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Senior Specialist, External Quality Operations

Mallinckrodt Pharmaceuticals

Remote · USFull-time$80–129K/yrSeen todaySeen in employer's feed today

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At a glance

Compensation
$80–129K/yr
Location
Remote · US
Schedule
Full-time
Work Authorization
Not specified

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Job overview

The Senior Specialist, External Quality Operations supports externally manufactured pharmaceutical and biopharmaceutical products for Keenova. The role manages relationships with contract manufacturing organizations (CMOs) and cross-functional teams, oversees quality activities, and escalates issues to management. It also supports batch review and release, supplier governance, stability programs, audits, and quality-system projects. The position is fully remote, with limited travel as needed.

Skills & qualifications

RequiredNice to have

Skills

Quality SystemsDeviation ManagementChange ControlTrainingSupplier QualificationDocument Management SystemsCGMP RequirementsGDPISO 13485

Qualifications

Bachelor's in Scientific Discipline5+ Years Quality Specialist Experience

Full job description

Fully Remote

Bridgewater, NJ

Malvern, PA

Full time

JR000016029

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 Review

  • Preparation, 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 Governance

  • Management 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 Deputation

  • Quality 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 Program

  • Protocol review and approval

  • Data review and management

  • Audits

  • Drive the audit readiness program to always ensure audit compliance

  • Quality/QMS Projects

  • As 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 (https://www.keenova.com/careers/)

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 .

At Keenova, we know that we contribute to something that matters because we make quality products that impact patient lives. Our dynamic work environment provides unique experiences for employees to grow and develop.

Invest in your own career with Keenova and let’s do something dynamic together.

Keenova provides equal employment opportunities to applicants and employees without regard to race; color; gender; gender identity; sexual orientation; religions practices and observances; national origin; pregnancy, childbirth, or related medical conditions; protected veteran status; disability; or any other category protected by law.

Additional information on Keenova’s hiring practices may be found by clicking (https://secure.compliance360.com/ext/ESLKi3LFkqY=)

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