This job is no longer available.
You can view related vacancies or set-up an email alert notification when similar jobs are added to the website using the buttons below.

The Opportunity

We're looking for an Industrial Upstream Specialist II, working in the Pharmaceuticals & Medical Products industry in Durham, North Carolina, United States.

  • Execution of production processes to meet manufacturing and business requirements.
  • Involved in process scale-up, process optimization and process validation activities.
  • Adhering to and development of documentation, including standard operating procedures and batch records.
  • Coordinates inventory of consumables for production.
  • Generation and resolution of process deviations for the department. 
  • Inspects and maintains the production equipment and control systems.
  • Collaborates with process support and development groups to assure smooth process transition in manufacturing.
  • Coordinates training for a specific unit operation on the process floor.
  • Inputs, reviews, and trends batch production data to support campaign summary report completion.
  • Maintains company safety, health and environmental standards.

We are offering Competitive Compensation and Benefits.

Our Client

Our client is an award-winning clinical development company.  Improving lives globally with 20+ years experience in clinical research and strategic resourcing.  Elevating results with proven strategies, comprehensive solutions, and customized delivery models.

Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

Strong relationships provide you connections and access to great opportunities.  Industry expertise sets you up for success with helpful insights, career coaching, and professional training.  Grow and learn while you put your skills to work.  

Experience Required for Your Success
  • Technical degree with a minimum of 5 years experience, OR
  • University degree with a minimum of 4 years experience 
  • In-depth understanding of cGMP compliant production and documentation
  • Able to function in a fast-paced team environment to meet critical production timelines
  • Experience with process equipment and systems, including 1 or more of the following:  Fermentation, Ultrafiltration, Chromatography (Unicorn®), Centrifugation, Aseptic Practices and Dispensing, Material Handling, Depth Filtration
  • Experience with flexible/disposable single-use systems and technology transfers
What Do You Think?

Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.

Not exactly? Join Our Talent Community, and we'll let you know of additional opportunities.