Laboratory Operations Support (Project Management)

Eurofins PSS Insourcing Solutions; Malvern (AR); On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

Comprehensive medical coverage

401(k) with company match

Paid vacation and holidays

Job summary

A leading life sciences company is seeking a Laboratory Operations Support professional in Malvern, Arkansas. The role involves continuous improvement initiatives in laboratory operations and documentation management. Candidates should have a BS/MS in a scientific field and 1-5 years of GMP experience. Full-time position, offering competitive benefits and potential travel. Ideal for those seeking growth in the pharmaceutical industry.

Qualifications

• 1-5 years experience in a GMP environment.
• Pharmaceutical industry experience preferred.
• Ability to travel to the Spring House site (10%).

Responsibilities

• Initiate continuous improvement initiatives for Asset management.
• Maintain best business practices for Asset management.
• Resolve instrumentation documentation issues.

Skills

GMP experience

Documentation skills

SharePoint proficiency

Analytical skills

Education

BS/MS in a scientific field

Tools

Maximo/eCMMS

Job description

Laboratory Operations Support (Project Management)

Laboratory Operations Support (Project Management)

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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.

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.

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

• Initiate continuous improvement initiatives for Asset management and laboratory Operations and update impacted procedures
• Maintain and support best business practices for Asset management such as Share Point Asset management
• Work with managers, coordinators, and staff of labs to resolve instrumentation documentation issues
• Work with QA and compliance to initiate, investigate, and resolve quality issues
• Review QA’s monthly overdue work order list and research instrument service history and use to resolve documentation issues
• Review training documents to see which are coming due for their 3 year update
• Verify CAR-T data for regulatory submission and make SharePoint updates
• Verify regulatory submission needed, and make Share Point updates
• Facilitate change control closure and send out notifications to activity owners and approvers
• Make status updates to change control SharePoint
• Work directly with vendors to resolve instrumentation accuracy and inventory documentation issues
• Support inventory accuracy for laboratories in Malvern and Spring House sites
• Update Maximo/eCMMS to address inventory inaccuracies, and maintain eCMMs system’s accuracy
• Provide process improvement and instruction to decrease turn-around time for bringing instruments into service
• Research asset history for resolution of outstanding work orders
  
  
  

Qualifications

• BS/MS in a scientific field
• 1-5 years experience in a GMP environment
• Pharmaceutical industry experience
• Experience with SharePoint is preferred
• Ability to travel to Spring House site (10%)
• Authorization to work in the United States indefinitely without restriction or sponsorship
  
  
  

Additional Information

Position is full-time, Monday-Friday, generally 8 a.m. - 5 p.m., weekend work might be expected. Candidates currently living within a commutable distance of Malvern, PA are encouraged to apply. This role may require travel to the Spring House, PA site.

• Excellent full time benefits including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
  
  
  

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

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