Those who join Emergent BioSolutions feel a sense of ownership about their future. You will excel in an environment characterized by respect, innovation and growth opportunities. Here, you will join passionate professionals who advance their scientific, technical and professional skills to develop products designed-to protect life.

JOB SUMMARY

Reporting to the Senior Manager, Product Quality, this is a senior position requiring significant expertise/specialization in QA area with responsibility for day-to-day implementation of Quality Systems and Compliance functions appropriate for Emergent (EBSI) combination product(s) (devices).

The role is responsible for (1) QA lead for internal and external projects (2) independent oversight of commercial manufacture in compliance with Good Manufacturing Practice (GMP) requirements (3) executing Quality Management System requirements in support of commercial and developmental programs (4) ensuring the realization of industry best practices for GxP and (5) serving as quality approval proxy as required

This position is responsible for performing various functions as an owner, reviewer and/or approver. These functions include deviations, change controls, CAPAs, Complaints, Quality Risk Management validation and transfer protocols reports, trend evaluation and reporting, technical review design of history files (and its supporting documentation), review of critical procedures and processes, lead process changes and new product introduction, assist with regulatory responses, and develop and implement process improvements.

ESSENTIAL FUNCTIONS
Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions.

Individual will be assigned the responsibility for QA product/client relations and support while working with the client and different teams at the site. Oversight of quality systems as they relate to the multiple product/client and processes
Individual will be liaison between Quality Assurance and other departments to ensure Quality Assurance commitments are completed and to identify areas to improve data trends or process/ product outcomes. They will operate in a cohesive fashion
Must be capable to work independently and strategically to ensure day¬ to-day activities are carried out in support of the business goals
Quality oversight, with management support of external manufacturing, warehousing operations, validation, verification, and quality control of combination product(s) (devices) at Emergent
Responsible for product release, including batch documentation review, management of changes, complaints, deviations, validations, and product annual reviews to ensure completeness, accuracy, and compliance
Lead or assist in continuous improvement projects as assigned. Interacts with senior leadership, direct manager, peers, departmental or non-departmental personnel, internal customers, external clients and other cross functional peers across Emergent to gain alignment on sound quality decisions
Perform, review and approve risk assessments and propose risk mitigations and or corrective/preventive actions to reduce process/ product variation as part of the Quality Risk Management program
Lead Implementation of appropriate CAPA or risk mitigations for Quality related items
QA oversight of Validation activities including reviewing and approving validation (including Continued Process Verification (CPV)) and stability protocols and reports
QA oversight of product related stability activities including new and routine annual requirements
Performing review of Design History Files (DHF) for combination products and relevant supporting documentation
Write and implement Quality Plans (where appropriate) to ensure compliance to QMS
Trend evaluation and reporting and SPC analysis of trends to determine (when possible) proactive approaches to advert future quality issues with process/ product.
Annual product review generation, review and approval
Technical review and approval of critical SOPs and processes
Coordinate and work with Project Managers and Technical Transfer personnel on process changes and new product introduction
Support design and development activities with combination products
Quality oversight of Regulatory Affairs activities including with regulatory submissions
Developing and implementing process improvements

Other:

Participates in and lead Quality Assurance Process Improvement Teams
Participates in and lead inspection readiness, audits and regulatory inspections as needed
Provide guidance for ISO 13485 and ISO 14971 requirements for combination products
Other assigned responsibilities as established by Manager

Supervisory Responsibilities:

No direct reports but routinely act as a QA lead and provide guidance to other departmental personnel
Routinely represents QA management in direct discussions with clients.

The above statements are intended to describe the nature of work performed by those in this job and are not an exhaustive list of all duties. Nothing in this job description restricts managements right to assign or reassign duties and responsibilities to this job at any time which reflects management’s assignment of essential functions.

MINIMUM EDUCATION, EXPERIENCE, SKILLS

Bachelors of Science (Pharmacy, Chemistry, Microbiology or related field), Advanced degree (M.S., Ph.D., MBA) preferred. Minimum 8 years of cGMP experience including Manufacturing and Quality Assurance experience
2-3 years in a senior or leadership Quality Assurance role
Qualified Person experience preferable
Broad experience and thorough understanding of international GMP Quality Management System regulations for drugs and devices including ICH Guidelines, ISO 13485, FDA 21 CFR Parts 210, 211 and 820, European (EudraLex Volume 4) and Health Canada GMPs
Demonstrated experience owning, driving and leading Quality initiatives
Demonstrated experience working independently with internal and external partners
Experience as process owner for deviation, CAPA, change management, and self-inspection programs as well as managing 3rd party audits and inspections is preferable. Experience with quality risk management will be considered an asset.
Must be a self-starter with ability to work independently
Ability to manage and deliver multiple priorities, projects and tasks in a dynamic environment using own initiative with little instruction on routine work, general instructions on new assignments
Ability to operate efficiently in a complex matrix organization and international environment making sound decisions regarding compliance-related issues with minimal supervision.
Strong mature leadership and interpersonal influencing skills showing personal/departmental accountability and responsibility.
Strong verbal and written communication skills with well-structured communication and presentation ability to various audience levels.
Ability to lead Change Management activities and strong Project Management knowledge
Excellent communication skills, both written and verbal
Ability to exercise judgment to determine appropriate corrective actions
Ability to exercise judgment for defined practices and policies in selecting methods and techniques for obtaining solutions
Ability to use computer programs

There are physical/mental demands and work environment characteristics that must be met by an individual to successfully perform the essential functions of the job. This information is available upon request from the candidate.

As part of our team, you'll join talented and inspiring colleagues whose sense of purpose complements your own. We offer highly diverse career opportunities, a supportive culture, competitive salaries, flexible work arrangements and an extensive benefits package. Information submitted will be used by Emergent BioSolutions for activities related to your prospective employment. Emergent BioSolutions respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy.

Specialist II, Quality Assurance

Benefits

Job Description