Rise Technical Recruitment Limited
Process Development Manager (Pharma)
Rise Technical Recruitment Limited, Newtown, Pennsylvania, United States, 18940
Process Development Manager (Pharma)
Newtown, PA
$120,000 - $150,000
+ 401k match, annual pay-rises, PTO, tuition reimbursement, flexible holidays & many more excellent company benefits!
Are you ready to take ownership of technical operations within a growing pharmaceutical manufacturer?
Do you want to lead a team driving documentation, process development, and validation for FDA-approved oral solid products?
This is a leadership opportunity for someone who thrives at the intersection of R&D, Manufacturing, and Quality, taking the lead on the documentation, protocols, and technical reports that keep production running smoothly and compliantly.
You will play a key role in supporting new product introduction, process improvements, and regulatory submissions, while managing a capable team and shaping the technical backbone of the site.
You will join a business that values experience and initiative, somewhere you can step straight in, make an impact, and have real visibility with senior leadership.
If you have built your career in oral solid dosage and are looking for a genuine next step with authority, stability, and a team behind you, this role is not to be missed.
The Role:
Lead the technical services function for oral solid manufacturing projects
Manage documentation, validation, and process reports across departments
Support new product transfer and continuous improvement initiatives
Partner with R&D, Quality, and Manufacturing to ensure compliance and timely execution
The Person:
Bachelor's degree in Chemistry, Chemical Engineering, or Pharmaceutical Sciences
Hands‑on background in oral solid dosage manufacturing (tablets, capsules, etc.)
Experience leading or mentoring within Technical Services, R&D, or Manufacturing
Confident communicator with excellent organizational and documentation skills
#J-18808-Ljbffr
Newtown, PA
$120,000 - $150,000
+ 401k match, annual pay-rises, PTO, tuition reimbursement, flexible holidays & many more excellent company benefits!
Are you ready to take ownership of technical operations within a growing pharmaceutical manufacturer?
Do you want to lead a team driving documentation, process development, and validation for FDA-approved oral solid products?
This is a leadership opportunity for someone who thrives at the intersection of R&D, Manufacturing, and Quality, taking the lead on the documentation, protocols, and technical reports that keep production running smoothly and compliantly.
You will play a key role in supporting new product introduction, process improvements, and regulatory submissions, while managing a capable team and shaping the technical backbone of the site.
You will join a business that values experience and initiative, somewhere you can step straight in, make an impact, and have real visibility with senior leadership.
If you have built your career in oral solid dosage and are looking for a genuine next step with authority, stability, and a team behind you, this role is not to be missed.
The Role:
Lead the technical services function for oral solid manufacturing projects
Manage documentation, validation, and process reports across departments
Support new product transfer and continuous improvement initiatives
Partner with R&D, Quality, and Manufacturing to ensure compliance and timely execution
The Person:
Bachelor's degree in Chemistry, Chemical Engineering, or Pharmaceutical Sciences
Hands‑on background in oral solid dosage manufacturing (tablets, capsules, etc.)
Experience leading or mentoring within Technical Services, R&D, or Manufacturing
Confident communicator with excellent organizational and documentation skills
#J-18808-Ljbffr