What are the responsibilities and job description for the Vice President Quality Control 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.
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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 Control, 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 Control teams at both the Torrance and Vista sites, ensuring that all laboratory operations support the manufacturing operations and
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s business objectives, and that the laboratory operations comply with all the laws, regulations, and guidance applicable to pharmaceutical drug manufacturing.
Your Tasks
Lead, manage and develop the Quality Control teams at Torrance and Vista
Ensure that all laboratory operations support the manufacturing operations and
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s business objectives, including technical requirements and capabilities.
Ensure that all laboratory operations comply with pharmaceutical drug manufacturing laws, regulations, and guidance
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 Control teams
Guide the directors and managers of the Quality Control teams, and cultivate their ability to meet business needs, as well as fulfill technical 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 Control 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 analytical science and technology
Ensure responsiveness to customer inquiries and requests, contributing to timely and effective responses to customers RFP’s for projects and services
Stay abreast of developing analytical science and technology, championing the continuous improvement of analytical capabilities to advance
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s business
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 and 5 years of analytical laboratory experience in the pharmaceutical industry
Knowledge of GMP for drugs and 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
Ph.D. degree in Analytical Chemistry
Experience working at a CMO
Technical experience in drug substance analysis
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. An applicant who receives an offer of employment from the Company for a position as a U.S employee will be required to provide proof of vaccination status, or request and receive a disability or religious accommodation for which the applicant is entitled under applicable law, before their first day of employment or any later deadline specified by the Company in the offer letter. 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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