHSMS. Institute operational controls, monitor the key characteristics, carry out root cause analysis for the Non conformity and take CAPA. Ensure continual improvement in OHS & EMS Management Systems. Identify SHE training needs for awareness and Competence. Ensure SHE requirements wrt contracted services and service providers. Qualified B-tech (any stream).

Dishman Carbogen Amcis is looking for Senior Executive - Production to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes

Ensure 100% follow of cardinal site safety rules. Controlling the process by monitoring the process parameters for producing prescribed quality of output as per specified SOPs. Maintaining and running of various equipment s in proper order to ensure smooth running of soya chunks plant and maintaining records in respective log sheets. Intimate timely for requirement of raw material, chemicals, and spare parts etc. for continuous running of soya chunks plant. Responsible for raw material receipt and finished good transfer with proper communication with supervisor Ensure safety guards are properly fixed on rotating equipment, use of proper PPE`s at work premises and while handling hazardous chemical. Ensure good housekeeping in and around soya chunks plant with the help of helpers. Operator is responsible for loading ,unloading of raw material, finshed goods & chemical Ensure sampling at various process stages as per quality plan. Transferring of product to respective storage area and taking their stock daily. Ensure measures such as preventive and predictive Maintenance, lubrication are done as per schedules to avoid trouble. Attending routine break down and preventive maintenance. Responsible for control and reduction of downtime in shift. Maintain various records and reports in plant log book. Make regular checks of plant equipment and make adjustments, repairs for trouble shootings. Ensure to maintain site tidiness and general good housekeeping throughout the soya chunks plant. Operator is responsible to maintain GMP to co-ordinate with quality Department. Perform all other duties as assigned and required. Report to the shit incharge / Reporting Manager.

The Technical Department within the organization is a team responsible for producing the final products with required quality to help the business to deliver it to the committed costumers. This team also continuously work to strategically expand, preserve or improve products, standards or policies whilst sticking to regulatory guidelines related to the business prospectives. Responsibilities: Follow all ADM safety rules and regulations Operators in this position are responsible for the effective and efficient operation of oil storage tank. They will ensure that the equipment is fully operational and in good repair. Operate all equipment associated with the oil storage tank and its maintenance Work in a oil storage tank environment Troubleshoot, process and maintenance problems rectification as required. Operator is responsible for loading, unloading and oil issue to oil packing section. Maintaining good housekeeping in oil storage tank Maintaining and running of various equipment s in proper order to ensure smooth running of operation Maintaining records in respective log sheets. Intimate timely for requirement of raw material, chemicals, and spare parts etc. for continuous operation. Ensure sampling at various process stages as per quality plan. Operator is responsible to maintain GMP in co-ordination with quality department. Perform all other duties as assigned and required. Report to the shit InCharge / reporting manager.

;Follow all ADM safety rules and regulations Operators in this position are responsible for the effective and efficient operation of Crude oil filtration plant. They will ensure that the equipment is fully operational and in good repair. Operate all equipment associated with the Crude oil filtration and its maintenance Work in a Crude oil filtration as per stated in SOP Troubleshoot, process and maintenance problems rectification as required. Operator is responsible for running crude oil filtration plant with focus on minimum chemical and utility consumption Maintaining good housekeeping in Crude oil filtration as per GMP Maintaining and running of various equipment s in proper order to ensure smooth running of operation Maintaining records in respective log sheets. Intimate timely for requirement of raw material, chemicals, and spare parts etc. for continuous operation. Ensure sampling at various process stages as per quality plan. Operator is responsible to maintain GMP in co-ordination with quality department. Perform all other duties as assigned and required. Report to the shit InCharge / reporting manager.

JOB DESCRIPTION Job Title: Bioassay Analyst - Large molecules Job Location: Bangalore Department - BGRC Analytical About Syngene: Syngene ( www.syngeneintl.com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose of the Role: The candidate shall be responsible to perform the development, validation, and routine testing of bioassay/ELISA for Large Molecules (LMs), especially Monoclonal antibodies (mAbs) and other LMs. The candidate shall be responsible for method development, validation, and stability testing drug substance/drug product. The candidate shall be willing to work in shifts. Role Accountabilities: Shall develop and validate cell-based assays and binding assays (ELISA), SEC and CGE especially for monoclonal antibodies (mAbs), etc. Shall troubleshoot the problems for these methods. Must have strong knowledge of the development of cell-based bioassays for Monoclonal antibodies. Experience in Qualification and Validation of cell-based bioassays Shall have experience on Good documentation/laboratory practices such as ALCOA+ Broad knowledge on analysis of cell-based assays to derive relative potency software s (such as Softmax Pro and PLA) Basic cell culture technics and hands-on experience in maintaining of mammalian cells. Must have experience in handling various cell lines (adherent and suspension cell lines). Preparation of Mammalian cell banks for Bioassays. Experience in handling of primary and continuous cell lines like Revival, maintenance, cell bank preparation, and cryopreservation Shall prepare the raw datasheets, protocols, reports, and SOPs Handling of QMS (Incidents, deviations, Out of Specifications, change controls, etc.) for GMP activities Shall be responsible for procurement and inventory maintenance of Pharmacopeial Standards / Chemicals / Reagents / Consumables / Spares etc., required for the projects Shall adhere to the procedure of GxP/GMP/Safety and as per the procedure defined in the internal standard operation procedure Must have good hold on MS office (word, excel, ppt), outlook, and other essential tools required for routine activity Experience in developing and validating SEC, CGE methods is an added advantage especially for monoclonal antibodies (mAb) is an added advantage Experience in calibration and qualification of HPLC, UPLC, GC, and other QC laboratory instruments is added advantage Good communication and e-mail writing skills are required since the candidate needs to communicate with clients/external users situated overseas Commitment to safety Behavioral Skills Good Interpersonal skills Self-time management Good Team player Polite/Good Communication skills Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience 2-6 years Skills and Capabilities: Development, validation, and routine testing of Bioassay /ELISA, SEC, CGE for Monoclonal antibodies (mAbs) and other Large molecules Qualification and validation of cell-based bioassays Able to follow instructions and perform the tasks under the supervision of the Team leader Preparation and Maintenance of all the documents Experience in developing and validating SEC, CGE and HPLC methods for mAbs is an added advantage Theoretical knowledge in Chromatography and spectroscopy technique Good documentation/laboratory practices such as ALCOA+ Good knowledge of MS-office (word, excel, ppt) and E-mail writing skills Education M. Pharm/ M. Tech/ M.Sc. / B.Sc. (Biotechnology/Biochemistry) with 2-6 years experience in GMP environment (QC) Equal Opportunity Employer:

• experience In Production manufacturing, operation, process safety and manpower management production planning, unit process in Chemical / API Intermediate Industry. • To ensure execution of production operations as per SOP. Required Candidate profile • To co-ordinate for internal GMP activities • Knowledge of GMP & GDP procedure to follow. • Monitoring production planning to meet production targets • Equipment handling.

Role & responsibilities Primarily responsible for operation and clearing of Strip packing machine. Prepare the BMR and Logs-books and records of equipment and Batches. Maintain safety and clean work environment by following current GMP. Should have knowledge of BMR, BPR preparations and maintain staff record. Preferred candidate profile ITI in Mechanical or relevant field