107 Fg Jobs

YOUR ROLE We are seeking a talented and driven Supply Planner to join our team. The ideal candidate will be responsible for collecting, analysing, and interpreting complex data sets to drive informed business decisions. You will work closely & Directly with the Client & cross-functional teams to identify trends, patterns, and insights that will contribute to our company's growth. In this role you will play a key role in Rolling out weekly / monthly production plans to the factory Managing Inventory at the optimum level - making sure that there is no non-moving or slow-moving FG as well as no stock outs at warehouse / consumer Experience in S&OP planning Defining stock policies & ensure adher...

Ensure that all incoming, in-process, and outgoing Raw Materials (RM), Packing Materials (PM), and Finished Goods (FG) are inspected and QC-approved, and that identification and traceability are maintained at all stages from material inward to FG dispatch, including PM. Ensure calibration and maintenance of lab equipment. Ensure outsourced inspection services/service providers are evaluated and approved. Participate in the supplier evaluation process, including on-site supplier audits. Coordinate with Production and Purchase departments to report quality issues with RM/PM, processes, and FG. Preserve test samples for the defined period and dispose of them later with proper documentation and ...

Responsibilities: To take note of all day dispatches from Admin In charge and plan for palletizing accordingly. Inform time to time to concerned plant In Charge for about production planning and other details as packing Batch Quantity. Ensure Packing and palletizing is strictly as per SOP checklist and material dispatched as per dispatch checklist Ensure FG stock are properly placed in FG Godown and FG Godown are locked properly after working hours. Prepare Export /Domestic invoices for all dispatches as per SO/ Dispatch checklist Arrange for loading of FG to container / Other Vehicle and ensure that container is stuffed as per approved stuffing plan. Arrange for authentication of Export inv...

Company: Strides Pharma Science Ltd Department: Quality Control (QC) Position: Executive Job Location: Bangalore Qualification: M.Sc. (Chemistry), B-Pharm, M-Pharm Experience: 2 to 5 Years Skills required: Experience on Raw material, In-process, Finished product, Stability and Microbiological testing. Work experience on FDA regulatory plants Flexible to work in shifts Regards, Srinidhi S s.srinidhi@arcolab.com

Designation - Executive , Technical Assistant Department - Quality Control, ASL / MVC Qualification - MSC/ BSC / M.Pharm / B.Pharm Experience - 2 Years - 6 Years Job Location - Indrad (Ahmedabad - Mehsana highway) Key Skills - HPLC, Method Validation, Chemical Testing, Instrument Handling, Documentation Interested candidates can apply with their updated cv.

Note: Walk In Interview at Bharuch Date: - 02-11-2025 (Sunday) Designation: Store Officer-Sr. Officer Location: Dahej, Bharuch Experience: 2 to 7 years in API Qualification: M.Sc. / B.Sc. / M.Com / B.Com Required Candidate profile Roles and Responsibilities: -2 to 7 years of experience in API Plant in RM/ PM/ Finish Good section (Shift Operation)

1 Plan Delivery as per sales orders and customer delivery scheduled. 2 Packing of FGs as per SOP for customer required items as per priority 3 SO approval 4 FG materials stores (multiple locations) management 5 Stores hygiene 6 Planning for Standard products Stocks Categorised and review std product list Maintain proper stocks 7 Maintain prper FIFO 8 On going Perpetual inventory Take stock of 5 to 10 SKUs daily. 9 Inventory reconciliation 1 or 2 Physical inventory Stock taking in year and reconsiliation of the same after proper autorisations. 10 Delivery management 11 Customer Inspection co-ordination Intimate to customer 15days before the planned visit date 12 Dispatch plan 13 Vehicle arran...

QC Head 1 Pos based in Kathua, Jammu & Kashmir. The ideal candidate brings 12 - 15 yrs exp. and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Mana...

The ideal candidate brings 1-6 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Lead microbiology practices including EM, MLT, sterility assur...

Role & responsibilities Candidate should be able to Manage daily RM/PM warehouse store activity starting form receipt to dispensing with enforcing regulatory norm all times. Candidate should lead and manage the team. Candidate Managing FG store activity starting from inward and FG dispatches inline to supply chain management requirement. Familiar with GST regulation. Candidate will be responsible for accountability of manpower utilization, departmental discipline, maximum utilization of the available resources. Candidate should have Manage the final storage and distribution of pharmaceutical products, ensuring compliance with strict quality and regulatory standards. Candidate have to Maintai...

QC Head 1 Pos based in Kathua, Jammu & Kashmir. The ideal candidate brings 12 - 15 yrs exp. and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Mana...

The ideal candidate brings 1-6 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Lead microbiology practices including EM, MLT, sterility assur...

About The Role Project Role : Application Developer Project Role Description : Design, build and configure applications to meet business process and application requirements. Must have skills : SAP Fieldglass Contingent Workforce, API Management Good to have skills : NA Minimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Developer, you will engage in the design, construction, and configuration of applications tailored to fulfill specific business processes and application requirements. Your typical day will involve collaborating with team members to understand project needs, developing innovative solutions, and ensur...

Gaining an understanding of the client's needs and requirements and communicating them and the quality standards to the production teams. Devising ways to improve the manufacturing process to ensure higher-quality goods. Required Candidate profile Strong attention to detail, observation, organizational, and leadership skills. Knowledge of quality control procedures and legal standards. Good technical and IT skills. Perks and benefits Bonuses Flexible Work Arrangements Paid Time Off

Role & responsibilities Perform routine and non-routine analytical testing of raw materials, intermediates, finished products, and stability samples. Operate and maintain laboratory instruments such as HPLC, GC, UV-Vis, FTIR, Dissolution testers , etc. Prepare standard and sample solutions as per method of analysis and SOPs. Review and interpret analytical data, identify discrepancies, and report out-of-specification (OOS) results. Perform method validation, verification, and transfer activities under supervision. Maintain and calibrate laboratory equipment per schedule. Document all activities accurately and in a timely manner in laboratory notebooks and analytical reports. Ensure complianc...

About AkzoNobel Since 1792, weve been supplying the innovative paints and coatings that help to color peoples lives and protect what matters most Our world class portfolio of brands including Dulux, International, Sikkens and Interpon is trusted by customers around the globe Were active in more than 150 countries and use our expertise to sustain and enhance the fabric of everyday life Because we believe every surface is an opportunity Its what youd expect from a pioneering and long-established paints company thats dedicated to providing sustainable solutions and preserving the best of what we have today while creating an even better tomorrow Lets paint the future together, For more informati...

PRIVIJ Consultants Engineering Pvt. Ltd is looking for M.E.P. Project Engineer to join our dynamic team and embark on a rewarding career journey Prepare, schedule, coordinate, monitor and control the assigned engineering projects Monitor compliance to applicable codes, practices, QA/QC policies, performance standards and specifications Cooperate and communicate effectively with the client and project team Functional planning and execution of particular work packages within the given parameters Implementing Project driven changes and requests Evaluation of customers specifications Ability to lead multiple projects and partner with management / functional managers to resolve conflicts and obta...

QC Head 1 Pos based in Kathua, Jammu & Kashmir. The ideal candidate brings 12 - 15 yrs exp. and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Mana...

The ideal candidate brings 1-6 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Lead microbiology practices including EM, MLT, sterility assur...

URGENT REQUIREMENT!!! Job Description: Job Details: Position Title: Instrumentation Engineer/Supervisor (Third Party Contract) Contract Duration: 6-8 months Location: Hazira, Surat & ONGC Mumbai High Platform - Offshore Experience: 7-10 years Type: Third-Party Contract Passport Mandatory Job Summary: We are seeking an experienced Instrumentation Engineer for a 6-8 months contract to support our projects in Hazira, Surat, and ONGC Mumbai High Offshore. The ideal candidate will have 7-10 years of experience in the oil and gas industry, with a strong background in both onshore construction and offshore operations. This is a third-party contract role where you will be responsible for a range of ...

Key Responsibilities: Coordinate with Production, Quality, SRE, and Commercial teams for daily dispatch activities. Monitor truck loading & unloading operations efficiently. Handle ERP transactions and maintain basic computer records. Maintain Finished Goods (FG) stocks as per defined stock norms. Oversee packing operations to ensure compliance with standards. Prepare and maintain dispatch-related documents and check sheets . Ensure regular maintenance of FG trolleys . Implement and follow 5S & Safety practices . Demonstrate effective material handling skills . Track and monitor truck timings to meet delivery schedules. Qualifications & Skills Graduate / Diploma (preferred in Logistics, Supp...

Diploma / B.E.- Mechanical / Electrical Engineer with 3+ years of experience as Stores Executive. Role ensures accurate inventory records, timely material dispatches & compliance with GMP, ISO & other quality standards applicable to pharma industry. Required Candidate profile Knowledge of pharma machinery parts (eg. tablet press, granulators, blenders) is a plus. Responsible for overseeing the receipt, storage & distribution of pharmaceutical machinery parts & components. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Planning - Ensuring despatches are as per plan - Meeting the quality, quantity, on time requirements by planning accordingly Inventory - Organizing and maintaining inventories, and ensuring optimal stock levels using inventory management principles Warehouse Management Overseeing receiving, warehousing, distribution and maintenance operations. Setting up layout and ensure efficient space utilization. Product Assembly – Planning for product assembly through manpower and line management Manpower Management - Allocating manpower for packing, loading and unloading, etc. to meet the delivery requirements Shipping/Transport Management - Ensuring trucks are loaded and unloaded properly, and that al...

As a Control & Safety System Engineer, you will be responsible for the following tasks: - Elaborating/revising technical specifications (DCS/SIS) - Developing/revising control-command architectures (ICSS) - Participating in basic and/or detailed ICSS studies - Monitoring internal and/or external interfaces - Participating in activities to validate the installation aspects of control, safety, fire, and gas systems (quantity of cabinets, loop types) - Preparing functional specifications: functional analysis, control narrative, cause & effect matrices, logic diagrams In Nashik, your responsibilities will include: - Monitoring and interfacing with the engineering team at POC - Coordinating and p...

Key Responsibilities : 1. SOP & Compliance Management Ensure all Standard Operating Procedures (SOPs) related to the Warehouse are updated, valid, and implemented at all times. Monitor and maintain accurate records for all warehouse activities in compliance with cGMP and GDP norms. Oversee audit readiness and ensure timely closure of audit observations. 2. Training & Team Development Plan, schedule, and deliver regular training sessions for warehouse staff and support staff to enhance skills and maintain compliance standards. Build, motivate, and guide the team to achieve departmental objectives and maintain high performance levels. 3. Warehouse Operations Planning Strategically plan daily, ...