Pharmaceutical Sourcing Contracts Manager - 100% Onsite
Job Description
Job Description
Job Title: Sourcing Contracts Manager – 100% Onsite
Job ID: 258
Job Length: 6 Months (Renewable)
Compensation: Up to $105/hr. W2
Location: Alameda, CA
Must have: relevant contract writing experience.
Budget/Financial accumen and Excel experience are major plus.
· 6 Month contract, onsite
· Core hours are 9 am – 3 pm
· This team starts in the early molecule development phase up to manufacturing
· This contracts team is w/in supply chain, and they issue out all of the manufacturing contracts.
· They are very specific to contract manufacturing orders
· The team size is 2 contract workers and this is the 3rd worker
· The load is 500 per year the team processes between 3 workers (high volume end to end)
· Strong contract writing experience
· Ariba experience nice to have
· Top skills to look for:
· Experience in drafting SOW’s and Change Orders
· Testing or raw materials contract drafting experience
· Will accept candidates with experience drafting CRO contracts
· Technical Skills: Ariba, SAP, finance software
· Pharma/Biopharma
· GxP nice to have
· Excel (nice to have)
· Reconciliations
· Key skills sets that would make someone successful:
· Quick learner
· Very organized
· Methodical thinking and not missing steps is important
· They have had lawyers and contract writers that are successful
· Legal background
SUMMARY/JOB PURPOSE:
Client is seeking a Sourcing Contract Manager to join the Pharmaceutical Operations and Supply Chain (PSC) Contracts team, reporting to the lead for Contracts & Budgets & Outsourcing. You will be responsible for supporting the team in contract management activities such as administering, writing and execution of the contracts related to PSC team. Where required, this role will be required to support and assist in escalations and resolution of payments that have been committed to a supplier. You will support and collaborate with various internal and external business teams to address contracts and financial requests.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
- Write/draft Statement of Works (SoWs) and Change Orders (COs) associated with low-risk contracts leveraging the Agiloft Legal Contract Lifecycle Management (CLM) system.
- Advise and troubleshoot on existing agreements under the guidance of the assigned team member.
- Attend cross functional internal and external supplier meetings to ensure supplier contract terms and conditions are adequately addressed and contracts executed in a timely manner.
- Responsible for the routing, tracking and facilitating the timely progress of contracts from point of submission into PSC through to execution.
- Responsible for the creation of purchase requisitions to enable the PSC business to commence work with the scope of the executed contract.
- Where required assist and support continuous improvement activities to improve the team’s ability to deliver value to the business.
- Facilitate and support budget forecasting and accrual activities where required.
- Provide support during any financial audits at month or quarterly close, as needed.
- As applicable per designated PSC business, maintain GxP and financial audit inspection readiness.
Education/Experience:
- BS/BA degree in related discipline and 3 years of related experience; or,
- Equivalent combination of education and experience.
- May require certification in assigned area.
Experience/The ideal for Successful Entry into the Job:
- The ideal candidate must have 1-2 years of direct working experiences in the life-sciences industries emphasis on contract drafting and sourcing negotiations with preferably outsource services such as contract manufacturers (CMOs), and/or clinical research testing laboratories.
- Collaboration with multi-functional teams.
- Working knowledge of clinical and commercial supply chain contract terms and conditions.
- Experience in negotiating and drafting complex contract manufacturing, biologics and clinical and commercial supply chain related agreements.
- Experience in SAP, Ariba, Tableau and management of both clinical and commercial supply chain, required.
- Experience in Contract Life Management (preferred Agiloft) system.
Knowledge/Skills:
- Some understanding of the contract management process, including tracking, negotiation, approval and signature processes.
- Working knowledge of the drug discovery and development process and ability to understand risks and requirements associated with pharmaceutical contracting preferred.
- Ability to work effectively across a variety of functional groups such as Commercial, Research and Development, Chemistry Manufacturing Controls (CMC), Clinical Studies and Finance,) and all levels of management.
- Ability to work with vendors and effectively negotiated commercial terms.
- Flexible and willing to learn new procedures and skill sets.
- Must be detail oriented and have strong organizational skills.
- Ability to handle multiple tasks simultaneously.
- Ability to prioritize; must be responsible and conscientious.
- Ability to work under pressure to meet specific deadlines.
- Dedication to quality and reliability in all work tasks.
- Excellent verbal and written communications skills.
TechData is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.
Job Type: Contract
Benefits:
- Dental insurance
- Health insurance
- Vision insurance
Experience:
- life-sciences : 3 years (Preferred)
- contract drafting : 3 years (Preferred)
- contract negotiations: 1 year (Preferred)
- outsource services : 1 year (Preferred)
- SAP: 1 year (Preferred)
- Ariba: 1 year (Preferred)
- Tableau: 1 year (Preferred)
- Contract Life Management (preferred Agiloft) systems: 1 year
Company Descriptionwww.techdataservice.com