TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is with one of our Biot ech clients who researches develop and commercializes drugs. The company focuses primarily on antiviral drugs used in the treatment of HIV, hepatitis B, hepatitis C, and influenza, including Harvoni and Sovaldi.
Position: Sr. Manager, Supply Chain
Location: Remote
Duration: 18 Months
Job Type: Contract
Work Type: Remote
Job Description
Purpose of Role:
Manage the long-term planning/execution (0 to 5 years) of manufacturing and packaging of finished goods globally utilizing internal and external finished good suppliers to ensure product availability for our patients.
Core Accountabilities
Ensuring product availability for our customers globally
Developing the Master Production Schedule for assigned product(s)/franchise(s)
Managing/Relationship
Success Measured By:
Work closely with all other functions; Manufacturing/R&D/Regulatory Affairs/Quality/API group/Clinical and Legal
Become the SME for Rapid Response planning and reporting
Service
Product availability; No stockouts
Production Plan Stability
Inventory Policy Adherence (Adherence to target, Obsolescent Inventory Value)
Driving efficiencies in drug product supply chain by identifying and eliminating waste in design and processes
Core Responsibilities
Responsible for midterm to long-term network MPS in monthly buckets (months 4 – 48)
Monitor demand forecast and manage inventory levels and ensure changes are aligned with network supply plans
Responsible for supply chain modeling to
Support budgeting process
Maintain planning parameters
Evaluate demand scenarios
Define sourcing strategies
Proposes safety stock levels throughout the drug product supply chain and works with API supply chain to ensure alignment of inventory across DP and API
Works with API supply chain to ensure long range API purchase plans support master production plan and resolves issues where they may arise
Responsible for mapping market/product demand to SKUs and DCs
Responsible for rough cut capacity planning and monthly evaluation against existing capacity models to ensure feasible plans
Leads and support monthly Supply and Management meeting meetings to present network MPS and changes per planning cycle
Ensure Annual stability plans are met
Represents Global Supply Chain on CMC and CCPR teams to ensure changes will be implemented in a strategic and timely manner
Manage all changes and assess impact to supply chain to ensure no interruption to patient supply
Manage NPI introductions and ensures all launch timelines are met
May assist with the development and integration of new technologies and/or new processes as needed to support continuous improvement by seeking ways to improve planning performance
Responsible for resolving supply issues in short term across the network plan (next 3 months) and balancing for short-term network inventory
Publish 18-month rolling forecast to CMOs to ensure capacity availability
Work with drug substance team for API allocation to production plans & support master production plan / resolves issues where they may arise
Manages relationships with other departments (i.e. quality, mfg., AO, logistics, etc.) to resolve supply issues
Develops and implements strategies and goals for specific products.
Support And Advisory Responsibilities
Maintains and assists with the implementation of Supply Chain policies, procedures, techniques, standards, and systems.
Contributes to the development of complex new concepts, techniques and standards. Leads projects on process improvements at supply chain planning SME
Supports the execution of supply chain planning initiatives to achieve departmental targets.
Assists with the preparation of project plans and manages projects to successful and timely completion. Provides expertise to the team and functional areas to anticipate and identify complex project issues which pose a challenge to achieving strategic goals.
Reviews and assists with planning requirements for business operations. Acts as an advisor to meet schedules and/or resolve technical problems.
Develops and maintains documentation to reflect the effectiveness and efficiency of department activities. Simplifies externally-facing documentation to the benefit of customers.
Analyzes systems and processes and impact on business performance. Develops tools needed to support division Center of Excellence Service Teams action.
Frequently collaborates with other departments, to ensure functional area resources are sufficient to achieve project goals and objectives.
May recommend and assist with the integration of new technologies and/or new processes as needed, to reduce costs.
May assist in the development of operational functional requirements and business process flow architecture of ERP functions and features, in support of client’s existing and future business plans.
Knowledge, Experience, And Skills
Experience in pharmaceutical operations/cGMP environment highly desirable.
Able to develop solutions to a wide range of complex problems, which require the regular use of ingenuity and innovation.
Excellent verbal and written communication skills and interpersonal skills.
Demonstrates good planning and organizational skills coupled with strong time management skills.
Has an aptitude for working with computer systems to plan and manage supply chain requirements (Kinaxis RapidResponse, SAP, EBS, Logility, JDA)
Demonstrates strong analytical and problem-solving skills. Ability to exercise independent judgment in developing methods, techniques, and evaluation criteria for obtaining results.
Demonstrates up-to-date knowledge of business operating systems, distribution requirements planning, production scheduling, Oracle/DB2/Access databases and Microsoft applications (e.g., Excel) as relates to business needs.
Proficiency in ERP system software, with emphasis on Operations/Supply Chain functionality.
Good organizational and time management skills, including working knowledge of basic project management tools and techniques.
Solid working knowledge of relevant regulatory guidance, including pharmaceutical GMPs and ICH Q7A
Minimum Qualifications
8+ years of relevant experience in related field and a BS or BA; or 6+ years of relevant experience and a MA/MS/MBA.
Required Years Of Experience
8+ years of relevant experience in related field and a BS or BA; or 6+ years of relevant experience and a MA/MS/MBA.
Top 3 Required Skill Sets
Supply Planning experience with demonstrated analytical and problem-solving skills ,
ERP/ Planning System experience,
Solid working knowledge of relevant regulatory guidance, including pharmaceutical GMPs
Top 3 Nice To Have Skill Sets
Proficiency in Kinaxis Rapid Response or SAP,
Strong communication skills,
Able to develop solutions to a range of complex problems
Required Degree Or Certification
8+ years of relevant experience in related field and a BS or BA; or 6+ years of relevant experience and a MA/MS/MBA.
TekWissen® Group is an equal opportunity employer supporting workforce diversity.
TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.
Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.
TekWissen® is an equal opportunity employer supporting workplace diversity.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Management and Manufacturing
Industries
Staffing and Recruiting
Referrals increase your chances of interviewing at TekWissen ® by 2x