Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

Job Description

This position is Responsible for leading Quality Assurance Department in accordance with vision, values, and strategic goals of the company. It will involve overseeing and facilitating efficient quality operations, assuring consistent client service, implementing laboratory practices as applicable to current regulatory standards, working with client and agency audits and correspondence, maintaining certifications, Quality Assurance policy development, and maintenance, following up promptly on any quality and compliance related issues, and implementing respective CAPA actions to assure adherence to the required quality metrics. Other responsibilities are as follows:

Chairs Quality Management Oversight Meetings to monitor for trends, identify improvements, and assure the effectiveness of the Quality Management SystemImplements, prepares, and presents training programs as required to satisfy regulatory requirementsManages Quality Management SystemApplies industry experience to establish and implement best laboratory practices and quality system standards as related to compliancePerforms QA review and approvals as requiredMaintains current records for required certifications and/or accreditationsCommunicates with client and agency auditors, responds to findings, and effectively addresses concerns or findingsProvides information for monthly/quarterly reports to senior site managementIdentifies, implements, and assures adherence to effective quality control measuresMentors QA staff and provides leadership through demonstration of the vision, values, and strategic goals of the companyLeads complex projects through to completionCommunicates effectively with client staff membersPerforms other duties as assigned

QualificationsBachelor’s or Master’s degree in Chemistry or closely related science field from a four year college/university or equivalent education and job experienceAt least five years of bio/pharmaceutical chemistry/microbiology/biopharmaceutical experience with some data review responsibilities and a working knowledge of regulatory requirementsSolid understanding of chemistry/lab practices.Knowledge of auditing techniquesFamiliarity with at least one scientific technique (HPLC, GC, etc.)Self-confidence, leadership, ability to reason, make sound decisions, and delegateEmpathy and sensitivity towards othersMotivation to excel and inspire excellence in othersAbility to manage the work of others and see projects through to completionStrong communication including verbal, writing, and presentation skillsAbility to communicate effectively and relate well to peopleMental and emotional stability and maturityAbility to handle personal stress and diffuse stress in othersStrong organizational skills and ability to handle multiple prioritiesSets positive example for othersDedication to quality, ethics, and customer servicePride in appearance, conduct, and companyAbility to work effectively under pressure to meet deadlinesGood negotiation and reasoning skillsExcellent written and verbal communications skillsGood judgment and tact recognizing and solving problemsRecognized as understanding, interpreting, and following company policy

Additional Information

Position is full-time, Monday-Friday, 8 a.m.-5 p.m., with overtime as needed.  Candidates currently living within a commutable distance of San Diego, CA are encouraged to apply.

Target compensation: $80,000-$100,000/year

As a Eurofins Lancaster Labs employee, you will become part of a company that has received national recognition as a great place to work.  We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options.

To learn more about Eurofins, please explore our website www.eurofinsus.com .

 

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.