Supervisor, Chemistry Production

About the role

The Supervisor, Chemistry Production at LGC will oversee the chemistry production department, supervise manufacturing processes, and ensure quality standards are met. This role involves managing production schedules, supervising staff, evaluating quality control data, and training new employees.

Responsibilities

• 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, considering equipment and resource constraints.
• Oversee drug standards supervision and reconstitution.
• Operate production equipment; weigh, measure, and check raw materials to ensure proper ingredients and quantities are included in manufactured products.
• 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.
• Create and maintain quality in an ever-changing and developing environment.

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.
• Able to manage priorities and workflow.
• Versatile, flexible, and willing to work within constantly changing priorities.
• Acute attention to detail.
• Able 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.

Pay

The 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.