3M has a long-standing reputation as a company committed to innovation. We provide the freedom to explore and encourage curiosity and creativity. We gain new insight from diverse thinking, and take risks on new ideas. Here, you can apply your talent in bold ways that matter. **Job Description:** **Educational and Experience Requirements:** **Education:** + Bachelor’s degree in pharmacy (B Pharm) or Chemical Engineering. + Graduated from a reputed university or college, such as NITs, RECs, or Tier-1 state colleges. **Experience:** + 3 to 7 years of experience in manufacturing or production. **Job Description** **Mixing and Filling Operations** + Expert in **liquid-liquid** and **solid-liquid mixing** and filling processes. + Proficient in **packaging operations** with a focus on accuracy, hygiene, and efficiency. **Regulatory Compliance** + Implement and oversee manufacturing practices in strict adherence to **FDA** , **WHO** , and **cGMP** guidelines. + Ensure processes meet global **quality and safety standards** . **Project Management** + Successfully managed projects aimed at **cycle time reduction** , **productivity improvements** , and **line balancing** . + Demonstrated ability to drive cross-functional teams towards project milestones and KPIs. **Safety & Risk Analysis** + Conduct **Pre-Startup Safety Reviews (PSI)** , **HAZOP** , and **Process Hazard Analysis (PHA)** for new product introductions. + Lead all **Process Hazard Management** activities for existing products to ensure safe and reliable operations. **Process Analysis & Optimization** + Perform **process capability studies** , **What-if analyses** , and **variability studies** to optimize performance. + Define and refine key process parameters such as **cycle time** , **lead time** , **takt time** , and **line balancing** . **Process & Equipment Qualification** + Lead and support **process qualifications** , **change control** , and **IQ/OQ (Installation & Operational Qualification)** . + Accountable for **equipment calibration** and maintaining validation records. **Operational Excellence** + Foster **shop floor discipline** , **team engagement** , and a culture of **5S** , system adherence, and compliance. + Drive **continuous improvement** through **SPC (Statistical Process Control)** and **process mapping** . **Documentation & Training** + Manage **production reporting** and ensure all process documentation is up to date. + Conduct **training programs** for team members on SOPs and best practices. **Customer-Centric Quality Management** + Conduct **root cause analyses** for customer complaints and deviations. + Implement **Corrective and Preventive Actions (CAPA)** to drive continuous quality improvements. **Operational Management** + Monitor and maintain **line flow** , **output** , and **process control** for optimal production efficiency. **Capacity Planning & Resource Management** + Develop and execute **capacity plans** , **shift planning** , **material issuance** , and **manpower loading** . + Use **SAP** applications (preferred) for planning, tracking, and analysis. **Improvement Initiatives** + Spearhead **yield improvement** , **OEE (Overall Equipment Effectiveness)** , and **automation** projects. + Apply **Industrial Engineering techniques** like **cycle time** , **method** , and **work studies** to improve productivity, quality, and safety. **Process Redesign & Layout Optimization** + Identify opportunities and implement **process redesigns** , **layout modifications** , and **workflow enhancements** to boost efficiency and reduce waste. **1. Certifications** + **Six Sigma Green Belt** certification is preferred (not mandatory). **2. Regulatory & Industry Compliance** + Proven experience working with **FDA** , **WHO** , and **cGMP** standards. + Sound understanding of **ICH** and **WHO guidelines** related to pharmaceutical manufacturing and quality systems. **3. Technical Proficiency** + Hands-on experience in **commissioning and qualification processes** (IQ, OQ, PQ). + Familiarity with validation protocols and regulatory documentation. **4. Industry Exposure** + Demonstrated exposure to the **pharmaceutical** and **healthcare** industries, preferably in manufacturing or process engineering roles. **5. Corporate Experience** + Experience working in **multinational corporations (MNCs)** is preferred. + Ability to work within **structured environments** and adhere to global corporate policies. **6. Career Stability** + Shows a **stable career progression** with limited job-hopping. + Preference for candidates with **long-term tenures** in previous roles, reflecting reliability and commitment. Learn more about 3M’s creative solutions to the world’s problems at www.3M.com or on Instagram, Facebook, and LinkedIn @3M. **Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.** **3M Global Terms of Use and Privacy Statement** Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at 3M are conditioned on your acceptance and compliance with these terms. Please access the linked document by clicking here (http://multimedia.3m.com/mws/media/1274940O/3m-jobs-country-data-privacy-statements-external.pdf) , select the country where you are applying for employment, and review. Before submitting your application, you will be asked to confirm your agreement with the terms. At 3M we apply science in collaborative ways to improve lives daily as our employees connect with customers all around the world. Learn more about 3M's creative solutions to global challenges at www.3M.com or on Twitter @3M or @3MNews. 3M does not discriminate in hiring or employment on the basis of race, color, sex, national origin, religion, age, disability, veteran status, or any other characteristic protected by applicable law.