What are the responsibilities and job description for the Vice President Quality Assurance position at Clevelcrossing?
The Swiss based
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Group is a public, innovation-driven company specializing in the development and manufacturing of pepTides and oligonucleoTides. As a full service provider
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offers products for clinical development and commercial applications as well as a comprehensive catalog and exclusive custom synthesis. With 50 years of experience and subsidiaries in Switzerland, the United States, the United Kingdom and Japan,
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is the partner of choice for the biotech and pharma industry worldwide.
While professional experience and qualifications are key for this role, make sure to check you have the preferable soft skills before applying if required.
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Leading Partner in Tides
In order to continue our organic growth, we are constantly looking for talent.
Your Responsibilities
The Vice President of Quality Assurance, as a member of the
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Americas, Inc. Executive Committee, fulfills a critical role in intermediate and active pharmaceutical ingredient manufacturing operations. This individual oversees the Quality Assurance teams at both the Torrance and Vista sites, ensuring compliance with all the laws, regulations, and guidance applicable to pharmaceutical drug manufacturing together with the fulfillment of
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s business objectives.
Your Tasks
Lead, manage and develop the Quality Assurance teams at Torrance and Vista
Ensure compliance with all pharmaceutical drug manufacturing laws, regulations, and guidance, while assuring fulfillment of
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s business objectives
Take an active role in achieving expected financial performance, including management of costs and diligent use of resources, as well as engage in budgeting and cost accounting activities
Establish priorities and set goals for the Quality Assurance teams
Guide the directors and managers of the Quality Assurance teams, and cultivate their ability to meet business needs and to fulfill quality and compliance requirements
Identify and develop high-performance and high-potential individuals, actively supporting the development of their careers at
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Assure the Quality Assurance team is ready to support growth of the business, with a pipeline of needed skillsets and potential successors for managerial and leadership positions within the
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organization.
Provide leadership and guidance throughout the organization as a primary champion of GMP and pharmaceutical regulatory compliance
Ensure responsiveness to customer inquiries and requests, contributing to timely and effective responses to customers RFP’s for projects and services
Contribute to negotiation of quality agreements with customers, suppliers, and service providers
Stay abreast of developing GMP and other regulatory requirements and pursue continuous improvement throughout the organization
Take an active role in harmonizing and optimizing processes between the different
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sites, particularly between Torrance and Vista
Your Profile
Ph.D. Degree in science related field with a minimum of 5 years industry experience or Master’s Degree in science related field with a minimum of 8 years industry experience
Minimum of 10 years overall experience with 5 years of managerial experience in the pharmaceutical or medical device industry
Knowledge of GMP for APIs and applicable FDA regulations
Excellent written and oral communication skills
PC proficient with ability to efficiently and productively use Microsoft Word, Excel and PowerPoint
Ability to effectively organize, multitask, and work in a fast-paced, deadline driven work environment
Ability to lead, motivate and mentor others
Ability to communicate in a proactive and solution-focused manner, including keeping management aware of potential issues
Detail oriented with the ability to troubleshoot and resolve problems
Ability to work independently and manage one’s time
Communicate effectively and ability to function well in a team environment
Ability and willingness to be physically present at both the Torrance and Vista sites on a weekly basis
Preferred
Experience working at a CMO
Technical experience in drug substance manufacturing
Candidates for positions as US employees of
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Americas, Inc. (“Company”) must be in the process of or fully vaccinated against the COVID-19 virus and provide the Company with proof of vaccination as a condition of employment, except for U.S. employees who request and qualify under applicable law for disability and religious accommodation from the COVID-19 vaccine mandate. The Company is an equal opportunity employer and provides employment opportunities and makes employment decisions without regard to an individual’s disability, religion or on any other basis prohibited by law.
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