Internet Publishing in Brisbane, San Mateo, California | Fast Recruitment & Job Search

Strong understanding of project management methodologies

Demonstrated experience in leading cross-functional teams in a remote environment

Identify improvement opportunities in how we partner with and manage our 3PL vendors

Experience in e-commerce/retail operations, either vertically integrated or 3PL, with a focus on direct-to-consumer

Experience implementing Lean practices in a warehouse environment

Experience in apparel/luxury supply chain

Remains current with therapeutic areas under study, industry practices / trends and FDA requirements. Applies this knowledge to current programs.

BS/BA or MS/MA degree in related discipline or equivalent combination of education and experience

Develop and manage effective working relationships with Investigators and other key clinical opinion leaders

Partners with and maintains regular contact with key stakeholders including Regulatory, Clinical Development, Legal, Finance, and others as necessary

Experience with financial budgeting or reporting

Accountable for the oversight and execution of multiple clinical trials including:

Prior experience with HACCP requirements

Verify all HACCP documentation is completed by cooks, assembly clerks, and receiving clerks are done.

Assist in integrating good food handling procedures and HACCP requirements into production’s daily routine.

Work with airline account managers to conduct monthly Chefs Table exercises.

Conduct disciplinary write-ups as appropriate for failure to adhere to HACCP requirements.

Bachelor’s degree in Food Science or Biology or a minimum of 3 years’ experience in food, drug, or medical device industry.

Create and manage vendor profiles in SAP while obtaining and verifying W-9/W-8BEN Forms for new suppliers domestic and foreign alike.

3-way matching, and SAP experience is preferred

Excellent written and verbal communication skills

Experience working in a manufacturing company is a plus

Prepare weekly payment runs while ensuring all suppliers are paid in accordance with set credit terms outlined within the contracts.

Reconcile and maintain the Accounts Payable sub-ledger reports to the G/L.

Education, Experience And Skills Requirements

Any suitable combination of education, training, or experience is acceptable.

Evaluate new technologies and methodologies to support and advance analytical capabilities on the therapeutic products.

Handle and troubleshoot instrument issues such as on DNA sequencers and qPCR instruments.

Represent as subject matter expert on analytical molecular assays to support Chemistry, Manufacturing and Controls (CMC) team on new pharmaceutical products.

Supervise 2 Research Associate Contractors.

15+ years of experience in sales, marketing, and/or market access in the pharmaceutical or biotech industry

7+ years of experience building and leading sales teams with record of strong performance

New product launch experience is required

Experience leading teams in oncology or rare disease is strongly preferred

Experience working in both large and small biotech environments is preferred

Development: Collaborate with team members to understand professional development areas and support growth activities aligned to the goals of team members.

Education, Experience And Skills Requirements

Establish strong working relationships with cross-functional stakeholders from research, technology, program management, manufacturing, clinical, commercial, legal and finance

Strong project and time management skills ensuring effective and efficient decision making and issue resolution

Analyse internal business development processes and make recommendations for process improvement to drive efficiencies and improve deal execution and management

Knowledge of biopharma product development and commercialization experience; cell & gene therapy focus is a plus

Manage term sheet and contracting discussions for in-licensing transactions across technology, manufacturing, delivery, and other prioritized areas

Follow HACCP requirements for this area.

Monitor all inbound flights, store equipment, and assigned cages to be secured.

Monitor and secure all duty-free goods.

Work in storage areas that is refrigerated.

Restock, move, and rotate stock within storage areas (refrigerated and non-refrigerated storage areas).

Breakdown refuse containers for disposal.

Present data to management, cross-functional project teams, and external partners

6+ years of relevant CNS research post-PhD experience in an industry or academic setting

Experience with small molecule, gene therapy or nucleic acid therapy modalities for CNS diseases

Deep knowledge of genetic and pathophysiology of CNS diseases and relevant in vitro and animal models of diseases

Experience with advanced primary in vitro cell culture, e.g., iPSCs, Neuron Progenitor Cells (NPCs), iPSC-d Motor neurons (iMN)

Experience with transfection methods of relevant cell types (Lipofection, nucleofection, AAV transduction)

Learn on the job. Robust annual education and conference budget, including airfare and hotel costs

Covered health, dental and vision. Health, dental and vision insurance covered by Heirloom

Generous parental leave. 16 weeks paid leave for all Heirloom employees, regardless of primary/secondary caregiver status

Flexible time off. Flexible PTO for exempt (salaried) employees & 120 hours for full time non-exempt (hourly) employees

Stay healthy. Monthly health and wellness reimbursement

● Strong organizational and effective time management skills; ability to meet tight deadlines

· Manage receipt, storage and documentation of clinical samples from Tempest-led studies

· 0-3 years of post-doctoral experience (academia or industry)

· Experience in working with human biological samples (whole blood, plasma, tissue samples) and culture techniques

· Experience in working with rodent tumor models systems

· Experience working under and writing SOPs is beneficial

Experience with organizational design and development and talent management

Benefits administration and compensation experience are strong plusses

Manage supporting processes which drive the employee lifecycle, including role, responsibility and reporting changes and offboarding

8+ years experience in human resources with a focus on operations

Experience working with a PEO in an administrative capacity

Experience in emerging growth biotech companies

2+ years management experience, including people management

Bachelor’s or Master's degree in Business Administration, Operations, Supply Chain Management or related field

Strong understanding of procurement best practices and industry trends in highly regulated environments, specifically therapeutics or clinical supply chain management

Understanding of end-to-end supply chain business processes (Demand and Supply Planning, Inventory Management, Lifecycle Management)

Using market knowledge to mitigate supply chain risks; proactively seek information to predict, understand, and analyze risks and develop appropriate strategies

8+ years experience in Supply Chain or Procurement in Biotechnology companies; 6+ years experience with Master’s

Touch several different areas of Cutera’s business, including corporate law, data privacy, disputes, and commercial transactions

Learn the basics of regulatory research and interpretation

Partner with the business teams to provide guidance and advice

Learn about contract drafting and negotiation

If you are selected for our legal summer internship program, you will be compensated at $35.00 -$40.00 /hour.

Ongoing mentorship from individuals within our organization

Support various projects as needed for team leads & external collaborations including basic project management.

Knowledge of the following applications is highly preferred Concur, Ariba/SAP, SharePoint, Room Scheduler, Microsoft Teams.

Responsibilities (include, But Are Not Limited To)

Attend Leadership Team meetings and solicit agenda items, note action items, and upload meeting notes/updates to SharePoint site.

Support specific operations through scheduling leadership meetings, Function-Wide Town Halls, and department level event planning, etc.

Organize meetings and events including scheduling, coordinating room schedules, AV assistance and catering

Follow HACCP requirements for this area.

Basic math skills required. Addition, Subtraction and Multiplication.

Be able to work safely while following all safety requirements.

Pack trolleys with airline equipment in accordance with individual airline specifications to meet schedule.

Pack trolley to exact diagrams for drawer configuration and quantity of consumables.

Maintain organization of products in bond rooms.

Other duties as assigned by management

Setup and deliver food and equipment to workstations in the Food Department.

Ensure adherence and conformity of processes.

Ability to work as a team player

Will be exposed to extreme temperature changes and noise

Must be able to lift, push, pull, move product, equipment and supplies up to twenty-five(25) pounds

Benefits on offer for this contract position:

Broad experience in cell-based assays and automation is required

Experience in the biotechnology or pharmaceutical industry is preferred.

Strong interpersonal skills and dedication to collaboration with internal and external project teams is required

Experience with flow cytometry, quantitative PCR, and RNA preparation

Ability to learn new technologies and work collaboratively to make discoveries that promote the development oligonucleotide therapeutics.

Assist Transportation Manager as needed.

Write daily shift report (as per template provided by Transportation Manager) and email to Transportation Manager and General Manager.

Capture all working hours and control timekeeping and provide respective time adjustment sheets to HR and Transportation Manager.

Weekly pay, PTO, Paid Training, 401K after 6 months

Attend dispatch phone, send/receive fax and emails, in a timely manner.

Forward daily flight catering status (flight for number of PAX prepared) to KL.

Conduct management training regarding FSQ requirements to ensure compliance.

Oversee that FDA/Medina and standard requirements are documented to maintain compliance.

Ensure regularly audits of sanitation requirements are maintained in all areas of the facility.

3-5 years of experience in the food industry.

Experience in an SQF facility a plus.

USDA & FDA certification preferred.