Role & responsibilities Prepare Pre shipment Documents. Prepare Bank documents. Prepare Packaging labels. Audit Check list for Custom clearance purpose. Audit BL draft for Shipping line. Prepare Master report for shipment. Supervision of container stuffing in warehouse. Prepare Post shipment Documents Mailing and drafting Prepare way bill in portal. Prepare COO in DGI-Tonal Tracking shipments

Role & responsibilities Conduct in-process checks during various stages of sterile injectable manufacturing, including dispensing, compounding, filtration, filling, and sealing. Perform line clearance and area clearance before the start of manufacturing and packaging operations. Monitor aseptic practices and personnel hygiene compliance inside cleanrooms and controlled areas. Verify critical process parameters and environmental conditions during batch processing. Ensure compliance with SOPs, batch manufacturing records (BMR), and batch packaging records (BPR). Participate in visual inspection activities and oversee container-closure integrity checks. Monitor the usage and replacement of sterilized garments, materials, and equipment in aseptic areas. Raise deviations, non-conformances, and change controls as needed. Assist in investigations for OOS, OOT, or any batch-related quality issues. Provide training to operators and workers on GMP, GDP, and aseptic technique

WALK-IN INTERVIEW ALERT JD Join the growth journey with Opes Healthcare Location: 3rd Floor,Tulsi Plaza, Changodar, Ahmedabad. Date: 25th May 2025 (Sunday) Time: 09:00 AM to 02:00 PM Multiple Job Openings at Opes Healthcare-Ahmedabad. Were hiring passionate and dynamic individuals across multiple departments! Open Positions: 1. IPQA :Monitor all process check/Line Clearance/cGMP/Documentation Officer to Sr. Executive. B.Pharm/ M.Pharm | 02–07 yrs 2. Quality Control: RM Testing/HPLC/GLP/Documentation – Officer to Sr. Executive. B.sc/M.sc/B.Pharm/ M.Pharm | 02–07 yrs 3. F&D: Design & Develop formulation/Process Optimization/cGMP/Documentation/ – Officer to Sr. Executive. B.Pharm/ M.Pharm | 02–07 yrs 4. ADL: Stability Studies/HPLC/GLP/Documentation/Method Development – Officer to Sr. Executive. B.Sc/M.Sc/B.Pharm/M.pharm | 02–07 yrs 5. Production(Third party operation): Audit to Other company/Production planning/Material control/QMS-Officer to Sr. Executive. B.Pharm/M.pharm | 02–07 yrs 6. Purchase: Vendor management/ RM,PM,CAPEX,/Documentation/Market Analysis – Manager Any Graduate | 08–15 yrs 7. PDC(Packaging Development Cell): Review & Approved Artwork/Product packaging/cGMP/DGFT Guideline/Change control/Vendor Communication/Master Packaging card Preparation- Officer to Sr. Executive. B.sc/M.sc/D. Pharm/B.Pharm/Diploma in Packaging Technology| 03–07 yrs 8. Logistic: Pre & Post Documentation | Preparing Export Invoice | Tracking Shipment | Coordination with CHA - Officer to Sr. Executive Any Graduate| 01–05 yrs 9.PPMC: Production Scheduling | Material Requirement Planning | Inventory Management | Demand Forecasting - Officer Any Graduate| 01–02 yrs Contact Us: +91 8511849377 | +91 7486829377 career@opeshealthcare.com Let your career thrive with Opes Healthcare Employee Benefits: Employee Health Insurance| Employee Accidental Insurance|2nd & 4th Saturday Off| Attractive HR Policies| AC- Transportation Facility. Be a part of something impactful. See you at the interview!

Role & responsibilities Lead Pre Formulation studies for solid orals, oral liquids, external preparations, injectable products, and nutraceuticals. Design project strategies through comprehensive literature surveys. Conduct API and excipient characterization, drug and excipient ratio studies, and explore various manufacturing strategies. Develop and finalize QQ formulas in alignment with the requirements of the Business Development (BD) team. Coordinate with BD team to ensure timely project execution. Finalize specifications for finished products. Evaluate product stability during manufacturing, monitor stabilized batches, and prepare related reports. Enhance existing formulations and explore new dosage forms possibilities. Procure innovator products, conduct comparative characterization studies, and test products. Prepare product development reports (PDRs), identify critical material attributes (CMAs), critical process parameters (CPPs), and critical quality attributes (CQAs) for robust product development using Quality by Design (QbD) principles. Execute development studies and prepare comprehensive study reports. Optimize formulations and processes using QbD methodologies. Respond to queries related to commercial and under development products promptly. Ensure effective technology transfer of F&D products. Review and authorize documents related to stability, inuse stability, forced degradation, and Bioequivalence (BABE) protocols. Authorize formulation related activities for BABE projects and lead BABE projects as required. Perform any other tasks assigned by the Head of Department (HOD) or management. Preferred candidate profile Pharma industries only Formulation THANKS YOU REGARDS MILAP RATHOD (74868 29377) whtup HR DEPARTMENT OPES HEALTHCARE PRIVATE LIMITED

Role & responsibilities Lead, mentor, and manage the Pharmacovigilance QA team to ensure effective execution of QA activities. Develop, implement, and maintain QA processes, procedures, and tools aligned with regulatory guidelines (e.g., ICH, FDA, EMA). Monitor and ensure compliance of pharmacovigilance activities with applicable regulations and internal SOPs. Conduct risk assessments and develop mitigation plans to ensure PV compliance . Oversee the management and closure of CAPAs (Corrective and Preventive Actions) following audits or inspections. Plan, coordinate, and conduct internal and external audits of PV processes, systems, and vendors audits ( Risk Based Audit approach ). Lead audit preparedness activities and ensure timely resolution of audit findings. Collaborate with cross-functional teams to implement audit recommendations and continuous improvements. Maintain audit documentation and track audit metrics for management review. Ensure all QA activities support compliance with global pharmacovigilance regulations, including GVP (Good Pharmacovigilance Practices). Participate in regulatory inspections and provide QA support as needed. Review and approve quality documentation related to PV activities such as SOPs, training materials, and audit reports. Identify QA training needs for the PV team and develop training programs accordingly. Conduct and coordinate training sessions on quality standards, SOPs, and compliance requirements. Promote a quality culture and awareness within the PV department. Identify gaps and areas for improvement within PV and QA processes and implement best practices. Collaborate with PV operations and other departments to optimize workflows and enhance quality outcomes. Utilize metrics and KPIs to monitor quality performance and drive continuous improvement. Act as the key liaison between PV, QA, regulatory affairs, and other stakeholders. Provide guidance and support on quality-related matters to internal teams and external vendors. Facilitate effective communication to ensure alignment on quality expectations and deliverables. Plan, assign, and review work for QA team members and provide ongoing feedback and development opportunities. Facilitate team meetings and promote continuous communication and knowledge sharing within the team. Support recruitment, onboarding, and performance management of QA staff. Preferred candidate profile Bachelors degree in Pharmacy, Life Sciences, or related field (Master’s preferred). Extensive experience (typically 7+ years) in Pharmacovigilance with significant exposure to QA activities. Strong knowledge of global pharmacovigilance regulations, GVP, and quality management systems. Proven leadership and team management skills. Experience in conducting audits and managing CAPAs . Excellent communication, organizational, and problem-solving skills. Ability to work collaboratively with cross-functional teams and external vendors.

Role & responsibilities Preparation, Review and Execution of Process Validation Protocols and summary reports based on the Analytical results and Batch documents data.

Roles and Responsibilities Manage a team of ABMs (Area Business Managers) to achieve sales targets and expand market presence in assigned areas.

Role & responsibilities Collaborate on formulating and analyzing research strategies tailored to market and customer demands. Oversee commercial activities, securing approvals from manufacturers and our supply team. Assist in selecting manufacturers based on available equipment and machinery for specific products. Finalize quality and quantity formulas and product specifications, submitting them to manufacturers. Coordinate the preparation and arrangement of registration samples and artwork. Liaise with manufacturers to ensure commercial production aligns with our quality and quantity standards and product specifications. Collect and review documents from manufacturers. Coordinate with external laboratories for sample and product analysis according to our standards. Finalize active pharmaceutical ingredient (API) selection based on approved specifications submitted to relevant health authorities. Review and submit Product Information Files (PIFs) to manufacturers. Submit final quality and quantity standards and product specifications for new product launches. Coordinate with external F&D support teams. Review analytical data received and support regulatory affairs (RA) team with query responses. Arrange API and working substance samples, as well as analytical data like HPLC and certificates of analysis (COAs) for the F&D team. Review all documents from external sources and provide them to the RA team. Assist the supply team in sourcing API and primary material specifications. Review manufacturers' and Opes Healthcare's certificates of analysis for finished products. Provide troubleshooting support during new and existing product launches. Plan and execute plant visits during commercial production activities. Update management on critical changes, incidents, and market complaints. Review and approve all GMP documents including SOPs, change controls, deviations, batch manufacturing and packing records, process study protocols/reports, qualification documents, specifications, and standard testing procedures (STPs). Approve apex documents such as the Quality Manual, Validation Master Plan (VMP), and Site Master File (SMF). Design, review, and approve the Quality Management System (QMS) and associated documents. Drive initiatives for continuous improvement and operational excellence. Collaborate with other departments to ensure effective implementation of the designed quality management system. Manage activities related to registration batch manufacturing. Preferred candidate profile pharma THANKS YOU REGARDS MILAP RATHOD (7486829377) HR DEPARTMENT OPES HEALTHCARE PRIVATE LIMITED

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

Role & responsibilities We have an urgent requirement for an Area Business Manager for our Injectable Division . The ideal candidate will be a business generator capable of establishing strong partnerships with healthcare professionals, executing various pharmaceutical marketing activities, and working cross-functionally to provide solutions in a highly ethical and compliant manner. This is an individual contributor profile . Team handling is not a responsibility for this position. Roles and Responsibilities: Lead Generation and Account Management: Generate leads and convert them into business through effective account management, specifically focusing on hospital business . Develop and manage strong relationships with corporate hospitals and healthcare professionals in your assigned territory. Sales Effectiveness: Ensure consistent sales performance by meeting call averages, coverage, and daily activity reporting. Continuously achieve monthly and annual sales targets. Marketing & Brand Building - monthly basis: Execute marketing strategies like Promotion Campaigns , Continuing Medical Education (CME) , and Patient Experience Programs to enhance brand image and recall. Conduct market research to assess the feasibility of new products and services, as well as gather feedback on existing and newly launched services. Competitive Analysis: Monitor competitor activities in the assigned territory, providing timely and insightful reports to management. Identify trends and market opportunities to adapt strategies and stay ahead of the competition. Strategic Planning monthly basis: Create a strategic roadmap for every key account, ensuring alignment with business objectives and market demands. Coordinate with the HO team to ensure customer feedback and complaints are addressed through proper channels. Reporting and Planning: Daily reporting of field visits, activity details, and planning work schedules. Regularly attend company meetings, presentations, and briefings to stay informed on company goals and updates. Desired Candidate Profile: Educational Qualifications: Graduate: Any Graduate (preferably from a Pharma or Life Sciences background). Experience: Proven experience in Key Account Management for Hospital Business . Experience in selling Injectable therapies , antibiotics, vitamins , or other critical care products. Key Skills: Territory Knowledge : In-depth understanding of the assigned territory and market dynamics. Relationship Management : Strong rapport with doctors, paramedics, and other healthcare professionals. Data Analysis : Ability to analyse sales data and generate insights. Product Knowledge : Ability to effectively discuss the technical USPs of the companys products with healthcare professionals. Other Skills: Good communication skills and the ability to present complex information in a clear, professional manner. Strong organizational skills with the ability to manage time and prioritize effectively. Self-motivated and results-oriented with a proven track record of achieving sales targets. Job location: Ahmedabad & nearby periphery Preferred candidate profile pharma THANKS YOU REGARDS MILAP RATHOD (7486829377) call any time HR DEPARTMENT OPES HEALTHCARE PRIVATE LIMITED

Role & responsibilities Responsible for Pre-formulation studies for lab formulation development trials of solid orals, Oral Liquid, injectable, products, and Nutraceuticals product. To design strategy for projects through literature surveys. Respective API characterization, excipients characterization, drug and excipient study and its ratio. Worked on different manufacturing strategies for the development of products. To evaluate product for stability in manufacturing, monitor and review the stabilized batches. To study on existing formulations. Responsible for co-ordination, execution and monitoring of scale up activity, Responsible for Trial batches, Scale up batches, Optimization batches, Exhibit batches. Co- ordination with all cross-functional teams. TT sites and LL Sites To design/assist/support/ review for documents such as SOP, LNB, QQ, Risk assessment, PDR, MFR, Scale up BMR, stability protocol, qualification, validation documents, change controls, deviations, investigations and CAPAs etc. Preferred candidate profile pharma THANKS YOU REGARDS MILAP RATHOD (7486829377) any time call me or whtup HR DEPARTMENT OPES HEALTHCARE PRIVATE LIMITED