Manager, Quality Operations

Curia Aalborg ApS; New York (NY); On-site; USD 106,000 - 137,000; Full time

Benefits offered by this job

Generous benefits

Paid training

Career advancement

Education reimbursement

401K with matching

Learning platform

Job summary

Curia is seeking a Manager, Quality Operations in Rensselaer, NY to oversee conditions and activities in the API manufacturing areas to ensure cGMP compliance and lead the disposition team. This role requires hands-on leadership and cross-functional collaboration with site departments.

You will partner with site stakeholders to maintain data integrity, drive continuous improvement, and support batch record reviews and deviations management, while reporting metrics to site management.

Qualifications

• Bachelor's or Master's degree in Microbiology, Chemistry or related field.
• 8–10 years of GMP experience in FDA-regulated pharma with 2 years supervisory experience.
• Strong background in deviations, batch review and disposition.

Responsibilities

• Oversee quality operations in API manufacturing areas to ensure cGMP compliance.
• Lead disposition program and real-time batch record reviews.
• Collaborate cross-functionally with site departments and management.
• Maintain data integrity principles across the site.
• Escalate manufacturing quality issues through the NTM process.
• Develop leading indicator metrics for quality oversight.

Education

Bachelor's Degree in Microbiology, Chemistry or related field

Master's Degree in Microbiology, Chemistry or related field

Job description

Manager, Quality Operations in Rensselaer, NY

Build your future at Curia, where our work has the power to save lives

Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life‑saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives.

We proudly offer

• Generous benefit options (eligible first day of employment)
• Paid training, vacation and holidays (vacation accrual begins on first day of employment)
• Career advancement opportunities
• Education reimbursement
• 401K program with matching contributions
• Learning platform
• And more!

The Quality Operations Manager is responsible for oversight of the conditions and activities in the API manufacturing areas to ensure continual compliance with cGMP and also oversee disposition team. This position requires expertise in all aspects of manufacturing of APIs, ability to work hands on, strong leadership skills, and the ability to collaborate in a cross‑functional environment. The individual will work closely with all departments in the manufacturing environment and will report metrics to site management on a regular basis.

Responsibilities

• Assist the Site Quality Head with the development, implementation, and strict adherence to the quality assurance program
• Develop and/or review standards, policies, and procedures for all functions and departments involved with or related to the production and testing of all materials
• Ensures there is a robust batch disposition program including a holistic batch record review training for Ops and Quality
• Ensure that the data integrity principles are understood and implemented consistently throughout the site
• Ensures all operational deviations are appropriately investigated, product impact determined and documented within the Quality System prior to disposition
• Responsible to oversee site walkthrough program, identify key themes of improvement and drive improvement
• Responsible for developing and maintaining real time batch record review program in place
• Ensure there is a robust cleaning and sanitization program in place
• Develops and maintains a robust disposition review process involving all key stake holders, drives accountability for RFT and Yield to Release metrics
• Review and approve all major deviations initiated for manufacturing activities
• Partner with site stakeholders to achieve and maintain operational excellence, site quality compliance and a strong, site‑wide quality culture while achieving the site business goals. This includes also leading and supporting site‑wide cGMP training activities
• Communicate effectively with internal and external customers making sure that the Curia values and business goals are consistently achieved
• Ensure a robust line clearance process is in place and adhered
• Will act as an interface with customers for any batch record related queries, manufacturing deviations and yield to release data
• Ensures, any manufacturing quality issues are promptly escalated through NTM process
• Develop and maintain leading indicator metrics for good quality oversight on the floor

Qualifications

• Bachelor's Degree in Microbiology, Chemistry or related field
• Minimum 8 -10 years of related industrial GMP experience in an FDA-regulated pharmaceutical environment, including 2 years' supervisory experience, OR
• Master's Degree in Microbiology, Chemistry or related field with minimum 3 years of related industrial GMP experience in an FDA-regulated pharmaceutical environment, including 2 years' supervisory experience
• Strong background in deviations, batch review and disposition

Other Qualifications

• Must pass a background check
• Must pass a drug screen
• May be required to pass Occupational Health Screening

Preferred

• Advanced degree in related field
• Prior work experience in a CMO

Pay Range: $106,000-$137,000

Education, experience, location and tenure may be considered along with internal equity when job offers are extended.

Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regar