Pfizer - Good health is vital to all of us, and finding sustainable
solutions to the most pressing health care challenges of our world
cannot wait. That's why we at Pfizer are committed to applying science
and our global resources to improve health and well-being at every stage
of life. We strive to provide access to safe, effective and affordable
medicines and related health care services to the people who need them.
PROCESS SAFETY SENIOR MANAGER
ROLE DESCRIPTION
Provide
global process safety expert support to Pfizer Global Supply’s internal
and external supply network, to ensure key risks are appropriately
managed and compliance is maintained.
RESPONSIBILITIES
At
the direction of the Director/Leader Process Safety, establishes
effective global processes and guidance to identify evaluate and address
process safety risks at Pfizer locations.
Supports Pfizer locations through expert process safety mentoring, training and counselling.
Supports
PGS and R&D stakeholders by providing expert process safety
assistance in selection and development of key suppliers.
Leads or supports process safety risk assessments for site capital projects and new process introduction.
Participates in subject matter spe...t audits and assessments of Pfizer sites and suppliers.
Develops and delivers training programs in process safety topics.
QUALIFICATIONS
Undergraduate Degree in Chemical engineering.
Minimum 7 to 10 years relevant process safety experience in chemical, biological or drug product manufacturing.
Risk
assessment/risk management knowledge with the ability to explain risk
profiles and associated risk mitigation practices, therefore influencing
others to comply.
Active membership in at least one relevant professional body.
Good oral, written and interpersonal communications skills and the ability to work across multiple countries and cultures.
Ability to quickly assess EHS risks and consider business implications.
Non-standard Work Schedule, Travel or Environment Requirements:
Required to travel local and/or internationally around 30%.
Ability to periodically work flexible hours to accommodate international time zones.
Note: When the page opens, enter the Job Opening ID (1030728) in the Job ID Box, and click "Search"
REGIONAL QO LEADER, ASEPTIC ASIA
ROLE DESCRIPTION
Reporting
to the VP Aseptic Quality Operations, the Regional QO Leader Aseptic
Asia provides strategic and tactical leadership to the site quality
organizations for three global aseptic manufacturing sites:
Dalian, China;
WuXi, China
Perth, Australia.
The
Regional QO Leader Aseptic Asia ensures that Pfizer Quality Standards
and cGMP requirements for manufacture of aseptic products are
implemented and consistently followed.
The position will be a member
of the Aseptic Quality Leadership Team, and will be responsible for
actively developing and contributing to network initiatives.
RESPONSIBILITIES
GENERAL SCOPE OF RESPONSIBILITIES:
Provide
strategic and tactical leadership to Aseptic site QO units in Asia on
all matters related to quality and cGMP compliance.
Ensure consistency in achieving product quality and cGMP compliance across multiple manufacturing sites and global markets.
Ensure
that Pfizer Quality Standards and relevant drug substance/finished drug
product requirements for manufacture of Aseptic products are
implemented and consistently followed to establish site cGMP compliance.
Ensure efficient and effective resolution of critical product quality/cGMP compliance issues.
Provide support and guidance for major investigations and product quality and cGMP compliance issues as they occur.
Work closely with the Aseptic Operating Unit QO Leader to make decisions on Aseptic site quality and cGMP compliance issues.
Provides facilitation for key quality issues in preparation for AQRT’s.
Provide
support to sites where necessary for regulatory inspections (planning,
execution and closeout) including support in preparation of responses to
findings.
Evaluate site quality and cGMP compliance risk,
communicate risk and implement mitigation plans to reduce the risk to
Pfizer and to Pfizer’s customers.
Enable quality strategy and drive changes to support manufacturing product transfers associated with the sites.
Interface with relevant functions (Regulatory, GCMC, other PGS site quality, supply chain, procurement, etc.).
Endorse site QO budgets, staffing plans, QO organization and hiring/development of colleagues for key site QO positions.
Provide support and GMP review for major site capital projects.
Visit
sites to review organization, product issues, facilities, capital
projects, audit status, regulatory inspection status, complaints,
operations and related topics.
Provide performance management and development for direct reports (Site QO leaders).
Collaborates with counterparts in Regulatory, Manufacturing, Legal, Supply Chain and other groups on projects and issues.
Collaborates with site QO Center Leadership, Site Leaders and QO OpU Leaders on site quality initiatives and issues.
Ensuring
that sites monitor, trend and report Quality metrics in a highly
disciplined way to drive continuous improvement and ensure a compliant
state is maintained
Fostering a culture where innovation, science and risk-based quality and colleague engagement thrive.
Active member of the Aseptic Quality Forum
The
candidate must have a thorough understanding of quality systems and
global cGMP compliance requirements as they apply to commercial
manufacturing. Expertise and substantial experience in manufacturing
and/or quality oversight is required. Demonstrated experience in quality
decision-making in a highly complex environment is essential.
Additionally,
the successful candidate must be flexible with regard to changing and
conflicting priorities, able to easily shift gears in terms of behavior
and attitude in response to ambiguity and the needs of the situation.
Candidates
will need the ability to address obstacles with energy and
determination and exhibit commitment to change and passion for Pfizer's
best interests. Candidates should have the leadership skills necessary
to engage, influence and motivate colleagues at all levels in the
organization at all times, especially during periods of intense change.
QUALIFICATIONS
MINIMUM QUALIFICATION REQUIREMENTS:
EDUCATION:
BSc
in Chemistry, Microbiology, Engineering or related scientific field;
MSc, MBA or PhD in Pharmaceutical related field preferable.
EXPERIENCE:
Proven
leadership/facilitation skills and being able to involve several levels
of an organization to successfully meet the objectives.
Experience
working with complex organizational and ability to work across functions
and with all levels of the organization where the incumbent may not
have direct authority.
Strong organizing and planning skills and a high sense of urgency.
Demonstrated change agility to successfully manage high degree of complexity and priorities.
Experienced with Quality Risk Management tools.
Demonstrated ability to operate with agility in a highly diverse environment.
Proven
ability to work long-distance with direct reports and supervisor
maintaining effective communication across multiple levels of the
organization across diverse cultures.
Demonstrated excellence in developing & managing effective teams.
Minimum
15 years of relevant experience, including 10 years experience in the
pharmaceuticals and consumer industries, performing manufacturing,
technical services, research or QA functions.
Minimum 10 years QA-related experience is necessary and 5 years of site Quality management experience is preferred.
Demonstrated
knowledge of US, European and global cGMPs, compliance issues,
inspectional trends, industry quality assurance practices and systems,
and personal management skills.
Must be fluent in English and Mandarin.
The
candidate must have had center or site operational experience in a
GMP-regulated environment with a proven track record of effectively
supporting a moderate to large size quality unit.
The ability to
communicate effectively at all levels of the organization is essential.
Willingness to be inclusive and embrace team principles is necessary.
The
candidate must be self-motivated and flexible with the ability to work
effectively in a dynamic, problem-solving environment.
Note: When the page opens, enter the Job Opening ID (1027486) in the Job ID Box, and click "Search"
GCO DIRECTOR, KNOWLEDGE ARCHITECTURE
ROLE DESCRIPTION
Develop
and implement completely novel global Commercial Operations, Knowledge,
& Portal/Platforms Management practice, process, workflows,
operational data analytics and reporting, and technology infrastructures
within global Business Analytics and Insights (BAI) operation and
Global Commercial Operations (GCO).
Directly lead and contribute to
global operating model transformation, speed to market, significant
reductions in budget and efficiencies, and operational long-range value
delivery at enterprise levels for both Global Commercial Operations
(GCO) and Business Analytics and Insights (BAI).
This is a virtual role based in Europe, preferred location Walton Oaks, UK.
JOB FOCUS
Are
you energized by leading efforts in business transformation that have
direct impact on business performance through strategically enhanced
analytic and commercial operations service delivery? Are you motivated
by working with talented people from countries and cultures across the
globe, and by having opportunity to work across different functional
areas of expertise to execute new business models and ways of working
through the application of digital execution, virtual collaboration,
social technology, analytics, reporting, and digital knowledge
management?
An exciting opportunity has arisen to join Pfizer
Global Commercial Operations, Knowledge and Operations Knowledge
Architecture Center of Excellence. The global department is primarily
focused on leading business transformation efforts that focus on
launching and enabling global platforms and strengthening the operating
models of internal commercial services and analytics organizations at
Pfizer to meet the changing needs of business unit clients. The
available role is for an experienced lead with executive presence who
will be responsible for global projects with an EU regional emphasis in
stakeholder management and execution. Fundamental to the role is the
ability to influence without authority, lead change management, and
understand key stakeholders (business unit clients, analytics
colleagues, commercial operations colleagues) and their business
challenges in the EU markets at Pfizer. This opportunity manages highly
visible efforts with significant exposure to executive senior leaders at
Pfizer.
JOB DUTIES
Leads assessment,
research, design, development, execution, and measurement of new, GCO
and BAI portals/platforms, operations, and knowledge management
strategies globally and within regions.
Ideates, identifies,
designs, creates, implements and sustains operations & knowledge
management methods, tools, processes, and solutions for global GCO and
BAI implementation.
Executes responsibilities across program
development & management, technical & functional delivery, and
business partnership domains with senior GCO and Business Unit (BU)
stakeholders in one of the newest GCO/BAI functional areas of
exceptional complexity requiring a high degree of ingenuity, creativity,
business, analytic, operations, digital strategy expertise, and
influence.
Deploys significant leadership, influence, and
transformation management capability in unusually complex interactions
across multiple geographies, countries, and across GCO and BAI
matricies.
Executes both independently and as part of a solid line and complex matrix reporting team.
Acts
independently to uncover and resolve issues and create process and
technology solutions associated with the development and implementation
of operational programs, knowledge and expertise sharing, workflow,
tools, and reporting development, and works as part of a complex,
broader team.
RESPONSIBILITIES
Prime
consultant/implementer and Operations/Knowledge leader to GCO and BAI
regional and global teams to ideate, identify, design, create, implement
and sustain critical operating and knowledge management solutions
Collaboratively
build a knowledge management operating model to transform GCO and BAI
operations across the domains of people, process, and technology with
scalable frameworks
Provide global and regional expertise, insights,
and influence on knowledge asset management (understand and influence
workflow, develop knowledge maps, assess flow needs, and influence
change to drive greater efficiency, effectiveness, re-use, hard dollar
savings and value from BAI operations and GCO ); viewed as expert in
field within Pfizer
Plan and lead KA communication and transformation strategy and efforts globally and within region
Co-lead
and influence KA Collaboration initiatives, Communities of Practice
[CoP], Knowledge exchange comprised of all levels of GCO and BAI
colleagues with senior GCO, BAI, and BU functional executives
Develop, track, measure, and insight driven reporting of GCO and BAI KA KPIs to drive influence
Ensure
Global Knowledge Management solutions drive global transformation and
align with global and regional business partner requirements
Partner
with senior GCO & BAI leaders, Procurement, BT and external
vendors/suppliers to scope, develop, and implement sophisticated and
highly advanced, new KA processes and technology applications to
accomplish long-range GCO and BAI objectives
Identifies, designs, and
implements transformational KA approaches requiring significant senior
leadership, organizational, analytic and reporting, and operational
alignment and influence. Attuned to the technology enabled knowledge
management and information sharing trends within and outside the pharma
sector
QUALIFICATIONS
Educational qualification, MA/MS/MBA in Management, Marketing Research, Statistics, Operations, IT, Info Science required
Certification(s):
Knowledge Management, Technology, Statistics, Change Management,
Consulting, Business Process Management preferred
Proven seasoned experience in Technology, Consulting, BPO, Operations, Analytics
Critical competencies
Knowledge/Information Management
Analytics
Operations
Business Process & Workflow
Technology
Business Transformation
Learning Agility
Influence
Cross-cultural Awareness & Engagement
Business Partnership
CLICK HERE TO APPLY
Note: When the page opens, enter the Job Opening ID (1030728) in the Job ID Box, and click "Search"
DUE DATE: 29 April, 2016
Job Opportunities at Pfizer Nigeria
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