Skip to main content

Process Engineer

  1. United States
North Carolina
  1. Contract
Competitive
  1. Commissioning, Qualification and Validation
30-08-2024
34916
Process Engineer - Pharmaceuticals - 12-Month Contract

Our client, a global Pharmaceutical manufacturing organization are looking for a talented Process Engineer to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States.


Main Responsibilities
  • The Process Engineer will help the Process Engineering team manage Project Change Controls, identify equipment bill of materials, identify spare parts, and perform other process equipment engineering tasks to get the respective systems ready for IV/OV, performance qualification, and commercial operations.
  • The individual must be comfortable with shifting week to week priorities based on a dynamic project environment.
  • The individual must be willing to be onsite (Holly Springs, NC) during “core” working hours (9-4pm), M-F.

Knowledge and Skill
  • Minimum 2 years of pharmaceutical industry experience required. Five plus years is preferred.
  • Prepare for and facilitate cross-functional meetings related to Project Change Controls. Prepare meeting minutes and follow up with action item owners to drive on-time completion.
  • Collaborate with the maintenance systems organization to manage schedule and deliverables related to spare parts and maintenance requirements. Coordinate with Process Engineers to ensure tasks are completed on time. Contribute as SME as availability permits.
  • Perform other process engineering tasks as requested:
  • Review vendor turnover package documentation
  • Monitor system punch list and drive punches to closure
  • Support commissioning, qualification, and validation (CQV) team activities (reviewing protocols, reviewing SOPs, contacting vendors for information, equipment troubleshooting, etc.)

Desired (but not required) Skills
  • General knowledge of DeltaV automation structure (S88 model)
  • General knowledge of EIDA
  • General knowledge of Kneat
  • Software;
  • Full Microsoft Office Package

If this role is of interest to you, please apply now! 

 #LI-MC1
Save as a job alert
List #1

Similar Jobs

Cleaning Validation Engineer

Salary

Competitive

Location

Cork

Salary

Competitive

Sector

Commissioning, Qualification and Validation

Job type

Contract

Location

Cork

Description

Cleaning Validation Engineer - Pharmaceuticals - Cork, Ireland - 12-Month Contract  Would you like to grow your career, whilst contributing to scientific innovations that are transforming

Reference

34106

Expiry Date

01/01/0001

Jack Steadman

Author

Jack Steadman
Read more
CIP Validation Documentation Engineer

Salary

Competitive

Location

Raleigh

Salary

Competitive

Sector

Commissioning, Qualification and Validation

Job type

Contract

Location

East Coast

Description

CIP Validation Documentation Engineer - Raleigh - 12-month contract Our client, a global Pharmaceutical manufacturing organization are looking for a talented CIP Validation Documentation Engineer

Reference

32698

Expiry Date

01/01/0001

Mark Chaumeton Read more
Technical Writer Cleaning Validation

Salary

€30 - €52 per hour

Location

County Limerick

Salary

Competitive

Sector

Commissioning, Qualification and Validation

Job type

Permanent

Location

Midlands (Ireland)

Description

Technical Writer Cleaning Validation - Limerick - 12-Month Contract Ireland is a hive of activity for the Life Sciences Sector at present with global players setting up new and expanding existing

Reference

33589

Expiry Date

01/01/0001

Christopher Hutchinson Read more

Send us your CV

Our candidates are the cornerstone of our organisation and we are always looking to connect with new professionals who are seeking their next contract assignment or career opportunity.