Manufacturing Project Manager

Manufacturing Project Manager

LGC Clinical Diagnostics develops and manufactures a comprehensive portfolio of diagnostic quality solutions and component materials for the life sciences industry. We partner with IVD assay developers, pharmaceutical, CRO, and academic institutions in commercialization activities across the entire diagnostic pipeline. Laboratorians and diagnostic professionals across disciplines rely on LGC's products to support accurate and reliable diagnostic results.

Each day, our staff, scientific expertise, operational efficiency, and superior quality systems are ready to support the range of advanced technologies that collectively improve patient outcomes.

Job Description

In this role, you will coordinate manufacturing tasks and develop detailed manufacturing instructions outlining necessary raw materials, testing procedures, components, and resources. Your main responsibility will involve analyzing testing data from various platforms and troubleshooting issues to ensure accurate product manufacturing. You will serve as the expert on manufacturing products in production, such as panels, serological / NAT controls, bulk plasma, and urinalysis controls. Effective communication is key with customers, interested parties, team members, participants, partners, and team members to meet timelines and deliverables. You will oversee manufacturing design control and new product development tasks, identifying development needs and addressing any issues in the manufacturing or design process. You will demonstrate and inspire internal capabilities to meet customer requirements. You will act as the manufacturing Subject Matter Expert for New Product Development and new custom product opportunities. This role embodies LGC's values of Passion, Curiosity, Brilliance, Integrity, and Respect, emphasizing strong work ethic, meeting requirements, and adherence to company policies and industry regulations.

Responsibilities

• Oversee day-to-day manufacturing product / product management, ensuring tasks are done according to standard operating procedures following cGMP and ISO 13485 quality systems.
• Align with all cGMP, ISO 9001 and / or ISO 13485 regulatory requirements (as per the site's regulatory status).
• Monitor and maintain stock inventory with planning used in all products to ensure availability.
• Provide technical guidance on new products, existing products, and panels.
• Participate in evaluating, developing, improving, or providing technical support for product manufacturing.
• Effectively collaborate to transition new products into Manufacturing, including developing relevant documentation.
• Collaborate with Marketing / Customers to define design goals and determine feasibility of custom products.
• Collaborate with the R&D Team to transition new products into Manufacturing.
• Work with QC Team to ensure product testing is up to date, assist with crossover studies when required.
• Communicate technical aspects of LGC products to support internal and external customers.
• Lead troubleshooting investigations to resolution for any manufacturing area / customer complaint with little or no assistance.
• Act as a liaison for technical communication with custom product team and manufacturing.
• Maintain working knowledge of urinalysis, toxicology, and infectious diseases; pursue continuous education for the expansion of product lines.
• Maintain all product testing data, metrics for the department; track and report as required.
• Travel required on an as-needed basis.

Qualifications

Minimum Qualifications :

Bachelor's degree or equivalent experience (minimum of 5 years), with a focus on Biology, Chemistry, or a related scientific field.

Experienced in a Life Science setting, with a background in cGMP / ISO conditions, involving clean rooms within a manufacturing department capacity for over 5 years.

Proven team-building training and leadership skills.

Strong technical competence and problem-solving abilities, with the capacity to troubleshoot complex manufacturing problems.

Proficient with Microsoft Office Suite, including Word, Excel, PowerPoint, and Outlook.

Preferred Qualifications :

Master's degree with a focus on Biology, Chemistry, or a related scientific field.

8+ years of experience in a Life Science setting, specifically in a cGMP / ISO environment, with involvement in clean rooms within a manufacturing department.

SAP / Oracle ERP system experience.

Experience with 5S and Lean implementation.

Label printing software experience.

Competencies & Behaviours :

Resonates and operates in line with LGC's core value behaviors : Passion, Curiosity, Integrity, Brilliance, and Respect.

Outstanding communication and people skills, adept at operating successfully within a team atmosphere.

Diligent with a commitment to producing high-quality work under tight deadlines.

Adaptable, with the capacity / flexibility to respond to the demands of a growing / changing company.

Additional Information

Join LGC and become part of a team that values collaboration, integrity, and brilliance in all we do. We are committed to encouraging a workplace where everyone can thrive and contribute to our mission.

Our values :

PASSION

CURIOSITY

INTEGRITY

BRILLIANCE

RESPECT

Equal opportunities

LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, parental responsibilities, religion, or belief. Shortlisting, interviewing, and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership.

For more information about LGC, please visit our website www.lgcgroup.com