Manufacturing Project Manager

Manufacturing Project Manager – Kindeva Drug Delivery Our Work Matters At Kindeva we make products that save lives, ensuring better health and well‑being for patients around the world. The Impact You Will Make In this role you will lead projects to introduce new products, processes, and technologies within operations, applying technical product and process knowledge to the development of cross‑functional project plans. You will maintain schedules, budgets, and cost of goods (COGs) related to the technical development of manufacturing processes across Kindeva commercial sites and outsourced partners. Key Responsibilities Lead development of Project Charter and document initial requirements in line with stakeholder expectations. Scope project requirements to support new product introduction, product line extension, technical transfers, and product optimization projects. Work with the engineering team to ensure specification/requirement compliance in design, system performance, quality, and COGs. Ensure projects are executed within Health, Safety, Environmental and GMP requirements. Participate in phase gate reviews internally, with external partners, and customers. Project unit costs and CAPEX spend from development to commercialization. Creation, management and communication of detailed project plans with foresight to escalating constraints. Ensure that a relevant risk management and contingency plan are in place. Provide oversight and direction to ensure technical aspects of the project are executed. Represent Operations on Development project teams to ensure technical feasibility and alignment with commercial capabilities. Provide technical process input to NPI early‑stage and new business proposals. Work closely with Development and Engineering functions to ensure smooth transition of products, equipment and processes into commercial operations. Anticipate technical hurdles and identify mitigation strategies. Identify, define and solve complex problems, and establish metrics to aid decisions. Demonstrate knowledge of the organization’s risk and opportunities within the market. Demonstrate expert insight into the organization’s risks and opportunities within the market. Skills & Experience 5+ years’ experience in project management. 3+ years’ experience in a regulated industry such as pharmaceutical or food & beverage is preferable. Degree qualified in an engineering or science‑related technical discipline. Proven leadership in new product development is desirable. Experience with ISO 13485, 21 CFR 210/211/820 is desirable. Strong project management skills with experience using tools like MS Project, or similar. Financial experience in budgeting, cost control, and analysis is required. Track record of detailed program / project management exhibiting comprehensive planning and thorough communication. Action‑oriented to remove barriers and achieve results within a changing environment. Computer literate, familiar with Microsoft Word and Excel. Key Capabilities Excellent interpersonal and communication skills, both written & oral at all levels. Able to work both as part of a cross‑functional team but also act independently. Proficient in leading teams, as well as coordinating and communicating project requirements. Comfortable working with detailed technical information but also able to see the overall business picture. Demonstrate an expert understanding of functional project frameworks and project management concepts, techniques, tools, and best practices. Demonstrate flexibility, strategic thinking and drive to succeed. Able to deliver results accurately within demanding time frames. Adapt to changing priorities, timelines, and expectations without compromising quality. Maintain a high standard of accuracy, completeness, and documentation. Champion data integrity and a right‑first‑time culture. What We Offer Attractive compensation package. Company pension scheme (up to 10% employer contribution). 25 days holiday per year (plus bank holidays) plus service days after 5 years. Private Medical Insurance. Company sick pay. Employee Assistance Program with 24/7 confidential helpline support for employee and immediate family. Life assurance of four times life cover salary. Flexible working hours. Wellness programmes. Employee recognition program. Employee development. Free on‑site parking. Discount and cashback at many retailers. Cycle to work scheme. Flu vaccinations. Employee referral scheme. Additional Information Working Hours: 37.5hrs per week Location: Derby Road, Loughborough All applicants must be eligible to work in the UK. Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral. Kindeva is an Equal Opportunity Employer. Seniority level Mid‑Senior level Employment type Full‑time Job function Project Management and Information Technology Industries Pharmaceutical Manufacturing #J-18808-Ljbffr