20 External Manufacturing Jobs

General Manager - Contract Manufacturing Job Description Role Overview The General Manager - Contract Manufacturing will lead the strategic planning and execution of all outsourced production activities. This pivotal role ensures that external manufacturing partners meet the company's quality standards, production schedules, and financial objectives. The GM will manage vendor relationships, negotiate contracts, and drive continuous improvement initiatives across the third-party manufacturing network. Key Responsibilities Vendor Management: Identify, evaluate, and manage relationships with contract manufacturers (CMs) and suppliers. Contract Negotiation & Administration: Negotiate contracts, ...

Roles and Responsibilities Manufacturing of external preparations like ointments, creams, gels, liquids, Solutions, emulsions Ensure compliance with regulatory requirements, company policies, and procedures during external manufacturing activities. Maintain accurate records of batch records, stability studies, and analytical results of finished products, including ointments, creams, gels, liquids, Desired Candidate Profile 5-10 years of experience in a similar role as an Approved Manufacturing Chemist (AMC) or equivalent position. Bachelor's degree in Pharmacy (B. Pharma) from a recognized institution. Strong understanding of pharmaceutical regulations such as GMP guidelines and cGMP princip...

Role Overview: As a Data Product Analyst at Opella, you will be a part of the global Digital Data & Analytics team with a focus on enabling data-driven decision-making across the Manufacturing, Maintenance, EM (External Manufacturing), and Product Portfolio domains. Your responsibilities will include designing semantic layers in Snowflake, developing insights through Power BI dashboards (KPIs) and ad-hoc reporting, and ensuring the integrity and quality of data integration across multiple systems. You will act as a key liaison between business functions, data engineers, and architects to bridge business insights with enterprise data solutions. Key Responsibilities: - Seamlessly collaborate w...

Key Responsibilities: Identify, evaluate, and onboard suitable contract manufacturing partners (domestic and international). Manage day-to-day coordination with third-party manufacturers for production, quality, and supply chain activities. Negotiate commercial terms, finalize agreements, and ensure adherence to company policies. Monitor production schedules, delivery timelines, and cost optimization at partner sites. Coordinate with internal departments (Quality, Regulatory, Procurement, and Supply Chain) to ensure smooth operations. Ensure compliance with cGMP, regulatory, and company quality standards across all CMO sites. Drive continuous improvement initiatives to enhance efficiency and...

Role & responsibilities : Main Role purpose is Supply chain - Sourcing. , Global Sourcing , He/ She will regularly influence C-level from both internal and external worlds by advising senior leaders across multiple stakeholder groups to set the direction from sourcing strategies and related initiatives in line with EMS business unit and corporate goals. Brief of Responsibilities Establishing strong relationships with internal business stakeholders and governance global team; building a strong understanding of strategic business direction, requirements, compliance and priorities across assigned suppliers and/or spend categories. Developing in depth Regional Sourcing strategies Evaluating supp...

Responsibilities: * Ensure Contract Manufacturing is done with OEMs with compliance and company policies & procedures * Manage supplier relationships * Negotiate contracts & prices * Oversee inventory management * Coordinate purchasing activities

USV, a top-15 pharmaceutical company in India, excels in the diabetes and cardio sectors. We have a presence in over 65 countries with our dynamic team of over 7,000 across generations. Our commitment to brand building is evident in our popular products like Glycomet GP, Ecosprin AV, Jalra, Tazloc, Glynase, MVI and more. Candidate should be resident or ready to relocate either Palghar or Boisar / Virar (Mumbai) Should know regulated market CMO Knowledge of dosage forms like OSD, Semisolids, Liquids, parentals Quality- Should know to deliver products with all quality standards. SAP-Material Planning (RM/PM); Inventory control. Supply Planning-finished goods replenishment, production planning....

Job Overview: The purpose of the role is to liaise with internal and external Stakeholders to ensure timely delivery of New Product Developments (NPDs). The roles & responsibility include (but not limited to) scouting new product opportunities, develop and drive plans with reasonable negotiation, effective tracking and risk mitigation and achieve deadlines and milestones across stakeholders, teams and management, to ensure projects are completed successfully and as per timelines aligned Qualification: Graduate (Preferably Engineering) + MBA / PGDBM/ M.tech (Tier-2 or Tier-3 Institutes preferred Location : Kurla Mumbai Preferred candidate profile Minimum 3-4 years experienced in planning and ...

Role & responsibilities To be well versed about coordination and collaboration with Quality functions of third party manufacturing (CMO) sites and CMO team for compliance of product, facility, systems, procedures. and for documents required from third party for various purpose; review, RA submission etc. Must have knowledge and know how on regulatory pathway for registration of product as per third party and or loan license norms/rules and requirement of documentation for regulatory submissions. Incumbent is expected a good reviewer and investigator To know the function of oversight of CMO sites for batch/lot releases as applicable form the manufacturing (Feed supplements and Pharma products...

Role & responsibilities Identify 3rd parties for execution of lab development work Identify 3rd parties with different capabilities ( evaluate different chemistry capability) To understand their analytical capabilities Facility visit and Preliminary facility assessment report covering all the capabilities To co- ordinate with safety and quality team for audit and approval To co -ordinate between 3rd party and internal legal team to finalize CDA SWOT analysis of 3rd party lab Statutory and Legal compliance of 3rd party - confirmation from SCM to be co ordinated Collection of last 3 years audited finance report and to share with finance team to understand the financial stability of the organiz...

Responsibilities: Operation Control and Monitoring Multiple CMO Sites. Check Plan Vs Achievement on a regular basis. Provide information to Production coordinator daily via Daily Performance report. Check availability of resources at contract site to meet schedule. Check documents availability in case of change in product. Provide batch no. requisition to coordinator as per plan. Ensure timely SAP posting and dispatches. Monitor Schedule OTIF. OTIF Tracking at respective CM sites, On Time in Full (OTIF) delivery Supply deliveries as volumes committed & requirement. To Co-ordinate with Stores and contract manufacturing site for the timely shortages, availability, and release of RMs and PMs. F...

Candidate is responsible for sourcing the company who are looking for third Party Manufacturer. Identify and onboard reliable third-party manufacturers. Experience in Home Care/Laundry Care private label or contract manufacturing preferred.

Responsible for day-to-day activities of Pharma manufacturing , prepare documentation as per cGMP norms. Working Experience on External preparations Coordinate with other depart for smooth running of plant Capable of handling external Audits Required Candidate profile Min Exp 2 to 10 years in Quality department of a reputed pharmaceutical Company Knowledge of working in GMP Co. MS Office (MS Word & MS Excel) / ERP software. and good time management skills Perks and benefits Performance linked incentive & annual bonus extra

Role & responsibilities Technology transfer and scale-up activities at external/Third-party manufacturing/CMO sites. Coordinate and execute along with CMOs/internal teams for feasibility trials and commercial production. Evaluate & assure the equipment for capacity and process suitability at manufacturing site. Prepare and review documentation for feasibility/Trial batches, scale-up, exhibit /validation batches, and for commercial production. Plan, execute and monitor exhibit /validation batches for regulated markets at CMO/Third party manufacturing sites Ensure timely execution and readiness of CMOs for product transfers, validations and commercial Production. Troubleshoot technical issues ...

Technology transfer, scale-up at external/Third-party manufacturing/CMO sites. Coordinate with CMOs/internal teams for trials, validation and commercial production. Documents preparation for scale-up, validation and timely execution at CMOs. Food allowance Provident fund Health insurance

Position Overview : We are seeking a skilled and strategic-minded General Manager to lead our External Manufacturing division. The successful candidate will play a pivotal role in coordinating and optimizing our external manufacturing operations, ensuring seamless collaboration with partners, and maintaining the highest standards of quality, compliance, and efficiency. Key Responsibilities: Coordinate and facilitate effective communication between third-party vendors and internal stakeholders to ensure the fulfillment of company requirements and timely query resolution. Review production plans and coordinate with demand planning, supply planning, and Contract Manufacturing Organizations (CMO...

Overseeing the quality assurance function at our manufacturing sites located in Baddi & Rudrapur. Ensure that all products manufactured at the sites adhere to the required quality standards, regulatory requirements, and internal procedures. Required Candidate profile M.Sc/B.Pharm/M.Pharm 12+ year QA experience in a regulated pharma/CDMO environment Strong knowledge of cGMP, ICH & regulatory guidelines Hands-on experience in audits, documentation, quality systems

Role & responsibilities To be well versed about coordination and collaboration with Quality functions of third party manufacturing (CMO) sites and CMO team for compliance of product, facility, systems, procedures. and for documents required from third party for various purpose; review, RA submission etc. Must have knowledge and know how on regulatory pathway for registration of product as per third party and or loan license norms/rules and requirement of documentation for regulatory submissions. Incumbent is expected a good reviewer and investigator To know the function of oversight of CMO sites for batch/lot releases as applicable form the manufacturing (Feed supplements and Pharma products...

Role & responsibilities : Main Role purpose is Supply chain - Sourcing. , Global Sourcing , He/ She will regularly influence C-level from both internal and external worlds by advising senior leaders across multiple stakeholder groups to set the direction from sourcing strategies and related initiatives in line with EMS business unit and corporate goals. Brief of Responsibilities Establishing strong relationships with internal business stakeholders and governance global team; building a strong understanding of strategic business direction, requirements, compliance and priorities across assigned suppliers and/or spend categories. Developing in depth Regional Sourcing strategies Evaluating supp...

BE / B TECH Chemical 2 to 10 YRS for CMO, Outsourcing ,toll manufacturing ,Contract manufacturer ,third-party manufacturer, 3P ,External manufacturing