Sterile Liquids Production Specialist

Sterile Liquids Production Specialist

20 May 2024
Pennsylvania, Westpoint 00000 Westpoint USA

Sterile Liquids Production Specialist

Vacancy expired!

Job Description

Employee Responsibilities:

  • Support pilot plant operations for the GMP manufacturing of sterile, biologic, and vaccine clinical supplies. Interfaces with a large network including multiple research, commercialization, commercial supply, and other pilot plants teams
  • Lead and/or participate in various pilot plant process improvement projects with respect to compliance, efficiency, etc., working with cross-functional teams (e.g. operations, engineering, EM, quality, etc.)
  • Revise/author GMP documentation (e.g. SOP's, logs, etc.).
  • Conduct investigations of minor deviations (NOE's) and author associated reports.
  • Create and review logbooks and other GMP documentation; collaborate with hourly and salary staff for corrections as needed.
  • Review utility reports and troubleshoot as necessary
  • Manage/maintain department production metrics
  • Support GMP, safety, and training initiatives

Qualifications

The Ideal Candidate would possess:

  • Analytical problem solving skills
  • Cross functional leadership skills
  • Technical writing experience – including batch documentation, investigations, protocols
  • Strong computer, scientific, and organizational skills
  • Excellent communication (oral and written) and attention to detail
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies

Minimum Qualifications:

  • Bachelor’s/Master’s degree in engineering, biomedical engineering, chemistry, biology, or related field
  • Minimum of 2 years in a technical or operations support role
  • Sterile process manufacturing and/or formulation development
  • Knowledge of manufacturing equipment and Good Manufacturing Practices
  • Project management
  • Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

Position is full-time Monday through Friday with overtime as needed.Candidates currently living within a commutable distance of West Point, PAare encouraged toapply.

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 websitewww.eurofinsus.com.

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

All your information will be kept confidential according to EEO guidelines.

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