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Process Engineer

vor 2 Monaten

Lucerne, Schweiz Randstad Vollzeit
Jobdescription

On behalf of one of our clients, we are seeking a highly motivated individual to fill an open position to support drug substance tech transfer and commercial manufacture within their External Manufacturing Network. This is an exciting opportunity to work with key strategic external partners, grow technical experience in biologics or vaccines manufacturing, and work on high visibility network initiatives. Our team strives to provide technical excellence in our work and be strong partners, collaborators, and leaders within the large molecule line of business at our company.

 

Contract: temporary contract via Randstad

Start date: 01/11/2024

Duration: 1 year

Location: Luzern or 100% remote from Switzerland

 

Responsibilities include:

  • Work with external partners to achieve business goals and to establish a common culture that benefits both our company, external partners, and patients
  • Lead and act as the primary interface on technical issues between technical operations and external partner drug substance manufacturers
  • Responsible for technical transfer activities, as applicable, through authorship and/or review of required GMP documentation (Master Batch Records, change control, protocols, reports, qualifications, etc.) and regulatory filings.
  • Responsible for technical activities for the commercial manufacturing process at the external partner, which includes authorship of change control, management of process improvement projects, statistical analysis of process performance, and investigation of atypical events
  • Develops solutions to complex technical issues that require a high degree of ingenuity, creativity and innovation. Requires understanding and application of principles, concepts, practices, and standards that govern the manufacturing of sterile products.
  • Provide on-site coverage at external partner in support of commercial and / or tech transfer person in plant activities
  • Translate understanding of GMP requirements and current regulations and develop standardized work to meet these requirements by partnering with operations, quality, and external partners
  • Ensure that external partners are inspection ready for all routine inspections and / or inspections related to new product introductions or transfers, in concert with operations, quality, and regulatory
  • Responsible for participation in creating, sharing, and adopting best practices and business process strategies

 

Education Minimum Requirement:

  • Bachelor’s degree in Chemical/Biochemical Engineering, Pharmaceutical Science, or Chemistry/Biology, or other related science or engineering field

 

Required Experience and Skills:

  • Minimum of 7 years post-bachelor's degree experience in a GMP functional area or support of a GMP functional area, such as Operations, Technical Operations, Technology or Engineering
  • Ability to work independently as well as excellent organizational skills
  • Strong professional and interpersonal communication skills
  • Must be able to multi-task and work within tight deadlines
  • Strong analytical problem-solving skills, root cause analysis, and risk assessment/mitigation
  • Proven team building skills
  • Excellent command of English (both written and oral) and German as an advantage
  • Travel will be a requirement of this position at approximately 20%

 

Preferred Experience and Skills:

  • Experience in biologics drug substance manufacturing
  • Project management experience
  • Experience in deviation management and/or change control and/or equipment support
  • Knowledge of worldwide regulatory requirements, experience supporting regulatory inspections.

 

If you are ready to take the next step in your career and meet the qualifications, we invite you to apply and become part of a dedicated team.