3 Senior CDMO Project Manager Jobs in Devens, MA
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VERANOVA is Hiring a Senior CDMO Project Manager Near Devens, MA
Company DescriptionVeranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation.
Job SummaryThe Senior Project Manager is responsible for driving all activities for key commercial production of exclusive products at the Veranova Devens manufacturing site. They are the primary interface for the customer on technical and project issues and work closely with the site General Manager, site Technology Manager, Business Development, and program core team to ensure the program is on time and on budget.
This is a hybrid role with three days onsite at our Devens, MA facility.
Principal Accountabilities
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice .
Job SummaryThe Senior Project Manager is responsible for driving all activities for key commercial production of exclusive products at the Veranova Devens manufacturing site. They are the primary interface for the customer on technical and project issues and work closely with the site General Manager, site Technology Manager, Business Development, and program core team to ensure the program is on time and on budget.
This is a hybrid role with three days onsite at our Devens, MA facility.
Principal Accountabilities
- Serves as the primary interface to commercial clients on technical and project issues. Ensures that each program milestone is delivered in line with agreed objectives. This may be one or more clients dependent upon the size of the program.
- Responsible for building strong relationships of trust and collaboration with the team, ensuring that the needs of the customer as well as the cross functional team are met.
- Partners with the Production Technology Manager to ensure the production schedule is maintained; assist with mitigating scheduling conflicts, and support manufacturing investigations.
- Directs, leads, and motivates a multi-disciplinary team and holds team members accountable to deliver results. Helps drive a culture of achievement and accountability within the teams.
- Responsible for identifying and solving complex problems across varying and multiple workstreams with inter-connected parts.
- Accountable for managing all program communication (i.e., weekly customer meetings, Quarterly Business Reviews, KPIs, project spend, presentations to the Leadership Team).
- Ensures that all key stakeholders are knowledgeable of program KPIs, plans, program status and decisions through regular reporting and communication.
- Works collaboratively with Business Development in addressing out of scope deliverables and preparing project proposals.
- BS in Chemistry, Chemical Engineering, or equivalent discipline.
- Must have CDMO industry experience
- Minimum of 6 years’ experience hands on process, analytical, or manufacturing experience.
- Minimum of 6 years’ experience managing large commercial programs for key clients.
- Experience collaborating with operations and executive management to drive profitability.
- Exceptional program communication experience is essential (verbal and written).
- Experience with facilitating weekly customer meetings, Quarterly Business Reviews, and presentations to the Leadership Team.
- Strong interpersonal skills with the ability to influence without authority, motivate with enthusiasm, and develop productive working relationships with key stakeholders.
- Ability to work effectively across all levels of the organization, including executive management.
- An understanding of cGMP’s as they relate to drug substance manufacturing referred.
- Experience with the regulatory aspects of the drug approval process preferred.
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice .
Job Summary
JOB TYPE
Full Time
SALARY
$126k-157k (estimate)
POST DATE
05/28/2024
EXPIRATION DATE
07/16/2024
WEBSITE
stiteler.net
HEADQUARTERS
Charleston, SC
SIZE
<25
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