FATSAT-Projects - GMP - Oral Solid Dosage
You dont just execute projects you drive them.
You understand GMP OSD manufacturing and complex validation environments.
And youre ready to take ownership of a critical tableting area revamp.
This is your opportunity to step into a Manager / Engineering role where your expertise in commissioning & qualification (C&Q) directly shapes manufacturing excellence.
You will lead the qualification activities for the revamping of a pharmaceutical Oral Solid Dosage (OSD) tableting manufacturing area
You will:
- Own Design Qualification FAT SAT Qualification Handover & Close-Out
- Drive commissioning and qualification of OSD process equipment & computerized systems
- Lead C&Q activities on capital projects on time and within budget
- Author and approve validation strategies protocols & reports
- Interface cross-functionally with engineering QA MS&T suppliers & contractors
- Support audits and health authority inspections as SME
Youll operate within a structured stage-gate project environment and influence across organizational boundaries
What You Bring
- Degree in Engineering or Science (Mechanical Chemical Life Sciences etc.
- 5 years in pharmaceutical validation ideally within OSD in GMP environments
- Experience managing complex capital projects
- Strong problem-solving and communication skills
- Experience with inspections and regulatory interactions
- Project & change management expertise
- English and French fluent
About this contract:
- Starting Date 01. April
- 6 Months
- 100 % on-Site
Why This Role
- Lead instead of follow
- Influence instead of execute only
- Deliver measurable impact within a high-standard GMP environment
- Strengthen your profile in capital project C&Q leadership
FATSAT-Projects - GMP - Oral Solid DosageYou dont just execute projects you drive them.You understand GMP OSD manufacturing and complex validation environments.And youre ready to take ownership of a critical tableting area revamp.This is your opportunity to step into a Manager / Engineering role wh...
FATSAT-Projects - GMP - Oral Solid Dosage
You dont just execute projects you drive them.
You understand GMP OSD manufacturing and complex validation environments.
And youre ready to take ownership of a critical tableting area revamp.
This is your opportunity to step into a Manager / Engineering role where your expertise in commissioning & qualification (C&Q) directly shapes manufacturing excellence.
You will lead the qualification activities for the revamping of a pharmaceutical Oral Solid Dosage (OSD) tableting manufacturing area
You will:
- Own Design Qualification FAT SAT Qualification Handover & Close-Out
- Drive commissioning and qualification of OSD process equipment & computerized systems
- Lead C&Q activities on capital projects on time and within budget
- Author and approve validation strategies protocols & reports
- Interface cross-functionally with engineering QA MS&T suppliers & contractors
- Support audits and health authority inspections as SME
Youll operate within a structured stage-gate project environment and influence across organizational boundaries
What You Bring
- Degree in Engineering or Science (Mechanical Chemical Life Sciences etc.
- 5 years in pharmaceutical validation ideally within OSD in GMP environments
- Experience managing complex capital projects
- Strong problem-solving and communication skills
- Experience with inspections and regulatory interactions
- Project & change management expertise
- English and French fluent
About this contract:
- Starting Date 01. April
- 6 Months
- 100 % on-Site
Why This Role
- Lead instead of follow
- Influence instead of execute only
- Deliver measurable impact within a high-standard GMP environment
- Strengthen your profile in capital project C&Q leadership
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