611 Sops Jobs - Page 9

1. Assist in machine operation, assembly line tasks, or quality inspection. 2. Read and follow technical drawings, SOPs, and work instructions. 3. Conduct routine maintenance checks under supervisor guidance. 4. Record production data and ensure adherence to quality standards.

You will be responsible for downstream operations related to recombinant proteins at PU 3 for Sanzyme Biologics, Karakapatla unit. This includes handling tasks such as TFF for micro and ultra filtration systems, continuous centrifuge operation, chromatography systems management with audit trailing, column packing and unpacking for high-scale BPG columns, buffer preparations, sterilization of process materials, and working in shifts as required. In addition, you should be well-versed in clean room procedures, integrity testing, documentation practices, SOPs, and hierarchy within the organization. A suitable candidate for this position should hold a B.Tech or M. Sc in Biotechnology, Biochemist...

As a Manager Financial Compliance for a global building material manufacturer, your primary responsibility will be to lead financial compliance efforts to ensure statutory, tax, and legal adherence. This includes finalizing financial statements, overseeing audits, driving internal control improvements, managing risks, and providing strategic financial support to various teams within the organization. You will also be involved in tax audits, compliance training, and adhering to budget constraints. Your day-to-day tasks will involve preparing financial statements and schedules in compliance with Ind AS and the Companies Act, ensuring accurate book closure and account scrutiny with both locatio...

As a Quality Control Microbiologist and Analyst at Nat Habit, you will play a crucial role in ensuring the quality and authenticity of our 100% natural beauty and wellness products inspired by ancient ayurvedic solutions. You will be part of a team dedicated to bringing natural living habits to our customers by providing freshly made products free from chemicals and preservatives. Your responsibilities will include following approved SOPs and finished product specifications for analysis, conducting tests on raw materials, intermediary materials, and finished goods, as well as reporting on your findings. You will be involved in standard and special tests such as MLT, GPT, environment monitori...

You are invited to apply for the position of Quality Assurance Officer in the Pharma industry. This role specifically targets male candidates with a Pharma background. The Quality Assurance Officer will be based in Indore (Rajendra Nagar) and will be responsible for ensuring quality standards in compliance with regulatory requirements. Candidates with a qualification of B.com/B.pharma/B.tech and a minimum experience of 5 to 8 years in QA Pharma are preferred for this role. As a Quality Assurance Officer, your responsibilities will include maintaining quality training programs in adherence to FDA and other regulatory guidelines. This involves keeping training records up-to-date and revising p...

As an Engineer A&C Master Software at our company serving pharmaceutical and nutraceutical companies worldwide, you will be responsible for the control architecture design and PLC/HMI/SCADA software programming as per requirements. Your main duty will be developing the Master Application Program in PLC for products utilizing IEC61131 compliant programming language. It is essential to ensure thorough testing and a first-time-right approach before releasing the software program to the operation and manufacturing teams. You will be accountable for the design, creation, and testing of PLC Level 1 module software code to release Product code PLC Level 1 modules. Additionally, your role will invol...

As the Administration Head at the API manufacturing plant in the Pharmaceutical Manufacturing industry, you will play a crucial role in overseeing all administrative functions. Your responsibilities will include ensuring compliance with industry regulations, maintaining facility standards, managing staff welfare, and ensuring efficient operations across departments. You will be responsible for regulatory and statutory compliance, ensuring that the plant adheres to all relevant local and national pharmaceutical regulations. This includes maintaining alignment with Good Manufacturing Practices (GMP) and liaising with regulatory authorities like CDSCO, FDA, and others for inspections, certifica...

As a Senior Operations Analyst within our innovative organization specializing in affordable healthcare services, you will play a pivotal role in ensuring the continued delivery of exceptional healthcare services to our clients and consumers. Your expertise will contribute to the efficiency and effectiveness of our operational processes, ultimately improving the healthcare marketplace and consumer services we offer. Your primary responsibilities will revolve around production operations, including scheduling coordination, monitoring, and maintaining variance operational processes. This will involve tasks such as data management, operations workload management, and ongoing quality and perform...

You will be joining B S R & Co. LLP, a member of the B S R & Affiliates network of firms registered with the Institute of Chartered Accountants of India. With a presence in 14 cities in India, the firm boasts over 120 partners and employs more than 5,000 professionals. Specializing in audit, other assurance, and taxation services, B S R & Co LLP serves a diverse client base that includes Indian businesses, multinationals, and listed companies across various industry sectors. Our commitment is to consistently enhance audit quality, provide a rewarding experience for our employees, and embrace advanced technology. Your responsibilities will include conducting controls assessment in both manual...

We are searching for a Warehouse Supervisor to oversee warehouse operations, inventory management, audits, and team handling at our Bengaluru location. As a Warehouse Supervisor, you will play a key role in ensuring efficient warehouse workflows, accurate stock management, and a smooth supply chain process while upholding compliance with company policies. Your responsibilities will include overseeing day-to-day warehouse activities such as receiving, storing, and dispatching goods, as well as ensuring smooth inbound and outbound processes with proper documentation and tracking. It will be essential to maintain optimum warehouse space utilization for efficient operations. You will need to con...

As a Quality Assurance Specialist, you will be responsible for reviewing paper and electronic batch records to ensure completeness, clarity, and compliance with Good Manufacturing Practices (GMP). Your role will involve assessing the documentation related to raw materials and releasing them for production. You will provide quality support by contributing to the development of Corrective and Preventative Actions (CAPAs) and offering guidance to various departments on GMP aspects. Additionally, you will review and approve quality assurance controlled documents such as Standard Operating Procedures (SOPs), batch records, and work instructions. In this position, you will be tasked with evaluatin...

You will be responsible for documentation and execution of qualification activities. This includes preparation, review, and execution of URS (User Requirement Specification), DQ (Design Qualification), FDS (Functional Design Specification), UTM (User Traceability Matrix), IQ (Installation Qualification), OQ (Operational Qualification), PQ (Performance Qualification), RQ (Requirement Qualification) documents. Your responsibilities include the review of miscellaneous qualification documents and preparation and review of risk assessments for equipment and systems. You will be responsible for new project-related FAT (Factory Acceptance Test) and SAT (Site Acceptance Test). You will review and co...

At Allucent, you will play a crucial role in helping small-medium biopharmaceutical companies navigate the world of clinical trials to deliver life-changing therapies to patients worldwide. As a Sr. Clinical Research Associate Contractor (Sr.CRA) on our remote A-team, you will have the opportunity to independently manage and monitor investigational sites, ensuring adherence to trial protocols, SOPs, regulations, and Good Clinical Practice standards. Your responsibilities will include maintaining the highest quality standards for trial monitoring activities, overseeing site activities to ensure protocol compliance, preparing detailed reports, updating CTMS systems, and providing support to th...

The Business Transformation Lead position at 91Blackboard in Ahmedabad is a unique opportunity for individuals passionate about enabling Indian MSMEs to succeed with clarity, strategy, and impact. As a boutique consulting and coaching firm, we focus on blending structured problem-solving with human-centric leadership development through our 4D methodology (Determine, Diagnose, Develop, Deliver). We are seeking individuals who enjoy working directly with business owners, simplifying complexities, and creating practical solutions that make a real impact. In this hands-on role, you will collaborate closely with founders and business leaders to identify operational bottlenecks, drive business im...

We are looking for a meticulous Junior Engineer to contribute to the efficient maintenance and operation of our API manufacturing facility at Synnat Pharma. As a Junior Engineer, you will be integral to ensuring the reliability of our mechanical and electrical systems, contributing to our commitment to quality and compliance. This role involves a blend of hands-on equipment maintenance, detailed record-keeping, and active participation in equipment validation and qualification processes. You will collaborate closely with senior technicians and engineers, assisting in breakdown maintenance, equipment installation, and process improvement projects. Your dedication to following safety procedure...

The Assistant Manager position in the Quality Assurance department at ZLL-SEZ Oncology Injectable (Alidac) requires an experienced individual to fulfill the critical role. As an Assistant Manager, you will report to the Associate Manager and be responsible for various tasks including preparing and reviewing validation/qualification protocols, reports, certificates, and thermal studies protocols and reports. You will also be required to develop validation schedules, plans, and ensure the timely execution of all validation/qualification activities. In addition, providing training on SOPs, qualification/validation protocols, investigation, GMP, etc., will be part of your responsibilities. Your ...

Job summary We are looking for an individual to perform filling/washing and sterilization operations within GMP (Good Manufacturing Practices), regulatory, and organizational guidelines. The objective is to produce products within defined volumes and timelines, ensuring compliance with quality standards, GMP, and regulatory requirements as per schedule. Roles & Responsibilities - Perform filling, washing, sterilization operations as per the day plan, executing batch production records. - Participate in filling area line clearance activities and perform machine cleaning operations. - Handle material dispensing and issuance from the warehouse. - Issue discrepancies, work with cross-functional ...

As an HR Operations Specialist with 4-6 years of experience, you will be responsible for various HR activities including Onboarding, Insurance, PF, compliance, Internal Audit, Documentation and filing, policies, and SOPs. Your key responsibilities will include: - Onboarding new hires across different Business Units to ensure a smooth and positive experience from pre-joining to post-joining period. - Renewal of insurance plans and timely processing of claims. Serve as the primary point of contact for the Insurance Vendor. - Manage labor law compliances such as PF and ESI, including additions, nominations, declarations, transfers, and withdrawals of PF/ESI cases. Ensure compliance with regulat...

You will be responsible for end-to-end compliances under EOU/EHTP (Export Oriented Unit) scheme, which includes submitting applications to customs authorities with all necessary documents to seek approval for duty exemption on imported goods. Additionally, you will be tasked with the accounting of duty-free goods, tracking their utilization and movements, availing duty exemption under relevant notifications, addressing discrepancies in inward shipments, and availing export incentives if applicable. Moreover, you will need to submit statutory reports to Customs authorities and STPI authorities on a monthly and quarterly basis respectively. In addition, your role will involve end-to-end compli...

As a Senior Technical Documentation Specialist, you will be responsible for planning, creating, and maintaining detailed documentation to support software products, infrastructure, and internal systems. You will collaborate with cross-functional teams to produce user-friendly content that enhances understanding and efficiency across the organization. Your key responsibilities will include creating high-quality documentation such as user manuals, API guides, FAQs, and release notes tailored to technical and non-technical audiences. You will work closely with Development Heads, Technical Architects, and Operation Heads to gather information and ensure documentation accuracy and alignment with ...

The role of Solutions CoE Manager involves leading legal solutioning and project transitions within the Legal Support Services practice. As an experienced and strategically minded individual, you will be responsible for overseeing U.S. claims litigation processes, legal operations, and client engagement. Your key responsibilities will include leading the solutioning and transition of legal support engagements, participating in client due diligence sessions, designing and delivering training for new engagements, working directly with client stakeholders to capture requirements, and building reusable solution assets. Additionally, you will collaborate with delivery teams to ensure seamless kno...

You will be responsible for executing internal audits to optimize audit coverage in alignment with the organization's internal policies and external/regulatory requirements. Your key responsibilities will include planning and conducting internal audits for all activities within the organization, coordinating with internal auditors firms, overseeing management of control lapses, preparing reports for management and the board, ensuring compliance with action on internal audit observations, monitoring and adhering to timelines for audit completion, evaluating controls over operations, financial reporting, and compliance with rules and regulations, designing SOPs, updating RCMs, performing ICOFR...

DESCRIPTION AHS Specialists provide dedicated support to third-party Sellers. We eliminate frustration and consult with Sellers on best ways to address opportunities for their business on Amazon's e-commerce platforms. The objective of this role is to deliver sustainable results that improve Seller's Performance, while aligning to Amazon requirements. We use Standard Operation Procedure and judgment to provide guidance to Sellers on complex cases. The successful AHS Specialist will have a high degree of soft-skills, the ability to empathize with others and capable of succeeding in a fast-paced environment. AHS Specialist will also be analytical and customer service-oriented. The AHS Speciali...

As a Manager in Quality Assurance, Production, and Customer Service, you will be responsible for ensuring the consistent quality of seeds through the implementation and management of quality systems. Your role will involve handling customer complaints, conducting root cause analysis, and driving continuous improvement initiatives to enhance customer satisfaction and ensure regulatory compliance in QA, seed production, processing, storage, and distribution. Your key responsibilities will include acting as the primary point of contact for quality-related customer complaints, recording, investigating, and resolving complaints related to seed germination, genetic purity, physical admixture, mois...

You will be responsible for performing various activities on behalf of the Marketing Authorization Holder. Your main responsibilities will include maintaining oversight of the Pharmacovigilance (PV) system in all relevant aspects, such as SOPs & Training, contractual arrangements, databases, compliance data, audit/inspection plans, PV systems of local affiliates, and ensuring that all PV processes are conducted in accordance with pertinent regulations. Additionally, you will oversee the preparation and maintenance of the PV System Master File, maintain an overview of safety profiles and any emerging safety concerns of all Marketing Authorization Holder products, manage the signal management ...