11381 Qc Jobs - Page 31

Position Title: Assistant Manager - Production Position Type: Regular - Full-Time Requisition ID: 37306 We are passionate about food. But we’re even more passionate about our People! About The Role To supervise and co-ordinate the processing and packing operation of production line, ensuring the product is packed within the product specifications. To manage production costs by optimizing productivity / yield, while utilizing the staff / equipment in a safe, effective and hygienic manner. Manager The Team Roles and Responsibilities & Key Deliverables: Make sure performance of subordinates is achieved against their agreed KPI’s. Performance appraisals are carried out every three months and once per year. Full implementation of training / development plan for all subordinates. Ensure it meets within training budget and work skills plan. Reduce Staff turnover Always communicate with shop floor staff reference performance output, recognizing staffs’ achievements on monthly basis. Keeps staff up to date with any changes to company procedures or policy. People Management Identify goals and individual KPI’s and develop team and their individual capability. Measure performance using organizational tools (PEP). Demonstrate open, positive and constructive communication and enact McCain Foods Code of Conduct behaviors by providing support to all production department personnel in activities. This is to improve teamwork, motivation, leadership, and job specific knowledge on a routine basis as well as monthly and annual review. Measured through quick response and implementation of corrective actions and line team reaching required agreed targets. Do monthly recognition program in monthly review meetings to batter engagement and motivation. Improve our voice survey results score year on year and prepare plan for improvement based on gap analysis Ensure Execution Of The Packing Plan Drive Safety Culture down the line and achieve ZERO TRIR through Functional Objectives. Give indent of all raw materials and packing materials to concern department. Follow RTP plan as per Monthly Plan shared by Planner and ensure 100% schedule Adherence. Meeting daily plan, maximum 5 percent deviation is allowed of specified output and excluding raw material issues. Ensure all areas are properly manned to meet operational requirements. All equipment is in good running order and set up to comply with the final product specifications. Ensure timely CIP as per validation study and work on optimization of CIP time. Drive MDI program across line and achieve OEE to meet annual Production target. Oversee that efficiency standards are maintained and subsequent planned production volumes are packed. Discuss major casual labor issues to HR on daily basis and maintain the effectiveness of personal in order to achieve the optimum labor utilization. Communicate packing out-put, downtime or quality issues on daily basis to concern person. Achieve all BOP’s related process and packing. Ensure Annual BOP training to team members. Maintenance Duties Check production consumables stock and make sure inventory level with limit. Assists with engineers during breakdowns. Ensure daily checks to be filled by subordinates. Report any defects in equipment performance to the Engineering Executives, control room operator and engineers. Manage Product Cost Manage production reports on a daily basis-ensuring yield, labor and burdens are within budget and match the cost sheet. Inform any deviation to manager on daily basis regarding cost. Check records of all waste generated within the process / packing area and investigate whenever excessive waste is found. Ensure all operation work procedures adhered to for optimal packing efficiencies / yield. Educate and train employees to ensure they are fully aware of all standards required within the process / packing area. Maintain DDS meetings and do daily Gemba Walks. Financial Management Of Department Develop and apply strong financial management approach to annual production department budget ensuring compliance with all financial management policies, audit requirements and reporting Set with Production Manager, and meet, all production department SCA’s. (Cost Saving Projects) . Provide written explanations as required, at month end and at the end of the financial year including any deviation. Initiate and recommend projects for capital consideration. Provide support for projects in the form of savings/benefits and improvements to safety and plant performance. Product Quality NPD & Hygiene Communicate with the QC concerning corrective action reports related to quality problems that occur within the packing area. Ensure operations are maintaining all quality checks within specified parameters, ensuring traceability. All non-conformance products are identified / recorded and reason for non-conformance been recorded. Customer complaints and restricted products are within the specified targets. Ensure proper execution of NPD (New Product Development), launched and all process conditions are noted and recorded. Maintain GMP in plant. Ensure Compliance With All Statutory Requirements & McCain Policies Fulfill legal compliance with all relevant legislation Fulfil compliance with McCain policies and systems Full compliance with food safety standards. Carries out monthly safety inspection of the production area Operational Safety: - No loose wires or electrical panels are open to the environment (Only engineers have access to electrical panels). All floors are kept dry to minimize slips. All staff in the packing area wear Personnel Protective Equipment (PPE). Train an update all staff in relation to all safety issues within the production area. Anticipates and identifies safety related problems, takes corrective action to resolve the safety issue. Maintain BOS system Make sure operators and shift executives are filled near misses and first add. Control Department Overhead Expenses All expenses are within the operational budget. All expenses are within the specified services budget. About You BE/B-tech in Electrical /Mechanical Engineer/Food Technology. Should have min. 8 years’ experience in the Food Industry Must be People Manager with at least 3 years experience. Apply Now if you are looking to be part of a flourishing and energetic environment! Join a recognized brand known throughout households across the globe! McCain Foods is an equal opportunity employer. As a global family-owned company, we strive to be the employer of choice in the diverse communities around the world in which we live and work. We recognize that inclusion drives our creativity, resilience, and success and makes our business stronger. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, age, veteran status, disability, or any other protected characteristic under applicable law. McCain is an accessible employer. If you require an accommodation throughout the recruitment process (including alternate formats of materials or accessible meeting rooms), please let us know and we will work with you to find appropriate solutions. Your privacy is important to us. By submitting personal data or information to us, you agree this will be handled in accordance with McCain’s Global Privacy Policy and Global Employee Privacy Policy , as applicable. You can understand how your personal information is being handled here .

We’re Hiring: MEP BIM Modeler (3 YEAR + BIM EXPERIENCE) Location: Plot No. 73, Pocket 2, Jasola Vihar, New Delhi, Delhi 110025 Salary: ₹20,000 – ₹40,000 per month (based on Skill) Joining: Immediate Serene BIM Studios is expanding, and we’re looking for a talented MEP BIM Modeler to join our growing team! Role Overview: You’ll be working on high-quality BIM models for LOD 400 Mechanical, Electrical, and Plumbing services. You will need accuracy, knowledge of clash detection resolutions, and engineering concepts. Key Responsibilities: Develop detailed and clash-free BIM models for MEP services Coordinate with architectural and structural teams for seamless integration Ensure LOD compliance and maintain project documentation Support QA/QC processes for BIM deliverables Requirements: Proficiency in Revit (MEP) and Navisworks Strong understanding of MEP systems and BIM workflows Ability to interpret drawings and specifications accurately 3+ years of relevant experience preferred Why Join Us? At Serene BIM Studios, we value precision, creativity, and collaboration. You’ll be part of a team that works on world-class projects with cutting-edge BIM practices. 📩 Apply now or share with someone who might be a perfect fit! 🌐 www.serenebimstudios.com 🔗 https://www.linkedin.com/company/serene-bim-studios

Job opening for QC Officer for Reputed API / Intermediate Manufacturing company at Khambhat - Gujarat.

Job description Job Title: Project Coordinator – Civil / MEP (PMC Role) Experience Required: 10+ Years Department: Project Management Reports To: Project Manager / Project Director Job Summary: We are seeking a highly experienced and proactive Project Coordinator for a Project Management Consultancy (PMC) role. The candidate will be responsible for end-to-end coordination of industrial and commercial projects involving civil, architectural, and MEP works. The role demands strong communication, multitasking, and execution control to ensure timely delivery, quality, and compliance across all project phases—from inception to handover. Key Responsibilities: Project Lifecycle Coordination: Coordinate all activities from project initiation to handover . Interface between client, consultants, contractors , and internal teams. Ensure timely mobilization of resources , site readiness, and kickoff procedures. Cross-Disciplinary Coordination (Civil + MEP): Coordinate and align works between civil, structural, architectural , and MEP disciplines . Conduct regular coordination meetings with discipline leads to ensure seamless integration of works. Monitor and resolve inter-disciplinary clashes (civil-MEP interfaces). Client & Consultant Interaction: Act as a single point of contact (SPOC) for clients and consultants for technical and project progress updates. Attend client meetings; circulate MoMs, action plans, and progress trackers . Ensure that client/consultant instructions are implemented effectively and documented properly. Schedule & Progress Monitoring: Track project milestones and ensure timely execution per the master schedule . Assist in preparation and monitoring of micro-level schedules (weekly/fortnightly plans). Identify delays or risks early and drive corrective actions. Documentation & Reporting: Prepare and maintain Daily/Weekly/Monthly Progress Reports (DPR/WPR/MPR) . Maintain logs of RFI, drawing revisions, approvals, material tracking , and other critical project records. Ensure proper documentation of decisions, deviations, and approvals. Quality, Safety, and Compliance: Coordinate QA/QC processes with discipline leads and client representatives. Ensure that works are executed in line with design, specifications, codes , and safety norms . Support in managing audits, inspections, and compliance checks. Required Skills & Qualifications: Bachelor’s Degree in Civil Engineering (additional MEP knowledge is a plus). Minimum 10 years of experience in industrial/commercial project coordination, preferably with PMC or EPC firms. Strong understanding of Civil and MEP works execution & interfacing. Excellent knowledge of construction sequencing, method statements, and cross-functional coordination. Proficiency in MS Office, AutoCAD, MS Project / Primavera. Strong leadership, interpersonal, and stakeholder management skills. Fluent in written and spoken English (regional language proficiency is an advantage). Willingness to work on-site and manage multiple teams. Job Type: Full-time Benefits: Food provided Health insurance Provident Fund Schedule: Day shift Ability to commute/relocate: Pune, Maharashtra: Reliably commute or planning to relocate before starting work (Required) Work Location: In person Application Deadline: 10/07/2025 Job Type: Full-time Benefits: Food provided Health insurance Provident Fund Language: English (Preferred) Work Location: In person

About Sun Pharma: Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of US$ 5.4 billion. Supported by 43 manufacturing facilities, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe. Job Summary Integration Specialist – LIMS, will be responsible for the integrating various lab instruments/software with LIMS application for successfully establishing paperless environment in QC/R&D Labs. This role requires a deep understanding of laboratory workflows, Instrument connectivity techniques, strong technical skills, and the ability to work closely with cross-functional teams to ensure the LIMS meets the needs of the organization Roles and Responsibilities • Support in QC/R&D lab instrument integration with LIMS application, at the time of LIMS implementation at various locations of SUN Pharma. • Develop and execute test scripts, and relevant documentations required as part of validation activity. • Configure LIMS software to meet the specific needs during Instrument integration activity. • Provide training and support to end-users, ensuring they are proficient in using the LIMS. • Troubleshoot and resolve any issues related to LIMS performance, functionality, and integration with other systems/instruments. • Maintain comprehensive documentation of the LIMS implementation process, including user guides and technical manuals. • Shall be aware about documentation of LIMS application as per GMP. Shall be able to create and manage documentation of LIMS application to ensure system is in compliance state. Qualifications and Preferences Qualifications: • Bachelor's degree in Information Technology, or Computer Science or related field. • Minimum of 4-5 years of experience in LIMS implementation & Instrument Integration activity, preferably in a pharmaceutical or biotech environment. • Strong understanding of laboratory processes and workflows. • Deep understanding of Lab Software functionality such as Empower, LabSolutions, Chromeleon. • Strong command on Data extraction / connectivity methodologies techniques for port based instruments such as balances, pH etc. • Proficiency in LIMS software (Expertise on CaliberLIMS is preferred) • Strong analytical and problem-solving skills. • Excellent communication and interpersonal skills. • Experience with regulatory compliance requirements (e.g., FDA, GMP, GLP). Preferred Qualifications: • Advanced degree in Life Sciences, Information Technology, or a related field. • Familiarity with laboratory instruments and their integration with LIMS • Experience with Caliber LIMS is preferred. • Good documentation skills to create and manage GxP documents. Selection Process: Interested Candidates are mandatorily required to apply through the listing on Jigya. Only applications received through Jigya will be evaluated further. Shortlisted candidates may need to appear in an Online Assessment and/or a Technical Screening interview administered by Jigya, on behalf on Sun Pharma Candidates selected after the screening rounds will be processed further by Sun Pharma

Position Summary Embark on a fulfilling career journey with BGH, where innovation meets compassion in healthcare. Join our dynamic team at the forefront of medical excellence, with a focus on Chemistry, Hematology, Transfusion Medicine, Microbiology, and Anatomical Pathology. Elevate your skills in our cutting-edge Point of Care department, where professionals like MLAs, MLTs, Senior MLTs, Charge MLTs, and PAs collaborate seamlessly. Embrace the excitement of 24/7 core lab operations, spanning days, nights, evenings, weekends, and STATs. Be part of our dedicated Microbiology and Histology teams, where your commitment to community care truly shines. At BGH, we're not just a workplace – we're a family, united by cohesiveness, professionalism, and a shared passion for making a positive impact. Join us in shaping the future of healthcare, where every day brings new opportunities for growth and success! Responsible to the Charge Technologist(s) in the Division(s) in which they are working and to the Lab Manager for performing phlebotomy and ECG tracings (site specific), as well as, preparing and organizing specimens for analysis and various duties in different divisions of the lab. Duties do not require interpretation, assessment or the exercise of independent judgment. Required EDUCATIONAL REQUIREMENTS: Successful Completion of an approved Laboratory Assistants training program and Certification with other professional organizations (i.e., CSMLS, OSMT). OR Technologist current registered with the College of Medical Laboratory Technologist of Ontario. Supervisory, verbal and written communication skills. Ability to organize, prioritize and meet deadlines. Students and new graduates actively pursuing certification are welcome to apply. Duties Blood Specimen Procurement Performs phlebotomy on Inpatients and Outpatients and BG Emergency. Implements good quality venipuncture - adult and paediatric. Implements good quality capillary collection – adult and paediatric. Maintains accurate patient identification and specimen labelling at all times. Recognizes suitability of specimens and the need for requests. Advises Technologists on Diagnosis, STATS, A.S.A.P, etc. Operates Lab computer – ordering test, logging specimen in, receiving, etc. ECGs - TMH Requires special training. Performs electrocardiograms (ECG). Responsible for good quality ECG tracings – adult and paediatric. Enters ECG into computer. Copies and dispenses ECG as required. Completes ECG process with special attention to Pre-Op ECG. Departmental Maintains pleasant and professional rapport with patients and other customers at all times. This key position has direct interaction with all the laboratories main customers, thus has a direct effect on laboratory reputation. Maintains good infection control practices. Helps with documentation and phone enquiries, as required. Assists with compiling statistics when necessary. Participates in quality assurance activities. Orientates and trains new staff/students. Assists in developing, reviewing and amending department policies and procedures. Prepare Hospital Incident Forms. Lab Tests/Set-Up – May Be Site Specific Prepares referred out specimens for appropriate outside labs for special testing and documents as required. Prepares specimens for shipment to QHC Laboratories as required. Performs inventory. Performs temperature readings. Change charts. Packaging and unpacking blood. Stocking POCT refrigerator. Maintenance (centrifuge, tachometers, timers, etc.). Sorts, centrifuges and distributes laboratory specimens entering the Laboratory. Maintains good quality sterile techniques. May place specimens on Hematology, or Biochemistry, analysers with special training. Assists with send outs. Assists with sample separating (centrifuging). Assists with worksheets. Assists with units Haematology May place specimens on analysers after special training. Chemistry Assists with aliquoting and identifying Assist with the setup of tests (eg. drugs screens, pregnancy). May place specimens on analysers after special training. Performs urinalysis (excluding microscopic). Microbiology (Site specific) Receives all microbiology samples. Answer phone calls and transfer to MLT as required. Plating microbiology samples and cultures as required. Restocking microbiology supplies. Subculture QC organisms. Equipment maintenance. Discard microbiology samples once complete. Construct Public Health kits. Equipment/Supply Procurement/Maintenance Troubleshoots problem with ECG, Holter, and Events machines and calls for service when required. Obtains weekly order from stores and organizes and puts order away. Keeps supply of Kleenex, Javex and towels, etc. in each division. Maintains and cleans blood taking room and ECG room. Assists with general maintenance and clean up of equipment and instruments. Assists with housekeeping and glassware washing. Safety Maintains a safe environment by: Following established safety, WHMIS, infection control and waste disposal policies. Maintaining a clean and organized work area. Cleaning phlebotomy trays. Keeping equipment cleaning records (eg. ECG). Weekly cleaning and minor maintenance of ECG machines. Follow infection control policies eg. Isolation, universal precautions. Working with needles and blood requires special care - all staff are to use safety equipment supplied and specified gloves, goggles, safety devices, lab coats, etc. Minimizes risks to self, other staff, patients and visitors through: Familiarity with policies and procedures regarding safety. Attendance at safety training including fire safety, back care and W.H.M.I.S. training. Reporting of hazards and incidents. Related Duties Contributes to Department by performing related tasks as required. Maintains patient confidence and protects Health Centre operations by keeping information confidential. Maintains skills/knowledge by attending educational sessions and keeping informed of Health Centre policies and procedures. Models QHC Vision and Values At Quinte Health, guided by our core values of Imagine It's You, Value Everyone, We All Make a Difference, and Stronger Together, our family of four hospitals holds a central role in the mission to enhance lives and foster healthier communities. We operate as a cohesive team, uniting all our hospitals, to deliver local and regional healthcare services. In partnership with our communities, we strive to improve access to high-quality care, right in their own neighborhoods. Our sense of fulfillment is deeply rooted in the impactful work we do, a sentiment shared by our dynamic teams of staff, dedicated physicians, and committed volunteers. They not only care passionately for our patients but also for each other, embodying our core values at every turn. We don't just serve our communities, we actively contribute to them. Quinte Health is woven into the fabric of our local landscape, with our team members residing, raising their families, and often retiring right here in the communities they cherish. We are on a constant lookout for compassionate and dedicated individuals to join our team. Our diverse array of exciting roles encompasses positions that span multiple hospitals, as well as opportunities situated within a single hospital. Join us as we live out our values in providing exceptional healthcare close to home Physical Demands Analysis Physical Requirements Able to communicate and respond clearly on the telephone and face-to-face. Able to sit 2-6 hours per day at a computer table or bench. Able to stand and/or walk 3-5 hours a day. Able to lift no greater than 28 pounds on an occasional basis. Frequent bending or leaning depending on section of Laboratory where working. Able to work at a moderate pace maintaining accurate results. Must be able to see objects close up, reading requisitions, computer screens. Must be able to distinguish between colors, depending on section of Laboratory where working. Must have good manual dexterity. Mental Requirements Able to concentrate on details despite frequent interruptions. Attention to detail is essential. Able to follow both written and oral directions and remember in detail daily requirements and routine. Able to comprehend and utilize written materials. Able to cope with a high paced, sometimes high stress, work environment. Able to interact positively with a variety of individuals from various socio-economic backgrounds. Equal Opportunity We thank all interested candidates for their response, however, only those chosen for an interview will be contacted. Quinte Health is an equal opportunity employer committed to meeting needs under the Canadian Charter of Rights and Freedom and the Ontario Human Rights Code. Our Recruitment process follows the Accessibility for Ontarians with Disabilities Act in order to provide a fair and equitable process for all candidates. Applicants requiring accommodation through the recruitment/interview process are encouraged to contact the Human Resources Department at 613-969-7400 x2577 or

Job Title Assistant Project Manager Job Description Summary This role is responsible for planning, organizing, and managing resources to ensure that projects are completed on time, within budget, and to the required quality standards. Assistant Project Manager will work closely with architects, contractors, and other stakeholders to ensure that projects are executed according to plan. Job Description About the Role: Monitor execution at site to ensure that civil/external works are carried out as per approved drawings, specifications, and design intent. Review and ensure workability and adherence to standards in method statements submitted by contractors for each civil work item (e.g., subgrade preparation, concreting, paver laying, trenching, backfilling, manhole construction). Ensure alignment of site execution with approved methodologies, especially for infrastructure services and external development works. Maintain all documentation related to assigned external civil works (inspection reports, checklists, site instructions, as-built records). Anticipate and flag imminent bottlenecks in external work progress; recommend and implement corrective actions to avoid delays. Advise contractors on improving productivity of labour and equipment for civil works (e.g., batching, curing, rework minimization). Monitor procurement and delivery of civil-related materials, equipment, and labour (e.g., kerbstones, concrete, pipes etc) in accordance with work schedules; suggest improvements where necessary. Assist QA/QC team in verifying quality of civil works, including compaction, levels, slopes, and materials testing. Support safety team in implementing safety standards, particularly for high-risk external works like excavation, trenching, lifting operations, and road works. Escalate to the project manager any issues concerning civil work progress, safety violations, quality deviations, or resource shortages. Monitor milestones and budgets related to civil infrastructure, and initiate actions to minimize rework or non-conformance costs. Participate in risk management for external works, identifying potential issues (e.g., water table, unstable soil, third-party services) and suggesting mitigations. Ensure implementation of system requirements for civil works during installation and testing (e.g., manholes, inspection chambers, slope testing for drainage). Ensure the Construction & Safety Management Plan is implemented for all external civil activities. About You B.E Civil with 5 to 10 years of experience in buildings. Technical awareness of civil, electro-mechanical, and architectural works Excellent organizational and motivational skills Outstanding attention to detail and observation ability Exceptional communication and interpersonal abilities Why join Cushman & Wakefield? As one of the leading global real estate services firms transforming the way people work, shop and live working at Cushman & Wakefield means you will benefit from; Being part of a growing global company; Career development and a promote from within culture; An organisation committed to Diversity and Inclusion We're committed to providing work-life balance for our people in an inclusive, rewarding environment. We achieve this by providing a flexible and agile work environment by focusing on technology and autonomy to help our people achieve their career ambitions. We focus on career progression and foster a promotion from within culture, leveraging global opportunities to ensure we retain our top talent. We encourage continuous learning and development opportunities to develop personal, professional and technical capabilities, and we reward with a comprehensive employee benefits program. We have a vision of the future, where people simply belong. That's why we support and celebrate inclusive causes, not just on days of recognition throughout the year, but every day. We embrace diversity across race, colour, religion, sex, national origin, sexual orientation, gender identity or persons with disabilities or protected veteran status. We ensure DEI is part of our DNA as a global community - it means we go way beyond than just talking about it - we live it. If you want to live it too, join us. INCO: “Cushman & Wakefield”

Date: 15 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Manufacturing Services Key Result Areas Role-specific Active involvement in all upstream manufacturing activities. Perform error free operation by eliminating operational gaps in advance. Active trouble shooting to minimize the various risks prior to execution and during execution. Initiate and process upstream deviations /investigations and closure. Pre -execution activity: Area and equipment readiness. Issuance of raw material /consumables and issuance batch records. Upstream process execution: Batch process operation /unit operation (including CIP, SIP and preparation upstream accessories), close monitoring of batch performance and data. Follow and practice on-line documentation all the time. Follow cGMP practices during the manufacturing activity and operations associated activities with QA, QC and EAM. Attend the training session of EHS, cGMP and HRD. Ensure process equipment's/instruments are in Qualified in state. Verify PM, check the log books and ensure the clean room requirements in order to get line clearance from QA for batch execution. Active coordination with inter-depts. for sample submission, closure of documentation and timely execution and contribution for the assigned tasks. Perform on-line documentation, cGMP compliance in all the manufacturing activity, and timely closure of executed documents and batch records. Ensure the Quality system is followed in day today upstream operations. Identify the gaps in the system to improve. Active involvement in all upstream manufacturing activities. Perform error free operation by eliminating operational gaps in advance. Active trouble shooting to minimize the various risks prior to execution and during execution. Initiate and process upstream deviations /investigations and closure. Technical /Functional Skill Expertise in Upstream unit operations (CHO based mammalian expression systems). Strong Hands on experience with SUB (Up to 2000 L scale) Exposure to handle of Bio-similar proteins and Mabs projects in cGMP area. Sound knowledge and awareness of GMP controls, Quality systems and regulatory aspects Experience on risk assessment tools and change management. Experience on the Equipment Qualification and commission aspects

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description Key Responsibilities: 24 × 7 audit readiness. Responsible to work in different shifts. Participation in internal, external, regulatory audits. Ensure 100% participation in training’s against CAPA’s. Responsible for initiation and investigation on LIR, OOS, OOT & boarder line results and reporting them to the in-charge. Supporting to share required documents from QC to RA/ other requirement. Determining team priorities in accordance with the plant’s needs, while coordinating with the team leader / Manger. Follow up the housekeeping, cGMP, GLP and Safety Guideline in laboratory. Sampling and analysis of RM / FG / intermediates / cleaning samples based on requirement and result entry in analytical sheet, QA form, LIMS and online documentation as per data integrity norms. Perform analytical test according to the monograph and SOP. Responsible for calibration and verification of instruments. Maintaining of reserved samples room and chambers / autoclaves / incubators. Help to in charge in preparation of documents related to department (like STP’s, SOP’s and etc.) Ensure the sampling of finished products, Raw material, Intermediate and sending sample to outside laboratory for analysis. Must be ensured sampled, approved and rejected labels timely as require. Responsible to maintain the stock record of chemicals and reconciliation of standards. Any other job assigned by the Manger -QC Manger or group leader-QC Qualifications The ideal candidate will have: Education: B.Sc. / M.Sc. in Chemistry. Experience: Minimum 5 years of industrial experience. Preferred Industries: API / Pharma. Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description Key Responsibilities: 24 × 7 audit readiness. Responsible to work in different shifts. Participation in internal, external, regulatory audits. Ensure 100% participation in training’s against CAPA’s. Responsible for initiation and investigation on LIR, OOS, OOT & boarder line results and reporting them to the in-charge. Supporting to share required documents from QC to RA/ other requirement. Determining team priorities in accordance with the plant’s needs, while coordinating with the team leader / Manger. Follow up the housekeeping, cGMP, GLP and Safety Guideline in laboratory. Sampling and analysis of RM / FG / intermediates / cleaning samples based on requirement and result entry in analytical sheet, QA form, LIMS and online documentation as per data integrity norms. Perform analytical test according to the monograph and SOP. Responsible for calibration and verification of instruments. Maintaining of reserved samples room and chambers / autoclaves / incubators. Help to in charge in preparation of documents related to department (like STP’s, SOP’s and etc.) Ensure the sampling of finished products, Raw material, Intermediate and sending sample to outside laboratory for analysis. Must be ensured sampled, approved and rejected labels timely as require. Responsible to maintain the stock record of chemicals and reconciliation of standards. Any other job assigned by the Manger -QC Manger or group leader-QC Qualifications The ideal candidate will have: Education: B.Sc. / M.Sc. in Chemistry. Experience: Minimum 5 years of industrial experience. Preferred Industries: API / Pharma. Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Company Description Founded in 2018 with a passion for organic farming, Rus Organic offers a selection of high-quality organic products. In October, we launched our first product range, a line of organic cold-pressed juices. Proudly based in India, Rus Organic is committed to advancing our reach both domestically and internationally. Join us as we grow and innovate in the organic industry. Role Description This is a full-time on-site role for a Quality Assurance Specialist, located in Bhiwandi. The Quality Assurance Specialist will be responsible for managing and monitoring quality control processes and ensuring compliance with Good Manufacturing Practices (GMP). Daily tasks include conducting quality audits, maintaining quality management systems, and collaborating with production teams to implement quality improvements. 1. FSSC implementation is followed at each floor or each department 2. Plan MRM and internal audits 3. QC testing - improvisation wrt our product category ( currently we are doing mainly pH , brix) 4. FSSAI and legal metrology related tasks (we can take away this from pratiksha and totally give it to a new person) 5. Routinely follow whether conditions of license requirements are fulfilled 6. Initiate activities for food safety culture building 7. Organic certification Qualifications Proficiency in Quality Control, Quality Assurance, and Quality Management practices Experience and knowledge in Good Manufacturing Practice (GMP) Strong skills in Quality Auditing Excellent attention to detail and analytical skills Strong communication and interpersonal skills Ability to work collaboratively in an on-site setting Previous experience in the food and beverage industry is beneficial Bachelor's degree in Quality Management, Food Science, or related field

Job Location: Office location only (Utran, Surat, Gujarat) Job Summary Building test cases for websites and mobile applications. Executing test plans manually and/or building automated testing routines. Create automation scripts. Communicating about bugs via bug tracking systems. Ensuring high-quality standards including functionality and code quality. Finding high-level usability problems in navigation, workflow, and reporting. Responsibilities and Duties Intimate understanding of web applications. Experience in Requirements Analysis. Good Understanding of SDLC Process. Expert at Building Test Cases. Exposure to automation scripts using Selenium webdriver. Good English communication skill to document bugs. Good in Functional Testing. Experience in reporting the bugs using Bugzilla/Jira/Mantis or any other bug tracking tool. Experience in Regression testing. Experience in Coordinating with Test Managers/Team leads/Scrum Master. Required Experience, Skills and Qualifications Software Testing, Software Troubleshooting, QA/QC, Preparing Test Cases, Agile methodology, Selenium, jMeter Benefits Every 1st and 3rd Saturday full day off Flexible timing Freely working environment Paid leaves / Leave encasement Job Type: Full-time Pay: ₹12,000.00 - ₹30,000.00 per month Benefits: Leave encashment Paid time off Application Question(s): Are you from Surat Local Candidate? Education: Bachelor's (Preferred) Language: Gujarati (Required) Location: Utran, Surat, Gujarat (Required) Work Location: In person

Company: Manish Jewellers Pvt. Ltd. Location: Mumbai Industry: Gold Jewellery Manufacturing & Wholesale Employment Type: Full-Time Experience Required: Fresher to 1 year (Jewellery industry experience preferred but not mandatory) Monthly Salary Range: Rs. 15,000 - 18,000 Role Overview We are seeking a smart, dependable, and detail-oriented Inventory Assistant to support our daily inventory operations. This role involves maintaining accurate product data, managing jewellery tags, assisting with packaging and storage, and contributing to creative content generation using AI tools. The ideal candidate is tech-friendly, organized, and eager to learn. Accuracy, discipline, and adaptability are crucial in this high-value industry. Key Responsibilities Product Data & Inventory Management: Enter product details (weight, karat, type) into IMS (Inventory Management System) Generate barcode tags and attach them accurately to products Upload and manage product images and preview links Support stock audits and physical verification Ensure proper bin placement and systematic storage of jewellery Track product movement between departments with proper logging Packaging & Dispatch Support: Assist in safe, clean, and organized packaging for clients or exhibitions Cross-check tagging and quantity before sealing parcels Maintain accurate records of packed and dispatched items Workflow & Communication: Update Trello or internal dashboards with inventory status Immediately flag discrepancies to QC or Production Coordinator Organize jewellery trays and maintain a neat, disciplined stockroom layout Coordinate with team via Slack, WhatsApp, or Email as per task requirement AI-Powered Creative Support: During non-peak hours, use AI tools such as Gemini, ChatGPT, Midjourney , or similar platforms to generate product creatives, visual mockups, and written content Experiment with tools like Sora or Veo 3 to help create product videos, short reels, or jewellery showcase clips Assist in organizing product imagery into moodboards or promotional assets for internal and marketing use Maintain a clean archive of all AI-generated outputs for team reference and feedback First 3 Months Expectations Learn internal IMS and tagging system thoroughly Issue 100% error-free tags and entries Keep trays and bins organized with up-to-date labels Demonstrate punctuality and careful handling of all jewellery items Begin contributing to basic creative tasks using AI tools under guidance Assist seamlessly in daily stockroom and dispatch operations Tools You’ll Use IMS (Internal Inventory Software) — training provided Excel / Google Sheets Barcode printer and tag machine Slack / WhatsApp / Email for internal coordination AI platforms: Gemini, ChatGPT, Midjourney, Sora, Veo 3 (training/guidance provided as needed) Required Skills & Qualifications Minimum 12th pass or graduate in any stream Fresher to 1 year of work experience (jewellery or warehouse experience is a bonus) Basic computer literacy — typing, Excel, printing, internet usage Strong attention to detail and accuracy in repetitive tasks Ability to handle physical inventory with care and discipline Curiosity and willingness to experiment with new tools and technologies Work Environment & Expectations Formal dress code — you’ll work around high-value products Personal phones not allowed during work hours Daily update of stock movement logs required Expected to assist other departments (Dispatch/QC) when needed Cleanliness, organization, and discipline are strictly maintained Creative tasks using AI are expected during downtime Ideal Candidate Traits Eager to learn and grow in a structured, tech-integrated role Disciplined and consistent in repetitive yet sensitive tasks Trustworthy with high-value items and confidential information Comfortable using digital tools for both operational and creative work Respectful of internal structure and escalation protocols What We Offer Structured hands-on experience in inventory and product management Exposure to emerging AI tools in a real business context Training in jewellery-specific product handling, tagging, and creative tools Supportive work culture with potential for role expansion Competitive salary with performance-based appraisals

Who Are We HaystackAnalytics is a HealthTech company creating clinical genomics products, which enable diagnostic labs and hospitals to offer accurate and personalized diagnostics. Supported by India's most respected science agencies (DST, BIRAC, DBT), we created and launched a portfolio of products to offer genomics in infectious diseases. Our genomics based diagnostic solution for Tuberculosis was recognized as one of top innovations supported by BIRAC in the past 10 years, and was launched by the Prime Minister of India in the BIRAC Showcase event in Delhi, 2022. Role Overview The Scientist will play a critical role in the development, implementation, and automation of bioinformatics pipelines for our NGS sequencing services. The ideal candidate will have hands-on experience with various NGS data analysis, familiarity with automation tools, and a strong problem-solving mindset. What We Want You To Do Design, develop, and optimize scalable NGS data analysis pipelines for WGS, WES, RNA-Seq, and metagenomics projects involving human, bacteria, fungi, algae, and other organisms. Conduct high-quality, end-to-end bioinformatics analyses—QC, alignment, variant calling/annotation, transcriptomics, and metagenomic profiling. Integrate automation solutions for routine and customized bioinformatics analyses, improving efficiency, reproducibility, and scalability. Conduct custom NGS data analysis and prepare robust detailed reports Work closely with wet-lab teams, product managers, and clients to refine requirements, troubleshoot issues, and deliver robust analytical reports. Maintain detailed records of workflows, protocols, pipeline releases, and validation procedures. Stay up-to-date with the latest bioinformatic methods, algorithms, and NGS technologies; evaluate and implement new solutions as needed. Address client queries and support custom project requirements. What Are We Looking In You PhD or MSc with +8 years relevant experience in Bioinformatics, Transcriptomics, Genomics, Metagenomics or related disciplines. Experience with building bioinformatics pipelines for various NGS data analysis workflows Assisting in drafting and completing manuscripts for publication Experience with handling various different databases and tools Perform statistical analysis on the datasets Comfortable working on Linux OS system Ability to read, interpret and curate scientific literature Excellent communication skills (oral and written) and attention to detail Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow, instructions, meet deadlines, and comply with company policies Experience of 2-4yrs+ in Python & experience of 3-5 yrs in Bash scripting Experience with pipeline orchestration tools (Nextflow or Snakemake) will be a bonus Skills: bash scripting,bioinformatics,statistical analysis,transcriptomics,python,ngs data analysis,ngs,automation tools,automation,pipeline,genomics,pipeline orchestration tools (nextflow, snakemake),metagenomics

Job Summary: To control the quality of incoming material and final product at the plant Key Responsibilities: Carry out testing of raw materials as per ITP (Internal Testing Plan) Visually inspect and/or test every incoming delivery of course and fine aggregates for its quality before acceptance. Conduct daily testing of concrete specimens. Ensure that all tests are carried out as per procedures given in Business Operating System and in Indian standards. Ensure compliance with all QA/QC protocols as per BOS. Ensure that all test equipments are properly operated and maintained. Ensure safe operation of the laboratory and all related equipment Plant calibration along with other plant team members Timely submission of reports to external and internal customers Ensure the health and safety of oneself, colleagues, vendor partners by complying with the Company policies, procedures, guidelines, rules and regulations of occupational health and safety at work Qualifications & Experience: Education: Civil Diploma/ Graduate Experience: 3 – 5 Years from RMC or Aggregate or Construction industry

At Mace, our purpose is to redefine the boundaries of ambition. We believe in creating places that are responsible, bringing transformative impact to our people, communities and societies across the globe. To learn more about or purpose, culture, and priorities, visit our strategy site. Within our consult business we harness our unique combination of leading-edge practical expertise and project delivery consultancy to unlock the potential in every project. The Project It is a large hospital in Ahmedabad. Our Values Shape The Way We Consult, And Define The People We Want To Join Us On Our Journey, They Are Safety first - Going home safe and well Client focus - Deliver on our promise Integrity - Always do the right thing Create opportunity - for our people to excel. Management of the implementation of a quality management system and its effectiveness in meeting business, statutory, legal, and contractual requirements. Engages with business stakeholders to manage compliance to requirements, supporting a resilient business that manages risks effectively. The role is a key enabler to change and business improvement. You’ll Be Responsible For Delivers delegated elements of an annual business plan to time and budget. Manages and facilitates external certification audits. Provides expertise and guidance in supporting achievement of new certifications where appropriate. Responsible for organising and facilitating internal audits in the audit programme. Accountable for leading audits and producing audit reports. Utilises comprehensive expertise and investigates and interprets root cause analysis of instances of non-conformance, including recommending corrective measures and long-term preventative measures. Coordinates reviewing of management system content for appropriateness, improvement, and implementation. Contributes to the identification of new systems and processes to drive efficiency, recommending improvements and innovations. Ensures information for quality reports is available, accurate and delivered within agreed timescales. Accountable for the production of communication articles, plans and communication collateral. Coordinates activities reported in management reviews, collating, analysing, and presenting data and key metrics, analyses trends and provides recommendations and guidance. Provides recommendations for action to mitigate risk and improve management system effectiveness. Provides specialised expertise and knowledge to support on business development activities. Accountable for the development and delivery of training. Manages and monitors performance of a supply chain, including support to suppliers as appropriate through training, guidance, and audits of their QMS capabilities. Works collaboratively towards the common goal of net zero carbon transition, and share responsibility for the proactive identification and management of the associated carbon emissions and reductions during the delivery of work. You’ll Need To Have Bachelor's degree in civil. Experience of projects of a similar nature. Mace is an inclusive employer and welcomes interest from a diverse range of candidates. Even if you feel you do not fulfil all of the criteria, please apply as you may still be the best candidate for this role or another role within our organization.

Job Summary: We are seeking a dedicated and detail-oriented QC Microbiologist with 2 to 4 years of experience in pharmaceutical/biotech microbiology labs. The ideal candidate will be responsible for performing microbiological testing to ensure compliance with GMP standards and regulatory requirements. Key Responsibilities: Perform routine microbiological testing including: Sterility testing Water and air sampling Environmental monitoring (EM) Bioburden and endotoxin testing Identification of microorganisms Microbial limit tests Maintain microbiological data and logbooks. Participate in media fill validations and aseptic process simulations. Prepare and review SOPs, protocols, and reports related to microbiology activities. Ensure all testing and documentation complies with GMP, USP, EP, and regulatory guidelines. Support microbiological investigations (OOS, deviations, CAPAs). Operate and maintain laboratory instruments such as autoclaves, incubators, particle counters, etc. Coordinate with production, QA, and validation teams for sample planning and testing timelines. Assist in audits and regulatory inspections as needed. Qualifications: · B.Sc. / M.Sc. in Microbiology, Biotechnology, or related life science discipline. · 2 to 4 years of hands-on experience in QC Microbiology within a regulated pharmaceutical or biotech environment. · Knowledge of cGMP, GLP, and regulatory guidelines (FDA, EMA, WHO). · Familiarity with microbiological techniques and cleanroom classifications. · Good documentation practices and understanding of data integrity principles. · Proficiency in MS Office and LIMS (Laboratory Information Management System) is a plus. Job Type: Full-time Pay: ₹300,000.00 - ₹800,000.00 per year Benefits: Provident Fund Ability to commute/relocate: Pondicherry, Puducherry: Reliably commute or planning to relocate before starting work (Required) Experience: APIs: 5 years (Required) Work Location: In person

Stantec is a global leader in sustainable engineering, architecture, and environmental consulting. The diverse perspectives of our partners and interested parties drive us to think beyond what’s previously been done on critical issues like climate change, digital transformation, and future-proofing our cities and infrastructure. We innovate at the intersection of community, creativity, and client relationships to advance communities everywhere, so that together we can redefine what’s possible. The Stantec community unites approximately 32,000 employees working in over 450 locations across 6 continents. About The Role Our Environmental Engineering team provides vital support to projects across varied projects including environmental compliance, environmental due diligence, environmental assessment, Environmental data management, Air and odour quality modelling, remediation, ecology, waste management, climate and sustainability. With this in mind, we are looking for Associate Principal Environmental Engineer, A leader and Subject Matter Expert to join our team to work on a variety of projects and grow capabilities of Environmental Engineering team. The opportunity You'll join a global team of Environmental professionals where you will have the opportunity to contribute to the continued growth of the team and connect with the large global community. You’ll be involved in a range of engineering projects throughout Australia, New Zealand, UK, North America and Middle East. Your own career will benefit greatly, you will be working alongside some of the smartest engineers in the industry ensuring your design and delivery capability is excelled. In This Role You Will Be Empowered To Lead a team of environmental professionals to provide support to Stantec’s global operations. Plan, coordinate, and manage a diverse range of projects. Manage project scope, schedule, budget, and coordination of regional and Pune project teams. Prepare technical correspondence, technical reports, work plans, investigations, grant applications, and project specifications including cost estimates and budgets. Participate in proposal development, technical conference presentations, and support with general marketing and business development activities. Coordinate multiple projects and interface with regional Stantec offices. Manage data, QA/QC, interpretation, evaluation/comparison to applicable regulatory standards. Provide management, guidance, training, and oversight of staff. Be an engaged leader, working alongside other teams, actively coaching, and supporting the career development of staff. Plan and take responsibility for employee recruitment, engagement, and retention. Your Capabilities And Credentials Strong technical skills and experience in various Environmental fields. Demonstrated ability to handle multiple priorities and assignments. Must be able to successfully work both collaboratively and independently. Strong technical writing and verbal communication skills in English with excellent interpersonal skills, including an aptitude for value-based leadership and people management. Ability to effectively communicate with other technical professionals, clients, and regulatory stakeholders. Ability to effectively discuss and make presentations related to project plans, milestone updates, and technical issues with stakeholders. Strong leadership of multidisciplinary teams on complex, time sensitive projects of varying sizes with a demonstrated ability to handle multiple assignments and priorities concurrently. Education And Experience Master’s degree qualified, Environmental Engineering or Environmental Science, with 12-15 years relevant experience Competent technically in all relevant fields of Environment. Ability to interface with clients, respond quickly, and deliver projects with a supporting engineering team. Primary Location: India | Pune Organization: Stantec IN Business Unit Employee Status: Regular Travel: No Schedule: Full time Job Posting: 02/05/2025 08:05:58 Req ID: 1000901

Stantec is a global leader in sustainable engineering, architecture, and environmental consulting. The diverse perspectives of our partners and interested parties drive us to think beyond what’s previously been done on critical issues like climate change, digital transformation, and future-proofing our cities and infrastructure. We innovate at the intersection of community, creativity, and client relationships to advance communities everywhere, so that together we can redefine what’s possible. The Stantec community unites approximately 32,000 employees working in over 450 locations across 6 continents. Primary Purpose Of Job As a Senior Medical Planner, you will play a key leadership, oversight and content expertise for strategic, master facility, functional space planning and medical planning on health sector projects collaborating with regional teams for delivering high-quality projects in the buildings business line. You will be involved in the development of integrated design proposals, while leading and mentoring others and collaborating with team members to contribute to the final deliverables in collaboration with the Project Leader. The ideal candidate will possess advanced technical expertise, while leading and mentoring others and collaborating with team members to contribute to the final deliverables—bringing inspiration to your daily practice. Key Accountabilities To be a medical planner for the design of major healthcare projects , ranging on average from 80,000 sqft to 800,000 sqft in typical project size Be responsible for the clinical planning of the full range of care services from preventative, outpatient, acute or post-acute healthcare facilities, through various stages of design, following “best practices” and applying Evidence Based Design Lead the architectural design and delivery of Stantec projects across in healthcare sector. Provide strategic direction and technical guidance for all architectural design aspects, ensuring alignment with project goals, timelines, and client requirements. Be responsible for facilitating QA/QC oversight of strategic, facility master planning and medical planning aspects of project design Take ownership of the development of conceptual, detailed, and construction drawings using Revit, AutoCAD, and other relevant tools. Mentor junior architects and collaborate with multi-disciplinary teams to ensure effective project integration and execution. Contribute to the strategic growth of the architectural team, sharing knowledge, and promoting best practices within the discipline. Ensure all architectural work adheres to Stantec’s Core Values, Quality Systems, and Project Quality Procedures. Collaborate closely with the Global Health Sector and Business Center leadership to ensure successful project and business outcomes. Foster a collaborative environment with internal teams and external stakeholders, including clients and consultants. Serve as a local leader to inspire our team, represent healthcare design, and reinforce the global brand of Stantec Help build and maintain the design culture of the studio Person Specifications Degree qualified (or equivalent) in Architecture with a Master’s or equivalent professional qualification preferred. A minimum of 8–10 years of professional experience , with a proven track record in leading in healthcare planning, design, and project management experience. Proficiency in advanced architectural software packages, including Revit Architecture, AutoCAD, MS Office, Sketchup and dRofus. Experience with Bentley Microstation and Photoshop is advantageous. In-depth knowledge of healthcare design principles, and technical detailing, with a focus on delivering projects to international standards. Significant experience in leading project teams, with a strong ability to mentor and guide junior architects and technicians. Excellent communication skills (both written and verbal) with the ability to effectively interact with clients, consultants, and multidisciplinary teams. Expertise in project management and client relationships, with the ability to manage multiple projects simultaneously while meeting deadlines and maintaining quality. Strong leadership, organizational, and problem-solving skills, with the ability to drive projects from conception through to completion. Experience in the North America, UK and Middle east market and a strong understanding of regional design codes, building regulations, and construction practices is highly desirable. Creative and innovative approach to design, with an emphasis on practical, functional, and sustainable solutions. Self-motivated, adaptable, and enthusiastic, with a passion for continuous professional development and growth. Primary Location: India | Pune Organization: Stantec IN Business Unit Employee Status: Regular Travel: No Schedule: Full time Job Posting: 22/04/2025 03:04:13 Req ID: 1000885

HR Contact Number - 84258 42750 Datacenter experience preferred Roles and Responsibilities: · Prepartion PO Material ordering against BOQ & also as per the site requirements · Coordination with procurement team to ensure timely delivery of materials on site · Regularly attending to site meetings with architect, consultants, PMC and client · Monitoring the onsite project work along with architect, consultants, PMC and client · Submission of Daily and weekly progress reports to PMC and architect · Prepartion of Project billing and invoice submission · Ensure Testing commissioning as per site requirements · Coordinated daily activities with the PM, sub-contractors to ensure the safe/efficient handover of electrical systems · Keeps equipment operational by following manufacturer’s instructions and established procedures; requesting repair service · To keep a check that the contracts are kept current and being updated with change orders if any on a regular basis · Preperation of Final bills, handing over documentation and as built drawing closure · Coordinating with sub-contractor with help of PM and Engineer to accomplish desired project goal within schedule. · Ensures that Company policies and project procedures are being adhered to · Ensure implementation and monitoring of the Company’s Safety and Environment Policies and QC Plans · Contributes to team effort by accomplishing related results as needed · Directs and maintains discipline and morale of the project staff along with PM. · All jobs as assigned by the VP- Projects/PM/MD Qualification & Preferred Skills · BE/Diploma (Electrical) experience in handling electrical projects · Excellent communication skill · Teamwork & Leadership skills preferred · IT Skills – MS Excel, Word, Powerpoint. · Familiarity with Google Workspace is preferred. · Excellent in organising &documentation skills · Ability to work in a team and remain professional all times Employment Type: Full Time, Permanent Job Types: Full-time, Permanent Pay: Up to ₹45,000.00 per month Ability to commute/relocate: Jamnagar, Gujarat: Reliably commute or planning to relocate before starting work (Required) Application Question(s): What is your current salary? Experience: Electrical: 1 year (Required) Work Location: In person

Domain SME / BA for Manufacturing for LS:Job Summary: Senior Business Analyst with strong domain expertise in Life Sciences manufacturing. This hybridrole blends the analytical rigor of a BA with the strategic insight of a Subject Matter Expert (SME). You will collaborate with clients to analyze businessneeds, define compliant and scalable technology solutions, and bring industry best practices to digital transformation initiatives.KeyResponsibilities:Business Analysis & Solution Design:Elicit, analyze, and document business and functional requirements from Life Sciences manufacturingstakeholders.Translate client needs into actionable user stories, use cases, and process flows for development and solutioning teams.Collaborate witharchitects and delivery teams to design solutions aligned with manufacturing operations and regulatory standards.Domain Advisory:Act as a trustedadvisor to clients by providing insights into industry best practices across GMP, batch processing, MES, QA/QC, and shop floor integration.Guide clients inaligning technology solutions with compliance requirements (e.g., 21 CFR Part 11, GAMP 5, GMP).Contribute to validation strategies and regulatoryreadiness for digital systems.Client Engagement & Pre-Sales Support:Participate in discovery workshops, assessments, and solution ideation sessions withprospective clients.Support proposal development with domain input, business case justifications, and solution outlines.Help craft roadmaps for digitaltransformation initiatives, particularly around MES, ERP, LIMS, or other manufacturing IT systems.Thought Leadership & Enablement:Stay up-to-date withLife Sciences manufacturing trends and bring forward innovative ideas (e.g., digital twins, real-time release, AI in QA).Contribute to internal knowledgerepositories and mentor junior BAs or team members on domain topics.Required Qualifications:Bachelor degree in Life Sciences, Engineering, or a relatedfield.8+ years of experience as a Business Analyst, with 3+ years in the Life Sciences manufacturing domain.Deep understanding of manufacturingoperations, systems (MES, ERP, LIMS), and regulatory frameworks.Strong communication and collaboration skills and the ability to work with bothbusiness and technical stakeholders.Proficiency in tools such as Visio, JIRA, Confluence, and data visualization/reporting platforms

Job Summary: To control the quality of incoming material and final product at the plant Key Responsibilities: Carry out testing of raw materials as per ITP (Internal Testing Plan) Visually inspect and/or test every incoming delivery of course and fine aggregates for its quality before acceptance. Conduct daily testing of concrete specimens. Ensure that all tests are carried out as per procedures given in Business Operating System and in Indian standards. Ensure compliance with all QA/QC protocols as per BOS. Ensure that all test equipments are properly operated and maintained. Ensure safe operation of the laboratory and all related equipment Plant calibration along with other plant team members Timely submission of reports to external and internal customers Ensure the health and safety of oneself, colleagues, vendor partners by complying with the Company policies, procedures, guidelines, rules and regulations of occupational health and safety at work Qualifications & Experience: Education: Civil Diploma/ Graduate Experience: 3 – 5 Years from RMC or Aggregate or Construction industry

Job Summary: To control the quality of incoming material and final product at the plant Key Responsibilities: Carry out testing of raw materials as per ITP (Internal Testing Plan) Visually inspect and/or test every incoming delivery of course and fine aggregates for its quality before acceptance. Conduct daily testing of concrete specimens. Ensure that all tests are carried out as per procedures given in Business Operating System and in Indian standards. Ensure compliance with all QA/QC protocols as per BOS. Ensure that all test equipments are properly operated and maintained. Ensure safe operation of the laboratory and all related equipment Plant calibration along with other plant team members Timely submission of reports to external and internal customers Ensure the health and safety of oneself, colleagues, vendor partners by complying with the Company policies, procedures, guidelines, rules and regulations of occupational health and safety at work Qualifications & Experience: Education: Civil Diploma/ Graduate Experience: 3 – 5 Years from RMC or Aggregate or Construction industry

We’re Hiring : QA QC Engineer /Jr. Engineer (for Spool) Department . Company: Gujarat Infrapipes Pvt Ltd Location: Vadodara (Por - Karjan highway), Gujarat Perk’s and benefits - Free Bus transportation facilities + Personal Medical insurance No. of vacancy - 10 + Vacancies Required Core skills : Stage wise QA QC Spool work Awareness of fabricated related work. Handling Q.A/Q.C. Procedures & various third Party inspection Well versed in ASME & other related manufacturing codes/standards He should have good knowledge of Non destructive (Ultrasonic testing, radiography examination, magnetic particle testing, die penetration testing, etc) & destructive examinations. Preparing of QAP in line with code/client specification Documentation as per ISO & ASME. Handling the inspection for raw material and finished products as per customer requirements. Years of experience : 1-5 years Salary : Best in industry For quick Apply! Send your resume to giplhr@gujaratinfra.com Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹34,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com . Job Summary Responsible for execution of Quality Systems to ensure that Apotex meets its regulatory and GMP compliance obligations for Third Party manufactured products and products supplied by Apotex under contract to Third Party Organizations. This includes Quality Systems to support New Product Launch and Submission batches. Interact with internal groups involved in Third Party Operations (e.g. RA, Supply Chain, Projects and other Quality groups as needed). Job Responsibilities Conduct the timely quality review of 3rd party full executed batch documents pertaining to Annual/New Product launch/Submission batches (where Apotex is the Marketing Authorization Holder) for accuracy and compliance to procedure to ensure that documents are in full compliance with cGMP, and regulatory standards. Escalate to QA Release team any non-conformance reports (related deviations, OOS/OOT) associated with Annual/New Product Launch / Submission batches to ensure that incidents were satisfactorily investigated and to confirm that the batch to be released has not been adversely impacted and to escalate issues timely wherever appropriate. Review vendor Certificate of Manufacture and Certification of Analysis as part of full review of execute batch record for Launch batches to confirm that product has been manufactured, packaged/labelled, tested and stored in accordance with vendor master production documents Responsible to Coordinate / Follow up with third party manufacturing sites for responses to any non-conformance identified during batch review. Responsible for timely compilation of batch release documents under guidance of Global External Manufacturing Quality. Responsible for timely updation of batch release tracker associated with batch release activity. Coordinate with third party manufacturing sites and internal stakeholders for obtaining required documents for release of batches in US and Canada market. Escalate to QA Release team any critical non-conformances that may impact compliance of the batch. Support in the development of SOPs to ensure efficient and compliant External Quality functions. Coordinates a centralized documentation control system for External Quality. Coordinates the routing for review, issuance and archiving of External Quality controlled documents. Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned. Job Requirements Education Bachelor’s Degree in Science or a College Diploma in Pharmaceutical Technology, or a related field. Knowledge, Skills and Abilities Strong knowledge of Global cGMPs (HC, FDA and EU) and the QA/QC systems associated with the manufacture of human drug products. Detail-oriented, accurate and reliable. Ability to manage multiple priorities in a fast-paced environment. Superior organizational skills, analytical thinking and inter-personal communication skills. Ability to work independently or as part of a team. Ability to build strong working relationships with Third Party partners. Demonstrates personal leadership and accountability. Experience At least 6-7 years of progressive Quality experience in QA or QA/QC roles. Experience with Microsoft Computer Products (Word, Excel, Access, PowerPoint). Experience with SAP and TrackWise is an asset. At Apotex, we are committed to fostering a welcoming andaccessible work environment, where all everyone feels valued, respected, and supported to succeed. We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.