The posting
Job Title
Senior Specialist, External Quality Operations
Requisition
JR000016029 Senior Specialist, External Quality Operations (Open)
Location
Bridgewater, NJ
Additional Locations
Malvern, PA
Job Description Summary
The Senior Specialist, External Quality Operations supports externally manufactured products for Keenova with a product portfolio that includes pharmaceutical and biopharmaceutical products. The position is responsible for building, maintaining and managing the relationship with their counterparts at the CMO and cross-functional team members. The position is responsible for appropriate escalation to Manager/Director level management and above.
Job Description
Key Responsibilities:
- Batch ReviewPreparation, review and approval of CMO documentation for batch production Review of batch records, addressing discrepancies and escalating where required to management. Preparation of disposition and release certification for reviewed batch records.
- CMO GovernanceManagement and oversight of third-party supplier activities relating to the manufacture, packaging and testing of product. Regular telephone and email communication with CMOs to ensure timely manufacture and resolution of quality issues for product. Continuous monitoring of product and performance from CMOs.
- Quality Support and DeputationQuality record management; deviations, change controls, CAPAs Monitoring cold-chain transportation, for both qualification and routine CMO Maintenance Input into Technical Quality Agreements Post-launch support for quality activities in various countries, as needed Management of delegated projects
- Stability ProgramProtocol review and approval Data review and management
- AuditsDrive the audit readiness program to always ensure audit compliance
- Quality/QMS ProjectsAs required. Champion continuous improvement efforts for projects identified at the CMOs or within Keenova
Qualifications:
Education
Bachelor’s Degree in scientific discipline, preferred +5-7years’ experience working as a Quality Specialist.
Experience
Direct experience working with Quality Systems (deviations, change controls, training, supplier qualification and document management systems)
Preferred Skills
Knowledge of cGMP requirements for pharmaceutical manufacturing and knowledge of GDP and ISO 13485
Organizational Relationship/Scope:
Reports to: Senior Manager, External Quality Operations
Working Conditions:
This position works in a remote, office type environment. Limited travel as needed.
Keenova offers employees a Total Rewards package which includes competitive pay and benefits. To learn more about our Total Rewards benefits please visit: Keenova Careers | Serve and Grow with Purpose | Keenova
The expected base pay range for this position is $80k– $129k. Please note that base pay offered may vary depending on factors including job-related knowledge, skills, and experience.
This position is eligible for a bonus in accordance with the terms of the applicable program. Bonuses are awarded at the Company’s discretion.
Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
#LI-REMOTE
#LI-GN1
At Keenova, we believe that no one should be alone in their pursuit of better health. This purpose drives us as we pair quality therapeutics with human support—showing up in big moments and small to help patients find comfort and confidence.
We bring deep expertise and resolve to every therapeutic area we serve, including immunology, urology, men’s health, orthopedics, critical care, and pediatric endocrinology. We work with patients, care partners, and physicians to help them navigate healthcare system complexity and access therapies that make a meaningful difference.
We are Keenova—keen to solve, keen to serve. Learn more at www.keenova.com.



