Jobs Posted through July 4, 2008



Jobs That Crossed My Desk Through August 2, 2009

Contact the person whose information appears at the top of each listing. Listings of each executive search person are separated by string of stars. Multiple listings submitted by one recruiter are separated by straight lines.

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Jim Brown Associates

15 Southwind Circle

Marina Bay – The Breakers

Richmond, CA 94804-7405

Phone: (510) 235-4472

FAX: (510) 235-4482

e-mail: jim@

Senior Manager Marketing—Bay Area

Our client is building a revolutionary new tool for spine and orthopedic applications, the company is run by a CEO and team who have successfully launched other medical devices companies, all with revolutionary products on the market.

They are looking for someone to lead all of the marketing efforts, to include:

1. Work closely with the engineering team to enhance product development and product definition.

2. Work closely with physicians (customers) to enhance both product development and sales.

3. Public relations / marcom / publication management

4. Convention / Tradeshow management

5. Clinical Marketing – from trials to product launch

Must be Hands-on, and want to grow with the company. Entreprenurial attitude – will do whatever it takes to get the business done, and wants to participate as part of a team. We like ambitious people, who stay focused and possess a strong work ethic. MBA preferred, with a track record of making things happen and demonstrated success working with engineers in product development role.

This is a great opportunity if you want to grow with a small company, and be a part of the future of medicine.

_________________________________________________________________________

Surgical Product Manager—Bay Area

CANDIDATES MUST HAVE SURGICAL INSTRUMENT MARKETING EXPERIENCE.

Essential Duties and Responsibilities include but are not limited to: (Other duties may be assigned)

· Develop sales materials and track promotional programs.

· Manage the current product lines.

· Analyze sales data and compile competitive information.

· Interface with R&D to develop line extensions and product improvements.

· Provide timely and effective communications with the direct and indirect sales force.

· Assist the sales efforts by creating useful information and materials to increase the usage of the company’s products.

· Work with vendors to insure that materials are produced on time and within budget.

· Provide accurate sales forecasts for manufacturing.

· Initiate ECNs to update and maintain the current products.

( Provide timely information concerning sales trends and performance to budget.

· Use data to effectively respond to market changes.

· Provide timely marketing input and assist in the R&D efforts.

· Provide product information and training for the sales force.

· Provide regular communications to the sales force, which will increase their knowledge and selling effectiveness.

· Act as the main in-house contact to provide technical information and support for the sales force.

• Utilize knowledge gained from experiences and input from customers and in-house personnel to develop sales programs and support materials to increase the sales of our current products.

• Work with the Director of Marketing to develop marketing plans and strategic objectives.

• Responsible for implementing marketing and sales strategic plans.

• Will be responsible for providing marketing input for product enhancements and line extensions.

• Develop marketing programs that add value to our products and improve customer satisfaction and increase sales.

• Use strong communication and analytical skills to provide sales trends and forecasts.

Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required.

• BA or BS degree (MBA preferred).

• Must have excellent verbal and written communication skills.

• Requires 2-3 years of medical sales and marketing experience.

• Must have a good understanding of the medical environment to effectively respond to market concerns and provide technical support for the company’s products, particularly orthopedic arthroscopic products.

• Must work well with outside vendors and design companies to produce written materials, and also with inside personnel across all departments in order to successfully manage the product line. An in-depth understanding of how the products are used and factors that can influence the buying decision is essential. Also requires the ability to make decisions concerning the format and design of product support materials. International medical marketing experience is a plus.

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Doug Lehner, National Account Manager

The Scientific Instrumentation Group

Email: DLehner@

Management Recruiters of Baltimore-Timonium

Website:

Phone: 443 921-9067 direct - 410 252-6616 x260 - 866 277-4049 toll free

Our client is a diversified, global technology leader that helps customers innovate with confidence, enhance their competitiveness, and boost their efficiency. Be a part of a team that solves real, complex problems for their customers, where what you do helps make a difference in the world, and where you are rewarded for your efforts with excellent compensation and benefits! Our client is currently looking for an Environmental Health and Safety Manager.  Qualified applicants must have:

·         Experience developing and maintaining programs for improved safety performance and regulatory compliance.

·         Experience conducting emergency response teams, evacuation drills and with first aide.

·         Proven track record of running teams and a minimum of 5 years of related experience.

·         Chemical handling experience.

·         Must have BS/BA degree in Science Field.

If this isn’t the right fit for you and you know someone that I should be talking to, please pass this along.  Also, if you know anyone you could refer, even just to network with, it would be greatly appreciated.

If you have interest in this position and would like more in depth information about this position, please respond with an updated resume and the best time to for you and I to talk further. 

Also, if you would like to confidentially discuss other career opportunities in the life sciences field if this is not the best fit or location for you. Please just respond with the best time for you and I to talk further.

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ann@,

10300 So. De Anza Blvd. Suite B

Cupertino, CA  95014

Interested in job below? Create a profile including a Word version resume online:

Demand Generation Campaign Manager (life sciences)

Crawford Communications Group () is seeking a qualified Demand Generation Campaign Manager for a temp-to-perm consulting engagement with one of our leading technology clients located in Sunnyvale. Please note that no phone calls will be accepted. Local San Francisco Bay Area candidates only please.

The successful candidate has managed full cycle demand generation campaigns from creation to execution. Must have proven capabilities for analyzing program metrics, tracking response rates, campaign optimization, reporting and converting leads to sales.

You Have:

 

• 5 – 8 years marketing experience, with at least 3 years experience in online marketing/project management and/or e-commerce. Must have worked within the life sciences industry.

 

• Power user knowledge of Eloqua, , web based marketing analytics tools and CRM dashboards.

 

• Hands on capability to create, manage and deliver a variety of marketing campaigns and deliverables: direct marketing, e-commerce, telemarketing, SEM, affiliate marketing, live and online customer events/meetings, webinars, tradeshows and conferences, collateral, Twitter and other social networking tools.

 

• A solid understanding of customer segmentation, product, sales and promotion analysis.

 

• Proven ability to translate product positioning and attributes to audience-specific messages and value propositions.

 

• The ability to develop detailed audience profiling data in order to optimize campaigns, audience reach and conversion to sales.

 

• Excellent verbal/written communication skills. Must have the ability to communicate with team members at varying levels, conceptually and tactically.

 

• Outstanding overall leadership competence including an entrepreneurial spirit and drive to succeed.

 

• Proficiency with the Microsoft Office Suite and web analytics tools.

 

• A bachelors’ degree or equivalent in Marketing, Business Administration.

• A program portfolio with relevant work samples.

Duration: ASAP for 3-6 months, with the potential to convert to permanent employment.

Hours/location: 40 hours/week onsite in Sunnyvale.

Rate: $40 - $50 per hour, D.O.E, as a w-2 employee of Crawford Communications Group.

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Interested candidates should send a resume or CV to Ariel Holland, hollanda@.

The Pan Asian Cohort Study (PACS) is an NIH funded study to investigate diabetes and its risk factors within Asian American ethnic subgroups in a San Francisco Bay area cohort. (). The PACS capitalizes on existing patient electronic medical records in an ambulatory care setting.

The PACS is hiring a Data Quality Analyst starting immediately for Summer 2009 (to continue for three months into this Fall) and to start up again in Summer 2010. The Data Quality Analyst will participate in developing the PAC database by refining data from the electronic health records. He or she will profile and refine the quality of demographic, clinical, laboratory, pharmacologic, and diabetes outcome data for the cohort population.  The Data Quality Analyst will work closely with a Statistician and Information Analyst to ensure proper loading of quality data into the PAC database for the stated purposes of this research.

Responsibilities:

- Start: immediately. End: 3 months.

- Compensation: $18,000 per summer.

- Explore existing clinical, patient-level data with the assistance of Statistician and Information Analyst.

- Profile data, investigate patterns and outliers in an effort to refine the consistency and quality of the data using SQL, SAS, JMP, and other analytic software with appropriate supervision.

- Partner with the Information Analyst and Statistician to efficiently build tables and data sets for the research team.

- Propose, develop, and implement algorithms for investigating and cleaning data.

- Maintain security of patient-level data in a HIPPA compliant manner.

- Perform other tasks and responsibilities as needed.

Qualifications:

Required: Candidates must meet the following criteria.

- Bachelor's degree in Information Management, Informatics, Bioinformatics, Statistics, Computer Science, Mathematics or related field. Master’s degree or PhD desired. At least 1 introductory course in statistics.

- At least 2 years experience with SQL.

- Demonstrated experience with managing large relational data sets. Consciousness in size and computing efficient with large data sets.

- Excellent analytic, research, and communication skills.

Preferred: Strong candidates should also meet the following criteria.

- Experience with Microsoft SQL Server 2005.

- Experience with clinical information.

- Experience working on a research team.

- Demonstrated responsibility of patient data in a HIPPA compliant manner.

- Experience with SAS 9.x and Enterprise Guide.

- Experience with JMP.

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Please contact

John Malloy

262 966 2522 Wisconsin

803 826 6398 South Carolina

414 322 7891 Cell

Executive Search and Outplacement

santee

File #546A7C1E0D2E22

A client I have worked with for several years now has asked us to find two separate research scientists/engineers. One needs to know bioabsorbable materials, the other PFTE. They are located near Columbia, SC. I know all the managers and executives well and these are very good jobs. Both need to be filled by PhD level people (Masters might fit with more experience.). They would look at someone with as little as five years experience out of school.

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This came in over the transom. The job is in the Boston area. If

interested, contact Eric directly.

Eric Smith

Eric Smith

UX Account Manager

A Q U E N T

O: 206-545-3622 | C: 206-779-0314 | F: 206-632-6927 | AIM: smittyinseattle

esmith@ | go/UXDesign |

in/smittyinseattle

Subject: Information Visualization

From: Eric Smith

I work with Aquent, the world¹s largest creative staffing firm, where I

focus on the UX discipline. There is a client of ours (a rather large

bio/pharma company) who is looking for what they are calling a Scientific

Information Visualization Designer. The full job description and some info

on myself is at .

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Jobs That Crossed My Desk Through July 26, 2009

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Jay Feeley, National Account Manager

The Medical, Life Sciences & Biotech Group

My Profile: Jay Feeley

Mailto: jfeeley@

Management Recruiters of Baltimore-Timonium

Website:

Phone: 443 921-9069 direct  -  410 252-6616 x224  -  866 277-4049 toll freeMy name is Jay Feeley, and I am a National Executive Recruiter specializing in the Medical Device Arena.  I am currently recruiting for a RA Program Director, and RA Program Manager, and a Sr. Quality Engineer for a very well established medical device company specializing in class III Vascular/Cardiac devices and disposables.

Location: Arizona (Relocation assistance available)

Must-Haves to Interview

RA Program Director

-Bach degree in life or eng science

-10 RA exp, min

-7 in mgr role

-comprehensive knowledge of US, European, and int'l regulations and standards (class III PMA. class II 510K) *** Must have experience writing and submitting PMA’s and 510K’s.

___________________________________________________________________________________

RA Program Manager

-Bach degree in life or eng science

-6-8 yrs RA exp, min 3 in mgr role

-comprehensive knowledge of US, European, and int'l regulations and standards (PMA. 510K)

_____________________________________________________________________________________

Sr. Quality Engineer

-BS + 7 yrs or Masters

-+ 3 yrs med device exp, new product development a must, extensive knowledge of FDA, GMP/GLP, ISO, ASTM, AAMI, CEN, -ASQ (Quality Eng Cert) or equivalent

__________________________________________________________________________________________________

If this isn’t the right fit for you and you know someone that I should be talking to, please pass this along.  Also, if you know anyone you could refer, even just to network with, it would be greatly appreciated.

If you have interest in this position and would like more in depth information about this position, please respond with an updated resume and the best time to for you and I to talk further. 

Also I am happy to confidentially discuss other career opportunities in the medical device field if this is not the best fit or location for you. Please just respond with a resume and/or the best time to talk.

Thank you for your time and have a great day!

*************************************************************************************************

Qualified candidates please reply to:

Christina Lehrman

clehrman@

tel:  925-242-1010 x 104

Below is our update on the med device positions we are currently working on.  We have positions in the SF bay area as well as other locations across the country.  You are welcome to pass this along to anyone that may be interested.  If you have any questions, please feel free to get in touch anytime.  Also, you may review the detailed job descriptions posted on our site at .

 

Most Urgent Positions:

▪ Director of Regulatory Affairs (SF Bay Area)

▪ Director of Regulatory Affairs (NM)

▪ Sr. Product Marketing Manager

▪ Principal International Regulatory Affairs Specialist

REGULATORY, QUALITY & CLINICAL AFFAIRS

Regulatory Affairs Director (SF Bay Area)

▪ Minimum of 7+ years experience in US and OUS medical device Regulatory Affairs management and execution

▪ Strong knowledge of IDE, PMA, 510(k), ISO, and QSR requirements required

▪ Experience with PMA supplements and manufacturing changes

▪ Bachelors Degree in scientific or health related field

_________________________________________________

Regulatory Affairs Director (NM)

▪ 10+ years of medical device experience

▪ PMA experience required

▪ Experience working with the OIVD at the FDA is a requirement

▪ Bachelors Degree in scientific or health related field

_________________________________________________

Principal International Regulatory Affairs Specialist

▪ Minimum of 5 years experience in US and OUS class III medical device Regulatory Affairs management and execution

▪   Strong knowledge of IDE, PMA, 510(k), ISO, and QSR requirements required

▪ Working knowledge of US and OUS clinical research regulations and techniques

▪ Demonstrated ability to effectively implement and manage complex global regulatory program

▪ Bachelors Degree in scientific or health related field required

_______________________________________________

Sr. Global Regulatory Affairs Director (S. CA)

▪ Minimum of 10+ years experience in US and OUS medical device Regulatory Affairs management and execution

▪ Emphasis is on international RA management

▪ Strong management skills, at least 3 yrs of senior management experience

▪ Bachelors Degree in scientific or health related field

___________________________________________________________

Sr. Regulatory Affairs Specialist (S. CA)

▪ At least 5 years of US and International medical device regulatory submission/approval experience, to include FDA, MDD, MHLW, TGA, and TPP

▪ 510(k), IDE and PMA experience (desired)

▪ Knowledge of FDA, EU, MHLW, TGA, and TPP requirements

▪ Bachelor’s degree in related field

Regulatory Affairs Certification (desired)

▪ ______________________________________________________________

R&D, MANUFACTURING & OPERATIONS ROLES

(Senior) Manufacturing Engineer (S. CA)

♣         BS degree in Mechanical or Materials Engineering is required.  3+ yrs med device experience.

♣         Knowledge of mechanics of materials and strong problem solving skills. 

♣         ISO/GMP training and project management/leadership skills a strong plus.

▪ Experience with statistical and analytical methods and strong mechanical design skills including test methods and test-fixture design required. 

_________________________________________________________

Process Development Manufacturing Engineer (S. CA)

▪ BS degree in Mechanical or Materials Engineering is required

▪  A minimum of three years of experience

▪ Knowledge of mechanics of materials and strong problem solving skills

▪ ISO/GMP training and project management/leadership skills a strong plus

▪ Experience with statistical and analytical methods and strong mechanical design skills including test methods and test-fixture design required.  

______________________________________________________________

Process Development Manufacturing Engineering Manager (S. CA)

▪ BS degree in Mechanical or Materials Engineering is required

▪  A minimum of 5 years of manufacturing exp in medical device industry

▪ Strong management skills

▪ ISO/GMP training and project management/leadership skills a strong plus

▪ Experience with statistical and analytical methods and strong mechanical design skills including test methods and test-fixture design required.  

______________________________________________________________

SALES, MARKETING & BUSINESS DEVELOPMENT

Sr. Product Marketing Manager

▪ OR experience is required (laparoscopic/endoscopic device experience would be a major plus)

▪ 5+ yrs med device marketing experience

▪ BA,BS degree

▪ Strong downstream marketing experience is a requirement

▪ Travel 30%+

______________________________________________________________

Director of Marketing

▪ Strong background in DTC/DTP (direct to consumer/patient) marketing experience

▪ 4+ yrs experience in Product Management

▪ Consultant and Ad Agency experience

▪ Sleep medicine or pulmonary device experience is a plus

▪ Travel 30% - 40%

_____________________________________________________

Clinical Specialist - CRM (location would be in FL)

▪ BA/BS

▪ 3 - 4+ yrs experience as clinical specialist in medical device industry

▪ Cardiac rhythm management device experience

 

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Please contact Cheryl Heinla if interested. Her email address is

Cheryl.Heinla@.

*

1)Food Science - Research for 3 months temporary. Must have

Research/Formulations experience. (I.e. someone with only QC will not

be considered). Hayward.

2) Jr. Mechanical Engineer - Biotech - rapid diagnostics. Prototyping,

machining, some electronic work. Hayward. Temp to hire.

3) Documentation for pharmaceutical. Must have excellent writing skills.

Location is Hollister. Temp 6 months.

4) Research Asst. in DMPK. 1-3 yrs. exp. with HPLC, LC/MS, other

molecular techniques. South SF. Temp 6 months.

5) Research Assoc for small molecule resuspending. Molecular biology

techniques. South SF. Temp 6 months.

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If you or someone you know is interest please contact Muara directly at:

Maura E. Markowitz, CSAM, National Account Manager

The Engineering & Manufacturing Group

My Profile:  Maura Markowitz

Mailto: mmarkowitz@

Management Recruiters of Baltimore-Timonium

Website:

Phone: 443 921-9051 direct  -  410 252-6616 x285  -  866 277-4049 toll free

I am currently recruiting for an RA Program Director and an RA Program Manager for a medical device company specializing in vascular, urology and medical device disposables.

Location:

Tempe, AZ (relocation assistance is available)

Position Description (RA Program Director):

Manages the Regulatory Affairs department while also participating on project teams as the Regulatory Affairs core team member.

Responsible for the supervision of a regulatory submissions group, the development of a regulatory strategy on new medical devices, and high-level supervision of the preparation and submission of the Food and Drug Administration (FDA) submission packages in an accurate and timely manner including, but not limited to: 510(k)’s, IDE’s, and PMA’s.  Also responsible for managing, developing, coaching and mentoring direct reports.

Requirements:

§  Bachelor’s Degree in life Science or Engineering

§  10 years Regulatory Affairs Experience

§  7 years in a management level role

§  Comprehensive know of US, European, and int'l regulations and standards (class III PMA. class II 510K)

Position Description (RA Program Manager):

This position manages the domestic (U.S.) and international activities of related product lines for the Regulatory Affairs department according to the company’s corporate procedures and policies; U.S. Government policies, primarily the Food and Drug Administration (FDA); applicable State requirements; and European and international regulations and standards.

This position coordinates domestic and international submission preparation and approval by the company, and FDA or appropriate international body in a timely manner. Responsible for determining RA strategies for relevant products. This position must recognize potential regulatory issues in day-to-day activities that involve product development through the manufacturing process.

Requirements:

§  Bachelor’s Degree in life Science or Engineering

§  6+ years Regulatory Affairs Experience

§  3 years in a management level role

§  Comprehensive know of US, European, and int'l regulations and standards (class III PMA. class II 510K)

If this isn't the right fit for you and you know someone that I should be talking to, please pass this along. Also, if you know anyone you could refer, even just to network with, it would be greatly appreciated.

If you have interest in this position and would like more in depth information about this position, please respond with an updated resume.  Once I have had the opportunity to review your resume, I will be in touch to discuss this position in further detail.

Thank you for your time and have a great day

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To learn more about this position along with immediate attention

please call 813 321 1670 and send a copy of your resume attached as a

WORD document to:  juang@.

My name is Juan Garcia. I represent The Fountain Group, which is a

Professional Contract Staffing Firm based out of Tampa, FL. We are

seeking qualified candidates to join our growing family of

professionals. We are currently seeking a Conformance Investigator for

a prominent client of ours in Berkeley, CA.

Contact recruiter if interested. It is a temporary position

Position description:

Purpose:

Senior technical professional who investigates and resolves complex

discrepancies in a timely manner.  Leads multi-discipline teams to

determine root cause and identify effective corrective actions

Thoroughly understands manufacturing processes, procedures, equipment

and personnel expectations to evaluate discrepancies.

Resolves discrepancies that are site wide, cross process unit or

quality system issues

Tasks:

Influences direction of complex investigations and communicates with

all levels of employees

Recognized as an authority in multiple areas and provides leadership

and guidance to others

Exhibits leadership in conformance efforts

Innovative in identifying root causes and effective corrective actions

Coordinate and perform discrepancy investigations,

obtain/analyze/assess appropriate data/information, generate

appropriate written documentation to support rationale/justification

for decisions made regarding potential impact/risk and product

disposition

Administer the periodic review and evaluation of corrective actions to

determine effectiveness/patterns or recurring problems that suggest

the need for improvements

BS 8+ years

MS 6+ years

PhD 4+ years

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Contact Rod Pagan

Manufacturing Manager

Summary:

Manage the daily and long term objectives of the sterile filling and

packaging areas and manufacturing projects.  Conduct departmental

operations in compliance with GMPs, SOPs and FDA guidelines.  Assist

in the management of department personnel.  Assume responsibility for

the GMP, environmental heath and safety procedure awareness, and

compliance within the respective area.

Duties:

Manage departmental employees; train, discipline, motivate, mentor and

develop in order to accomplish departmental goals within GMP/OSHA/SOP

and FDA guidelines.  Manage the department within budgetary cost

savings constraints while meeting or exceeding internal and external

customer needs.  Manage OEE, Material Variance, Schedule Attainment,

etc… Responsible for the job certification and training programs for

the department.

Manage departmental equipment, operations enhancement/improvements and

manufacturing projects.  Manage attendance, scheduling and performance

appraisals for departmental associates.  Involved in hiring process of

new associates.

Technical complaint investigations and failure investigations.

Participate on LEAN teams, review boards, in scheduling/performance

meetings and provide cross-departmental services.  Implement and track

improvements.

Write, rewrite, amend documentation, protocols, reports and SOP’s.

Support LEAN initiatives.  All other duties as assigned.

Education:

BS in Engineering, Chemistry, Biology or related field; Supervisory

and management courses recommended.

Experience:

 5- 8 years in aseptic pharmaceutical filling and packaging.

Special Skills:

Strong communication and interpersonal skills, technical knowledge of

aseptic filling and packaging operations, extreme attention to detail,

time management ability, good organizational skills, flexible,

effective problem solver and solid leadership qualities.  Ability to

write technical documents.

*************************************************************

Jay Feeley, National Account Manager

The Engineering and Manufacturing Group

Email: jfeeley@

Management Recruiters of Baltimore-Timonium

Website:

Phone: 443 921-9069 direct - 410 252-6616 x224 - 866 277-4049 toll free

Jay is currently recruiting for a Quality Systems Manager for a medical device company with facilities in 22 nations on six continents; the Company distributes its products in over 120 countries under some of the most well established brand names in the surgical device/disposables industry.

Location: Central, PA (Company will assist with Relocation)

Job Summary: This position will be responsible for managing the various aspects of the Quality and Management Systems including: CFR and ISO compliance, internal audits, complaint handling, corrective and preventive actions, document control, labeling control, complaint handling as well as process and software validation. The position will provide primary liaison to the rest of the company on regulatory matters.

Must-Haves to Interview

oBS technical/Life science degree

o3+yrs management exp at least 3 people

oexperience with improving performance issues & firing

o5+ yrs medical device experience-Class II or III

owork with cross functional teams

-Strong working knowledge of FDA 820 (QSR) and ISO 13485

- Working knowledge of CAPA, Complaint controls systems, risk management

- knowledge of basic submission-510k or PMA

-understanding labeling requirements a plus

-RA understanding (one or more) : understanding international submission, work with EU, involved in FDA audits, some type of response to FDA

If this isn't the right fit for you and you know someone that I should be talking to, please pass this along. Also, if you know anyone you could refer, even just to network with, it would be greatly appreciated.

If you have interest in this position and would like more in depth information about this position, please respond with an updated resume and the best time to for us to talk further.

Also I am happy to confidentially discuss other career opportunities in the medical device field if this is not the best fit or location for you. Please just respond with a resume and/or the best time to talk

__._,_.___

***************************************************************************************

Makro Technologies Job Alert

Biologist - I ()

Makro Scientific

Rahway, NJ

***********************************************************

Quality Complaint Handling Coordinator

Regulatory Regulatory Affairs Manager

Human Resources Director, Human Resources

What is Resume Inbox address?

hr@

access | closure

645 Clyde Avenue | Mountain View CA 94043

*************************************************************************************************

Contact:

Charles Jo

Recruiter/Sourcer

Saratoga, CA 95070-1590

408.668.4220 cell | charlesj@

Biotech/Pharma | Medical Devices/Instrumentation | IT/Engineering/Web |

Social Ventures/Non-profits

Multiple job openings at Medicines360 (San Francisco, CA) a non-profit

pharma startup

MISSION

Medicines360's mission is to develop new, affordable and innovative

therapies to address health inequities, particularly for women and children

living in poverty in the U.S. and globally.

* Director Clinical Operations

* Clinical Trial

Manager

* Finance Manager

* Senior Executive

Assistant

Updated list at:

*************************************************************************************************

Charles Jo is a in-house recruiter for Acclarent right now.

Acclarent is ramping up!! Please tell your group to go to their website and

if they are interested in a position they should send their resume to:

Charles Jo

Contract Recruiter

Acclarent

650.687.5404 ................
................

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