Supervisor, Chemistry Production

LGC is a leading, global life science tools company, providing mission‑critical components and solutions into high‑growth application areas across the human healthcare and applied market segments. Our high‑quality product portfolio is comprised of mission‑critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers’ products and workflows and are valued for their performance, quality and range. Our tools play a key role in customer workflows from discovery applications through to commercial manufacture and enable its customers to bring new diagnostics and therapies to market, progress research and development, optimise food production, and continuously monitor and enhance the quality of food, the environment and consumer products. Job Description Are you ready to take your career to the next level in a dynamic and innovative environment? As the Supervisor, Chemistry Production at LGC, you will have the unique opportunity to lead a team of passionate professionals in creating world‑class chemistry products. Your role will be pivotal in ensuring flawless production processes and maintaining the highest standards of quality. We are looking for an exceptionally skilled individual to join our team and help us achieve our ambitious goals! The essential functions of this position are as follows Provide oversight of the chemistry production department. Supervise and perform manufacturing processes for custom and catalog products. Supervise the effective working of manufacturing personnel and prepare production schedules, taking into consideration equipment and/or resource constraints, ensuring a commitment to both quality and company policies. Oversee drug standards supervision and reconstitution. Operate production equipment; weigh, measure, and check raw materials to ensure manufactured products contain proper ingredients and quantities. Evaluate quality control testing data and determine further actions as needed for product release. Prepare products according to approved Manufacturing Control Procedures, cGMP, and ISO 13485 quality system. Perform required batch record reviews for completeness and GDP. Record, compile, and analyze research data relevant to product development and evaluation procedures. Propose and evaluate formulation strategies for production and distribution. Review, initiate, and implement changes in Manufacturing documents and SOPs as needed, through the Document Control System. Maintain a clean room environment to align with regulatory requirements, GMP, and SOPs. Prepare regulatory documents as appropriate when needed. Train new employees. Lead and coach employees to meet production goals and maintain morale. Resolve conflict within the area of responsibility. Interact with all co‑workers and management in a positive, supportive, and cooperative way. Prepare performance evaluations and measure improvement goals. Develop professional skills to enhance job expertise and awareness of Company policies for GMP, SOP, and safety regulations. Create and maintain quality in an ever‑changing and developing environment. Qualifications Minimum Qualifications Bachelor’s Degree or equivalent experience in Chemistry, Pharmacy, Pharmacology, physical science, or a related field. More than 2 years’ experience in the Medical Device field or a closely related sector. Previous experience working with computer systems and software pertaining to product manufacturing and inventory management. Production flow management experience. General management and leadership experience. Excellent written and oral communication skills. Strong organizational, problem‑solving, and analytical skills. Ability to manage priorities and workflow. Versatility, flexibility, and a willingness to work within constantly changing priorities. Acute attention to detail. Ability to work independently and as a member of various teams. Good judgment with the ability to make timely and sound decisions. Ability to read, analyze, and interpret technical procedures. Ability to effectively present information and respond to questions. Strong knowledge of production flow processes. Working and applied knowledge of GMP (Good Manufacturing Practices) and standard laboratory practices. Preferred Qualifications More than 5 years’ experience in the Medical Device or a related industry and 2 years of management experience preferred. Proficient in ERP systems, QAD preferred. Knowledge of regulatory requirements. Knowledge of product/process validation. Additional Information Pay Range for this position is: Minimum pay rate: $79,000 USD Maximum pay rate: $119,000 USD The salary range provided covers the minimum and maximum amounts projected for this role. The base salary will be influenced by factors like experience, skills, and location. All your information will be kept confidential according to EEO guidelines. 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 positive and inclusive culture ensures that we can compete and succeed in our goals while encouraging respect and innovation. Our values:

PASSION

CURIOSITY

INTEGRITY

BRILLIANCE

RESPECT

Equal opportunities LGC is committed to valuing every job applicant and employee for their distinct skills 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 procedures will always be performed without bias related 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 scienceforasaferworld #J-18808-Ljbffr LGC