Hovione
is an independent family owned international group of companies.
From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated
Contract Development and Manufacturing Company
dedicated to helping
Pharmaceutical
Customers bring new and off-patent drugs to market.
Our people are the main asset for our continued success.
Reaching over **** team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites.
Working at Hovione means reaching for
innovation
and
excellence
in everything we do: for our clients, our partners and, above all, our patients.
That is why we are In it for life.
Responsibilities
Guarantees cGMP
compliance
in all activities and systems related to Projects and Products execution.
Assures that working practices are streamlined and aligned with the actual needs of each project.
Implements policies, procedures and methods to evaluate and to continuously improve the quality of products and operations throughout the products lifecycle.
Provides global supplier qualification services in support of new product introduction and existing products.
Collaborates with suppliers and Procurement to assure the quality of their products, materials, components and/or operations.
Rigorously, accurately, efficiently and professionally manage all quality activities for the assigned projects and / or products in accordance with applicable cGMP, quality operational standards / procedures and legal regulations, ensuring the site is always "audit ready"
Promote the importance of high-quality levels and the importance of a continuous improvement culture in relevant company activities
Act as a catalyst for change and improvement in performance/quality
Provide an example of professionalism
Assigned projects may relate to any of the following (non-exhaustive) areas: Raw Materials, Suppliers, Specifications, Production Processes, Change Control, Deviations, Quality agreements, Qualification and Validation, Stability Programs, Batch Release, Equipment Cleaning, Client Audits, Internal Audits, Customer Complaints, Customer requirements, PQR
Efficiently, accurately and reliably ensure that project and / or product activities are delivered in compliance with cGMP requirements and maintenance of the company Quality Management System is assured
Manage and participate in Quality Product key activities for the assigned product / projects, and introduction of new products; including (but not limited to) preparation, review and approval of auxiliary documentation, protocols and quality related reports
Prepare for and support internal and external site audits and inspections, conducting regular reviews and periodically following-up action plans as necessary
Ensure inspection readiness in work completed and Act in an advisory capacity for all internal and external site audits
Periodic follow-up of ongoing deviations and Change Controls (PdAs) to assure timely closure of deviations and approval of PdAs, as appropriate
Prepares SOPs, department
IOPs
, quality related reports and change control documents (PdAs) as required and appropriate
Review process master
documentation
, revision of executed batch documentation and product specifications as required and appropriate
Ensures that
SOPs
and IOPs are up to date, compliant and supports efficient production
Review regulatory documentation and co-ordination of site documentation to support regulatory requirements
Authorize the usage of production equipment/utilities when qualification required
Solve challenges related to compliance problems by providing collaborative and timely support to all areas and departments, escalating as required
Ensure the effective and proactive flow of information between stakeholders, representing the team as appropriate
To assure and promote compliance on Health, Safety and Environment in the area and activities for which is responsible, or in which participates
To maintain a regular presence on manufacturing floor, providing on-the-job support, developing a sense of collaboration with operational areas and performing a general oversight of activities, as required.
Accurately use and maintain all information systems
Support the generation / reporting of KPIs for the team
Develop and accumulate strong QA expertise, sharing knowledge of new developments and methodologies within the area
Co-ordinate and assist with the analysis and investigation of customer complaints that may arise, ensuring all complaints are investigated and closed out within specified timeframes
Be an advocate for safe operating and high-quality performance, alerting ascending colleagues to any potential risks, discrepancies, deviations or non-conformance in accordance with Hovione internal procedures, suggesting optimizations or improvements, including those that have the potential to mitigate unnecessary complexity
Apply and develop knowledge of Quality Assurance and participate in area processes, procedures and projects with the guidance of more senior colleagues
Perform to ensure all assigned tasks are delivered on time, safely, efficiently, reliably and in a cost-effective manner
Execute professional activities in compliance with GMP and HSE guidelines, internal and external requirements as well as promote the implementation and maintenance of Hovione ´s policies, systems and procedures (COPs, HBR, SOPs and others)
Undertake any additional tasks commensurate with the role as and when required
Carry out assigned tasks and duties in a safe manner, in accordance with instructions, and to comply with environmental, health & safety rules/procedures, regulations and codes of practice.
Qualifications
University, or equivalent, qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar scientific field (mandatory)
Requires educational / training experience in a
QA GMP
environment within the
Pharmaceutical
Industry (desirable)
Experience of working in a GMP operational environment (desirable)
Training and experience of GMP standards (desirable)
Experience of working with
Regulatory Affairs
and a basic knowledge of the function (desirable)
Knowledge of
GMP
practices
Fluency in
English
is a requirement
Computer literate with good working knowledge of the MS Office package
Good
documentation
skills and attention to detail
Must have the Knowledge, Experience and Skills to conduct their tasks in accordance with the rules and procedures set down
Hovione is a proud Equal Opportunity Employer
Inclusion
and
diversity
are key to us.
At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect.
We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity.