Supervisor, Chemistry Production

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:

• Bachelors 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: $79000 USD

Maximum pay rate: $119000 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

Remote Work :

No

Employment Type :

Full-time